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Clinical Trial Summary

A Study to Evaluate the Safety and Tolerability of IMR-687 in Subjects with Beta Thalassemia


Clinical Trial Description

A phase 2, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, PK, and PD of IMR-687 (phosphodiesterase (PDE) 9 inhibitor) administered once daily (qd) orally for 36 weeks in 2 populations of adult subjects with β-thalassemia: Population 1 (Transfusion Dependent Thalassemia (TDT) subjects) and Population 2 (Non-Transfusion Dependent Thalassemia (NTDT) subjects). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04411082
Study type Interventional
Source Imara, Inc.
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Status Terminated
Phase Phase 2
Start date October 16, 2020
Completion date May 4, 2022