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Clinical Trial Summary

This is a first-in-human, Phase 1/2, open-label, dose escalation and dose expansion and combination study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy of PT886. Patients with the following tumor types will be eligible for screening: unresectable or metastatic gastric adenocarcinoma, gastroesophageal junction (GEJ) adenocarcinoma, and pancreatic ductal adenocarcinoma (PDAC).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05482893
Study type Interventional
Source Phanes Therapeutics
Contact Phanes Therapeutics
Phone 858-766-0852
Email clinical-trials@phanestx.com
Status Recruiting
Phase Phase 1/Phase 2
Start date March 15, 2023
Completion date April 2026

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