Private company

Daiichi Sankyo

Logo: Daiichi Sankyo Company, Limited, CC BY 2.5, via Wikimedia Commons5

Japanese pharmaceutical company

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 1,278 billion in revenue in 2022. The company owns the American pharmaceutical company American Regent.3 Wikipedia text CC BY-SA 4.0

Last updated Oct 21, 2026.

Overview

2005Founded1
  • Industrypharmaceutical industry1
  • HeadquartersChūō1
  • Founded inTokyo1
  • Websitewww.daiichisankyo.co.jp
  • Legal formkabushiki gaisha1
  • LEI353800XGIU2IHQGC95044
  • StatusActive4
  • LEI statusIssued and current4
  • Registered address日本橋本町三丁目5番1号, 103-8426 東京都 中央区, Japan4
  • Registered withLegal Affairs Bureau, 0100-01-0956404

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 1,278 billion in revenue in 2022. The company owns the American pharmaceutical company American Regent.3

Corporate structure

Daiichi Sankyo sits at the top of its group. 3 entities, 2 countries on record. Switch between the flow chart and the network, and select any entity to see its details.

  • Daiichi Sankyo 東京都 中央区, Japan

Built from parent and subsidiary links from GLEIF, the Global Legal Entity Identifier Foundation (CC0); subsidiaries, stakes and holdings from Wikidata (CC0). Each entity in the chart links to its source.

The story

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 Jokichi Takamine, who patented the isolation of adrenaline. Takamine was president of Sankyo Co., Ltd from March 1913 until July 1922.

In 1990, Sankyo acquired the German 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.

Acquisitions

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.

It acquired U3 Pharma in June 2008, contributing a therapeutic anti-HER3 antibody to the company's anticancer portfolio. The company closed U3 Pharma in 2015.

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. The shutdown of Plexxikon was announced in 2022 as Daiichi Sankyo pivots to focus on more antibody-drug conjugate therapies.

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. On September 29, 2014, Daiichi Sankyo agreed to acquire Ambit Biosciences for approximately $410 million, the deal enabled Daiichi to gain the 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.

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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 following is an illustration of the company's major mergers and acquisitions and historical predecessors (this is not a comprehensive list):

Kickbacks, 2015

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 their own staff in their 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."

From Wikipedia’s article on Daiichi Sankyo, shared under CC BY-SA 4.0.6

Leadership

Who has led Daiichi Sankyo, and when. Pick a name to see everywhere that person has worked.

Board members and other officers (1)

Products and brands

This list is not comprehensive.

Oncology

Enhertu (trastuzumab deruxtecan, fam-trastuzumab deruxtecan-nxki in the United States only)

Ezharmia (valemetostat) (available only in Japan)

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Turalio (pexidartinib) (available only in the United States)

Vanflyta (quizartinib)

Zelboraf (vemurafenib)

Cardiovascular

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)

Nustendi (fixed dose combination of bempedoic acid and ezetimibe)

Other

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)

