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Clinical Trial Summary

This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with tislelizumab in participants with advanced solid tumors. Participants will receive study drug(s) until progressive disease, unacceptable toxicity, withdrawal of consent, death, or another discontinuation criterion is met, whichever occurs first. The maximum length of receiving study drug(s) for a participant is up to 2 years.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06233942
Study type Interventional
Source BeiGene
Contact Study Director
Phone 1.877.828.5568
Email clinicaltrials@beigene.com
Status Recruiting
Phase Phase 1
Start date April 12, 2024
Completion date September 28, 2027

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