Key Insights

Highlights

Success Rate

82% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 72/100

Termination Rate

13.8%

8 terminated out of 58 trials

Success Rate

81.8%

-4.7% vs benchmark

Late-Stage Pipeline

2%

1 trials in Phase 3/4

Results Transparency

25%

9 of 36 completed with results

Key Signals

9 with results82% success

Data Visualizations

Phase Distribution

57Total
P 1 (56)
P 3 (1)

Trial Status

Completed36
Terminated8
Recruiting6
Active Not Recruiting4
Unknown2
Not Yet Recruiting1

Trial Success Rate

81.8%

Benchmark: 86.5%

Based on 36 completed trials

Clinical Trials (58)

Showing 20 of 20 trials
NCT06899061Phase 1Active Not RecruitingPrimary

Modular Clinical Pharmacology Study to Evaluate the Drug-drug Interaction Potential and Relative Bioavailability of Saruparib

NCT02347228Phase 1TerminatedPrimary

Evaluate Safety, Tolerability, PK, Preliminary Clinical Activity of OB318 in Patients With Advanced Solid Malignancies

NCT05417594Phase 1RecruitingPrimary

Study of AZD9574 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Malignancies

NCT03363893Phase 1CompletedPrimary

Modular Study to Evaluate CT7001 Alone in Cancer Patients With Advanced Malignancies

NCT07643870Phase 1Not Yet RecruitingPrimary

Human ADME Study of [14C]-AZD1390

NCT07223047Phase 1RecruitingPrimary

A Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986523 Alone and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Malignancies

NCT06760481Phase 1Active Not RecruitingPrimary

Phase I/Ib Trial of TIraGolumab, AtEzolizumab, and RadScopal Radiation in Patients With Advanced Solid Malignancies (TIGER)

NCT06927297Phase 1Recruiting

Phase I Study of the Safety, Tolerability, and Efficacy of an Engineered Mitochondrial Vaccine in Advanced Solid Tumors

NCT07368478Phase 1RecruitingPrimary

A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK), and Preliminary Efficacy of BC2027 in Patients With Advanced Solid Malignancies

NCT05159700Phase 1Active Not Recruiting

A Phase I Study, Evaluating the Safety, Pharmacokinetics and Efficacy of PRJ1-3024 in Subjects With Advanced Solid Tumors

NCT06388902Phase 1SuspendedPrimary

A Phase I Study of BR115 for Injection Alone in Subjects With Advanced Solid Malignancies

NCT06028074Phase 1RecruitingPrimary

Safety and Tolerability Study of GIM-122 in Subjects With Advanced Solid Malignancies

NCT04521413Phase 1Active Not RecruitingPrimary

Safety and Efficacy Study of CFI-402411 in Subjects With Advanced Solid Malignancies

NCT02398747Phase 1CompletedPrimary

Japanese Phase I Study of AZD2014 in Advanced Solid Malignancies

NCT05315167Phase 1Recruiting

A Phase I/II Study to Evaluate the Safety, Pharmacokinetics and Efficacy of PRJ1-3024 in Subjects with Advanced Solid Tumors

NCT05469919Phase 1CompletedPrimary

An Open-Label Phase 1 Study of Ceralasertib in Japanese Patients With Advanced Solid Malignancies

NCT05573724Phase 1CompletedPrimary

Drug-drug Interaction Study With AZD5305 and Itraconazole in Patients With Advanced Solid Malignancies

NCT02740985Phase 1CompletedPrimary

A Phase 1 Clinical Study of AZD4635 in Patients With Advanced Solid Malignancies

NCT03084471Phase 3CompletedPrimary

An Open-Label, Multi-Centre, Study to Assess the Safety of Fixed-Dose Durvalumab + Tremelimumab Combination Therapy or Durvalumab Monotherapy in Advanced Solid Malignancies.

NCT04353102Phase 1CompletedPrimary

A Study to Evaluate the Safety, Tolerability and How YH002 Enters, Moves Through and Exits the Body in Subjects With Advanced Solid Malignancies

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