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Taiho Pharmaceutical

Full company profile

uuid0004sx3

Namestring
Taiho Pharmaceutical
Legal namestring
Taiho Pharmaceutical Co., Ltd. (大鵬薬品工業株式会社)
Websiteurl
taiho.co.jp
Company typeenum
Private
Founded yearint
1963
Descriptiontext

Taiho Pharmaceutical Co., Ltd. (大鵬薬品工業株式会社) is a Japan-headquartered pharmaceutical company founded in 1963 and operating today as a wholly-owned subsidiary of Otsuka Holdings Co., Ltd. The company runs two principal business segments. The first is prescription pharmaceuticals, anchored in oncology with 84.4% of FY2025 sales coming from cancer-related products and approximately 70% of pipeline dedicated to oncology indications, including major commercial products such as the TS-1/Teysuno oral fluoropyrimidine combination, Lonsurf (trifluridine/tipiracil) for metastatic colorectal cancer, Abraxane (nab-paclitaxel) for pancreatic and breast cancer, and INQOVI for acute myeloid leukemia. The second is a consumer healthcare (OTC) segment distributing branded Japanese products such as Tiovita Drink (~140 million bottles sold annually in FY2025), Solmack, Harncare, Pitas, and Zenol through pharmacy, drug store, and retail channels nationwide.

Taiho's underlying technology rests on two proprietary drug discovery platforms. The first is Cysteinomics (シスタイノミクス創薬), a 10+ year internally developed platform that selectively forms covalent bonds with cysteine amino acids in target proteins, enabling drug development against historically undruggable targets; the platform has produced approved agents in Japan, the U.S., and Europe. The second is AraLinQ™, a next-generation antibody-drug conjugate (ADC) platform acquired via the March 2025 purchase of Araris Biotech AG (a $400 million upfront deal) that features site-specific conjugation, defined binding sites, favorable physicochemical properties and blood stability, and the ability to load multiple payload types — already producing ARC-02, a CD79b-targeting ADC that entered Phase 1 trials in April 2026. R&D activity is supported by two main drug discovery centers in Tsukuba (Japan) and Zurich (Switzerland).

Taiho monetizes through three revenue streams: prescription drug sales to medical institutions in Japan (sales-led, MR-promoted), OTC consumer healthcare sales through retail pharmacy and drug-store channels with disclosed retail pricing typically ¥1,000–¥5,000 per unit, and licensing / co-development royalties and milestone payments from international partners including Cullinan Oncology/Therapeutics, Merck (via Astex), Arcus Biosciences, and others. The group's geographic footprint spans 16 countries with 21 overseas locations and a 60.2% overseas-sales ratio in FY2025; corporate-venture activity is conducted through Taiho Ventures, LLC (the largest CVC fund size among Japanese pharma CVCs, est. 2016) and Taiho Innovations (domestic CVC, est. 2019). FY2025 consolidated sales were ¥243 billion (~$2.43 billion) with 2,918 group employees and an R&D-to-sales ratio of 32.9%.

Short descriptiontext

Taiho Pharmaceutical is a Tokyo-based, Otsuka Holdings-owned pharmaceutical company that develops and markets oncology prescription drugs (84.4% of FY2025 sales) and Japanese consumer healthcare brands via proprietary Cysteinomics covalent-chemistry and AraLinQ ADC drug discovery platforms, generating ¥243 billion in FY2025 revenue.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1,001–5,000
akta.pro rankint
HeadquartersTokyo, Japan
HQ citystring
Tokyo
HQ countrystring
Japan
HQ regionstring
Asia
Markets served

Serves global market

Offices15 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
oncology pharmaceuticals, cancer therapeutics, consumer healthcare products, drug discovery platforms, prescription medications
Industry1 code
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Biological Products, (No Disgnostic Substances)2836
Product category
Oncology Pharmaceuticals
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1Prescription Pharmaceutical Products
TypeOthers
Description

Medical-use prescription drugs sold primarily in Japan, including anticancer agents (TS-1, LonSurf, Abraxane, Jevtana), antiemetics (Aloxi, Akaliz), and specialty drugs. Revenue generated through prescription sales to medical institutions.

