Recruiting
Phase 1
Phase 2

MDMA

Sponsor:

Anya Bershad, MD, PhD

Code:

NCT05770375

Conditions

Schizophrenia

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

Interventions

MDMA 40mg

MDMA 80mg

MDMA 120mg

Study Details

Brief summary:

Impaired social motivation, or "asociality," is a negative symptom of schizophrenia (SCZ) and a cause of significant functional impairment in the illness. Whereas many symptoms of schizophrenia can be treated with antipsychotic medications, deficits in social motivation persist, leading to significant social disability in patients. There is currently no effective treatment for this symptom of the illness. One promising and unexplored avenue to enhance social motivation in schizophrenia is ± 3,4-methylenedioxymethamphetamine (MDMA). MDMA is a psychostimulant that shares some pharmacological properties with amphetamines, but in addition, has pronounced pro-social effects, increasing the motivation to engage socially. In healthy volunteers, it produces feelings of empathy and closeness with others and increases attention to positive social cues, perhaps partly through its effects on the social bonding hormone, oxytocin. MDMA has shown promise in other psychiatric conditions such as PTSD. Thus, MDMA could offer a unique therapeutic benefit in patients with SCZ who suffer from impaired social motivation. The investigators plan to take the first step in testing MDMA as a treatment for these social deficits by testing the tolerability of the drug in patients with SCZ. This will be an open-label, ascending-dose, within-subject trial in which participants will receive 40mg, 80mg, or 120mg of MDMA. The doses will be administered in ascending order, but doses will be stopped if subjects experience moderate or greater psychotic symptoms at 24 hours. This trial will assess the tolerability of the drug in this population and guide in the selection of a maximum well-tolerated dose for future studies. The primary tolerability measure will be clinician-rated psychotic symptoms (disorganized speech, delusions, hallucinations) collected at 24 hours after MDMA administration. The results of this project will lay the foundation for further investigations of MDMA and other psychoactive compounds as a treatment for debilitating and difficult-to-treat social deficits in schizophrenia. Future studies will examine interactions between the effects of psychoactive compounds and nonpharmacologic psychosocial interventions targeting social symptoms.

Conditions

Schizophrenia

Study ID

NCT05770375

Start date

Sep 1, 2024

Status verified date

Jul, 2026

Completion date

Mar 1, 2028

Anticipated

Primary completion date

Mar 1, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 60

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Ages 18-60
  • able to understand spoken English sufficiently to comprehend testing procedures
  • DSM-5 diagnosis of schizophrenia, based on clinical interview
  • clinical stability (i.e., no inpatient hospitalizations for six months prior to enrollment, no changes in medication in for 6 months prior to enrollment)

Exclusion Criteria:

  • no history of aggressive or suicidal behavior while psychotic
  • no history of IQ less than 70 or developmental disability, based on medical history
  • no clinically significant neurological disease (e.g., epilepsy), or cardiovascular condition (e.g. cardiac arrhythmia) based on medical history
  • no history of serious head injury (i.e., loss of consciousness longer than 1 hour, neuropsychological sequelae, cognitive rehabilitation treatment after head injury) based on medical history
  • no substance or alcohol use disorder in the past six months
  • no sedatives or benzodiazepines within 24 hours of testing
  • no positive urine toxicology screen or visible intoxication on the day of assessment
  • no women who are pregnant or think that they might be pregnant, based on self-report and urine test
  • not currently taking SSRIs or SNRIs
  • no history of NMS or serotonin syndrome
  • No prolongation of the QTc interval on EKG

Study Design

Enrollment

20 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: MDMA

Each subject will receive 3 doses of MDMA in ascending order: 40mg, 80mg, 120mg.

Interventions

MDMA 40mg

MDMA 40mg

MDMA 80mg

MDMA 80mg

MDMA 120mg

MDMA 120mg

Primary outcome measure

  • Positive and Negative Syndrome Scale for Schizophrenia (PANSS): Disorganized speech. [ Time Frame: 24 hours after each drug session ]
  • Positive and Negative Syndrome Scale for Schizophrenia (PANSS): Delusions [ Time Frame: 24 hours after each drug session ]
  • Positive and Negative Syndrome Scale for Schizophrenia (PANSS): Hallucinations [ Time Frame: 24 hours after each drug session ]

Central Contacts and Locations

Central contacts

Locations

UCLA

Recruiting

Los Angeles, California, United States, 90025

Contacts

More Information

Sponsor

Anya Bershad, MD, PhD

Last update posted

Jul 17, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Anya Bershad, MD, PhD on 2026-07-17.