Founded in 1781. Starting as a medicine wholesaler, Takeda produced blockbuster drugs including Alinamin, Leuprorelin, and Prograf. Through the Shire acquisition, Takeda entered the global top 10 and transformed into a global pharmaceutical company with rare diseases and plasma-derived therapies at its core.
1781
Strategic Decision
Founded as a Medicine Wholesaler
The Trade Name and Trust Mechanism That Sustained 130 Years as a 'Medicine Distribution Company'
1915
Takeda Pharmaceutical Laboratory Established
1915Takeda Pharmaceutical Laboratory Established
1943
Trade Name Changed to Takeda Pharmaceutical Industries
1943Trade Name Changed to Takeda Pharmaceutical Industries
1949
Stock Listed on Tokyo Stock Exchange
1949Stock Listed on Tokyo Stock Exchange
1954
Strategic Decision
Launched OTC Drug Alinamin
The Competitive Advantage in OTC Drugs Born from the Combination of Advertising and Distribution Control
1960
Divisional System Introduced
1960Divisional System Introduced
1963
Shonan Factory Newly Established
1963Shonan Factory Newly Established
1973
Developed Blockbuster Drug Lilacillin
1973Developed Blockbuster Drug Lilacillin
1974
Shinbei Konishi Became President
1974Shinbei Konishi Became President
1977
Partnered with Abbott Laboratories of the U.S.
1977Partnered with Abbott Laboratories of the U.S.
1977
Strategic Decision
SMON Litigation Response
A Decision That 'Definitively Processed' Drug Harm Risk on the Financial Statements, Preparing Management Preconditions
1980
Strengthened R&D Investment. Annual R&D Expenditure Reached 20 Billion Yen
1980Strengthened R&D Investment. Annual R&D Expenditure Reached 20 Billion Yen
1988
Tsukuba Research Laboratories Newly Established
1988Tsukuba Research Laboratories Newly Established
1989
Strategic Decision
Launched Leuprorelin
The Structure Where 'Retreat-Ready Concentration' Created a Precedent for Japan-Originated Global Drug Discovery
1991
Launched Takepron
1991Launched Takepron
1992
Organizational Reform of Research Laboratories Implemented
1992Organizational Reform of Research Laboratories Implemented
1993
Launched Blockbuster Drug Prograf
1993Launched Blockbuster Drug Prograf
1996
Company System Introduced
1996Company System Introduced
1997
Takeda America R&D Center Newly Established
1997Takeda America R&D Center Newly Established
1997
Launched Blopress
1997Launched Blopress
1997
Actos Approved in the U.S.
1997Actos Approved in the U.S.
2005
Strategic Decision
Began Divestiture of Non-Focus Businesses
The Structure Where Phased Separation of Diversified Businesses Created Capacity for Concentrated Drug Discovery Investment
2008
Strategic Decision
Acquired Millennium Pharmaceuticals of the U.S.
The Embedding of the 'Buying Time' Concept That Formed the Starting Point for the Chain of Massive Acquisitions
2011
Shonan Research Laboratories Newly Established
2011Shonan Research Laboratories Newly Established
2011
Strategic Decision
Acquired Nycomed
The Structure Where a 1 Trillion Yen Weakness-Reinforcement Acquisition Did Not Directly Translate to Corporate Value Enhancement
2016
Strategic Decision
Christophe Weber Became CEO
The Internal Absence of Global Talent Structurally Determined the Long Tenure of a Foreign CEO
2016
Long-Listed Products Divested
2016Long-Listed Products Divested
2017
Acquired ARIAD
2017Acquired ARIAD
2017
Wako Pure Chemical Industries Divested
2017Wako Pure Chemical Industries Divested
2019
Strategic Decision
Acquired Shire
The 6.2 Trillion Yen That Exposed the Divergence Between 'Business Base Expansion and Corporate Value'
2020
OTC Drug Business Divested
2020OTC Drug Business Divested
2026
Julie Kim Scheduled to Become CEO
2026Julie Kim Scheduled to Become CEO
View Performance
RevenueTakeda Pharmaceutical:Revenue
Non-consol. | Consolidated (Unit: ¥100M)
¥4.6T
Revenue:2025/3
ProfitTakeda Pharmaceutical:Net Profit Margin
Non-consol. | Consolidated (Unit: %)
2.3%
Margin:2025/3
View Performance
PeriodTypeRevenueProfit*Margin
1957/3Non-consol. Revenue / Net Income¥16B--
1958/3Non-consol. Revenue / Net Income¥20B--
1959/3Non-consol. Revenue / Net Income¥22B--
1960/3Non-consol. Revenue / Net Income¥25B--
1961/3Non-consol. Revenue / Net Income¥31B--
1962/3Non-consol. Revenue / Net Income¥43B--
1963/3Non-consol. Revenue / Net Income¥56B--
1964/3Non-consol. Revenue / Net Income¥74B¥5B7.3%
1965/3Non-consol. Revenue / Net Income¥95B¥6B6.6%
1966/3Non-consol. Revenue / Net Income¥93B¥6B6.6%
1967/3Non-consol. Revenue / Net Income¥104B¥6B5.9%
1968/3Non-consol. Revenue / Net Income¥117B¥9B7.3%
1969/3Non-consol. Revenue / Net Income¥140B¥12B8.6%
1970/3Non-consol. Revenue / Net Income¥160B¥14B8.9%
1971/3Non-consol. Revenue / Net Income¥172B¥13B7.6%
1972/3Non-consol. Revenue / Net Income¥171B¥8B4.8%
1973/3Non-consol. Revenue / Net Income¥188B¥7B3.8%
1974/3Non-consol. Revenue / Net Income---
1975/3Non-consol. Revenue / Net Income---
1976/3Non-consol. Revenue / Net Income¥274B¥7B2.6%
1977/3Consolidated Revenue / Net Income¥317B¥10B3.2%
1978/3Consolidated Revenue / Net Income¥348B¥13B3.7%
1979/3Consolidated Revenue / Net Income¥389B¥20B5.1%
1980/3Consolidated Revenue / Net Income¥438B¥23B5.1%
1981/3Consolidated Revenue / Net Income¥451B¥22B4.9%
1982/3Consolidated Revenue / Net Income¥484B¥25B5.0%
1983/3Consolidated Revenue / Net Income¥519B¥26B5.0%
1984/3Consolidated Revenue / Net Income¥531B¥24B4.5%
1985/3Consolidated Revenue / Net Income¥544B¥22B4.0%
1986/3Consolidated Revenue / Net Income¥552B¥23B4.2%
1987/3Consolidated Revenue / Net Income¥571B¥28B4.9%
1988/3Consolidated Revenue / Net Income¥633B¥38B5.9%
1989/3Consolidated Revenue / Net Income¥687B¥39B5.6%
1990/3Consolidated Revenue / Net Income¥694B¥37B5.3%
1991/3Consolidated Revenue / Net Income¥691B¥44B6.4%
1992/3Consolidated Revenue / Net Income¥710B¥34B4.7%
1993/3Consolidated Revenue / Net Income¥720B¥48B6.6%
1994/3Consolidated Revenue / Net Income¥728B¥48B6.5%
1995/3Consolidated Revenue / Net Income¥772B¥51B6.6%
1996/3Consolidated Revenue / Net Income¥801B¥60B7.4%
1997/3Consolidated Revenue / Net Income¥839B¥71B8.5%
1998/3Consolidated Revenue / Net Income¥842B¥82B9.6%
1999/3Consolidated Revenue / Net Income¥845B¥92B10.8%
2000/3Consolidated Revenue / Net Income¥923B¥120B12.9%
2001/3Consolidated Revenue / Net Income¥963B¥147B15.2%
2002/3Consolidated Revenue / Net Income¥1.0T¥236B23.4%
2003/3Consolidated Revenue / Net Income¥1.0T¥272B25.9%
2004/3Consolidated Revenue / Net Income¥1.1T¥285B26.2%
2005/3Consolidated Revenue / Net Income¥1.1T¥277B24.7%
2006/3Consolidated Revenue / Net Income¥1.2T¥313B25.8%
2007/3Consolidated Revenue / Net Income¥1.3T¥336B25.7%
2008/3Consolidated Revenue / Net Income¥1.4T¥355B25.8%
2009/3Consolidated Revenue / Net Income¥1.5T¥234B15.2%
2010/3Consolidated Revenue / Net Income¥1.5T¥298B20.3%
2011/3Consolidated Revenue / Net Income¥1.4T¥248B17.4%
2012/3Consolidated Revenue / Net Income¥1.5T¥124B8.2%
2013/3Consolidated Revenue / Net Income (Parent)¥1.6T¥149B9.5%
2014/3Consolidated Revenue / Net Income (Parent)¥1.7T¥107B6.3%
2015/3Consolidated Revenue / Net Income (Parent)¥1.8T-¥146B-8.2%
2016/3Consolidated Revenue / Net Income (Parent)¥1.8T¥80B4.4%
2017/3Consolidated Revenue / Net Income (Parent)¥1.7T¥116B6.6%
2018/3Consolidated Revenue / Net Income (Parent)¥1.8T¥187B10.5%
2019/3Consolidated Revenue / Net Income (Parent)¥2.1T¥135B6.4%
2020/3Consolidated Revenue / Net Income (Parent)¥3.3T¥44B1.3%
2021/3Consolidated Revenue / Net Income (Parent)¥3.2T¥376B11.7%
2022/3Consolidated Revenue / Net Income (Parent)¥3.6T¥230B6.4%
2023/3Consolidated Revenue / Net Income (Parent)¥4.0T¥317B7.8%
2024/3Consolidated Revenue / Net Income (Parent)¥4.3T¥144B3.3%
2025/3Consolidated Revenue / Net Income (Parent)¥4.6T¥108B2.3%
Management Policy: 20252026
*Management plan not yet publicly disclosed