taiho.co.jp
2Consumer Healthcare (OTC) Products
TypeOthers
Description

Over-the-counter products including Tiovita Drink series (vitamin supplements), Solmack gastrointestinal products, Harncare urinary products, Pitas throat products, Zenol pain relief products, and other health supplements sold through retail pharmacies and drug stores.

taiho.co.jp
3Licensing and Co-development Royalties
TypeLicensing Royalties
Description

Revenue from licensing agreements, co-development partnerships, and milestone payments from international partners including Cullinan Oncology, Merck, and others for jointly developed oncology drugs.

biospace.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components6 values
Technology or R&D, Personnel, Operations, Supply Chain, Marketing or Sales, Infrastructure
Pricing details2 tiers
1Tiovita Drink series
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Tiovita Drink: Manufacturer suggested retail price varies by size (50mL, 100mL, etc.). Annual sales approximately 140 million bottles (FY2025).

taiho.co.jp
2Healthcare products (Solmack, Harncare, Pitas, Zenol)
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Various OTC products with retail prices ranging from approximately ¥1,000-5,000 depending on product and package size.

taiho.co.jp
GTM typeB2B and B2C
B2B and B2C
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1Taiho Ventures
Description

Strategic corporate venture capital arm of Taiho Pharmaceutical, established 2016, focusing on oncology biotech investments.

taiho.co.jp:443
+2 more records
Core offering1 text field

Taiho Pharmaceutical develops, manufactures, and commercializes prescription pharmaceutical products, with a primary focus on oncology drugs for cancer treatment, alongside a portfolio of consumer healthcare (OTC) products. The company operates proprietary drug discovery platforms, including the Cysteinomix platform for cancer metabolism and the AraLinQ ADC platform for antibody-drug conjugates, to advance its pipeline of small molecules and biologics across global markets.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Taiho Pharmaceutical operates two main business segments: Consumer Healthcare products (OTC medicines and health products) and Prescription Pharmaceuticals (primarily oncology-focused). Consumer Healthcare includes traditional medicines like Tiovita Drink (energy drink, ~140M bottles/year), Solmack (digestive liquid), Harncare (urinary issues), Pitas (throat troches), Zenol (topical analgesics), Bup-4 Lady (overactive bladder), and Efil (antibacterial spray). Prescription Pharmaceuticals focuses heavily on oncology with products like TS-1, Lonsurf, Abraxane, Yondelis, and pipeline candidates including Zipalertinib (EGFR inhibitor in FDA review), ARC-02 (ADC in Phase 1), and INQOVI. The company also operates advanced drug discovery platforms: Cysteinomix (coval binder technology with approved agents in JP/US/EU) and AraLinQ ADC technology (acquired 2025) for next-generation cancer therapies. R&D spending represents approximately 32.9% of sales with about 70% of pipeline in oncology.

Product and service1 record
1Lonsurf (trifluridine/tipiracil)
Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership10 partners
Strategic tierStrategicTypeTechnology or IntegrationAnnounced on2026-03-30
Description

Platform license agreement granting Taisho Pharmaceutical access to Biocytogen's proprietary RenNano® fully human heavy chain-only antibody discovery platform for internal R&D programs. Taisho will use RenNano® mice to generate and screen fully human HCAbs in vivo for antibody discovery research.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-01-07
Description

Merck's KANDLELIT clinical development program for calderasib (MK-1084) includes Taiho Pharmaceutical as collaborator. Phase 3 KANDLELIT-007 trial evaluating calderasib with KEYTRUDA in first-line KRAS G12C-mutant NSCLC. Collaboration originally established with Astex Pharmaceuticals.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-12-01
Description

Joint research agreement with JFCR and NEC Corporation to develop new cancer vaccines using whole-genome information. Initiative aims to identify shared neoantigens for creating personalized cancer vaccines and demonstrate their therapeutic efficacy.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2025-12-01
Description

Collaboration with JFCR and Taiho Pharmaceutical to develop cancer vaccines using whole-genome data and AI technology from NEC. Part of joint research agreement for neoantigen vaccine development.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-10-19
Description

Taiho exercised option for exclusive license to casdatifan (HIF-2α inhibitor) in Japan and certain territories in Asia based on 2017 agreement. Casdatifan is currently in Phase 3 trial for kidney cancer, with Japan participation expected in 2026. Exercise includes payments and potential royalties.

