|Daiichi Sankyō kabushiki gaisha|
TOPIX Large 70 Component
TOPIX 100 Component
Nikkei 225 Component
|Founded||Tokyo, Japan (2005) (by merger)|
|Headquarters||Daiichi Sankyo Building A/B 3-5-1, Nihonbashi-honcho, Chūō-ku, Tokyo 103-8426, Japan|
|Revenue||$ 9.028 billion USD (FY 2019) (¥ 981.8 billion JPY) (FY 2019)|
|$ 1.276 billion USD (FY 2019) (¥ 138.8 billion JPY) (FY 2019)|
Number of employees
|15,348 (as of March 2020)|
|Footnotes / references|
Daiichi Sankyo Company, Limited (Japanese: 第一三共株式会社, Hepburn: Daiichi Sankyō Kabushiki-gaisha) is a global pharmaceutical company and the second-largest pharmaceutical company in Japan. It achieved JPY 981.8 billion in revenue in 2019. The company owns the American biotechnology company Plexxikon, American pharmaceutical company American Regent, German biotechnology company U3 Pharma, and recently sold Ranbaxy Laboratories in India. Daiichi Sankyo Co., Ltd. is the producer of Benicar (Olmesartan), an angiotensin II receptor antagonist and top selling drug in the U.S. Global sales of Olmesartan in 2013 were 300.2 billion yen.
Daiichi Sankyo, Inc. (DSI) began operating in the U.S. in 2006. It is the U.S. subsidiary of Daiichi Sankyo Company, Limited, and a member of the Daiichi Sankyo Group. The organization, which includes U.S. commercial operations and global clinical development (Daiichi Sankyo Pharma Development), is headquartered in Basking Ridge, New Jersey.
Daiichi Sankyo Company, Limited is a full member of the European Federation of Pharmaceutical Industries and Associations (EFPIA) and of the International Federation of Pharmaceutical Manufacturers and Associations (IFPMA).
Daiichi Sankyo was established in 2005 through the merger of Sankyo Company, Limited (三共株式会社, Sankyō Kabushiki Kaisha) and Daiichi Pharmaceutical Company, Limited (第一製薬株式会社, Daiichi Seiyaku Kabushiki Kaisha), which were century-old pharmaceutical companies based in Japan. Sankyo Co., Ltd. was founded by Dr. Jokichi Takamine, who patented the isolation of adrenalin. Takamine was also the first president of Sankyo Co., Ltd from March 1913 – July 1922. In 1990, Sankyo acquired Luitpold-Werk Group, a pharmaceutical company based in Munich. In 2019, Luitpold renamed itself after its American Regent brand. American Regent, now based in the United States, is a subsidiary of Daiichi Sankyo.
As of 2015, Daiichi Sankyo was being "closely monitored" after settling charges concerning payment of remuneration to physicians in the form of speaker fees as part of company's Physician Organization and Discussion program, in violation of the False Claims Act, an anti-kickback statute.
Daiichi Sankyo agreed to pay the United States and state Medicaid programs $39 million to settle allegations by the United States Department of Justice over kickbacks to doctors. As part of the company's Physician Organization and Discussion program which ran from 2005 through 2011, Daiichi Sankyo paid physicians improper kickbacks in the form of speaker fees to induce physicians to prescribe Daiichi Sankyo's drugs, including Azor, Benicar, Tribenzor and Welchol. Allegedly, payments were made to physicians even when physician participants in PODs took turns “speaking” on duplicative topics over Daiichi-paid dinners, the recipient spoke only to members of his or her own staff in his or her own office, or the associated dinner was so lavish that its cost exceeded Daiichi Sankyo's own internal cost limitation of $140 per person.
“Schemes such as this are particularly abhorrent,” said Inspector General Daniel R. Levinson for the U.S. Department of Health and Human Services. “Manufacturers and physicians who engage in them are cheating Medicare and Medicaid out of millions of dollars and threatening programs upon which many elderly and disabled Americans rely. My office will take whatever steps necessary to guard against improper alliances between manufacturers of drugs and those who prescribe them. Through our corporate integrity agreement we will be closely monitoring Daiichi Sankyo.”
In 2006, Daiichi Sankyo acquired Zepharma, the OTC drugs unit of Astellas Pharma. On June 10, 2008, the company agreed to take a majority (64%) stake in Indian generic drug maker Ranbaxy, with a deal valued at about $4.6 billion.
The acquisition of Plexxikon, a Berkeley, California-based pharmaceutical start-up company, was completed on April 4, 2011 for $805 million and an additional $130 million in milestone payments, pending on the success of Vemurafenib (Plexxikon's lead program) an oral, novel drug that targets the oncogenic BRAF mutation present in about half of melanoma cancers and about eight percent of all solid tumors. Daiichi Sankyo is retaining US co-promotion right of the (Roche licensed) drug.
