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Takeda

Total Trials
15
Recruiting
15
Phases
Phase 4, Phase 3, Phase 2, Phase 1, Phase 1, Phase 2

Takeda Pharmaceutical Company Limited is Japan's largest pharmaceutical company and one of the top ten global biopharmaceutical companies by revenue, with a significant and growing clinical trials presence following major acquisitions including Shire (2019) and ARIAD Pharmaceuticals (2017). Headquartered in Tokyo with its global R&D center in Cambridge, Massachusetts, Takeda's trial portfolio focuses on oncology/hematology, gastroenterology, neuroscience, rare diseases, and plasma-derived therapies.

In oncology, Takeda's most recognized asset is brigatinib (Alunbrig), an ALK inhibitor for ALK-positive non-small cell lung cancer, and ixazomib (Ninlaro), the first oral proteasome inhibitor approved for multiple myeloma. Through the ARIAD acquisition, Takeda gained ponatinib (Iclusig) for CML and ALL with the T315I mutation. The hematology/rare disease portfolio — substantially expanded by the Shire acquisition — includes treatments for hemophilia A and B, von Willebrand disease, hereditary angioedema, Fabry disease, and Gaucher disease, each supported by ongoing natural history studies, registry-based surveillance, and interventional trials.

Takeda's gastroenterology program includes vedolizumab (Entyvio), a gut-selective integrin inhibitor approved for Crohn's disease and ulcerative colitis, with active trials in primary sclerosing cholangitis and other GI inflammatory conditions. The neuroscience pipeline targets attention deficit hyperactivity disorder, major depressive disorder, and bipolar disorder. Takeda participates in the Innovative Medicines Initiative and other public-private partnerships for antimicrobial resistance, dengue, and norovirus vaccine development.

Frequently Asked Questions — Takeda

What rare blood disorders does Takeda research in clinical trials?
Takeda inherited one of the most comprehensive hemophilia and rare bleeding disorder portfolios in the world from the Shire acquisition. Active trial programs include: recombinant FVIII products for hemophilia A (including extended half-life formulations and subcutaneous delivery), FVIII gene therapy (in collaboration with Biomarin), factor replacement therapy for hemophilia B, subcutaneous fitusiran (an siRNA targeting antithrombin) for hemophilia A and B with and without inhibitors, and lanadelumab (Takhzyro) for hereditary angioedema prophylaxis. Takeda also conducts observational registries for rare enzyme deficiencies including Fabry and Gaucher disease to generate long-term real-world evidence.
What is vedolizumab and what GI conditions is Takeda testing it in?
Vedolizumab (Entyvio) is a humanized monoclonal antibody that selectively blocks the α4β7 integrin, a receptor that mediates lymphocyte homing to the gastrointestinal tract. By targeting gut-specific immune trafficking without systemic immunosuppression, vedolizumab offers a favorable safety profile compared to TNF inhibitors. It is approved for moderately to severely active Crohn's disease and ulcerative colitis in adults and children. Takeda is actively studying vedolizumab and next-generation gut-selective agents in primary sclerosing cholangitis (a rare bile duct disease complicating IBD), pouchitis following colectomy for UC, and eosinophilic esophagitis.
How does Takeda approach early-phase oncology trials?
Takeda runs an active early-phase oncology trial program centered at Dana-Farber Cancer Institute, MD Anderson Cancer Center, MSK, and other major academic centers globally. The program focuses on hematologic malignancies — including myeloma, AML, and ALL — where Takeda has established therapies and is seeking to optimize regimens and develop successors. In solid tumors, Takeda's ARIAD heritage continues with ponatinib combinations in CML and Ph+ ALL, and the company is exploring antibody-drug conjugates and KRAS-targeted agents in solid tumors. Phase 1 trials typically require patients to have exhausted standard options; enrollment is managed by each site's clinical trials office.

Clinical Trials by Takeda

NCT06562543 Phase 4
Recruiting

A Trial to Evaluate the Safety and Activity of Fruquintinib in Minority Populations With Advanced, Previously Treated Colorectal Cancer

Colorectal Cancer
NCT07286058 Phase 3
Recruiting

Continuation Study of Zasocitinib in Adults With Psoriatic Arthritis

Psoriatic Arthritis
NCT05037760 Phase 2
Recruiting

A Study of Elritercept Alone or Together With Ruxolitinib in Adults With Myelofibrosis

Myelofibrosis
NCT07422480 Phase 3
Recruiting

A Study to Compare Elritercept With Epoetin Alfa to Treat Anemia in Adults With Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes (MDS) Who Need Regular Blood Transfusions

Myelodysplastic Syndrome
NCT07229911 Phase 1
Recruiting

A Study of TAK-781 in Healthy Volunteers and in Participants With Non-Cirrhotic Primary Sclerosing Cholangitis (PSC)

Healthy Volunteers
NCT06577363
Recruiting

A Survey of Maribavir Tablets in Participants With Cytomegalovirus Infection

Cytomegalovirus (CMV)
NCT05879757
Recruiting

Real-world Usage of HyQvia in Multiple Myeloma Adults With Secondary Immunodeficiency

Multiple Myeloma
NCT07436728 Phase 1, Phase 2
Recruiting

A Study of TAK-505 in Adults With Solid Tumors

Malignant Solid Tumors
NCT05100069
Recruiting

Survey of Brigatinib Used To Treat People With Non-Small Cell Lung Cancer

Non-small Cell Lung Cancer (NSCLC)
NCT06565078
Recruiting

A Database Survey to Evaluate the Safety of Immune Globulin Subcutaneous (Human), 20% Solution in Participants With Primary Immunodeficiency

Primary Immunodeficiency Diseases (PID)
NCT06405087 Phase 3
Recruiting

A Long-Term Extension Study of Vedolizumab in Children and Teenagers With Ulcerative Colitis (UC) or Crohn's Disease (CD)

Ulcerative Colitis
NCT05156983 Phase 3
Recruiting

A Study of TAK-330 to Reverse the Effects of Factor Xa Inhibitors For Adults Needing Urgent Surgery

Coagulation Disorder
NCT05677971 Phase 3
Recruiting

Study to Check the Safety of Fazirsiran and Learn if Fazirsiran Can Help People With Liver Disease and Scarring (Fibrosis) Due to an Abnormal Version of Alpha-1 Antitrypsin Protein

Alpha1-Antitrypsin Deficiency
NCT06677892
Recruiting

A Study of Maribavir in Adults With Post-transplant Cytomegalovirus (CMV) Infection in Belgium

Cytomegalovirus (CMV)
NCT07129343 Phase 3
Recruiting

A Study of Recombinant Von Willebrand Factor (rVWF) in Chinese Participants With Von Willebrand Disease (vWD)

Von Willebrand Disease (VWD)
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