A Study of IMR-687 in Subjects With Sickle Cell Disease

Status Terminated

Clinical Trial Summary

A Study to Evaluate the Safety and Efficacy of IMR-687 in Subjects with Sickle Cell Disease

Clinical Trial Description

A phase 2b, randomized, double-blind, placebo-controlled, multicenter study of subjects with sickle cell disease (SCD; homozygous sickle hemoglobin [HbSS], sickle-β0 [HbSβ0] thalassemia, or sickle-β+ [HbSβ+] thalassemia) to evaluate the safety and efficacy of the phosphodiesterase type 9 (PDE9) inhibitor, IMR-687, administered once daily (qd) for 52 weeks. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04474314
Study type	Interventional
Source	Imara, Inc.
Contact
Status	Terminated
Phase	Phase 2
Start date	August 13, 2020
Completion date	May 4, 2022

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