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Takeda Pharmaceutical Company Ltd

🇯🇵Japan
Ownership
-
Established
1925-01-01
Employees
-
Market Cap
$47.5B
Website
http://www.takeda.co.jp/

Clinical Trials

1.3k

Active:51
Completed:775

Trial Phases

5 Phases

Phase 1:244
Phase 2:187
Phase 3:393
+2 more phases

Drug Approvals

6

SFDA:6

Drug Approvals

INSTIGAR 30 mg Delayed-Release Capsule

Approval Date
Jul 18, 2025
SFDA

XEFO 8MG TAB

Approval Date
Jul 18, 2025
SFDA

ACTOSMET 15/850 mg tablet

Approval Date
Jul 18, 2025
SFDA

LUPRON DEPOT 3.75MG-VIAL

Approval Date
Jul 18, 2025
SFDA

DUETACT 30/2 mg tablet

Approval Date
Jul 18, 2025
SFDA

INSTIGAR 60 mg Delayed-Release Capsule

Approval Date
Jul 18, 2025
SFDA

Clinical Trials

Distribution across different clinical trial phases (1018 trials with phase data)• Click on a phase to view related trials

Phase 3
393 (38.6%)
Phase 1
244 (24.0%)
Phase 2
187 (18.4%)
Not Applicable
97 (9.5%)
Phase 4
90 (8.8%)
phase_1_2
5 (0.5%)
phase_2_3
2 (0.2%)

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

Not Applicable
Not yet recruiting
Conditions
Healthy Volunteers
Primary Sclerosing Cholangitis
Interventions
Drug: TAK-781
Drug: Placebo
First Posted Date
2025-11-17
Last Posted Date
2025-11-17
Lead Sponsor
Takeda
Target Recruit Count
134
Registration Number
NCT07229911
Locations
🇺🇸

ICON, Salt Lake City, Utah, United States

A Study About the Diagnosis and Management of Hereditary Angioedema (HAE) in Egypt

Not yet recruiting
Conditions
Hereditary Angioedema (HAE)
First Posted Date
2025-10-20
Last Posted Date
2025-10-20
Lead Sponsor
Takeda
Target Recruit Count
100
Registration Number
NCT07218393
Locations
🇪🇬

Mansoura university hospital, Al Mansurah, Egypt

🇪🇬

Alexandria university_Clinical Research Center, Alexandria, Egypt

🇪🇬

Ain shams university hospital_Pediatrics, Cairo, Egypt

and more 4 locations

A Study of TAK-188 in Adults With Advanced or Spreading Solid Tumors

Not Applicable
Not yet recruiting
Conditions
Advanced or Metastatic Solid Tumors
Interventions
Drug: TAK-188
First Posted Date
2025-10-03
Last Posted Date
2025-10-24
Lead Sponsor
Takeda
Target Recruit Count
223
Registration Number
NCT07205718
Locations
🇺🇸

UCLA Health-Santa Monica Cancer Care (Cancer Care - Santa Monica), Santa Monica, California, United States

🇺🇸

Yale School of Medicine - Smilow Cancer Hospital - Center for Thoracic Cancers, New Haven, Connecticut, United States

🇺🇸

Florida Cancer Specialists - Lake Nona, Orlando, Florida, United States

and more 12 locations

A Study of Vortioxetine in Japanese Pediatric Patients With Major Depressive Disorder

Not Applicable
Recruiting
Conditions
Major Depressive Disorder
Interventions
Drug: Placebo tablets
First Posted Date
2025-10-02
Last Posted Date
2025-11-17
Lead Sponsor
Takeda
Target Recruit Count
180
Registration Number
NCT07204314
Locations
🇯🇵

Kaku Mental Clinic, Chūōku, Fukuoka, Japan

🇯🇵

Shikoku Medical Center for Children and Adults, Zentsujichó, Kagawa-ken, Japan

🇯🇵

Yokohama City University Hospital, Kanazawachō, Kanagawa, Japan

and more 17 locations

A Study of Agalsidase Alfa Enyzme Replacement Therapy in Chinese Children and Adults With Fabry Disease

Not yet recruiting
Conditions
Fabry Disease
First Posted Date
2025-09-23
Last Posted Date
2025-09-23
Lead Sponsor
Takeda
Target Recruit Count
200
Registration Number
NCT07187440
Locations
🇨🇳

Peking University First Hospital, Beijing, China

🇨🇳

Peking University Third Hospital, Beijing, China

🇨🇳

Peking Union Medical College Hospital, Beijing, China

and more 15 locations
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News

Beacon Biosignals Secures $86M Series B to Advance AI-Driven Brain Health Diagnostics

Beacon Biosignals raised an oversubscribed $86 million Series B funding round to build the world's largest neurodiagnostic dataset and advance AI-driven biomarkers for brain health.

XOMA Royalty Reports Strong Q3 2025 Results with Multiple Strategic Acquisitions and Key Pipeline Milestones

XOMA Royalty Corporation reported robust financial performance in Q3 2025, receiving $43.9 million in royalties and milestones from partners in the first nine months of 2025, including $14.3 million in Q3 royalties.

Takeda's Mezagitamab Shows Sustained Kidney Protection 18 Months After Treatment in IgA Nephropathy

Takeda's Phase 1b study demonstrates that mezagitamab (TAK-079) maintains stable kidney function in IgA nephropathy patients through Week 96, 18 months after the last dose.

Accipiter Biosciences Emerges with $12.7M Seed Funding to Develop AI-Designed De Novo Protein Therapeutics

Accipiter Biosciences has emerged from stealth with $12.7 million in seed financing co-led by Takeda and Flying Fish Partners to develop de novo multifunctional biologics for complex diseases.

VOQUEZNA Shows Rapid Relief of Nighttime GERD Symptoms in Phase 3 Trial

VOQUEZNA (vonoprazan) demonstrated significant improvement in nocturnal GERD symptoms in patients with Non-Erosive Reflux Disease, with 59.9% and 56.4% heartburn-free nights for 10mg and 20mg doses respectively versus 43.3% for placebo.

Abeona Therapeutics Appoints Gene Therapy Expert James Gow as Senior VP of Clinical Development

Abeona Therapeutics has appointed James A. Gow, MD, MBA, MS, MHCM, as Senior Vice President, Head of Clinical Development & Medical Affairs, effective immediately.

Halozyme Acquires Elektrofi for $750M to Expand Ultra-High Concentration Drug Delivery Technology

Halozyme Therapeutics has agreed to acquire Elektrofi for $750 million upfront plus up to $150 million in milestone payments, gaining access to breakthrough Hypercon microparticle technology.

Ultragenyx Appoints Eric Olson as Chief Business Officer to Lead Rare Disease Pipeline Expansion

Ultragenyx Pharmaceutical appointed Eric Olson as Chief Business Officer and Executive Vice President effective September 22, 2025, following Thomas Kassberg's planned retirement after 14 years with the company.

Crystalys Therapeutics Emerges with $205M Series A to Advance Gout Treatment Dotinurad

Crystalys Therapeutics launched with $205 million in Series A funding to develop dotinurad, a URAT1 blocker for gout treatment that is already approved in Japan, China, Philippines, and Thailand.

Star Therapeutics Secures $125M Series D to Advance Von Willebrand Disease Drug VGA039 Through Phase 3 Testing

Star Therapeutics raised $125 million in Series D funding co-led by Sanofi Ventures and Viking Global Investors to advance its Von Willebrand disease drug VGA039 through late-stage clinical testing.

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