Historical Background

Until the 1990s, Takeda Pharmaceutical grew as a comprehensive pharmaceutical company with prescription drugs at its core while also encompassing OTC drugs and peripheral businesses. However, as drug development became larger in scale and R&D costs soared, the recognition grew that business dispersion would lead to a decline in competitiveness, and from the 2000s the company advanced selection and concentration, clearly pivoting to become a pharmaceutical-specialist company centered on drug discovery. Under this strategy, blockbuster drugs in areas such as gastrointestinal and central nervous system were successively launched, forming a growth phase that drove performance in the 2000s.

Meanwhile, this dependence on blockbuster drugs inherently contained the risk of future revenue decline accompanying patent expiration, and the difficulty of maintaining a stable pipeline through in-house drug discovery alone became apparent. In response, Takeda utilized corporate acquisitions aimed at globalization and pipeline expansion, transforming its business structure through the Nycomed acquisition in 2011 and the Shire acquisition in the latter half of the 2010s. While these acquisitions contributed to expanding growth areas, they also brought rapid expansion in corporate scale and increased financial burden, creating the current management challenge of how to balance profitability and capital efficiency as a giant enterprise.

Management Guidelines

Through the 2019 acquisition of Shire, Takeda Pharmaceutical significantly expanded its business domains and geographic reach, establishing itself as a global pharmaceutical company of exceptional scale for a Japan-originated enterprise. By building a business portfolio centered on rare disease areas, its international presence in research and development, sales, and manufacturing improved markedly, and it acquired the foundation to face the global market independently. On the other hand, the acquisition of approximately 6 trillion yen in scale led to a significant increase in interest-bearing debt, bringing major changes to the company's financial structure.

Post-acquisition, Takeda positioned the recovery of its financial base as the top priority, and it took several years to reduce debt through divestiture of non-core businesses and generation of cash flow. In this process, there were also phases where allocation of management resources toward R&D investment and new drug creation was constrained, and the primary management issue became how to balance the scale of a giant enterprise with drug discovery capabilities. Based on these experiences, the company aims for management that simultaneously achieves growth investment and financial discipline, and has set its management guideline as sustainably creating value as a global company through business operations based on profitability criteria.

Author's Questions

  • Why did Takeda judge the 6 trillion yen Shire acquisition as the 'only realistic option'?

    In the latter half of the 2010s, Takeda Pharmaceutical should have had multiple options available, including strengthening in-house drug discovery, gradual alliances and smaller acquisitions, and region-focused growth. Among these, why did the company choose a 6 trillion yen acquisition carrying significant financial risk, effectively abandoning other growth scenarios? How were the competitive environment, time horizon, and quality and quantity of the pipeline evaluated?

  • Why was Takeda unable to replicate the successful experience of blockbuster drugs from the 2000s?

    In the 2000s, Takeda Pharmaceutical built a highly profitable structure through successive launches of blockbuster drugs from in-house discovery. However, if one assumes the same model continued, why could the same results not be replicated? How did the successful experience of that time influence decision-making in the face of changes in the R&D environment and competitive conditions, and in particular, why was the option of focusing on antibody drugs and rare diseases not adopted?

  • Why was CEO Weber not dismissed despite prolonged underperformance in corporate value?

    After the Shire acquisition, Takeda Pharmaceutical's stock price and capital efficiency languished over an extended period, yet CEO Christophe Weber continued in his position. This fact raises many unclear points about the extent to which performance evaluation was based on shareholder returns, and how the board of directors verified the CEO's management decisions. It is possible that continuity of management was prioritized after the irreversible decision of the massive acquisition, but as a result, the extent to which the board held management accountability is not necessarily clear from the outside.

