RecruitingPhase 3NCT07549412
A Study of Precemtabart Tocentecan With or Without Bevacizumab Compared to Trifluridine/Tipiracil Plus Bevacizumab in Participants With Previously Treated Metastatic Colorectal Cancer (PROCEADE-CRC-03)
Studying Esophageal atresia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- EMD Serono Research & Development Institute, Inc.
- Principal Investigator
- Medical ResponsibleEMD Serono Research & Development Institute, Inc.
- Intervention
- Precemtabart tocentecan(drug)
- Enrollment
- 1020 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2026 – 2029
Study locations (3)
- Profound Research LLC at Cancer and Leukemia Center, Troy, Michigan, United States
- GenesisCare North Shore (Oncology), St Leonards, New South Wales, Australia
- Icon Cancer Centre Chermside, Chermside, Queensland, Australia
Collaborators
Merck KGaA, Darmstadt, Germany
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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