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Clinical Trial Summary

A Phase 1 Study to Investigate the Safety, Tolerability, Pharmacokinetics/Pharmacodynamics, and Antitumor Activity of NM1F as Monotherapy and in Combination with Pembrolizumab in Subjects with Locally Advanced/Metastatic Solid Tumors


Clinical Trial Description

This is a Phase 1, multicenter, open-label, two-parts, FIH study to evaluate the tolerability, safety, PK/PD, and preliminary anti-tumor activity of NM1F as monotherapy and in combination with pembrolizumab (Keytruda®) in subjects with unresectable locally advanced, or metastatic solid tumors. The study consists of two parts : NM1F monotherapy dose escalation (Phase 1a), NM1F dose escalation in combination with a fixed dose of pembrolizumab (Phase 1b). For each subject in the two parts, the study will include a screening period (up to 28 days), a treatment period (1 year and 2 years for Phase 1a and 1b, respectively, or until treatment discontinuation), and a follow-up period . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05746897
Study type Interventional
Source Hefei TG ImmunoPharma Co., Ltd.
Contact Xiaohu Zheng, Doctorate
Phone +86-13956959849
Email xiaohu.zheng@tgimmunopharma.com
Status Recruiting
Phase Phase 1
Start date April 13, 2023
Completion date September 30, 2027

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