A Study of ATR-101 for the Treatment of Congenital Adrenal Hyperplasia

Status Completed

Clinical Trial Summary

This is a Phase 2 multicenter, single-blind, multiple dose study to evaluate the safety and efficacy of orally administered ATR-101 in subjects with classic congenital adrenal hyperplasia (CAH). Treatment duration will range from a minimum of approximately 2 months to 6 months per subject. A subject may receive a minimum of one dose level or up to a maximum of 5 dose levels, in sequentially increasing dose strengths. Each dose level will last 28 days.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02804178
Study type	Interventional
Source	Millendo Therapeutics, Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	May 18, 2016
Completion date	August 17, 2017

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See also
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