Strategic tierStrategicTypeTechnology or IntegrationAnnounced on2025-06-04
Description

Technical verification collaboration using SyntheticGestalt's SG4D10B molecular foundation AI model (world's largest molecule-specialized foundation model trained on 10 billion compound data points) to enhance Taiho's cysteinomics drug discovery platform. Aims to improve prediction accuracy for covalent drugs targeting historically undruggable proteins.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-03-01
Description

Taiho Pharmaceutical acquired Araris Biotech AG in March 2025 to strengthen biologics and ADC research and development capabilities. Gained access to AraLinQ™ ADC technology platform for next-generation antibody-drug conjugate development. ARC-02 Phase 1 trial initiated based on this technology.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-05-12
Description

Agreement for Taiho to acquire Cullinan Pearl and co-develop Cullinan's EGFR inhibitor CLN-081/TAS6417 (zipalertinib) for NSCLC treatment. Deal included $275 million upfront payment with milestone payments and profit-sharing arrangements. Zipalertinib NDA accepted by FDA in April 2026.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2020-01-01
Description

Collaborative research partnership established 2020 for comprehensive drug discovery research targeting difficult-to-treat cancers. Particularly focused on brain tumors and brain metastases using Taiho's brain-penetrating compound discovery platform combined with MD Anderson's external research expertise.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2020-01-01
Description

Strategic collaboration in oncology established in 2020 involving Taiho Pharmaceutical, Astex Pharmaceuticals, and Merck & Co. for oncology drug discovery and development.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Japanese pharmaceutical company with leading oncology franchise including the DXd antibody-drug conjugate platform (Enhertu, Datroway). Direct comparable in Japanese oncology pharma with overlapping ADC and targeted oncology development priorities.

TypeDirect peer
Description

Major Japanese oncology-focused pharmaceutical company (Roche subsidiary), with strong franchise in solid tumors and hematologic cancers. Highly comparable therapeutic focus and Japanese market footprint.

TypeDirect peer
Description

Japanese pharmaceutical company with concentrated oncology franchise (Xtandi, Vyloy, Padcev via Pfizer partnership). Comparable in shifting toward specialty/oncology focus and global development footprint.

TypeDirect peer
Description

Japanese pharmaceutical company with oncology franchise including Opdivo (co-developed with BMS) and pipeline in solid tumors. Comparable mid-size Japanese oncology-focused pharma peer.

TypeDirect peer
Description

Japanese pharmaceutical company with oncology portfolio (Lenvima) plus neurology/PAD areas. Comparable Japanese specialty pharma with overlapping oncology priorities and global commercial footprint.

TypeBroad incumbent
Description

Japan's largest pharmaceutical company with oncology alongside GI, rare diseases, and neuroscience. A larger, more diversified incumbent covering the same Japanese-pharma oncology category with broader portfolio.

TypeBroad incumbent
Description

Global biopharmaceutical leader with extensive oncology franchise (Tagrisso, Imfinzi, Enhertu in partnership with Daiichi Sankyo). Co-promotion and clinical collaboration partner context for KRAS/EGFR targeted therapy development.

TypeBroad incumbent
Description

Global biopharmaceutical company with major oncology portfolio including checkpoint inhibitors and ADCs (Opdivo partnership with Ono). Broader incumbent with overlapping oncology priorities.

TypeBroad incumbent
Description

Active oncology drug discovery collaborator with Taiho via Astex Pharmaceuticals on KRAS G12C program (calderasib/KANDLELIT-007 with Keytruda). Comparable in oncology pipeline and ADC/biologics interest.

TypeRegional player
Description

Japanese specialty pharmaceutical company focused on oncology, immunology, and rare diseases. Operates primarily in Japan/APAC comparable geographies with similar specialty-pharma positioning.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat6 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment2 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI capability8 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature2 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries9 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance1 record

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A2 records

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment3 records

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Taiho Pharmaceutical

Oncology Pharmaceuticalstaiho.co.jp

Taiho Pharmaceutical is a Tokyo-based, Otsuka Holdings-owned pharmaceutical company that develops and markets oncology prescription drugs (84.4% of FY2025 sales) and Japanese consumer healthcare brands via proprietary Cysteinomics covalent-chemistry and AraLinQ ADC drug discovery platforms, generating ¥243 billion in FY2025 revenue.