Author's Insights

A Pharmaceutical Company That Spent 240 Years Continuously Moving Upstream: Distribution → Manufacturing → OTC Drugs → Drug Discovery

When the first Chobei Takeda founded a medicine wholesale business in Doshomachi, Osaka in 1781, Takeda was not a company that 'made' medicine but one that 'distributed' it. As a broker of traditional Japanese and Chinese medicines, the sources of competitive advantage were trust relationships with suppliers and the ability to assess quality, and the company had no manufacturing function. The practice of successive heads adopting the name 'Takeda Chobei' was a mechanism for sustaining the business based on the trade name and trust rather than the individual, which was commercially rational. This structure was maintained for over 130 years, and Takeda established its position as a leading medicine wholesaler in Doshomachi. It was an era when distribution was the essence of the business.

The first turning point came with World War I in 1914. The disruption of pharmaceutical imports from Germany fundamentally shook the import-dependent business structure. In 1915, Takeda established the Takeda Pharmaceutical Laboratory in Osaka and embarked on in-house manufacturing. This was the transition from distribution to manufacturing. The next turning point was the launch of Alinamin in 1954. Against a backdrop of postwar nutritional deficiency, Takeda introduced a vitamin B1 derivative as an over-the-counter drug and built it into a nationally recognized brand through an advertising strategy featuring film star Toshiro Mifune and nationwide uniform-price distribution via the 'Takeda-kai.' Here, Takeda transformed from a company that merely 'makes' into one that 'sells.' However, at this stage it was still not yet a 'drug discovery' company.

The full-scale shift toward drug discovery accelerated from the 1980s onward. With the implementation of the substance patent system in 1976, the loophole of follow-on companies imitating drugs by merely changing the manufacturing process was closed, and the effectiveness of patents for drug discovery was enhanced. Takeda recorded R&D expenditure of 21 billion yen in FY1979, investing at double the level of competitors and clearly signaling its drug discovery-oriented direction. In 1989 Leuprorelin, in 1991 Takepron, and in 1997 Actos—blockbuster drugs were launched in succession. Leuprorelin in particular was born from a 'retreat-ready concentration' in which Kunio Takeda, then head of the U.S. subsidiary, discontinued antibiotic development and concentrated resources on cancer therapeutics. This successful experience became the prototype for the 'selection and concentration' strategy—the divestiture of diversified businesses including chemicals, food, and agrochemicals, and concentration of management resources on pharmaceuticals—pursued during Kunio Takeda's later tenure as president.

The 240 years of Takeda Pharmaceutical can be read as a trajectory of consistently shifting the business center of gravity ever further 'upstream': distribution → manufacturing → OTC drugs → prescription pharmaceuticals → global drug discovery. The pace of change was by no means rapid. After 130 years as a medicine wholesaler, 40 years as a manufacturer, and 30 years as an OTC drug maker, the company's form as a drug discovery-based international enterprise was finally established. Yet the direction has been consistent. Each era's transformation occurred in response to changes in the external environment—import disruption, nutritional demand, patent system reform, globalization—but each was a choice toward 'further upstream, toward higher value-added domains.' From distribution to drug discovery over 240 years. Both the slowness of this transition and its consistency reflect the essence of the company called Takeda Pharmaceutical.

2026-02-08 | by author
The Price of Not Cultivating Global Talent
The Acquisition Chain and the Difficulty of Recruiting and Dismissing a Foreign CEO

The 2008 acquisition of Millennium (approximately $8.9 billion) was Takeda Pharmaceutical's first full-scale massive overseas M&A. The decision to acquire cancer research capabilities and a U.S. base in a single stroke was made by President Yasuchika Hasegawa. On the extension of the Kunio Takeda strategy that had completed divestiture of diversified businesses and concentrated management resources on pharmaceuticals, the next phase entered with the recognition that 'in-house drug discovery alone takes too long,' and it became time to buy external research platforms. Viewed on its own, the Millennium acquisition was a rational decision, but this deal became the starting point for a chain of massive M&As that would span the next 15 years. Nycomed for approximately 1.1 trillion yen in 2011, ARIAD for 583.1 billion yen in 2017, and Shire for 6.2 trillion yen in 2019. Each acquisition had its own strategic rationale, but viewed as a whole, a chain structure emerges of 'compensating in the next acquisition for what was lacking in the previous one.' Millennium because drug discovery capabilities were insufficient, Nycomed because the sales network was insufficient, ARIAD because the pipeline was insufficient, Shire because the rare disease revenue base was insufficient. An escalation structure where one acquisition begets the next.

What accelerated this chain was a structural problem: the shortage of talent capable of managing global operations. Takeda Pharmaceutical had long been led by the two founding families—the Takeda family and the Konishi family—but in 2003 Yasuchika Hasegawa, a non-founding family member, became president, breaking free from founding family control. However, management talent capable of gripping the acquired overseas companies had not been sufficiently developed internally. With each successive acquisition of Millennium and Nycomed, the ability to manage local management teams and research organizations was tested, but the talent that could be dispatched from Japanese headquarters was limited. The more globalization was advanced through acquisitions, the more the shortage of talent to govern acquired companies became apparent. This structural contradiction led to the appointment of Christophe Weber as CEO in 2015.

Weber was from GlaxoSmithKline in the UK and had management experience at a major European pharmaceutical company. Chairman Hasegawa had been evaluating him as a successor candidate from the time of his COO appointment, and entrusted the CEO position after approximately one year. The decision to place a foreigner at the helm of Japan's largest pharmaceutical company was simultaneously a necessity of global management and a consequence of the failure to develop a successor internally. Under the Weber regime, the 6.2 trillion yen Shire acquisition was executed, but recouping the acquisition premium took longer than expected, and the stock price underperformed relative to peers over a prolonged period. Interest-bearing debt surged, and to restore finances, the company was forced to sell the OTC drug business including Alinamin for approximately 250 billion yen. Yet even when results did not materialize, the foreign CEO could not be easily replaced—because there was no one inside the company who could take over. Weber is scheduled to step down in 2026, but he will have held the top position for approximately 10 years.

What the 15-year chain of acquisitions confronts us with is the dual dilemma of a 'buying time' strategy. One is the business dilemma: patents on acquired businesses also expire, creating new 'insufficiencies' and necessitating ever-larger acquisitions. The other is the talent dilemma: the more globalization is accelerated through acquisitions, the more severe the shortage of management talent to govern acquired companies becomes, ultimately requiring the recruitment of a CEO from outside. And even when the externally recruited CEO fails to deliver expected results, the options for replacement are limited since there is no successor candidate. Both business and talent can be resolved in the short term by 'buying,' but the cost of skipping 'cultivating' comes back in another form. Whether this structure can be broken is the question facing Takeda Pharmaceutical after Shire.

