Key Insights

Highlights

Success Rate

75% trial completion

Clinical Risk Assessment

Based on trial outcomes

High Risk

Score: 62/100

Termination Rate

8.3%

1 terminated out of 12 trials

Success Rate

75.0%

-11.6% vs benchmark

Late-Stage Pipeline

8%

1 trials in Phase 3/4

Results Transparency

33%

1 of 3 completed with results

Key Signals

1 with results75% success

Data Visualizations

Phase Distribution

10Total
Not Applicable (1)
P 1 (1)
P 2 (7)
P 3 (1)

Trial Status

Completed3
Not Yet Recruiting3
Enrolling By Invitation1
Terminated1
Active Not Recruiting1
Recruiting1

Trial Success Rate

75.0%

Benchmark: 86.6%

Based on 3 completed trials

Clinical Trials (12)

Showing 12 of 12 trials
NCT04266093Enrolling By Invitation

Gene Therapy Follow up Protocol for Subjects Previously Enrolled in NCI Center for Immuno-Oncology Studies

NCT07038369Phase 1Active Not Recruiting

A Phase 1 Study of ATV-1601 in Patients With Advanced Cancer That Have AKT1 E17K Mutations

NCT07731828Phase 2RecruitingPrimary

Neoadjuvant Short-course Hypofractionated Radiotherapy Plus Adebrelimab and Platinum Chemotherapy in Locally Advanced Cervical Cancer: A Single-arm Phase II Trial

NCT07631884Phase 2Not Yet Recruiting

Exploratory Study on the Efficacy and Safety of Trastuzumab Rezetecan in the Treatment of HER2-Expressiong Advanced Solid Tumor

NCT07631871Phase 2Not Yet Recruiting

An Exploratory Study of Zanidatamab in HER2-positive Advanced Tumor After at Least One Line of Standard Therapy

NCT05824494Phase 2Not Yet Recruiting

Cadonilimab Plus Nab -Paclitaxel for Patients With Recurrent, or Metastatic Cervical Cancer Resistant to Immune Checkpoint Inhibitors

NCT02267876CompletedPrimary

Longitudinal Clinical Evaluation of the HPV Assay on the BD VIPER LT System With Cervical Specimens

NCT01627288Not ApplicableCompleted

Integrated Dose Escalation for Advanced, Localized Gynecologic Cancer (The IDEAL - GYN Trial)

NCT04096911Phase 2Unknown

Combination of PD-1 Monoclonal Antibody and HPV Vaccine in Patients With Cervical Cancer

NCT00950261Phase 2WithdrawnPrimary

Efficacy Study for Postoperative Chemoradiation Using Triweekly Cisplatin in Cervical Cancer Patients

NCT00190528Phase 3TerminatedPrimary

A Trial of Neoadjuvant Chemotherapy + Surgery vs. Surgery for Bulky Stage I/II Cervical Cancer

NCT00916500Phase 2CompletedPrimary

Concurrent Chemoradiation With Cisplatin Every 3 Week in Advanced Cervical Cancer

Showing all 12 trials

Research Network

Activity Timeline