What Taiho Pharmaceutical does

Taiho Pharmaceutical Co., Ltd. (大鵬薬品工業株式会社) is a Japan-headquartered pharmaceutical company founded in 1963 and operating today as a wholly-owned subsidiary of Otsuka Holdings Co., Ltd. The company runs two principal business segments. The first is prescription pharmaceuticals, anchored in oncology with 84.4% of FY2025 sales coming from cancer-related products and approximately 70% of pipeline dedicated to oncology indications, including major commercial products such as the TS-1/Teysuno oral fluoropyrimidine combination, Lonsurf (trifluridine/tipiracil) for metastatic colorectal cancer, Abraxane (nab-paclitaxel) for pancreatic and breast cancer, and INQOVI for acute myeloid leukemia. The second is a consumer healthcare (OTC) segment distributing branded Japanese products such as Tiovita Drink (~140 million bottles sold annually in FY2025), Solmack, Harncare, Pitas, and Zenol through pharmacy, drug store, and retail channels nationwide.

Taiho's underlying technology rests on two proprietary drug discovery platforms. The first is Cysteinomics (シスタイノミクス創薬), a 10+ year internally developed platform that selectively forms covalent bonds with cysteine amino acids in target proteins, enabling drug development against historically undruggable targets; the platform has produced approved agents in Japan, the U.S., and Europe. The second is AraLinQ™, a next-generation antibody-drug conjugate (ADC) platform acquired via the March 2025 purchase of Araris Biotech AG (a $400 million upfront deal) that features site-specific conjugation, defined binding sites, favorable physicochemical properties and blood stability, and the ability to load multiple payload types — already producing ARC-02, a CD79b-targeting ADC that entered Phase 1 trials in April 2026. R&D activity is supported by two main drug discovery centers in Tsukuba (Japan) and Zurich (Switzerland).

Taiho monetizes through three revenue streams: prescription drug sales to medical institutions in Japan (sales-led, MR-promoted), OTC consumer healthcare sales through retail pharmacy and drug-store channels with disclosed retail pricing typically ¥1,000–¥5,000 per unit, and licensing / co-development royalties and milestone payments from international partners including Cullinan Oncology/Therapeutics, Merck (via Astex), Arcus Biosciences, and others. The group's geographic footprint spans 16 countries with 21 overseas locations and a 60.2% overseas-sales ratio in FY2025; corporate-venture activity is conducted through Taiho Ventures, LLC (the largest CVC fund size among Japanese pharma CVCs, est. 2016) and Taiho Innovations (domestic CVC, est. 2019). FY2025 consolidated sales were ¥243 billion (~$2.43 billion) with 2,918 group employees and an R&D-to-sales ratio of 32.9%.

Taiho Pharmaceutical firmographics

Firmographics
Name
Taiho Pharmaceutical
Legal name
Taiho Pharmaceutical Co., Ltd. (大鵬薬品工業株式会社)
Website
https://taiho.co.jp
Company type
Private
Founded year
1963
Operating status
Operating
Headcount range
1,001–5,000 employees
Short description
Taiho Pharmaceutical is a Tokyo-based, Otsuka Holdings-owned pharmaceutical company that develops and markets oncology prescription drugs (84.4% of FY2025 sales) and Japanese consumer healthcare brands via proprietary Cysteinomics covalent-chemistry and AraLinQ ADC drug discovery platforms, generating ¥243 billion in FY2025 revenue.
Ownership category
akta.pro rank

Taiho Pharmaceutical industry classification

Industry
Product category
Oncology Pharmaceuticals
NAICS
Pharmaceutical Preparation Manufacturing (325412), Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834), Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)

Keywords

  • Oncology pharmaceuticals
  • Cancer therapeutics
  • Consumer healthcare products
  • Drug discovery platforms
  • Prescription medications

Where Taiho Pharmaceutical is headquartered

Location

Headquarters

HQ city
Tokyo
HQ country
Japan
HQ region
Asia

Offices15 records

Markets served

Taiho Pharmaceutical business model

Business model
GTM type
B2B and B2C
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Personnel, Operations, Supply Chain, Marketing or Sales, Infrastructure