2026-02-08 | by author
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1781
6

Founded as a Medicine Wholesaler

The Trade Name and Trust Mechanism That Sustained 130 Years as a 'Medicine Distribution Company'

Takeda Pharmaceutical's founding began not with product development but with medicine brokerage based on distribution and trust. The practice of successive heads adopting the name 'Takeda Chobei' was a mechanism for enhancing business continuity by attributing trust to the trade name rather than the individual. The fact that this structure was maintained for over 130 years demonstrates that a business centered on distribution and quality assessment was rational over the long term, even without manufacturing capabilities.

BackgroundDoshomachi's concentration of traditional medicine distribution and entry conditions for medicine wholesalers

In the late Edo period, Doshomachi in Osaka had established itself as a distribution hub for traditional Japanese and Chinese medicines, attracting medicine wholesalers from across the country. Merchants serving feudal domains and town-based medicine dealers had congregated, forming a commercial space where information and trust governed transactions. Medicine was a daily necessity, and demand remained stable through physicians and pharmacies, making the medicine wholesale trade a business of relatively high continuity.

At the same time, operating as a medicine wholesaler required adaptation to business practices including trust relationships with suppliers, the ability to assess quality, and collection of payments. Doshomachi was not merely a market but a place where norms and practices among peers had accumulated, and for new entrants, the process of learning and building trust was necessary.

DecisionThe first Chobei Takeda founded the business as a traditional medicine broker

In June 1781, the first Chobei Takeda founded a medicine wholesale business in Doshomachi, Osaka, and began selling traditional Japanese and Chinese medicines. He entered the trade as a medicine broker dealing in Chinese medicines and domestic drugs, serving physicians and pharmacies. The rationality of this era was reflected in the choice of a business based on distribution and trade rather than specific product development.

After founding, the practice of successive heads of the Takeda family adopting the name 'Takeda Chobei' became established. The formation of a mechanism for sustaining the business based on the trade name and trust rather than the individual allowed commercial judgment and trade relationships to be inherited across generations. This structure was maintained for over 130 years, and Takeda established its position as a leading medicine wholesaler in Doshomachi.

ResultA business structure based on distribution and trust persisted for over 130 years

Since its founding, the Takeda family operated as a medicine broker without manufacturing capabilities, with trust relationships with suppliers and the ability to assess quality as the sources of competitive advantage. This distribution-centered business structure was maintained even after the Meiji Restoration when importation of Western medicines began, and Takeda preserved its position as a leading medicine wholesaler in Doshomachi while adding the function of an importer.

The foundation of sustaining the business for over 130 years as a medicine wholesaler was later inherited as awareness of trade partner relationships and quality control during the transition to manufacturing and drug discovery. The starting point of Takeda Pharmaceutical was not a 'company that makes medicine' but a 'company that distributes medicine,' and this origin became the starting point for 240 years of business evolution.

The Trade Name and Trust Mechanism That Sustained 130 Years as a 'Medicine Distribution Company'

Takeda Pharmaceutical's founding began not with product development but with medicine brokerage based on distribution and trust. The practice of successive heads adopting the name 'Takeda Chobei' was a mechanism for enhancing business continuity by attributing trust to the trade name rather than the individual. The fact that this structure was maintained for over 130 years demonstrates that a business centered on distribution and quality assessment was rational over the long term, even without manufacturing capabilities.

TimelineFounded as a Medicine Wholesaler — Key Events
6/1781Founded as a medicine wholesaler
5/1871Began importing medicines from the West
1915
Takeda Pharmaceutical Laboratory Established
1943
Trade Name Changed to Takeda Pharmaceutical Industries
1949
Stock Listed on Tokyo Stock Exchange
1954
3

Launched OTC Drug Alinamin

The Competitive Advantage in OTC Drugs Born from the Combination of Advertising and Distribution Control

The launch of Alinamin was a decision to adapt vitamin B1 derivative research results cultivated in prescription pharmaceuticals to the OTC drug market. The combination of advertising featuring Toshiro Mifune and nationwide uniform-price distribution through the Takeda-kai was a design that simultaneously achieved brand awareness formation and maintenance of distribution order. This product, which grew to account for 37% of revenue, became the starting point that transformed Takeda Pharmaceutical from a manufacturing company into a consumer-oriented company.

BackgroundPostwar nutritional deficiency and expanding vitamin demand formed the OTC drug market

In postwar Japan, deteriorating food conditions and nutritional deficiency had become a social problem. Vitamin B1 deficiency disorders such as beriberi were widely recognized, and interest in nutritional supplementation was growing not only in medical settings but also among ordinary households. Vitamin preparations were broadening their demand base from medical use to general consumers.

Takeda Pharmaceutical had been engaged in vitamin research since before the war and had accumulated formulation technology for vitamin B1 derivatives. Meanwhile, the postwar business structure was weighted toward prescription pharmaceuticals, and full-scale development in the OTC drug field for general consumers was still underway. In response to changes in the market environment, there was room to adapt research results to the consumer market.

DecisionFull-scale entry into OTC drugs combining advertising strategy and distribution control

In March 1954, Takeda Pharmaceutical launched 'Alinamin,' an OTC drug with a vitamin B1 derivative as its active ingredient. Research results cultivated in prescription pharmaceuticals were converted into a consumer product, designed for nationwide sales from the outset. Simultaneously, a large-scale advertising campaign was conducted featuring film actor Toshiro Mifune.

On the sales side, distribution management was advanced through the 'Takeda-kai,' and by registering Alinamin as a resale-designated item, a nationwide uniform-price sales system was established. The design combining brand awareness through advertising with maintaining distribution order through price control was a decision aimed at establishing competitive advantage in the OTC drug market.

ResultGrew into a flagship product accounting for 37% of revenue, transforming the business composition

After launch, Alinamin expanded sales volume alongside the nationwide expansion of brand awareness. By fiscal 1955, vitamin preparations accounted for approximately 37% of the company's revenue, significantly impacting the business composition. Takeda Pharmaceutical established a business structure with OTC drugs as an earnings pillar in addition to prescription pharmaceuticals.

On the other hand, other pharmaceutical companies entered the vitamin preparation field in succession, and the competitive environment intensified. Takeda Pharmaceutical sought to stabilize its sales base by continuing distribution organization control and price management. Alinamin was the product that served as the catalyst for Takeda Pharmaceutical's transformation from merely a 'making' company to a 'selling' company.

