Trial Profile

A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Immunogenicity Profiles of the Recombinant Anti-HER2 and Anti-CD3 Humanized Bispecific Antibody (M802) in HER2-Positive Advanced Solid Tumors

Status: Not yet recruiting

Phase of Trial: Phase I

Latest Information Update: 04 Jan 2024

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At a glance

Drugs M 802 (Primary)
Indications Advanced breast cancer; Gastric cancer; HER2 positive breast cancer; Solid tumours
Focus Adverse reactions
Sponsors YZY Biopharma

28 Jul 2021 Planned End Date changed from 31 Mar 2021 to 31 Dec 2023.
28 Jul 2021 Planned primary completion date changed from 31 Dec 2020 to 30 Nov 2023.
28 Jul 2021 Planned initiation date changed to 28 Aug 2021.

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