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Clinical Trial Summary

This clinical trial will enroll subjects with HER2+ solid tumors and is conducted in two phases. The primary objective of Phase 1 is to determine the safety and tolerability of AB-201 in subjects with advanced HER2+ solid tumors. The primary objective of Phase 2 is to evaluate the efficacy of AB-201. Subjects will receive up to 3 doses of AB-201, followed by scheduled assessments of overall health and tumor response.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05678205
Study type Interventional
Source Artiva Biotherapeutics, Inc.
Contact AB-201-01 Study Team
Phone 858-267-4465
Email AB-201-01StudyTeam@ArtivaBio.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date August 1, 2023
Completion date April 2027

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