A Multicenter, Open-Label Phase 1/1b/Phase 2 Dose-Finding, Safety, and Pharmacokinetic Study of MBRC-101, an Anti-Epha5 Monomethyl Auristatin E (MMAE) Antibody Drug Conjugate, in Advanced Refractory Solid Tumors
MBRC-101-001 (MBrace): A study of MBRC-101 in Advanced Refractory Solid Tumors
Sponsor: MBrace Therapeutics
Enrolling: Male and Female Patients
IRB Number: AAAV4204
U.S. Govt. ID: NCT06014658
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this research is to determine the dose and dosing regimens of an investigational drug, MBRC-101, that are well tolerated, as well as to evaluate its safety in patients with advanced or metastatic solid tumors that have already received conventional therapy. MBRC-101 is not an approved treatment anywhere in the world. Investigational means that the drug has not been approved by any government authority responsible for the regulation of new medicines, such as the U.S. Food and Drug Administration (FDA). This is the first time MBRC-101 is being tested in humans.
Do You Qualify?
Are you 18 years or older? Yes No
Do you have a malignant solid tumor? Yes No
Submit
Cancel
You may be eligible for this study

Place Holder




For more information, please contact:
Research Nurse Navigator
cancerclinicaltrials@cumc.columbia.edu
212-342-5162