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Clinical Trial Summary

A Phase 1 study in subjects with LR-MDS to assess the safety and tolerability of JSP191 as a second-line therapy.


Clinical Trial Description

An open-label, single-arm, dose-escalation study designed to determine the potential safety, efficacy, maximum tolerated dose (MTD) or optimal biologic dose (OBD), and recommended phase 2 dose (RP2D) of JSP191 (briquilimab) monotherapy for LR-MDS subjects with documented cytopenia (red blood cell-transfusion dependent, thrombocytopenia, and/or neutropenia). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05903274
Study type Interventional
Source Jasper Therapeutics, Inc.
Contact Harold Pestana
Phone 201-221-9785
Email hpestana@jaspertherapeutics.com
Status Recruiting
Phase Phase 1
Start date June 19, 2023
Completion date July 2025