Clinical Trials Directory

Trials / Terminated

TerminatedNCT03936933

Pharmacodynamic Study Goserelin 3.6mg Injection Administered Subcutaneously in Premenopausal Patients with Breast Cancer

Two Arm, Multicentric, Randomized, Open Label, Parallel, Multiple Dose Study Subcutaneous Injection of Goserelin 3.6 Mg (Eurofarma) Vs ZOLADEX 3.6 Mg (AstraZeneca) Administered Subcutaneously in Premenopausal Patients with Breast Cancer.

Status
Terminated
Phase
Phase 3
Study type
Interventional
Enrollment
6 (actual)
Sponsor
Eurofarma Laboratorios S.A. · Industry
Sex
Female
Age
18 Years – 59 Years
Healthy volunteers
Not accepted

Summary

A two arm, multi centric, randomized, open label, parallel, multiple dose pharmacodynamic study in premenopausal patients with advanced breast cancer.

Detailed description

A phase III, two arm, multi centric, randomized, open label, parallel, multiple dose pharmacodynamic study in premenopausal patients with breast cancer

Conditions

Interventions

TypeNameDescription
DRUGGoserelin acetate 3.6 mg Injection3.6 mg, Subcutaneously at every 28 days
DRUGZOLADEX® 3.6mg Injection3.6 mg, Subcutaneously at every 28 days

Timeline

Start date
2020-10-30
Primary completion
2024-09-30
Completion
2025-01-30
First posted
2019-05-03
Last updated
2025-02-17

Locations

1 site across 1 country: India

Source: ClinicalTrials.gov record NCT03936933. Inclusion in this directory is not an endorsement.