Condition: Solid Tumor, Unspecified, Adult · Sponsor: MegaPro Biomedical Co. Ltd.
This is a first-in-human (FIH), multicenter, open-label, uncontrolled, Phase 1/2a study with dose escalation in patients with advanced solid tumors (Part 1) and cohorts of up to 15 patients per selected indication (Part 2). The solid tumor types in Part 2 will be decided by the sponsor prior to the start of Part 2, but not be solely based on the efficacy results in Part 1.
This description comes directly from the study's public registry record.
Summer Liao, MS · +886-3-5910360 · thliao@megaprobio.com
Always discuss trial participation with your own doctor first.
| Taipei Veterans General Hospital | Taipei, Taiwan | Recruiting |
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Source record: clinicaltrials.gov/study/NCT04643418