Key Insights

Highlights

Success Rate

79% trial completion

Published Results

315 trials with published results (15%)

Research Maturity

928 completed trials (45% of total)

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 72/100

Termination Rate

11.8%

246 terminated out of 2085 trials

Success Rate

79.0%

-7.5% vs benchmark

Late-Stage Pipeline

8%

174 trials in Phase 3/4

Results Transparency

34%

315 of 928 completed with results

Key Signals

315 with results79% success246 terminated

Data Visualizations

Phase Distribution

1,658Total
Not Applicable (282)
Early P 1 (28)
P 1 (622)
P 2 (552)
P 3 (154)
P 4 (20)

Trial Status

Completed928
Recruiting351
Unknown267
Terminated246
Active Not Recruiting122
Not Yet Recruiting92

Trial Success Rate

79.0%

Benchmark: 86.6%

Based on 928 completed trials

Clinical Trials (2085)

Showing 20 of 20 trials
NCT04847063Phase 1Recruiting

Individual Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Treatment of Peritoneal Carcinomatosis From Peritoneal Mesothelioma or Atypical Mesothelial Proliferation or From Ovarian, Colorectal, or Appendiceal Histologies

NCT04585750Phase 1Recruiting

The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)

NCT03762733Enrolling By Invitation

Tissue Acquisition and Genomics Analysis of Breast Cancer and Other Gynecologic Malignancies

NCT01441089Recruiting

Collection of Blood From Patients With Cancer, Other Tumors, or Tumor Predisposition Syndromes for Genetic Analysis

NCT05652283Phase 2RecruitingPrimary

Pamiparib Combined With Surufatinib for the Neoadjuvant Treatment of Unresectable Ovarian Cancer

NCT01767675Phase 2CompletedPrimary

Outcomes After Secondary Cytoreductive Surgery With or Without Carboplatin Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Followed by Systemic Combination Chemotherapy for Recurrent Platinum-Sensitive Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

NCT06465069Phase 1Recruiting

A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors

NCT07743164Phase 3Not Yet RecruitingPrimary

A Clinical Trial of Raludotatug Deruxtecan (R-DXd) With or Without Bevacizumab in Participants With Ovarian Cancer Who Have Progressed During Treatment With PARP-inhibitors Treatment on First Line Maintenance (MK-5909-008/ENGOT-ov107/GOG-3142 / REJOICE-Ovarian05)

NCT07059884Not ApplicableRecruiting

Distance-Based Exercise to Preserve Function and Prevent Disability

NCT07797283Phase 3Not Yet RecruitingPrimary

Phase 3 Study of INCB123667 Plus Bevacizumab Versus Bevacizumab Alone as First-Line Maintenance Therapy in Ovarian Cancer Overexpressing Cyclin E1

NCT04575961Phase 2Active Not RecruitingPrimary

Study of Pembrolizumab Combination With Chemotherapy in Platinum-sensitive Recurrent Low-grade Serous Ovarian Cancer

NCT07778498Phase 1Not Yet RecruitingPrimary

A Phase I/II, First-in-Human Study to Evaluate TJ102 in Participants With Advanced or Metastatic Ovarian Cancer and Other Solid Tumors.

NCT03170960Phase 1Active Not Recruiting

Study of Cabozantinib Alone or in Combination With Atezolizumab to Subjects With Locally Advanced or Metastatic Solid Tumors

NCT07843303Phase 2Not Yet RecruitingPrimary

Trastuzumab Rezetecan Plus Bevacizumab in Platinum-Sensitive Recurrent Ovarian Cancer

NCT07189871Phase 1Recruiting

177Lu-BetaBart in Patients With Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors

NCT04751435Not ApplicableRecruiting

Developing New Educational Materials About Genetic Testing for a Diverse Group of Cancer Patients

NCT06586957Phase 1Recruiting

A Study With NKT3964 for Adults With Advanced/Metastatic Solid Tumors

NCT07693894RecruitingPrimary

Innovative Ovarian Cancer Biomarker Assays

NCT07278336Phase 1RecruitingPrimary

A Study to Assess Adverse Events, Change in Disease Activity and How Intravenous (IV) ABBV901 Moves Through the Body Alone or in Combination With Other Anticancer Drugs in Adult Participants With Ovarian Cancer

NCT07814248Phase 1Recruiting

A Phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and Dose Expansion Study of the Peptide Drug Conjugate (PDC), TS-104, as a Monotherapy in Subjects With Select Advanced Solid Tumors

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