Key Insights

Highlights

Success Rate

86% trial completion

Published Results

17 trials with published results (17%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 49/100

Termination Rate

6.0%

6 terminated out of 100 trials

Success Rate

85.7%

-0.9% vs benchmark

Late-Stage Pipeline

5%

5 trials in Phase 3/4

Results Transparency

47%

17 of 36 completed with results

Key Signals

17 with results86% success

Data Visualizations

Phase Distribution

81Total
Not Applicable (22)
Early P 1 (3)
P 1 (23)
P 2 (28)
P 3 (4)
P 4 (1)

Trial Status

Completed36
Recruiting21
Active Not Recruiting17
Unknown9
Terminated6
Not Yet Recruiting5

Trial Success Rate

85.7%

Benchmark: 86.6%

Based on 36 completed trials

Clinical Trials (100)

Showing 20 of 20 trials
NCT05256225Phase 3Active Not RecruitingPrimary

Testing the Addition of Herceptin Hylecta or Phesgo to the Usual Chemotherapy for HER2 Positive Endometrial Serous Carcinoma or Carcinosarcoma

NCT02465060Phase 2Active Not Recruiting

Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)

NCT07285044Phase 2Recruiting

The Cancer Connected Access and Remote Expertise Beyond Walls Program to Provide In-Home Cancer Treatment and Improve Treatment Satisfaction in Cancer Patients Living in the Florida Panhandle and Surrounding Areas

NCT04152499Phase 1Active Not Recruiting

Phase I-II, FIH, TROP2 ADC, Advanced Unresectable/Metastatic Solid Tumors, Refractory to Standard Therapies (KL264-01)

NCT00791635Active Not Recruiting

Longitudinal Evaluation of Women Undergoing Pelvic Surgery for the Treatment of Gynecologic Cancer

NCT05059444Recruiting

ORACLE: Observation of ResiduAl Cancer With Liquid Biopsy Evaluation

NCT05139368Not ApplicableActive Not Recruiting

Hypofractionated Radiotherapy for the Treatment of Cervical or Endometrial Cancer

NCT01366144Phase 1Active Not Recruiting

Veliparib, Paclitaxel, and Carboplatin in Treating Patients With Solid Tumors That Are Metastatic or Cannot Be Removed by Surgery and Liver or Kidney Dysfunction

NCT07216105Phase 1Recruiting

FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors

NCT04839614Not ApplicableRecruitingPrimary

Concurrent Laparoscopic Hysterectomy and Weight Loss Surgery in Obese Patients With Endometrial Carcinoma or Endometrial Intraepithelial Neoplasia

NCT07662824Not ApplicableRecruiting

Flyte Device for Improving Urinary Incontinence Among Endometrial and Cervical Cancer Survivors Who Have Undergone Radiation Therapy

NCT04851119Phase 1Recruiting

Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors

NCT04567771Not ApplicableRecruiting

Comparison of Proton or Intensity Modulated Radiation Therapy After Surgery for Endometrial or Cervical Cancer

NCT05919264Phase 1Recruiting

FOG-001 in Locally Advanced or Metastatic Solid Tumors

NCT07741968Not ApplicableRecruiting

A Blended e-Health Intervention to Improve Fear of Progression in Women With Gynecologic or Breast Cancer

NCT07281547Phase 4Not Yet RecruitingPrimary

Low Dose Aspirin to Lower Inflammation and Prevent Endometrial Cancer in Postmenopausal Women With Non-atrophic Endometrial Changes and Pain

NCT07738315Phase 2Not Yet RecruitingPrimary

Elemene Liposomes in Endometrial Cancer

NCT07723235Not ApplicableNot Yet Recruiting

Web-based Lifestyle Program, mHealth and EMA Intervention, to Improve Weight Loss in Rural Stage I-III Postmenopausal Breast and Endometrial Cancer Survivors, HERO-C Trial

NCT05714553Phase 1Terminated

NUC-3373 in Combination With Other Agents in Patients With Advanced Solid Tumours

NCT05078047Phase 3Active Not Recruiting

Study Comparing the Standard Administration of IO Versus the Same IO Administered Each 3 Months in Patients in Response After 6 Months of Standard IO

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