The Competitive Advantage in OTC Drugs Born from the Combination of Advertising and Distribution Control

The launch of Alinamin was a decision to adapt vitamin B1 derivative research results cultivated in prescription pharmaceuticals to the OTC drug market. The combination of advertising featuring Toshiro Mifune and nationwide uniform-price distribution through the Takeda-kai was a design that simultaneously achieved brand awareness formation and maintenance of distribution order. This product, which grew to account for 37% of revenue, became the starting point that transformed Takeda Pharmaceutical from a manufacturing company into a consumer-oriented company.

TimelineLaunched OTC Drug Alinamin — Key Events
3/1954Launched OTC drug Alinamin
12/1957Secured 46.7% domestic market share in vitamin preparations
3/1971Significant profit decline due to vitamin preparation price cuts
1960
Divisional System Introduced
1963
Shonan Factory Newly Established
1973
Developed Blockbuster Drug Lilacillin
1974
Shinbei Konishi Became President
1977
Partnered with Abbott Laboratories of the U.S.
1977

SMON Litigation Response

A Decision That 'Definitively Processed' Drug Harm Risk on the Financial Statements, Preparing Management Preconditions

The phased booking of 20 billion yen in provisions for the SMON litigation was a decision to process the drug harm issue as a confirmed management loss rather than carrying it as an indefinite risk. In exchange for accepting short-term earnings deterioration, uncertainties regarding future compensation burdens were reduced, and the preconditions for management were secured toward strengthening R&D investment from the 1980s onward. It was a choice to organize the crisis and move forward.

BackgroundThe emergence of clioquinol drug harm and the filing of class action lawsuits

Takeda Pharmaceutical began selling clioquinol preparations—the cause of the SMON litigation—in 1959. At the time, clioquinol was widely used as an intestinal antiseptic, and prescriptions and sales expanded nationwide. However, from the 1960s onward, severe neurological symptoms including visual and walking impairments following diarrhea treatment were reported across the country, and the drug harm later known as SMON became a social problem.

Even after the government halted sales of clioquinol preparations in 1970, debate over the expanding number of victims and where responsibility lay continued. By the mid-1970s, class action lawsuits were filed nationwide, and the phase shifted to one simultaneously demanding legal and social responsibility from pharmaceutical companies. For Takeda Pharmaceutical, the SMON issue came to be recognized as a long-term risk that shook the premises of management.

DecisionPhased booking of 20 billion yen in provisions, anticipating future compensation

In 1977, Takeda Pharmaceutical decided to book litigation provisions in anticipation of future settlements and compensation related to the SMON litigation. Provisions were booked in phases from FY1977 through FY1980, reaching a cumulative total of approximately 20 billion yen. Even relative to the revenue scale at the time, this was a substantial burden, and was a decision that compressed profits in the short term.

This response demonstrated a posture of processing the drug harm issue as a confirmed risk in management terms, rather than responding to individual lawsuits on a case-by-case basis. The aim was to explicitly organize future uncertainties on the financial statements rather than deferring them, thereby preparing the preconditions for advancing R&D and business operations.

ResultSecured preconditions for R&D investment in exchange for financial burden

Through provisioning, Takeda Pharmaceutical bore a significant financial burden from the late 1970s through the early 1980s. The approximately 20 billion yen was a clear loss for the company at the time, reducing short-term profitability. On the other hand, uncertainties regarding future compensation burdens were resolved to a certain degree.

As a result, the SMON drug harm was repositioned from a risk that continuously constrained management to a past issue that had been addressed. In the strengthening of R&D investment and overseas expansion pursued from the 1980s onward, the litigation issue became less of a direct constraint, and the management environment was prepared for concentrated investment in drug discovery.

A Decision That 'Definitively Processed' Drug Harm Risk on the Financial Statements, Preparing Management Preconditions

The phased booking of 20 billion yen in provisions for the SMON litigation was a decision to process the drug harm issue as a confirmed management loss rather than carrying it as an indefinite risk. In exchange for accepting short-term earnings deterioration, uncertainties regarding future compensation burdens were reduced, and the preconditions for management were secured toward strengthening R&D investment from the 1980s onward. It was a choice to organize the crisis and move forward.

1980
Strengthened R&D Investment. Annual R&D Expenditure Reached 20 Billion Yen
1988
Tsukuba Research Laboratories Newly Established
1989

Launched Leuprorelin

The Structure Where 'Retreat-Ready Concentration' Created a Precedent for Japan-Originated Global Drug Discovery

The success of Leuprorelin was born from a concentrated investment that carried the risk of discontinuing antibiotic development. The decision made by Kunio Takeda at the U.S. subsidiary was a choice to bet on a single product rather than dispersing limited resources, and it became the foundational experience for the 'selection and concentration' strategy he would later deploy as president. The achievement of over 100 billion yen in global sales numerically validated that a Japanese company could deploy proprietary drug discovery through its own sales globally.

BackgroundStructural constraints preventing proprietary expansion in the U.S. market

In the mid-1980s, despite improving research capabilities, Japanese pharmaceutical companies had not yet reached the stage of building proprietary sales networks in Western markets. New drugs were limited to technology exports through licensing, and a structure of dependence on Western companies for sales and approval processes continued.

Takeda Pharmaceutical established a U.S. subsidiary through a joint venture with Abbott Laboratories in 1985, but initially lacked strong proprietary products and struggled to grow performance in the fiercely competitive U.S. market. Research capabilities were being accumulated, but the path to converting them into business results had not been established.

DecisionDiscontinuation of antibiotic development and concentration of management resources on Leuprorelin

Kunio Takeda, then head of the U.S. subsidiary, judged that survival in the U.S. market would be difficult as long as limited development resources were spread thin. He determined that the mainstream antibiotic field was too competitive and there was little room for a late entrant to prevail, and made the painful decision to discontinue development.

On that basis, management resources were concentrated on 'Leuprorelin,' which was under development as a cancer therapeutic. By introducing it as an improved formulation with reduced administration frequency, differentiation in the clinical setting was pursued, and a system was put in place to handle everything from regulatory compliance to sales in-house. It was a concentrated investment with readiness to retreat.

ResultAchieved global sales exceeding 100 billion yen, validating the proprietary deployment model

Leuprorelin, launched in the U.S. in 1989, rapidly expanded sales in the U.S. market on the back of its low administration frequency. As of FY1995, it recorded domestic sales of 21.7 billion yen, U.S. sales of 63.8 billion yen, and European/other sales of 15.3 billion yen, reaching a blockbuster level exceeding 100 billion yen globally.

Leuprorelin became the first product to validate the model of deploying Japan-originated drug discovery to the global market through a proprietary sales network. This success became the benchmark for Takeda Pharmaceutical's subsequent overseas investment decisions and formed the prototype for the 'selection and concentration' strategy that Kunio Takeda would later pursue as president.

