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NCT03316482

Leuprorelin Acetate DPS (Leuplin DPS) Treatment Quarterly in Patients With Central Precocious Puberty

Completed Phase 4 Last updated 2 June 2020
What this trial tests

Phase 4 trial testing Leuplin DPS 11.25mg in Central Precocious Puberty in 58 participants. Completed in 30 December 2019.

Timeline
11 June 2015
Primary endpoint
29 August 2019
30 December 2019

Quick facts

Lead sponsorJin Soon Hwang
PhasePhase 4
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment58
Start date11 June 2015
Primary completion29 August 2019
Estimated completion30 December 2019
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Jin Soon Hwang — full company profile →

Who can join

Adults 4 to 9, any sex, with Central Precocious Puberty. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A multicenter, open-label, prospective study to evaluate the safety and efficacy of leuprorelin acetate DPS (Leuplin DPS) treatment quarterly in patients with central precocious puberty

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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