Revenue model

  1. Prescription Pharmaceutical Products: Medical-use prescription drugs sold primarily in Japan, including anticancer agents (TS-1, LonSurf, Abraxane, Jevtana), antiemetics (Aloxi, Akaliz), and specialty drugs. Revenue generated through prescription sales to medical institutions.
  2. Consumer Healthcare (OTC) Products: Over-the-counter products including Tiovita Drink series (vitamin supplements), Solmack gastrointestinal products, Harncare urinary products, Pitas throat products, Zenol pain relief products, and other health supplements sold through retail pharmacies and drug stores.
  3. Licensing and Co-development Royalties: Revenue from licensing agreements, co-development partnerships, and milestone payments from international partners including Cullinan Oncology, Merck, and others for jointly developed oncology drugs.

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goTiovita Drink series
Unit PricingPay-as-you-goHealthcare products (Solmack, Harncare, Pitas, Zenol)

Go-to-market motion2 records

Distribution channels3 records

Marketing channels5 records

Taiho Pharmaceutical product offering

Product offering

Core offering

Taiho Pharmaceutical develops, manufactures, and commercializes prescription pharmaceutical products, with a primary focus on oncology drugs for cancer treatment, alongside a portfolio of consumer healthcare (OTC) products. The company operates proprietary drug discovery platforms, including the Cysteinomix platform for cancer metabolism and the AraLinQ ADC platform for antibody-drug conjugates, to advance its pipeline of small molecules and biologics across global markets.

Product overview

Taiho Pharmaceutical operates two main business segments: Consumer Healthcare products (OTC medicines and health products) and Prescription Pharmaceuticals (primarily oncology-focused). Consumer Healthcare includes traditional medicines like Tiovita Drink (energy drink, ~140M bottles/year), Solmack (digestive liquid), Harncare (urinary issues), Pitas (throat troches), Zenol (topical analgesics), Bup-4 Lady (overactive bladder), and Efil (antibacterial spray). Prescription Pharmaceuticals focuses heavily on oncology with products like TS-1, Lonsurf, Abraxane, Yondelis, and pipeline candidates including Zipalertinib (EGFR inhibitor in FDA review), ARC-02 (ADC in Phase 1), and INQOVI. The company also operates advanced drug discovery platforms: Cysteinomix (coval binder technology with approved agents in JP/US/EU) and AraLinQ ADC technology (acquired 2025) for next-generation cancer therapies. R&D spending represents approximately 32.9% of sales with about 70% of pipeline in oncology.

Differentiator

Problem solved

Functional benefit

Brands

  • Taiho Ventures: Strategic corporate venture capital arm of Taiho Pharmaceutical, established 2016, focusing on oncology biotech investments.
  • Taiho Innovations
  • Cysteinomix

Products and services

  • Lonsurf (trifluridine/tipiracil)

Companies that use Taiho Pharmaceutical

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles2 records

Taiho Pharmaceutical technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

AI capability8 records

Feature2 records

Taiho Pharmaceutical partnerships and signals

Strategic signal

Partnerships

Ten partnerships are on record, tiered strategic and core.

