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Study of Carbetocin Nasal Spray for the Treatment of Hyperphagia in Prader-Willi Syndrome

StatusCompleted
PhasePhase 3
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Notable Primary endpoint(s) modified Show 8 more changesShow less
    • Results posted: Oct 15, 2026
    • Trial completed
    • Primary completion date changed from estimate of Oct 2025 to Aug 19, 2025
    • Enrollment target: estimated 170 to confirmed 175
    • Eligibility criteria shortened, about 109 words
    • Secondary endpoints: 2 to 4
    • Site details revised at 13 of 30 sites
    • Publications: details revised at 1 of 1 entry
  2. Minor Re-verified, no change to tracked fieldsv22
  3. Minor Primary completion date: May 2026 to Oct 2025
    • Study completion date: Jun 2026 to Nov 2025
    • Eligibility criteria expanded, about 25 words
    v21
  4. Minor 2 versions Re-verified since Jul 1, 2025, no change to tracked fieldsv19-v20
  5. Minor Trial status: Recruiting to Active, Not Recruiting
    • Study sites: 33 to 30
    v18
Show 16 earlier versionsHide 16 earlier versions
  1. Minor Study sites: 31 to 33v17
  2. Minor Study sites: 26 to 31v16
  3. Minor Study sites: 25 to 26v15
  4. Minor Study sites: 23 to 25v14
  5. Minor Re-verified, no change to tracked fieldsv13
  6. Minor Study sites: 22 to 23v12
  7. Minor Study sites: 17 to 22v11
  8. Minor Study sites: 15 to 17v10
  9. Minor Study sites: 11 to 15v9
  10. Minor Study sites: 10 to 11v8
  11. Minor Study sites: 7 to 10v7
  12. Minor Study sites: 3 to 7v6
  13. Minor Re-verified, no change to tracked fieldsv5
  14. Minor Site details revised at 1 of 3 sitesv4
  15. Minor Trial status: Enrolling by Invitation to Recruiting
    • Site details revised at 3 of 3 sites
    v3
  16. Minor Study sites: 2 to 3v2
  1. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
12-week, randomized, double-blind, placebo-controlled, parallel-group study of carbetocin nasal spray for the treatment of hyperphagia in Prader-Willi syndrome (PWS)
Trial Details
NCT Number NCT06173531
Lead Sponsor ACADIA Pharmaceuticals Inc.
Conditions
(from sponsor)
Hyperphagia in Prader-Willi Syndrome
Enrollment 175 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov