Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04753164 · ClinicalTrials.gov registry record · Phase 2

Multicenter Study to Evaluate the Efficacy and Safety of Oral ACT-539313 in the Treatment of Adults With Moderate to Severe Binge Eating Disorder

A Phase 2 study, sponsored by Idorsia Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
136
Enrollment target

NCT04753164: Completed Phase 2 study, sponsored by Idorsia Pharmaceuticals.

NCT04753164 is a Phase 2 study that has completed, run by Idorsia Pharmaceuticals. The registered enrollment target is 136 participants, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04753164, a Phase 2 study, has completed, sponsored by Idorsia Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
136 participants
Enrollment target

Study Summary

Placebo-controlled study to evaluate the efficacy and safety of oral ACT-539313 in the treatment of adults with moderate to severe binge eating disorder

Primary Outcome

BE days per week is defined as the number of diary days with at least one confirmed BE episode during the applicable 14-day time interval divided by the total number of diary days, times 7.

Interventions

  • DRUG Placebo
  • DRUG ACT-539313

Trial Details

FieldValue
Enrollment Target 136 participants
Start Date 2021-02-16
Est. Completion 2022-03-25
Phase Phase 2
Idorsia Pharmaceuticals

34 total trials

What the finished NCT04753164 record still lists

NCT04753164 is an interventional study that assigns participants to a tested intervention. The registered 136 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT04753164 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04753164 about?

NCT04753164 is a clinical study titled "Multicenter Study to Evaluate the Efficacy and Safety of Oral ACT-539313 in the Treatment of Adults With Moderate to Severe Binge Eating Disorder". Placebo-controlled study to evaluate the efficacy and safety of oral ACT-539313 in the treatment of adults with moderate to severe binge eating disorder

What is the current status of trial NCT04753164?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 136 participants. The study started on 2021-02-16. Estimated completion is 2022-03-25.

What interventions are being tested in trial NCT04753164?

The interventions under investigation include: Placebo (DRUG), ACT-539313 (DRUG).

Who is sponsoring clinical trial NCT04753164?

This trial is sponsored by Idorsia Pharmaceuticals, which has 34 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04753164's enrollment target sits among peer trials

136 527th of 2000 higher than 1,469 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01555892 · 136 participants · Phase 1

    Cytotoxic T-Lymphocytes for EBV-positive Lymphoma, GRALE

  • NCT03216525 · 136 participants · Phase 3

    Alvimopan Versus Placebo in Patients Undergoing Radical Cystectomy on an Enhanced Recovery Protocol

  • NCT04476901 · 136 participants · Phase 2

    Administration of Allogeneic-MSC in Patients With Non-Ischemic Dilated Cardiomyopathy

  • NCT04603898 · 136 participants · NA

    Oxalate Formation From Ascorbic Acid

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04753164, the US trial registry maintained by the National Library of Medicine. NCT04753164 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.