Clinical Trial

Clinical Trial of TQB3126 for Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy in Breast Cancer Subjects

Not Yet Recruiting Phase 1/2
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Summary
The trial comprises Phase I dose escalation/expansion and Phase II combination therapy. Using a multicenter, open-label, non-randomized design, breast cancer patients will receive TQB3126 to assess its safety, tolerability, pharmacokinetics and preliminary efficacy.
Trial Details
NCT Number NCT07697443
Lead Sponsor Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Conditions Breast Cancer
Enrollment 306 participants
Start Date 2026-08
Primary Completion 2029-08 (estimated)
Study Completion 2030-08 (estimated)
Updated on ClinicalTrials.gov 2026-07-13