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Spots Global Cancer Trial Database for A First-in-human of Multiplle Doses of BB-1705 in Subjects With Locally Advanced/Metastatic Solid Tumors

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Trial Identification

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

Conditions

Solid Tumor

Interventions

BB-1705

Study Description

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.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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