The Structure Where 'Retreat-Ready Concentration' Created a Precedent for Japan-Originated Global Drug Discovery

The success of Leuprorelin was born from a concentrated investment that carried the risk of discontinuing antibiotic development. The decision made by Kunio Takeda at the U.S. subsidiary was a choice to bet on a single product rather than dispersing limited resources, and it became the foundational experience for the 'selection and concentration' strategy he would later deploy as president. The achievement of over 100 billion yen in global sales numerically validated that a Japanese company could deploy proprietary drug discovery through its own sales globally.

TimelineLaunched Leuprorelin — Key Events
3/1996Leuprorelin surpassed 100 billion yen in annual sales
1991
Launched Takepron
1992
Organizational Reform of Research Laboratories Implemented
1993
Launched Blockbuster Drug Prograf
1996
Company System Introduced
1997
Takeda America R&D Center Newly Established
1997
Launched Blopress
1997
Actos Approved in the U.S.
2005
4

Began Divestiture of Non-Focus Businesses

The Structure Where Phased Separation of Diversified Businesses Created Capacity for Concentrated Drug Discovery Investment

The business divestitures from 2001 onward were structural reform that eliminated the burden low value-added businesses had been imposing on the pharmaceutical-level cost structure, and secured investment capacity for new drug development. The design of transitioning through joint ventures to phased share transfers achieved irreversible specialization. Without this reform, the concentration of management resources necessary for subsequent massive overseas acquisitions would have been difficult.

BackgroundDiversified businesses structurally constraining the transformation to an R&D-driven enterprise

By the late 1990s, R&D expenditure of 20–30 billion yen per new drug had become the norm in the pharmaceutical industry, and the quality of R&D investment was determining corporate value. Takeda Pharmaceutical broadly held diversified businesses including chemical products, food, agrochemicals, and living environment in addition to prescription pharmaceuticals, with management resources in a dispersed state.

Particularly problematic was that business groups with different value-added levels were being operated as a unified entity under the cost structure and management systems of a pharmaceutical company. As new drug development costs increased while investment recovery in the Japanese market alone became difficult, a review of the business portfolio itself became unavoidable.

DecisionPresident Kunio Takeda led the phased separation of diversified businesses

President Kunio Takeda clearly championed the transition from diversification to specialization, and from 2001 began phased restructuring of diversified businesses. Businesses including urethane, vitamins, veterinary pharmaceuticals, agrochemicals, food, and living environment were separated through joint ventures and share transfers, and from 2005 onward divestitures were accelerated.

This reform was positioned not as short-term profit optimization but as structural reform to secure future R&D investment capacity. It was a decision to enhance competitiveness as an R&D-driven international enterprise by concentrating management resources on the pharmaceutical business.

ResultIrreversible transition to pharmaceutical specialization completed, forming the premise for global strategy

Through the diversified business restructuring from 2001 onward, Takeda Pharmaceutical's capital allocation clearly converged on the pharmaceutical business. A structure was put in place enabling concentration of management resources on R&D, global expansion, and the new drug pipeline, and organizational decision-making was also simplified.

On the other hand, business divestitures were accompanied by short-term revenue scale reduction, and the time horizon for R&D results to materialize lengthened. However, through this reform, Takeda Pharmaceutical shed its character as a diversified company and irreversibly transformed into an international pharmaceutical enterprise with R&D at its core. This structural transformation became the premise for the subsequent global strategy including the Millennium acquisition and Shire acquisition.

The Structure Where Phased Separation of Diversified Businesses Created Capacity for Concentrated Drug Discovery Investment

The business divestitures from 2001 onward were structural reform that eliminated the burden low value-added businesses had been imposing on the pharmaceutical-level cost structure, and secured investment capacity for new drug development. The design of transitioning through joint ventures to phased share transfers achieved irreversible specialization. Without this reform, the concentration of management resources necessary for subsequent massive overseas acquisitions would have been difficult.

TestimonyKunio Takeda (Takeda Pharmaceutical, then President)

Since I became president, I have reformed from diversification to specialization, having married off nearly all businesses outside of pharmaceuticals. Now that the reforms are nearing completion, the next stage is creating a system that makes managing a specialized company easy. I think the employees now understand where the company is heading.

The future of a pharmaceutical company ultimately depends on new drugs. The future of a company can be seen from how well-stocked its pipeline is. New drugs spend a long time in the pipeline, so the question for us is how to create new products and deliver them speedily to patients. We are now earnestly devising how to manage 'Takeda the global company.'

Source2002/10/21 Nikkei Business 'Editor-in-Chief Interview: Kunio Takeda'
TimelineBegan Divestiture of Non-Focus Businesses — Key Events
3/2000Veterinary pharmaceutical business JV'd with Schering-Plough (Takeda 40%)
1/2001Vitamin bulk business JV'd with BASF (Takeda 34%)
4/2002Food business JV'd with Kirin Brewery (Takeda Kirin Food, Takeda 49%)
10/2002Latex business transferred to Nippon A&L
11/2002Agrochemical business JV'd with Sumitomo Chemical (Sumika Takeda Agrochemicals, Takeda 40%)
4/2003Living environment business spun off (Nippon Enviro Chemicals)
3/2005Agreed to transfer 5 living environment business subsidiaries to Osaka Gas Chemical
6/2005Veterinary pharmaceutical JV fully transferred to Schering-Plough
1/2006BASF Takeda Vitamins fully transferred to BASF
4/2006Beverage and food business JV'd with House Foods
10/2007Beverage and food JV scheduled for transfer to House Foods
11/2007Agrochemicals scheduled for transfer to Sumitomo Chemical
2008
5

Acquired Millennium Pharmaceuticals of the U.S.

The Embedding of the 'Buying Time' Concept That Formed the Starting Point for the Chain of Massive Acquisitions

The Millennium acquisition was Takeda Pharmaceutical's first full-scale massive overseas M&A and embedded the concept of 'buying time through acquisitions' in subsequent management. The decision to deploy resources secured through diversified business divestitures toward external acquisition of drug discovery capabilities was rational, but the structural significance lies in the fact that this single deal became the starting point for the acquisition chain continuing through the 2011 Nycomed, 2017 ARIAD, and 2019 Shire acquisitions.

BackgroundIn-house drug discovery alone leaves the time horizon for global expansion uncertain

By the mid-2000s, Takeda Pharmaceutical had completed the restructuring of diversified businesses and put in place a structure for concentrating management resources on prescription pharmaceuticals. However, the Japanese market had limited growth potential due to drug price revisions and demographic shifts, and achieving a stronger presence in global markets through in-house drug discovery alone would require considerable time.

In this context, acquisition of overseas companies emerged as an option for simultaneously advancing strengthening of drug discovery capabilities and overseas expansion. It was necessary to externally acquire R&D platforms to reinforce the future pipeline early and clarify its positioning as an R&D-driven international enterprise.

