Key Highlights

Risk & Performance

Pipeline Risk Assessment

Pipeline Risk Assessment

Based on historical performance

Moderate Risk

Score: 40/100

Failure Rate

12.0%

3 terminated/withdrawn out of 25 trials

Success Rate

83.3%

-3.2% vs industry average

Late-Stage Pipeline

48%

12 trials in Phase 3/4

Results Transparency

27%

4 of 15 completed trials have results

Key Signals

2 recruiting4 with results

Enrollment Performance

Analytics

Phase 3
12(52.2%)
Phase 2
7(30.4%)
N/A
4(17.4%)
23Total
Phase 3(12)
Phase 2(7)
N/A(4)

Activity Timeline

Global Presence

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Clinical Trials (25)

Showing 20 of 25 trials
NCT04595565Phase 3Active Not Recruiting

Sacituzumab Govitecan in Primary HER2-negative Breast Cancer

Role: collaborator

NCT07541703Active Not Recruiting

Independent, External, Blinded Retrospective Validation of an AI-based Prognostic Assay in ER-Positive/HER2-Negative Early Breast Cancer

Role: collaborator

NCT06446882Not ApplicableRecruiting

Diagnostic HER2DX-guided Treatment for Patients wIth Early-stage HER2-positive Breast Cancer

Role: collaborator

NCT02513394Phase 3Active Not Recruiting

PALbociclib CoLlaborative Adjuvant Study

Role: collaborator

NCT07084558Not ApplicableRecruiting

ABCSG 61 / TEODOR : Neoadjuvant TrEatment Optimization Driven by Circulating Tumor DNA and endOcrine Responsiveness

Role: lead

NCT03822572Not ApplicableActive Not Recruiting

ABCSG C08-Exercise II: Trial of Endurance Exercise Following Adjuvant Chemotherapy for Colorectal Cancer

Role: lead

NCT00798070Phase 3Active Not Recruiting

Panther: A Study Comparing Biweekly and Tailored EC-T Versus Three Weekly FEC-T in Breast Cancer Patients

Role: collaborator

NCT01210313Completed

Physical Activity for Reduction of Recurrence Rate After Adjuvant Chemotherapy for Localised Colorectal Carcinoma

Role: lead

NCT01015625Not ApplicableCompleted

Primary Operation in SYnchronous meTastasized InVasivE Breast Cancer

Role: lead

NCT00295646Phase 3Completed

Tamoxifen Versus Anastrozole, Alone or in Combination With Zoledronic Acid

Role: lead

NCT00309478Phase 3Completed

Randomized Study Comparing CMF and Goserelin + Tamoxifen in Premenopausal Receptor-positive Patients

Role: lead

NCT00671645Phase 2Terminated

Preoperative Combined RadioChemo-Molecular Target Therapy With Capecitabine, Bevacizumab, and Radiotherapy

Role: lead

NCT00309491Phase 3Completed

Randomized Study Comparing Tamoxifen vs. Tamoxifen + Aminoglutethimide in Postmenopausal Receptor-positive Patients

Role: lead

NCT00309569Phase 3Completed

Randomized Study Comparing Pre- and Postoperative vs. Conventional Adjuvant Treatment in Receptor-negative Patients

Role: lead

NCT01523639Phase 2Terminated

A Randomized, Placebo-controlled, Double-blind Phase II Study Evaluating if Glucophage Can Avoid Liver Injury Due to Chemotherapy Associated Steatosis

Role: lead

NCT00512993Phase 3Completed

Postoperative Use of Zoledronic Acid in Breast Cancer Patients After Neoadjuvant Chemotherapy

Role: collaborator

NCT01367028Phase 2Completed

A Phase II Study of Neoadjuvant Trastuzumab+Docetaxel+NPLD+/-Bevacizumab in Her2-pos. Early Breast Cancer

Role: lead

NCT01434147Phase 2Completed

Preoperative Combined Induction Chemotherapy With Capecitabine, Oxaliplatin, Bevacizumab and Radiotherapy

Role: lead

NCT00297141Phase 2Completed

Preoperative Combined Radiochemotherapy for Patients With Rectal Carcinoma

Role: lead

NCT00297128Phase 2Completed

Preoperative Chemoradiation With Capecitabine and Cetuximab

Role: lead