On April 7, 2014, Daiichi Sankyo announced it had agreed to vote its shares in Ranbaxy in favor of Sun Pharma's acquisition of 100% of Ranbaxy through the merger process which entailed a share swap. The transaction is set to close in December 2014, pending shareholder, court and regulatory approvals and other customary conditions. On September 29, 2014, Daiichi Sankyo agreed to acquire Ambit Biosciences for approximately $410 million, the deal enabled Daiichi to gain the Phase III cancer compound quizartinib. On April 20, 2015, the company announced it had sold off the 8.9% stake in Sun Pharmaceutical Industries it acquired when acquiring Ranbaxy, raising $3.2 billion.
It transferred 41 of its products in Japan to Alfresa Holdings Corporation for JPY 4.2 billion in 2018 in order to focus on oncology. The company acquired ramosetron, nicardipine and barnidipine from Astellas Pharma in October 2019.
In January 2020, the company's market value rose above JPY 5 trillion after the U.S. Food and Drug Administration approval and release of Enhertu, an antibody-drug conjugate for cancer treatment. Daiichi Sankyo developed Enhertu in cooperation with AstraZeneca, which agreed in March 2019 to pay up to $6.9 billion to Daiichi Sankyo in exchange for a share of Enhertu's sales. The shutdown of Plexxikon was announced in 2022 as Daiichi Sankyo pivots to focus on more antibody-drug conjugate therapies.
The following is an illustration of the company's major mergers and acquisitions and historical predecessors (this is not a comprehensive list):
This list is not comprehensive.
- Enhertu (trastuzumab deruxtecan, fam-trastuzumab deruxtecan-nxki in the United States only)
- Turalio (pexidartinib)
- Vanflyta (quizartinib) (available only in Japan)
- Zelboraf (vemurafenib)
- Benicar (olmesartan medoxomil) (also sold as Benicar HCT, Azor, Olmetec, Rezaltas, Sevikar, and Tribenzor)
- Effient (prasugrel) (co-marketed with Eli Lilly and Company; also sold as Efient)
- Lixiana/Savaysa (edoxaban)
- Minnebro (esaxerenone) (available only in Japan)
- Nilemdo (bempedoic acid, only sold in the EU) (also sold as Nustendi)
- Canalia (teneligliptin, canagliflozin) (available only in Japan)
- Evoxac (cevimeline hydrochloride)
- Injectafer (ferric carboxymaltose injection)
- Memary (memantine hydrochloride) (available only in Japan)
- Nexium (esomeprazole) (only in Japan; marketed by AstraZeneca elsewhere)
- Pralia (denosumab) (only available in Japan; also sold there as Ranmark)
- Tarlige (mirogabalin) (only available in Japan)
- Tenelia (teneligliptin hydrobromide hydrate)
- Venofer (iron sucrose)
- Vimpat (lacosamide) (only available in Japan; co-marketed with UCB)
- Welchol (colesevelam HCl)
Select mid-stage and late-stage investigational candidates in Daiichi-Sankyo's pipeline include:
- Datopotamab deruxtecan (Dato-DXd)
- Patritumab deruxtecan (HER3-DXd)
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- "Luitpold Pharmaceuticals Renamed American Regent". American Pharmaceutical Review. 2 January 2019. Retrieved 17 December 2020.
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- "Ranbaxy promoters to sell stake to Japan's Daiichi". June 11, 2008. Retrieved April 29, 2014.
- "Daiichi Sankyo Intends to Purchase U3 Pharma for Roughly $236M". Genetic Engineering & Biotechnology News. Mary Ann Liebert, Inc. May 21, 2008. Retrieved July 6, 2008.
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- "Daiichi Sankyo To Acquire Plexxikon". Plexxikon. February 28, 2011. Archived from the original on 2011-03-06. Retrieved April 29, 2014.
- "GEN - News Highlights:Daiichi Sankyo to Acquire Ambit Biosciences for Up to $410M". GEN. 2014-09-29.
- "GEN - News Highlights:Daiichi Sankyo Sells Off Stake in Sun Pharma". GEN. 2015-04-21.
- "Daiichi Sankyo splits to offload old assets and focus on oncology ambition". The Pharma Letter. 1 August 2018. Retrieved 1 December 2020.
- "Daiichi Sankyo buys three drugs to boost presence in Asia". The Pharma Letter. 15 October 2019. Retrieved 1 December 2020.
- Takada, Noriyuki; Kawana, Yukihiro; Sakabe, Yoshinaru (28 January 2020). "Daiichi Sankyo harnesses 'old' R&D to strike cancer drug gold". Nikkei Asia. Retrieved 1 December 2020.
- Matsuyama, Kanoko (16 June 2019). "Drug devised to replace chemotherapy may reshape cancer care". The Japan Times. Retrieved 1 December 2020.
- Terry, Mark (29 March 2019). "AstraZeneca and Daiichi Sankyo Sign $6.9 Billion Deal for a Single Cancer Drug". BioSpace. Retrieved 1 December 2020.
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- Wells, Madeline (2022-01-12). "South SF company bought for $800 million is being shut down". SFGATE. Archived from the original on 2022-01-12.
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- "AZ, Daiichi Sankyo get early okay for DS-8201, now named Enhertu". PMLive. 23 December 2019. Retrieved 3 December 2020.
- Taylor, Phil (5 August 2019). "Daiichi Sankyo's pexidartinib is first FDA-approved drug for rare tumour". Pharma Phorum. Retrieved 3 December 2020.
