Condition: Von Hippel Lindau-Deficient Clear Cell Renal Cell Carcinoma · Sponsor: Jiangsu Hansoh Pharmaceutical Co., Ltd.
The aim of the Phase Ia portion is to identify the maximum tolerated dose or maximum acceptable dose MTD/MAD of HS-10516. The phase Ib portion will evaluate the preliminary efficacy of HS-10516 in patients with VHL Syndrome Associated Tumors.
This description comes directly from the study's public registry record.
Kan Gong, PhD · 13910394281 · kan.gong@bjmu.edu.cn
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| Peking University First Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06553339