Last reviewed · How we verify

NCT06984159

The Study Will Evaluate if Leuprolide Mesylate is Safe and Effective in the Treatment of Subjects With Advanced Prostate Carcinoma, When Administered as Two Injections Six Months Apart.

Completed Phase 3 Last updated 22 May 2025
What this trial tests

Phase 3 trial testing Leuprolide Injectable Emulsion (CAMCEVI®) in Advanced Prostate Cancer in 137 participants. Completed in 24 April 2024.

Timeline
12 July 2022
Primary endpoint
30 November 2023
24 April 2024

Quick facts

Lead sponsorChangchun GeneScience Pharmaceutical Co., Ltd.
PhasePhase 3
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment137
Start date12 July 2022
Primary completion30 November 2023
Estimated completion24 April 2024
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Changchun GeneScience Pharmaceutical Co., Ltd. — full company profile →

Who can join

18 and older, male only, with Advanced Prostate Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the Safety, Efficacy and Pharmacokinetics of Leuprolide Injectable Emulsion in Advanced Prostate Cancer

Publications & conference data

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

Verify or expand the search:

Other recruiting trials for Advanced Prostate Cancer

Currently open trials in the same condition.

Other Changchun GeneScience Pharmaceutical Co., Ltd. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06984159.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing