Condition: Squamous Cell Carcinoma of Head and Neck · Sponsor: Sichuan Baili Pharmaceutical Co., Ltd.
Phase Ib: To observe the safety and tolerability of SI-B001+SI-B003 in combination and to identify RP2D in locally advanced or metastatic head and neck squamous cell carcinoma indications. Initial efficacy, pharmacokinetic characteristics and immunogenicity were evaluated. Phase II: To evaluate the efficacy of SI-B001+SI-B003 two-drug combination chemotherapy. Safety and tolerance, PK/PD, immunogenicity were evaluated.
This description comes directly from the study's public registry record.
Sa Xiao, PHD · +8615013238943 · xiaosa@baili-pharm.com
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| Shanghai Oriental Hospital | Shanghai, Shanghai Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05668858