A Multicenter Randomized Double-Blind Parallel-Group Dose-Controlled Study Evaluating the Safety and Efficacy of RE104 for Injection in the Treatment of Patients with Postpartum Depression (PPD)
Brief description of study
The purpose of collecting your pregnancy information is to see if RE104 has any effects on pregnancy, its outcome, and the birth and health of a baby.
Clinical Study Identifier: s24-00310
ClinicalTrials.gov Identifier: NCT06342310
Principal Investigator:
Stephen Ross.
Other Investigators:
Daniel Edward Roberts,
Kelley O'Donnell,
Xiaojue Hu,
Joshua Siegel,
Richard J Zeifman.
If you are registered as a volunteer, please log in to contact the study team/express interest in this study.