From Wikipedia’s article on Daiichi Sankyo, shared under CC BY-SA 4.0.6

Subsidiaries and ownership

Subsidiaries

From Wikidata.1

Timeline

  1. 2005Founded Founded in Tokyo1

Calendar

Drug trials and FDA: coming up

  1. Nov 11, 2026Phase 3 trial readout expected Phase 3 trial of Trastuzumab deruxtecan, Taxane and others in Breast Cancer; HER2-positive; Metastatic, run by AstraZeneca: primary completion expected Nov 11, 2026 (ClinicalTrials.gov NCT04784715).7
  2. Jan 11, 2027Phase 3 trial readout expected Phase 3 trial of Dato-DXd, Osimertinib and others in Metastatic Non-small Cell Lung Cancer, run by AstraZeneca: primary completion expected Jan 11, 2027 (ClinicalTrials.gov NCT06417814).8
  3. Jan 31, 2027Phase 2 trial readout expected Phase 2 trial of DS-5141b in Duchenne Muscular Dystrophy: primary completion expected Jan 31, 2027 (ClinicalTrials.gov NCT04433234).9
  4. Jul 28, 2027Phase 3 trial readout expected Phase 3 trial of Dato-DXd, Durvalumab and others in Breast Cancer, run by AstraZeneca: primary completion expected Jul 28, 2027 (ClinicalTrials.gov NCT06103864).10
  5. Sep 1, 2027Phase 3 trial readout expected Phase 3 trial of Dato-DXd, Durvalumab and others in Breast Cancer, run by AstraZeneca: primary completion expected Sep 1, 2027 (ClinicalTrials.gov NCT05629585).11
  6. Oct 1, 2027Phase 3 trial readout expected Phase 3 trial of Trastuzumab Deruxtecan in Breast Cancer: primary completion expected Oct 1, 2027 (ClinicalTrials.gov NCT05950945).12

Drug trials and FDA: recently

  1. Jul 10, 2026Phase 3 trial completed Phase 3 trial of Datopotamab Deruxtecan, Rilvegostomig and others in Non-small Cell Lung Cancer, run by AstraZeneca: primary completion Jul 10, 2026, no results posted yet (ClinicalTrials.gov NCT06564844).13
  2. Jun 9, 2026Phase 3 trial completed Phase 3 trial of Trastuzumab Deruxtecan, Cisplatin and others in Locally Advanced or Metastatic Non-Small Cell Lung Cancer, run by AstraZeneca: primary completion Jun 9, 2026, no results posted yet (ClinicalTrials.gov NCT05048797).14
  3. May 22, 2026FDA approved a new use FDA approved an efficacy supplement for Datroway (datopotamab deruxtecan-dlnk), a new use or patient group (BLA 761394, supplement 3).15
  4. May 15, 2026FDA approved a new use FDA approved an efficacy supplement for Enhertu (fam-trastuzumab deruxtecan-nxki), a new use or patient group (BLA 761139, supplement 41).16
  5. Apr 27, 2026FDA approved a new use FDA approved an efficacy supplement for Enhertu (fam-trastuzumab deruxtecan-nxki), a new use or patient group (BLA 761139, supplement 39).17
  6. Dec 15, 2025FDA approved a new use FDA approved an efficacy supplement for Enhertu (fam-trastuzumab deruxtecan-nxki), a new use or patient group (BLA 761139, supplement 38).18
  7. Jun 23, 2025FDA approval FDA approved Datroway (datopotamab deruxtecan-dlnk), a new molecular entity, priority review (BLA 761464).19
  8. Mar 12, 2025Phase 3 trial completed Phase 3 trial of Trastuzumab Deruxtecan, Paclitaxel and others in Breast Neoplasms, run by AstraZeneca: primary completion Mar 12, 2025, results posted Jun 9, 2026 (ClinicalTrials.gov NCT05113251).20

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). Trials from ClinicalTrials.gov, as the sponsor registered them (expected dates are the sponsor's own and often move); approvals and advisory committee meetings from the FDA. The FDA does not publish its decision (PDUFA) dates. The full markets calendar

SEC filer profile

How Daiichi Sankyo is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARDaiichi Sankyo Company, LTD2
  • CIK0001340156
  • Incorporated inJapan2
  • Fiscal year endsMarch 312
  • Industry code (SIC)2834 Pharmaceutical Preparations2
  • Business address5-1, Nihonbashi 3-Chome, Chuo-Ku,, Tokyo, M0 103-84262
  • Phone(011) 81-3-5255-70412
  • On EDGAR sinceOct 3, 20052
  • Filings75 in all: 6-K (51), F-6EF (4), SC TO-C (3), SC TO-T/A (3), SC 13G (2), SC 13G/A (2), 15-15D (1), 15F-15D (1)2
    All 16 form types

    20-F (1), 3 (1), 4 (1), 8-K15D5 (1), CORRESP (1), EFFECT (1), F-6 (1), SC TO-T (1)

  • Latest filingsAnnual report (20-F) Sep 27, 2006

Sources

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