Condition: Advanced Solid Tumors · Sponsor: HighField Biopharmaceuticals Corporation
This is an open-label, single-arm, non-randomized, single-center, dose-escalation study designed to evaluate the safety and tolerability of HF50 in patients with HER-2 positive and HER-2 low-expression advanced solid tumors. The primary objectives are to assess the safety, tolerability, and determine the maximum tolerated dose (MTD) and/or recommended Phase II dose (RP2D) of HF50. Secondary objectives include evaluating the pharmacokinetic (PK) profile and preliminary antitumor activity of HF50.
This description comes directly from the study's public registry record.
Zelei Dai, MMedSc · +86 17691161216 · daisydzl@icloud.com
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| West China Hospital of Sichuan University | Chengdu, Sichuan, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06822998