  • BiocytogenstrategicTechnology or Integration · 30 March 2026Platform license agreement granting Taisho Pharmaceutical access to Biocytogen's proprietary RenNano® fully human heavy chain-only antibody discovery platform for internal R&D programs. Taisho will use RenNano® mice to generate and screen fully human HCAbs in vivo for antibody discovery research.
  • Merck & Co. (development partner)coreStrategic or Co-development Partner · 7 January 2026Merck's KANDLELIT clinical development program for calderasib (MK-1084) includes Taiho Pharmaceutical as collaborator. Phase 3 KANDLELIT-007 trial evaluating calderasib with KEYTRUDA in first-line KRAS G12C-mutant NSCLC. Collaboration originally established with Astex Pharmaceuticals.
  • Japanese Foundation for Cancer Research (JFCR)coreStrategic or Co-development Partner · 1 December 2025Joint research agreement with JFCR and NEC Corporation to develop new cancer vaccines using whole-genome information. Initiative aims to identify shared neoantigens for creating personalized cancer vaccines and demonstrate their therapeutic efficacy.
  • NEC CorporationcoreTechnology or Integration · 1 December 2025Collaboration with JFCR and Taiho Pharmaceutical to develop cancer vaccines using whole-genome data and AI technology from NEC. Part of joint research agreement for neoantigen vaccine development.
  • Arcus BiosciencescoreStrategic or Co-development Partner · 19 October 2025Taiho exercised option for exclusive license to casdatifan (HIF-2α inhibitor) in Japan and certain territories in Asia based on 2017 agreement. Casdatifan is currently in Phase 3 trial for kidney cancer, with Japan participation expected in 2026. Exercise includes payments and potential royalties.
  • SyntheticGestaltstrategicTechnology or Integration · 4 June 2025Technical verification collaboration using SyntheticGestalt's SG4D10B molecular foundation AI model (world's largest molecule-specialized foundation model trained on 10 billion compound data points) to enhance Taiho's cysteinomics drug discovery platform. Aims to improve prediction accuracy for covalent drugs targeting historically undruggable proteins.
  • Araris Biotech AGcoreStrategic or Co-development Partner · 1 March 2025Taiho Pharmaceutical acquired Araris Biotech AG in March 2025 to strengthen biologics and ADC research and development capabilities. Gained access to AraLinQ™ ADC technology platform for next-generation antibody-drug conjugate development. ARC-02 Phase 1 trial initiated based on this technology.
  • Cullinan Oncology / Cullinan PearlcoreStrategic or Co-development Partner · 12 May 2022Agreement for Taiho to acquire Cullinan Pearl and co-develop Cullinan's EGFR inhibitor CLN-081/TAS6417 (zipalertinib) for NSCLC treatment. Deal included $275 million upfront payment with milestone payments and profit-sharing arrangements. Zipalertinib NDA accepted by FDA in April 2026.
  • University of Texas MD Anderson Cancer CenterstrategicStrategic or Co-development Partner · 1 January 2020Collaborative research partnership established 2020 for comprehensive drug discovery research targeting difficult-to-treat cancers. Particularly focused on brain tumors and brain metastases using Taiho's brain-penetrating compound discovery platform combined with MD Anderson's external research expertise.
  • Astex Pharmaceuticals / Merck & Co.coreStrategic or Co-development Partner · 1 January 2020Strategic collaboration in oncology established in 2020 involving Taiho Pharmaceutical, Astex Pharmaceuticals, and Merck & Co. for oncology drug discovery and development.

Scale indicators9 records

Recent moves8 records

Expansion highlights6 records

Taiho Pharmaceutical competitors and assessment

Company assessment

Direct peers

  • Daiichi Sankyo: Japanese pharmaceutical company with leading oncology franchise including the DXd antibody-drug conjugate platform (Enhertu, Datroway). Direct comparable in Japanese oncology pharma with overlapping ADC and targeted oncology development priorities.
  • Chugai Pharmaceutical: Major Japanese oncology-focused pharmaceutical company (Roche subsidiary), with strong franchise in solid tumors and hematologic cancers. Highly comparable therapeutic focus and Japanese market footprint.
  • Astellas Pharma: Japanese pharmaceutical company with concentrated oncology franchise (Xtandi, Vyloy, Padcev via Pfizer partnership). Comparable in shifting toward specialty/oncology focus and global development footprint.
  • Ono Pharmaceutical: Japanese pharmaceutical company with oncology franchise including Opdivo (co-developed with BMS) and pipeline in solid tumors. Comparable mid-size Japanese oncology-focused pharma peer.
  • Eisai Co., Ltd. Japanese pharmaceutical company with oncology portfolio (Lenvima) plus neurology/PAD areas. Comparable Japanese specialty pharma with overlapping oncology priorities and global commercial footprint.

Broad incumbents

  • Takeda Pharmaceutical: Japan's largest pharmaceutical company with oncology alongside GI, rare diseases, and neuroscience. A larger, more diversified incumbent covering the same Japanese-pharma oncology category with broader portfolio.
  • AstraZeneca: Global biopharmaceutical leader with extensive oncology franchise (Tagrisso, Imfinzi, Enhertu in partnership with Daiichi Sankyo). Co-promotion and clinical collaboration partner context for KRAS/EGFR targeted therapy development.
  • Bristol-Myers Squibb: Global biopharmaceutical company with major oncology portfolio including checkpoint inhibitors and ADCs (Opdivo partnership with Ono). Broader incumbent with overlapping oncology priorities.
  • Merck & Co. Active oncology drug discovery collaborator with Taiho via Astex Pharmaceuticals on KRAS G12C program (calderasib/KANDLELIT-007 with Keytruda). Comparable in oncology pipeline and ADC/biologics interest.

