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Brief Title: A First-in-human of Multiplle Doses of BB-1705 in Subjects With Locally Advanced/Metastatic Solid Tumors
Official Title: A Phase I First-in-human, Open Label, Multicenter, Dose Escalation and Cohort Expansion Study to Investigate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of BB-1705 in Patients With Locally Advanced/Metastatic Solid Tumors
Study ID: NCT05217693
Brief Summary: The study consists of two phases: dose-escalation (Phase I) and cohort expansion (Phase II).
Detailed Description: Phase Ia is a dose escalation study to assess the safety and tolerability, and to determine the MTD or MAD and RP2D of BB-1705. Phase Ib is a cohort expansion study to explore one or more RP2Ds to further assess safety, tolerability, pharmacokinetics, and preliminary anti-tumor activity. Patients with locally advanced and unresectable or metastatic solid tumors who have progressed on prior lines of standard of care therapies will be enrolled in this study if eligible.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Beijing Cancer Hospital, Beijing, , China
Hunan Cancer Hospital, Changsha, , China
First affiliated hospital of Gannan medical university, Ganzhou, , China
Bliss Biopharmaceutical Co, Ltd, Hangzhou, , China
Zhejiang University School of Medicine - The First Affiliated Hospital, Hanzhou, , China
Linyi Cancer Hospital, Linyi, , China
Jiangsu Province Hospital, Nanjing, , China