A Study of IBI363 in Subjects With Advanced Malignancies
Phase Ib Study to Evaluate the Safety, Tolerability and Preliminary Efficacy of IBI363 Combination Therapy in Subjects With Advanced Malignancies
Innovent Biologics (Suzhou) Co. Ltd.
556 participants
Jun 15, 2024
INTERVENTIONAL
Conditions
Summary
This is an open-label, multicenter Phase Ib study to evaluate the safety, tolerability, and efficacy of IBI363 in advanced malignancies patients
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
In this group, patients will receive IBI363 and chemotherapy
In this group, patients will receive IBI363 and Investigator's Choice SOC
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06468098