Regional players

  • Kyowa Kirin: Japanese specialty pharmaceutical company focused on oncology, immunology, and rare diseases. Operates primarily in Japan/APAC comparable geographies with similar specialty-pharma positioning.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat6 records

Key risks6 records

Key highlights7 records

Customer concentration

Taiho Pharmaceutical social profiles

Digital presence

Taiho Pharmaceutical compliance and trust

Trust signal

Compliance1 record

Taiho Pharmaceutical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Taiho Pharmaceutical leadership team

Management profile

Number of profiles

Profiles3 records

Taiho Pharmaceutical subsidiaries and ownership

Company hierarchy

Subsidiaries9 records

Taiho Pharmaceutical funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Taiho Pharmaceutical M&A and investment

M&A and investment

M&A2 records

Investments3 records

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Taiho Pharmaceutical

What does Taiho Pharmaceutical do?

Taiho Pharmaceutical develops, manufactures, and commercializes prescription pharmaceutical products, with a primary focus on oncology drugs for cancer treatment, alongside a portfolio of consumer healthcare (OTC) products. The company operates proprietary drug discovery platforms, including the Cysteinomix platform for cancer metabolism and the AraLinQ ADC platform for antibody-drug conjugates, to advance its pipeline of small molecules and biologics across global markets.

Is Taiho Pharmaceutical a public or private company?

Taiho Pharmaceutical is a private company. It is classified as corporate owned and is currently operating.

When was Taiho Pharmaceutical founded?

Taiho Pharmaceutical was founded in 1963. It employs 1,001 to 5,000 people.

Where is Taiho Pharmaceutical based?

Taiho Pharmaceutical is headquartered in Tokyo, Japan, in the Asia region.

How does Taiho Pharmaceutical make money?

Three revenue lines are on record. Prescription Pharmaceutical Products are the primary driver. The others are consumer Healthcare (OTC) Products and licensing and Co-development Royalties.

Who are Taiho Pharmaceutical's main competitors?

Direct peers on record are Daiichi Sankyo, Chugai Pharmaceutical, Astellas Pharma, Ono Pharmaceutical and Eisai Co., Ltd.. Broad incumbents are Takeda Pharmaceutical, AstraZeneca, Bristol-Myers Squibb and Merck & Co.. Kyowa Kirin is listed as a regional player.

Does Taiho Pharmaceutical have an API?

No public API is recorded for Taiho Pharmaceutical.

What industry is Taiho Pharmaceutical in?

Taiho Pharmaceutical's product category is Oncology Pharmaceuticals. Its primary akta.pro industry code is HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering). Its NAICS code is 325412 and its SIC code is 2834.