DecisionPresident Hasegawa acquired Millennium for approximately $8.9 billion

In 2008, Takeda Pharmaceutical acquired Millennium Pharmaceuticals, a U.S. biopharmaceutical company, for approximately $8.9 billion. The decision was led by President Yasuchika Hasegawa, with the aim of acquiring cancer research capabilities and a U.S. business base in a single stroke. It was Takeda's first full-scale massive overseas acquisition.

The choice of an acquisition to obtain management control rather than phased alliances or licensing reflected the concept of 'buying time' for research capabilities. It was a decision to deploy the management resources secured through divestiture of diversified businesses toward external acquisition of drug discovery capabilities.

ResultAcquired cancer research platform but also became the starting point for a chain of massive acquisitions

Through the Millennium acquisition, Takeda Pharmaceutical acquired cancer research capabilities and a U.S. base, gaining a foothold to concretely advance its transformation into an R&D-driven international enterprise. At the same time, the management decision to invest a massive amount became a result of simultaneously taking on financial burden and integration risk.

This acquisition did not push up corporate value in the short term, but it was important in embedding the concept of 'buying time through acquisitions' within the organization. The Millennium acquisition became the starting point for the chain of massive acquisitions continuing through the 2011 Nycomed, 2017 ARIAD, and 2019 Shire acquisitions.

The Embedding of the 'Buying Time' Concept That Formed the Starting Point for the Chain of Massive Acquisitions

The Millennium acquisition was Takeda Pharmaceutical's first full-scale massive overseas M&A and embedded the concept of 'buying time through acquisitions' in subsequent management. The decision to deploy resources secured through diversified business divestitures toward external acquisition of drug discovery capabilities was rational, but the structural significance lies in the fact that this single deal became the starting point for the acquisition chain continuing through the 2011 Nycomed, 2017 ARIAD, and 2019 Shire acquisitions.

TestimonyHasegawa (Takeda Pharmaceutical, President)

Many pharmaceutical companies face a situation where patents on blockbuster drugs made with existing technologies are expiring, commonly called the 'patent cliff of 2010' in the pharmaceutical industry. Takeda is also losing patents on major products this year. Japan is a unique country where sales don't drop that much even when patents expire, but in the U.S. and elsewhere, generic manufacturers are eagerly waiting, and 3-4 months after patent expiration, sales of the company that developed the original product can drop to about 10% or disappear completely—fierce turnover occurs. As I mentioned earlier, the largest market for pharmaceutical companies is the U.S., so given this reality, being able to survive and win is one of the conditions for being a global company. To do that, I believe there is no choice but to continue producing attractive new drugs.

2011
Shonan Research Laboratories Newly Established
2011
9

Acquired Nycomed

The Structure Where a 1 Trillion Yen Weakness-Reinforcement Acquisition Did Not Directly Translate to Corporate Value Enhancement

The Nycomed acquisition functioned as weakness reinforcement through the bulk acquisition of an emerging market sales network and European business base, mitigating revenue decline during the patent expiration phase. However, the level of growth expected by the capital market relative to the over-1-trillion-yen invested capital was not realized, and the stock price evaluation remained limited. This is an example demonstrating the challenge that business weakness reinforcement and corporate value enhancement do not necessarily align, and also influenced the invested capital decisions in the subsequent Shire acquisition.

BackgroundPatent expiration of flagship products and lack of sales infrastructure in emerging markets

From the late 2000s through around 2010, Takeda Pharmaceutical faced successive patent expirations on flagship products and had challenges with the sustainability of sales growth from existing products. In particular, the diabetes drug Actos had high contribution to earnings, and the revenue decline from generic entry was seen as a medium-term drag on performance.

With limited growth potential in the domestic market and increasing price pressure in developed Western countries, there was a growing recognition that maintaining the sales base along the existing trajectory would be difficult. As of 2010, the weakness identified for Takeda Pharmaceutical was the thinness of its sales infrastructure in emerging markets.

In a situation of insufficient penetration into emerging markets, which accounted for the majority of growth in the global pharmaceutical market, the option of building a sales network from scratch existed, but the time and investment burden were expected to be large. Acquiring a company that already had a strong sales network in Europe and emerging markets was judged to be more effective for advancing the growth timeline.

DecisionAcquired Nycomed for approximately 1.1 trillion yen, acquiring sales network in bulk

In May 2011, Takeda Pharmaceutical agreed to acquire Nycomed, a Swiss pharmaceutical company, for 9.6 billion euros, approximately 1.1 trillion yen. The decision was led by President Yasuchika Hasegawa, and the consideration was entirely in cash with no new share issuance. Avoiding dilution was prioritized, and part of the funding was financed through borrowing.

Through the acquisition, Takeda Pharmaceutical acquired a sales network spanning Europe, Russia, Asia, and Latin America in bulk, along with a product portfolio including COPD therapeutics. In addition to future growth through R&D, the aim was to secure a business base to complement revenue in the short-to-medium term, with Nycomed's annual revenue said to be approximately 300 billion yen.

On the other hand, this acquisition marked a departure from zero-debt management, and the increased complexity of management accompanying the rapid expansion of the overseas business ratio was also recognized as a risk to factor in. There were also cautious views on whether growth commensurate with the invested capital of over 1 trillion yen would be achieved.

ResultGeographic diversification achieved but corporate value improvement commensurate with invested capital not realized

Through the Nycomed acquisition, Takeda Pharmaceutical's emerging market revenue expanded significantly and the geographic portfolio changed substantially. Sales scale in Europe also expanded, and from the perspective of geographic diversification, the business base was reinforced. The effect of avoiding a sharp decline in consolidated revenue during the patent expiration phase was to some degree achieved.

However, market evaluation was limited. While the post-acquisition performance contribution was stable, it did not substantially push up corporate value, and the stock price response remained muted.

The Nycomed acquisition contributed to reinforcing business weaknesses, but did not demonstrate the level of growth expected by the capital market relative to the over-1-trillion-yen invested capital. It confronted Takeda Pharmaceutical's management with the challenge that business base expansion and corporate value enhancement do not necessarily align.

The Structure Where a 1 Trillion Yen Weakness-Reinforcement Acquisition Did Not Directly Translate to Corporate Value Enhancement

The Nycomed acquisition functioned as weakness reinforcement through the bulk acquisition of an emerging market sales network and European business base, mitigating revenue decline during the patent expiration phase. However, the level of growth expected by the capital market relative to the over-1-trillion-yen invested capital was not realized, and the stock price evaluation remained limited. This is an example demonstrating the challenge that business weakness reinforcement and corporate value enhancement do not necessarily align, and also influenced the invested capital decisions in the subsequent Shire acquisition.

