# Debiopharm International SA: Phase 3 study closed enrollment, 56 enrolled (Central Precocious Puberty)

**Score:** 90/100

| Field | Value |
|---|---|
| Sponsor | Debiopharm International SA |
| Sponsor type | Industry (pharma, biotech, medtech) |
| Study | A Study to Assess the Efficacy, Safety, and Pharmacokinetics of Debio 4326 in Pediatric Participants With Central Precocious Puberty (LIBELULA™ Clinical Trial) |
| NCT ID | NCT06129539 |
| Phase | Phase 3 |
| Status | active not recruiting |
| Conditions | Central Precocious Puberty |
| Intervention types | drug |
| Target enrollment | 56 |
| Site countries | United States, Argentina, Brazil, Chile, Mexico |
| Posted | 2023-11-13 |
| Planned start | 2024-07-31 |
| Event | Enrollment closed (active, not recruiting) |
| Event date | 2026-10-23 |
| Last update posted | 2026-10-23 |

## Why this score
- Posted in the last two weeks.
- Industry sponsor (buys outsourced services).
- Enrollment closed: data management, monitoring and closeout ahead.
- Phase 3: multi-site, larger budget.

Source: ClinicalTrials.gov (U.S. National Library of Medicine) API v2 (https://clinicaltrials.gov/study/NCT06129539). Last refreshed: 2026-11-04T06:04:38.232Z.
From public ClinicalTrials.gov registrations. Sponsor and study level only: we never list investigators, contacts or participants. A registration describes a planned study and can change. Status changes are read from each study's current status, actual dates and latest posted update, not a full change history, so an update can be a correction rather than a new change. Verify on ClinicalTrials.gov.