A Study of HQK-1001 in Patients With Sickle Cell Disease

Status Completed

Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of three dose levels of HQK-1001 administered once daily for 26 weeks in subjects with sickle cell disease.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01322269
Study type	Interventional
Source	HemaQuest Pharmaceuticals Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	April 2011

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See also
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