Key Insights

Highlights

Success Rate

92% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

1.8%

1 terminated out of 57 trials

Success Rate

91.7%

+5.1% vs benchmark

Late-Stage Pipeline

2%

1 trials in Phase 3/4

Results Transparency

0%

0 of 11 completed with results

Key Signals

92% success

Data Visualizations

Phase Distribution

48Total
Not Applicable (8)
Early P 1 (2)
P 1 (35)
P 2 (2)
P 3 (1)

Trial Status

Recruiting26
Completed11
Not Yet Recruiting10
Withdrawn5
Unknown2
Active Not Recruiting1

Trial Success Rate

91.7%

Benchmark: 86.5%

Based on 11 completed trials

Clinical Trials (57)

Showing 20 of 20 trials
NCT06802172Not ApplicableRecruiting

Effect of Meal Timing During Cancer Treatment in Patients in Alaska: A Randomized Clinical Trial

NCT07583654Phase 1Recruiting

Safety, Tolerability, and Preliminary Antitumor Activity of Cationic Peptide-IL22BP mRNA in Advanced Solid Tumors

NCT07685548Not Yet RecruitingPrimary

AI-Driven Tumor Response Evaluation for Solid Tumors

NCT07337525Phase 1Recruiting

A First in Human Study of PLT012 in Participants With Solid Tumor Cancers

NCT07218874Not ApplicableCompleted

Feasibility and Acceptability of the Remote Oncology Symptom Assessment Application

NCT07193511Phase 1RecruitingPrimary

BEACON-1: Study of AVZO-103 as a Single Agent and in Combination Therapy in Patients With Locally Advanced or Metastatic Urothelial Cancer or Other Solid Tumors (AVZO-103-1001)

NCT05520099Active Not Recruiting

Observational Basket Trial to Collect Tissue to Develop and Train a Live Tumor Diagnostic Platform (ELEPHAS-02)

NCT07671534Phase 2RecruitingPrimary

Metronomic Gemcitabine, Mitomycin C, and Thalidomide for Advanced Solid Tumors

NCT07100925Phase 1Withdrawn

A Study of Tolododekin Alfa (ANK-101) in Renal Allograft Recipients With High Risk Cutaneous Squamous Cell Carcinoma

NCT07664397Phase 1Not Yet Recruiting

Imaging Study of [89Zr]DFO-YS5 for Cancer Detection

NCT06607692Phase 1RecruitingPrimary

Study in Children and Adolescents of 177Lu-DOTATATE (Lutathera®) Combined With the PARP Inhibitor Olaparib for the Treatment of Recurrent or Relapsed Solid Tumours Expressing Somatostatin Receptor (SSTR) (LuPARPed).

NCT07603479Phase 1Not Yet Recruiting

A Phase I Study of JL19001 Injection Alone or in Combination With Standard Therapy in Patients With Advanced Solid Tumors or Relapsed/Refractory B-cell Non-Hodgkin Lymphoma

NCT06885424Enrolling By InvitationPrimary

A Long-Term Follow-Up Study of Participants Treated With A2 Biotherapeutics (A2 Bio) Gene Therapy (GT) Products

NCT07467629Phase 1RecruitingPrimary

QLS5212 for Participants With Advanced Solid Tumors

NCT07583914Phase 1Not Yet RecruitingPrimary

Safety, Tolerability, and Preliminary Antitumor Activity of Non-Cationic Peptide-CD47 siRNA in Advanced Solid Tumors

NCT07584954Phase 1RecruitingPrimary

Phase I, Open-labeled, Dose-escalation, Dose-expansion Study Evaluating the Safety, Tolerance, Pharmacokinetics, and Activity of IUAb190708 in Patients With Advanced or Recurrent Solid Tumors

NCT07038343Phase 1RecruitingPrimary

AVENTINE-1: Study of AVZO-1418 as a Single Agent and in Combination Therapy in Patients With Locally Advanced or Metastatic Solid Tumors (AVZO-1418-1001)

NCT07052760Early Phase 1WithdrawnPrimary

Imaging of Solid Tumors Using DLL3 SPECT

NCT06682117Not ApplicableRecruiting

A Clinical Study of Personalized Self-DC Vaccine Targeting Neoantigen in Treatment of Advanced Solid Tumor

NCT07424547Phase 1Recruiting

Phase I Study of SYS6043 in Patients With Advanced/Metastatic Solid Tumors

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