Pivotal Trial of SAT-014 for Trauma and Stressor-Related Disorder Symptoms

NACompletedINTERVENTIONAL
Enrollment

110

Participants

Timeline

Start Date

December 9, 2024

Primary Completion Date

May 29, 2025

Study Completion Date

May 29, 2025

Conditions
Post-traumatic Stress DisorderAdjustment Disorders
Interventions
DEVICE

SAT014

SAT-014 in Combination with Baseline Conventional Treatment Participants in this arm will use the SAT-014 application for 6 weeks in combination with their baseline conventional treatment, which may include pharmacological therapy or simple counseling (excluding cognitive behavioral therapy and psychoanalytic counseling therapy). The aim of this study is to assess the efficacy and safety of SAT-014 for alleviating symptoms of trauma and stressor-related disorders, such as PTSD and adjustment disorder.

OTHER

Control

Baseline Conventional Treatment Participants in this arm will receive only conventional treatment, which includes the medication they were taking at baseline for the indication or the basic counseling therapy they were receiving at baseline.

Trial Locations (5)

Unknown

Kyung Hee University Hospital, Seoul

Samsung Medical Center, Seoul

Severance Hospital, Seoul

SMG-SNU Boramae Medical Center, Seoul

Wonju Severance Christian Hospital, Wŏnju

All Listed Sponsors
lead

S-Alpha Therapeutics, Inc.

INDUSTRY

NCT06734858 - Pivotal Trial of SAT-014 for Trauma and Stressor-Related Disorder Symptoms | Biotech Hunter | Biotech Hunter