Merck KGaA / MilliporeSigma (CDMO)
Darmstadt, DE · St. Louis, MO
Hybrid — also manufactures internal programs
22 confirmed programs
· 11 sponsors
· Last scored 2026-03-15
73.0
Signal Score
○ FDA Inspections
✓ Clinical Trials (22)
○ SEC Filings
○ Press
Quick Facts: Merck KGaA / MilliporeSigma (CDMO)
- Signal Score
- 73.0/100 (as of 2026-03-15)
- Quality Compliance
- Assessment pending
- Headquarters
- Darmstadt, DE · St. Louis, MO
- Modalities
- mRNA, Biologics, Cell Therapy
- Active CGT Programs
- 22 confirmed from ClinicalTrials.gov across 11 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 InspectionsNo US records on file
No FDA inspection records found for this manufacturer
Quality score requires FDA inspection data
Operations
—
No ClinicalTrials.gov facility matches confirmed for this manufacturer.
Programs
22
Sponsors11
ModalitiesmRNA, Biologics, Cell Therapy
22 active programs across 11 sponsors
Modalities: Biologics, mRNA, Cell Therapy
16 programs in advanced phases (Phase 2/3)
Source: ClinicalTrials.gov facility matching
NCT04792073
Study of Avelumab and/or Radiation Therapy in People With...
PHASE2
Active Not Recruiting
View all 22 programs →
Source: ClinicalTrials.gov · Retrieved Mar 20, 2026
Financial Stability
83.0
Publicly traded — financial transparency
Source: SEC EDGAR, press monitoring
Subsidiary of Merck KGaA
SEC FilingsParent: Merck KGaA
Publicly traded — financial transparency
Capacity
63.0
3 CGT manufacturing sites
Sites: Darmstadt, Germany, St. Louis, MO, Carlsbad, CA
Source: SEC EDGAR, press monitoring, company profiles
3 CGT manufacturing sites
3 CGT manufacturing sites
Clinical Activity 22 studies
NCT06110195
Study of Xevinapant With Radiation and Chemotherapy for Patients With Head...
PHASE1
Active Not Recruiting
NCT04792073
Study of Avelumab and/or Radiation Therapy in People With Advanced Merkel...
PHASE2
Active Not Recruiting
NCT04052204
Avelumab With Bempegaldesleukin With or Without Talazoparib or Enzalutamide...
PHASE1/PHASE2
Terminated
NCT03737721
The UNSCARRed Study: UNresctable Squamous Cell Carcinoma Treated With...
PHASE2
Terminated
NCT03747419
Avelumab and Radiation in Muscle-Invasive Bladder Cancer
PHASE2
Terminated
NCT03409458
A Dose Escalation and Confirmation Study of PT-112 in Advanced Solid Tumors...
PHASE1/PHASE2
Completed
NCT03271372
Adjuvant Avelumab in Merkel Cell Cancer
PHASE3
Active Not Recruiting
NCT02968940
Avelumab With Hypofractionated Radiation Therapy in Adults With Isocitrate...
PHASE2
Completed
NCT02584829
Localized Radiation Therapy or Recombinant Interferon Beta and Avelumab With...
PHASE1/PHASE2
Terminated
NCT02083679
Sym004 in Subjects With Stage IV Non-small Cell Lung Cancer
PHASE1
Terminated
NCT01390818
Trial of MEK Inhibitor and PI3K/mTOR Inhibitor in Subjects With Locally...
PHASE1
Completed
NCT01040832
EMD 1201081 in Combination With Cetuximab in Second-Line Cetuximab-Naïve...
PHASE2
Completed
NCT00813943
Cilengitide, Temozolomide, and Radiation Therapy in Treating Patients With...
PHASE2
Completed
NCT00689221
Cilengitide, Temozolomide, and Radiation Therapy in Treating Patients With...
PHASE3
Completed
NCT00633529
Safety of Adding IMO-2055 to Erlotinib + Bevacizumab in 2nd Line Treatment...
PHASE1
Completed
NCT00111839
Effects of Matuzumab in Combination With Pemetrexed for the Treatment of...
PHASE2
Completed
NCT00132522
EMD 273066 in Patients With Recurrent EpCAM Positive Ovarian, Prostate,...
PHASE1
Completed
NCT01077960
Safety and Efficacy Study of Serostim® Human Immunodeficiency...
PHASE3
Completed
NCT00071240
Growth Hormone to Increase Immune Function in People With HIV
PHASE2
Completed
NCT00294918
An Efficacy and Safety Trial of Serostim® in the Maintenance of the...
PHASE2/PHASE3
Completed
+ 2 more studies
Source: ClinicalTrials.gov · Retrieved Mar 20, 2026
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