- "FDA approves Turalio, the first therapy for rare joint tumor". The Pharma Letter. 3 August 2019. Retrieved 3 December 2020.
- Idrus, Amirah Al (21 June 2019). "FDA nixes Daiichi's blood cancer drug quizartinib after Japanese regulators wave it through". Fierce Biotech. Retrieved 3 December 2020.
- "First-in-class skin cancer drug approved". PMLive. 18 August 2011. Retrieved 13 May 2021.
- "Products". Daiichi Sankyo. Retrieved 2 December 2020.
- Elvidge, Suzanne (2 August 2017). "Daiichi spends $300M to settle Benicar suits". BioPharma Dive. Retrieved 3 December 2020.
- "Daiichi Sankyo says prasugrel hits goals in thrombotic stroke study". The Pharma Letter. 21 July 2020. Retrieved 3 December 2020.
- Weinberg, Ido (9 January 2015). "FDA approves edoxaban to reduce stroke risk, treat DVT and PE". Healio. Retrieved 3 December 2020.
- "FDA approves Daiichi Sankyo bloodthinner Savaysa". PharmaTimes. 9 January 2015. Retrieved 3 December 2020.
- Terry, Mark (8 November 2019). "Daiichi Sankyo's Hypertension Drug Hits Mark in Diabetic Nephropathy Trial". BioSpace. Retrieved 3 December 2020.
- "EC nod for Daiichi Sankyo's cholesterol lowerers Nilemdo and Nustendi". The Pharma Letter. 6 April 2020. Retrieved 13 May 2021.
- "New combination therapy for type 2 diabetes approved in Japan". The Pharma Letter. 3 July 2017. Retrieved 3 December 2020.
- Dey, Sushmi (9 October 2012). "Ranbaxy launches authorised generic of Daiichi's Evoxac in US". Business Standard India. Retrieved 13 May 2021.
- Steinberg, Julie (29 July 2020). "Daiichi Sankyo Still Faces Claims Over Injectable Anemia Drug". Bloomberg Law. Retrieved 3 December 2020.
- "Daiichi Sankyo Looking to Establish "Base Treatment" Position for Memary". Pharma Japan. 23 April 2012. Retrieved 3 December 2020.
- "AZ pockets $100 million in Daiichi Sankyo deal for Nexium". PharmaTimes. 29 October 2010. Retrieved 3 December 2020.
- "Daiichi Sankyo files Ranmark to treat giant cell tumor of bone in Japan". The Pharma Letter. 29 August 2013. Retrieved 3 December 2020.
- "Daiichi Sankyo debuts bone cancer drug Ranmark in Japan". The Pharma Letter. 17 April 2012. Retrieved 3 December 2020.
- "Daiichi Sankyo wins approval to compete with Lyrica in Japan". The Pharma Letter. 9 January 2019. Retrieved 3 December 2020.
- Haneda, Masakazu; Kadowaki, Takashi; Ito, Hiroshi; Sasaki, Kazuyo; Hiraie, Sonoe; Ishii, Manabu; Matsukawa, Miyuki; Ueno, Makoto (2018). "Safety and Efficacy of Teneligliptin in Patients with Type 2 Diabetes Mellitus and Impaired Renal Function: Interim Report from Post-marketing Surveillance". Diabetes Therapy. 9 (3): 1083–1097. doi:10.1007/s13300-018-0416-2. PMC 5984919. PMID 29637459.
- Bulik, Beth Snyder (1 April 2018). "Daiichi Sankyo partners with Crohn's & Colitis Foundation to draw attention to iron deficiency". Fierce Pharma. Retrieved 3 December 2020.
- "UCB and Daiichi Sankyo's Vimpat approved in Japan". The Pharma Letter. 4 July 2016. Retrieved 3 December 2020.
- "Daiichi Sankyo says FDA OKs Welchol for diabetes treatment". Reuters. 18 January 2008. Retrieved 3 December 2020.
- "Datopotamab deruxtecan – DS-1062 (TROP2 ADC)". ADC Review. Retrieved 17 December 2020.
- Hergert, Jessica (31 January 2021). "Relapsed/Refractory Metastatic NSCLC Tumors Respond to Datopotamab Deruxtecan in Early Trial". Cancer Network. Retrieved 13 May 2021.
- "Patritumab Deruxtecan – U3-1402 – HER3 ADC". ADC Review. Retrieved 17 December 2020.
- Seymour, Caroline (30 January 2021). "Patritumab Deruxtecan Shows Early Activity in Metastatic EGFR-Mutant NSCLC". Targeted Oncology. Retrieved 13 May 2021.
- "Daiichi Sankyo sets out plans for dissolution of Japan Vaccine". The Pharma Letter. 26 December 2018. Retrieved 3 December 2020.
- "Daiichi Sankyo sets up collaborations for valemetostat in B-cell lymph". The Pharma Letter. 25 February 2021. Retrieved 13 May 2021.
- "Daiichi Sankyo's Oncolytic Virus Gets Orphan Status". Pharma Japan. 12 July 2017. Retrieved 17 December 2020.