A Phase 1/2 Study to Investigate CRB-701 in Solid Tumors

Recruiting Phase 1 Phase 2 Interventional Study
Solid Tumor, Adult
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Treatment
Participants needed
348 (estimated)
Sponsor
Corbus Pharmaceuticals Inc. · Industry
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About This Trial
The goal of this clinical trial is to define a safe and effective dose of CRB-701 for participants with solid tumors that are expressing a protein called nectin-4. The main questions it aims to answer are: What is the the safe and effective dose of CRB-701? What cancers can be treated effectively with CRB-701? Participants will be asked to attend clinic and be given a intravenous infusion of CR…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Confirmed diagnosis of select advanced or metastatic nectin-4 expressing solid tumors that have progressed having exhausted all appropriate lines of therapy or have no other standard therapy with proven clinical benefit. In Part C, HNSCC participants may enroll as first-line t…
Contacts

Ian Hodgson, PhD

+1 (617) 963-0105

Clinical@Corbuspharma.com

CONTACT

Rodney Carter, BSc

Clinical@Corbuspharma.com

CONTACT