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Clinical Trial Summary

A first-in-human study using BDC-3042 as a single agent and in combination with pembrolizumab in patients with advanced malignancies


Clinical Trial Description

This study has four parts. Part 1 is a dose escalation of BDC-3042 as a single agent to determine the maximum tolerated dose (MTD), recommended Phase 2 dose (RP2D), or maximum protocol dose (MPD) recommended for Part 3. In Part 3, the selected dose will be administered as monotherapy to patients with selected advanced malignancies. Part 2 is a dose escalation of BDC-3042 in combination with pembrolizumab to determine the maximum tolerated dose (MTD), recommended Phase 2 dose (RP2D), or maximum protocol dose (MPD) recommended for Part 4. In Part 4, the selected dose will be administered in combination with pembrolizumab to patients with selected advanced malignancies. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06052852
Study type Interventional
Source Bolt Biotherapeutics, Inc.
Contact Bolt Biotherapeutics
Phone +1 650 434 8640
Email clinicaltrials@boltbio.com
Status Recruiting
Phase Phase 1/Phase 2
Start date October 11, 2023
Completion date March 2028

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