2016
4

Christophe Weber Became CEO

The Internal Absence of Global Talent Structurally Determined the Long Tenure of a Foreign CEO

Weber's appointment as CEO was a consequence of Takeda Pharmaceutical's failure to develop global management talent internally. Even as massive acquisitions accelerated and financial deterioration progressed under the externally recruited CEO, the absence of successor candidates constrained the options for replacement. The approximately 10-year tenure demonstrates the structural problem that while both business and talent can be resolved in the short term by 'buying,' the omission of 'cultivating' manifests in another form.

BackgroundThe structural challenge of the absence of a next-generation top executive capable of managing global operations

Takeda Pharmaceutical had long been led by the Takeda and Konishi founding families, but in 2003 Yasuchika Hasegawa, a non-founding family member, became president and the management structure underwent a major transformation. Under the Hasegawa regime, growth strategy was advanced centered on internationalization and large-scale acquisitions, including the Millennium and Nycomed acquisitions.

However, global management talent capable of governing acquired overseas companies had not been sufficiently built up internally. Even after the departure from founding family control, the options for a next-generation top executive with management experience at Western pharmaceutical companies were limited, and a structural gap had emerged between strategic execution capabilities and talent development.

DecisionChairman Hasegawa appointed Weber as President and CEO within approximately one year

In 2014, Takeda Pharmaceutical recruited Christophe Weber, formerly of GlaxoSmithKline in the UK, as COO. Chairman Yasuchika Hasegawa had positioned Weber as a future CEO candidate from the time of his COO appointment, and after evaluating his management abilities for approximately one year, appointed him President and CEO in 2015.

The decision to place a foreigner at the helm of Japan's largest pharmaceutical company was simultaneously a necessity of global management and a consequence of the failure to develop a successor internally. The fact that the COO position was abolished and authority was concentrated indicates a clear intent of top-level succession.

ResultAcceleration of large-scale acquisitions and financial deterioration made management tensions apparent

Under the Weber regime, Takeda Pharmaceutical further accelerated its large-scale acquisition strategy, executing the approximately 6.2 trillion yen Shire acquisition in 2019. While the business base in rare diseases and plasma-derived therapies expanded, interest-bearing debt surged and the financial position deteriorated significantly.

The continuation of massive acquisitions raised financial risk in exchange for growth expectations and also created tensions with traditional stakeholders including the founding families. CEO Weber is scheduled to step down in June 2026, but he will have held the top position for approximately 10 years. The fact that talent capable of succeeding him had not been developed internally was the structural factor that, as a result, made the long tenure possible.

The Internal Absence of Global Talent Structurally Determined the Long Tenure of a Foreign CEO

Weber's appointment as CEO was a consequence of Takeda Pharmaceutical's failure to develop global management talent internally. Even as massive acquisitions accelerated and financial deterioration progressed under the externally recruited CEO, the absence of successor candidates constrained the options for replacement. The approximately 10-year tenure demonstrates the structural problem that while both business and talent can be resolved in the short term by 'buying,' the omission of 'cultivating' manifests in another form.

TimelineChristophe Weber Became CEO — Key Events
1993Kunio Takeda became president (founding family)
2003Yasuchika Hasegawa became president (non-founding family)
4/2015Christophe Weber became President and CEO
6/2026Julie Kim scheduled to become CEO
2016
Long-Listed Products Divested
2017
Acquired ARIAD
2017
Wako Pure Chemical Industries Divested
2019
1

Acquired Shire

The 6.2 Trillion Yen That Exposed the Divergence Between 'Business Base Expansion and Corporate Value'

The Shire acquisition achieved a transformation of business composition by bulk-acquiring rare disease and plasma-derived therapy business bases, but the recovery of the 6.2 trillion yen in invested capital took longer than expected. The fact that the company was forced to sell the OTC drug business including Alinamin to rebuild finances demonstrated the limits of capacity relative to the acquisition scale. The structure where business base expansion and corporate value enhancement do not align is a challenge for Takeda Pharmaceutical that has continued since the Nycomed acquisition.

BackgroundShrinking domestic market and the time horizon of in-house drug discovery accelerated acquisition considerations

From the mid-2010s onward, Japan's pharmaceutical market continued in a situation where volume-driven revenue expansion was difficult to expect, due to population decline and drug price revisions. Takeda Pharmaceutical continued R&D investment in priority areas of gastroenterology, oncology, and neuroscience, but with a high domestic revenue ratio, there were limits to growth and profit margin improvement.

The U.S. market was recognized as a market where revenue and profit could be expanded simultaneously, given its high price levels and limited competition in the rare disease area. Expansion through in-house R&D risked a prolonged period before revenue contribution materialized, and the option of bulk-acquiring businesses with existing revenue was considered.

DecisionCEO Weber acquired Shire for approximately 6.2 trillion yen

In May 2018, Takeda Pharmaceutical announced its intention to acquire Shire, headquartered in Ireland, for approximately $62 billion, or approximately 6.2 trillion yen. The decision was led by CEO Christophe Weber, with consideration being a combination of cash and the company's own shares. The aim was to bulk-acquire the rare disease and plasma-derived therapy business and increase the U.S. revenue ratio.

The acquisition amount was among the largest ever for overseas M&A by a Japanese company, and a significant increase in interest-bearing debt was deemed inevitable. Recovery of invested capital was entrusted to post-integration cash flow, and whether growth commensurate with the acquisition premium could be realized became the most significant management challenge.

ResultBusiness composition transformed but recouping the acquisition premium takes time

Having completed the Shire acquisition in January 2019, Takeda Pharmaceutical sold the consumer healthcare business and European OTC drug business and repaid borrowings. Cost reductions and base consolidation improved operating cash flow, and the outstanding debt balance was progressively reduced.

However, recouping the premium paid at the time of acquisition took longer than expected. The revenue growth rate did not significantly accelerate compared to pre-acquisition levels, and the stock price underperformed relative to industry peers and equity indices over a prolonged period. While the reorganization of business composition and the rebuilding of finances progressed, the capital market's evaluation remained harsh against the 6.2 trillion yen of invested capital.

The 6.2 Trillion Yen That Exposed the Divergence Between 'Business Base Expansion and Corporate Value'

The Shire acquisition achieved a transformation of business composition by bulk-acquiring rare disease and plasma-derived therapy business bases, but the recovery of the 6.2 trillion yen in invested capital took longer than expected. The fact that the company was forced to sell the OTC drug business including Alinamin to rebuild finances demonstrated the limits of capacity relative to the acquisition scale. The structure where business base expansion and corporate value enhancement do not align is a challenge for Takeda Pharmaceutical that has continued since the Nycomed acquisition.

TimelineAcquired Shire — Key Events
5/2018Shire acquisition process commenced
1/2019Acquired Shire plc
2020
OTC Drug Business Divested
2026
Julie Kim Scheduled to Become CEO
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