Takeda
Boston, MA · Zurich, CH
Hybrid — also manufactures internal programs
99 confirmed programs
· 26 sponsors
· Last scored 2026-03-15
61.5
Signal Score
✓ FDA Inspections (2)
✓ Clinical Trials (99)
○ SEC Filings
✓ Press (2)
Quick Facts: Takeda
- Signal Score
- 61.5/100 (as of 2026-03-15)
- Quality Compliance
- Assessment pending
- Headquarters
- Boston, MA · Zurich, CH
- Modalities
- AAV, Cell Therapy
- Active CGT Programs
- 99 confirmed from ClinicalTrials.gov across 26 sponsors
- Data Sources
- FDA Data Dashboard, ClinicalTrials.gov, SEC EDGAR, press monitoring
- Scored By
- CDMO Signal — independent CGT manufacturing intelligence platform
Signal Score & Pillar Breakdown
Quality Compliance
—
No FDA inspection records found. This CDMO may operate under a different legal name or may not have US FDA-inspected facilities.
FDA Inspections2 on record
Warning Letters0
Last InspectionVoluntary Action Indicated (VAI) (2025-11-12)
Operations
—
No ClinicalTrials.gov facility matches confirmed for this manufacturer.
Programs
99
Sponsors26
ModalitiesAAV, Cell Therapy
99 active programs across 26 sponsors
Modalities: Cell Therapy, AAV
66 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov facility matching
NCT07205718
A Study of TAK-188 in Adults With Advanced or Spreading Solid Tumors
PHASE1/PHASE2
Recruiting
View all 99 programs →
Source: ClinicalTrials.gov · Retrieved Mar 20, 2026
Financial Stability
60.0
Private company
Financial assessment: 60.0/100
Source: SEC EDGAR, press monitoring
Profile-based financial assessment
SEC FilingsPrivate company
Private company
Financial assessment: 60.0/100
Capacity
63.0
2 CGT manufacturing sites
Sites: Boston, MA, Zurich, CH
Source: SEC EDGAR, press monitoring, company profiles
2 CGT manufacturing sites
Recent Press2 articles
2 CGT manufacturing sites
FDA Inspection History
2025-11
2024-10
NAI
VAI
OAI
| Date | Site | Type | Observations | Classification |
|---|---|---|---|---|
| 2025-11-12 | Singen (Hohentwiel) | Drug Quality Assurance | No | Voluntary Action Indicated (VAI) |
| 2024-10-16 | Cambridge, Massachusetts | Bioresearch Monitoring | No | No Action Indicated (NAI) |
Source: FDA Data Dashboard · Retrieved Mar 20, 2026
Clinical Activity 99 studies
NCT07422480
A Study to Compare Elritercept With Epoetin Alfa to Treat Anemia in Adults...
PHASE3
Recruiting
NCT07224100
Dose-Adjusted EPOCH With or Without Rituximab Plus Ponatinib for the...
PHASE2
Recruiting
NCT06980480
A Study of Gammagard Liquid (Immune Globulin Infusion, 10%) to Prevent...
PHASE3
Recruiting
NCT07217301
IBI363 vs Docetaxel in Patients With Advanced Squamous Lung Cancer After...
PHASE3
Recruiting
NCT07205718
A Study of TAK-188 in Adults With Advanced or Spreading Solid Tumors
PHASE1/PHASE2
Recruiting
NCT06377228
A Study of TAK-007 in Adults With Refractory Lupus Nephritis (LN) or...
PHASE1
Withdrawn
NCT06588868
Systemic Therapies in the Treatment of Cutaneous T-cell Lymphoma
NA
Recruiting
NCT06677892
A Study of Maribavir in Adults With Post-transplant Cytomegalovirus (CMV)...
NA
Recruiting
NCT06615921
A Study of Maribavir in Adults With Post-transplant Cytomegalovirus (CMV) Infection
NA
Completed
NCT05952804
IVIG for Infection Prevention After CAR-T-Cell Therapy
PHASE2
Recruiting
NCT05718297
Brigatinib Post Definitive Chemo-radiotherapy in Patients with ALK-fusion...
PHASE2
Withdrawn
NCT05748197
A Study of ADCLEC.syn1 in People With Acute Myeloid Leukemia
PHASE1
Recruiting
NCT05886478
A Study in Adults With Cutaneous T-cell Lymphoma (CTCL) Retreated With...
NA
Completed
NCT05737849
A Study to Learn About the Tests Looking for a Gene Mutation in Adults With...
NA
Withdrawn
NCT05721950
A Study to Learn About Brigatinib Treatment Information Available in Chinese...
NA
Active Not Recruiting
NCT05319353
A Study to Evaluate the Safety and Tolerability, Pharmacokinetics, and...
PHASE3
Recruiting
NCT05886491
A Study of GDX012 in Adults With Relapsed or Refractory Acute Myeloid Leukemia
PHASE1/PHASE2
Active Not Recruiting
NCT05571137
A Study on Cytomegalovirus (CMV) Infection Outcomes Among Hematopoietic Stem...
NA
Completed
NCT05735327
A Study of Brigatinib as Preferred First Therapy for Adults With Non-Small...
NA
Recruiting
NCT05757700
Study of 19(T2)28z1xx TRAC-Chimeric Antigen Receptor (CAR) T Cells in People...
PHASE1
Active Not Recruiting
+ 79 more studies
Source: ClinicalTrials.gov · Retrieved Mar 20, 2026
Recent News 2 articles
Sandoz expands biosim collab with Samsung Bioepis, sets sights on Takeda's Entyvio - Fierce Pharma
Sandoz expands biosim collab with Samsung Bioepis, sets sights on Takeda's Entyvio Fierce Pharma
Cristália Laboratory prepares for a global leap with the drug that has enabled quadriplegics to walk - NeoFeed
Cristália Laboratory prepares for a global leap with the drug that has enabled quadriplegics to walk NeoFeed
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