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DHRHealth Institute for Research and Development

Clinical Trial

A Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate the Efficacy and Safety of SPR001 (Tildacerfont) in Adult Subjects with Classic Congenital Adrenal Hyperplasia

Study Status:

Open for enrollment

Contact Information:

(956) 362-2396

Please contact us for more information or to learn if you are eligible to participate.

Study Purpose:

To evaluate the effect of tildacerfont in reducing A4 in subjects with CAH over 12 weeks.

Information: 

Principal Investigator
Surya N. Mulukutla, MD
Co-PI
Luis Cantu Jr.
Sponsor
Spruce Biosciences
Type of Trial
Interventional
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