drugset / Trial / NCT07869732
(Z)-Endoxifen in Girls With MAS-Associated Peripheral Precocious Puberty
Phase 2
Not yet recruiting
6 enrolled
Atossa Therapeutics, Inc.
National Institute of Dental and Craniofacial Research (NIDCR) · collab
NaSingle-groupOpen-labelTreatment
Summary
The goal of this clinical trial is to evaluate the safety, tolerability, and blood levels of (Z)-endoxifen in girls with McCune-Albright Syndrome that have peripheral precocious puberty. The main question it aims to answer \[is/are\]: Are there any safety concerns? Is there any evidence of efficacy? There is no comparison group. Participants will: * take a capsule once a day for 3 months; * have doctor visits (tele-health and in-person); * blood samples collected; and * complete questionnaires
Timeline
- Start
- 2027-03
- Primary completion
- 2028-06
- Completion
- 2028-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Endoxifen | Small molecule | — | Oral |