Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 50/100

Failure Rate

9.1%

1 terminated/withdrawn out of 11 trials

Success Rate

83.3%

-3.2% vs industry average

Late-Stage Pipeline

18%

2 trials in Phase 3/4

Results Transparency

20%

1 of 5 completed trials have results

Key Signals

2 recruiting1 with results

Enrollment Performance

Analytics

Phase 1
6(54.5%)
Phase 2
3(27.3%)
Phase 3
2(18.2%)
11Total
Phase 1(6)
Phase 2(3)
Phase 3(2)

Activity Timeline

Global Presence

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Clinical Trials (11)

Showing 11 of 11 trials
NCT06472245Phase 3Recruiting

Trial of Therapeutic Cancer Vaccine OSE2101 in Patients With Non-Small Cell Lung Cancer and Secondary Resistance to Immune Checkpoint Inhibitor

Role: lead

NCT05751798Phase 1Recruiting

Dose-finding and Dose Expansion Study of OSE-279 in Subjects With Advanced Solid Tumors or Lymphomas

Role: lead

NCT04837092Phase 1Completed

Phase I/II Study of FR104 First Administration In Patient With Renal Transplantation: FIRsT Study

Role: collaborator

NCT03806309Phase 2Active Not Recruiting

OSE2101+FOLFIRI, or FOLFIRI Maintenance After FOLFIRINOX-based Induction Therapy in Advanced or Metastatic PDAC

Role: collaborator

NCT03990233Phase 1Completed

A Trial of BI 765063 Monotherapy and in Combination With BI 754091 in Patients With Advanced Solid Tumours

Role: lead

NCT04882007Phase 2Completed

Study of OSE-127 vs Placebo in Patients With Moderate to Severe Active Ulcerative Colitis

Role: lead

NCT04713514Phase 2Active Not Recruiting

OSE2101 Alone or in Combination With Pembrolizumab vs BSC in Patient With Platinum-sensitive Recurrent OC

Role: collaborator

NCT02654587Phase 3Terminated

OSE2101 Versus Chemotherapy in HLA-A2 Positive Patients With Advanced NSCLC After Immune Checkpoint Inhibitor Failure

Role: lead

NCT04885361Phase 1Unknown

To Evaluate the Safety, and Immunogenicity of Vaccine Candidate Against COVID-19, in Healthy Adults

Role: lead

NCT03980080Phase 1Completed

Phase I Study to Assess the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Immunogenicity of OSE-127 in Healthy Subjects

Role: lead

NCT02800811Phase 1Completed

Safety, Tolerability, PK, PD, and Immunogenicity of Single and Multiple Ascending Intravenous Doses of FR104

Role: lead

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