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The future of tradingled quantum cancer immunotherapy project wins NEDO demonstration program slotNEC joined Taiho Pharmaceutical, JFCR, AIST, and Waseda University in a NEDO-backed quantum computing cancer immunotherapy demonstration program. The project targets neoantigen design to boost CD4-positive T-cell responses via MHC class II, using quantum computing with AI-driven scoring. Work runs from September 2026 to March 2029, using AIST's ABCI-Q platform.European BiotechnologyThe Strüngmann legacy, passed onThe Strüngmann family office launched the Strüngmann Award to recognize European biotech entrepreneurs, with a €100,000 prize. The 2026 winner is Jonathan Talbot of Mosanna and Melodia Therapeutics. The award will expand beyond Germany, Austria, and Switzerland to include more of Europe.Clinical Trials ArenaTaiho, Cullinan report improved PFS in Phase III NSCLC trialTaiho, Cullinan, and Taiho Oncology reported Phase III REZILIENT3 trial results showing zipalertinib plus chemotherapy improved progression-free survival in EGFR exon 20 insertion NSCLC. Median PFS was 14.5 months versus 8.5 months with chemo alone, and objective response rates were 65% versus 40.3%. Interim overall survival analysis showed a hazard ratio of 0.72.FinancialContent Business PageArticles from Taiho Oncology, Inc. and Taiho Pharmaceutical Co., Ltd. and Cullinan Therapeutics, Inc.Taiho Oncology, Taiho Pharmaceutical, and Cullinan Therapeutics presented Phase 3 REZILIENT3 trial results at the IASLC 2026 World Conference on Lung Cancer in Seoul. The trial evaluated zipalertinib plus chemotherapy versus chemotherapy alone in first-line treatment of EGFR exon 20 insertion mutation-positive non-small cell lung cancer.AInvestThe Exon 20 Trial Already Passed. The September Show Is About Magnitude — and Who Gets PaidCullinan Therapeutics will present zipalertinib lung-cancer trial data on September 14, after the Phase 3 REZILIENT3 trial met its primary endpoint in August. The muted stock reaction reflects market anticipation, with magnitude of benefit now critical for commercial viability against Johnson & Johnson's Rybrevant. Cullinan shares 50% U.S. profits with Taiho, limiting upside despite $356M cash reserves.FierceBiotechCullinan tees up J&J fight—and $100M payday—as Taiho-partnered drug hits phase 3 cancer goalTaiho Pharmaceutical and Cullinan Therapeutics reported a positive phase 3 trial result for their combination therapy of zipalertinib and chemotherapy in treating NSCLC patients with EGFR exon 20 insertion mutations. This success positions the partners to seek FDA approval for first-line use, potentially triggering up to $100 million in payments from Taiho to Cullinan. The drug will enter a competitive market currently dominated by Johnson & Johnson's Rybrevant, with additional competition expected from AstraZeneca's recently acquired Zegfrovy.GurufocusZipalertinib Plus Chemotherapy Meets Primary Endpoint of ProgresTaiho Oncology, Inc., Taiho Pharmaceutical Co., Ltd., and Cullinan Therapeutics, Inc. announced that their REZILIENT3 trial met its primary endpoint of progression-free survival for the combination of zipalertinib and chemotherapy in first-line treatment for non-small cell lung cancer patients. The trial demonstrated a statistically significant improvement in progression-free survival, and the companies plan to pursue U.S. regulatory approval based on these results. Full trial results are expected to be presented at an upcoming international medical conference.Investing.comZipalertinib trial meets primary endpoint in lung cancer study By Investing.comTaiho Oncology, Taiho Pharmaceutical, and Cullinan Therapeutics announced that the Phase 3 REZILIENT3 trial for zipalertinib met its primary endpoint of progression-free survival in patients with EGFR exon 20 insertion mutations. The study demonstrated a statistically significant improvement in progression-free survival compared to chemotherapy alone, prompting the Independent Data Monitoring Committee to recommend unblinding the study. The companies plan to pursue U.S. regulatory approval for the combination regimen following discussions with the FDA.FinancialContent Business PageZipalertinib Plus Chemotherapy Meets Primary Endpoint of Progression-Free Survival in Planned Interim Analysis of Phase 3 REZILIENT3 Trial in First-Line EGFR Exon 20 Insertion Mutation Non-Small CellTaiho Oncology, Taiho Pharmaceutical, and Cullinan Therapeutics announced that the Phase 3 REZILIENT3 trial met its primary endpoint of progression-free survival for zipalertinib combined with chemotherapy in treating EGFR exon 20 insertion mutation non-small cell lung cancer. The combination demonstrated a statistically significant and clinically meaningful improvement in progression-free survival compared to chemotherapy alone, with manageable safety results. The companies plan to pursue U.S. regulatory approval for this regimen following discussions with the FDA.Stock TitanCullinan Phase 3 Trial Meets PFS Endpoint in EGFR NSCLCTaiho Oncology, Taiho Pharmaceutical, and Cullinan Therapeutics announced that the Phase 3 REZILIENT3 trial met its primary endpoint of progression-free survival for zipalertinib combined with chemotherapy in treating EGFR exon 20 insertion non-small cell lung cancer. The Independent Data Monitoring Committee recommended unblinding the study due to these statistically significant results, with safety profiles deemed manageable. The companies plan to pursue U.S. regulatory approval for this combination regimen following discussions with the FDA.