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Clinical Trial Summary

This is a Phase 1,open-label, multi-center, first-in-human, 2-part (Part 1: dose escalation and Part 2: expansion) study, evaluating multiple doses and schedules of intravenously (IV) administered NTX-1088, with or without pembrolizumab, in patients with advanced solid malignancies (i.e., locally advanced or metastatic).


Clinical Trial Description

This is a Phase 1, open-label, multi-center study whose principal Part 1 stage objective is to determine the recommended Phase 2 dose (RP2D) of the anti-PVR monoclonal antibody (mAb) as a single agent and combined with the anti-PD-1 mAb pembrolizumab in patients with advanced solid malignancies. In the Part 2 stage, the antitumor activity of NTX-1088 alone or combined with pembrolizumab will be evaluated in patients with malignancies known to express PVR. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05378425
Study type Interventional
Source Nectin Therapeutics Ltd
Contact Keren Paz, PhD
Phone 201-218-1774
Email keren@nectintx.com
Status Recruiting
Phase Phase 1
Start date September 1, 2022
Completion date December 2025

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