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goserelin

Generic: GOSERELIN ACETATE·Brand: ZOLADEX, Zoladex

goserelin: 20 clinical trials tracked.

goserelin evidence translation

What we can confirm

20 tracked trials

No verified listed developer

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about goserelin, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence6 indications · 8 study sponsors
Clinical Trials (20)showing 10 most recent

preEMBER: A Phase 2, Open-label Study Evaluating Imlunestrant in Premenopausal Women With Estrogen Receptor-Positive, HER2-Negative Breast Cancer

NCT07287098·Phase 2·LLY
Recruiting

Primary endpoint: Change from Baseline in Antigen Kiel (Ki-67) Expression

InterventionalRandomizedopen600 targetStarted 2026-05Completion 2029-1250 sites · Belgium, France, Germany, United StatesEli Lilly and Company

Phase 2 Randomized Trial to Examine Ovarian Function Suppression for Breast Cancer (OFS)

NCT07158021·Phase 2·MYOV
Recruiting

Primary endpoint: Proportion of participants with ultrasensitive estradiol concentration > 10 pg/ml

InterventionalRandomizedopen75 targetStarted 2026-01Completion 2028-011 site · United StatesUniversity of Michigan Rogel Cancer Center

A Phase 1, Open Label, Randomized, 2-sequence, 2-period, Cross-over, Single Center Study to Assess the Bioequivalence of Follitropin Alfa Solution for Injection in Prefilled Pen (Test) and Follitropin Alfa Powder and Diluent for Solution for Injection in Vial (Reference) in Healthy Downregulated Male Participants

NCT07097259·Phase 1
Completed

Primary endpoint: Baseline Adjusted Area Under the Serum Concentration-Time Curve From Time Zero to Last Quantifiable Sampling Time After Administration (AUC0-t, adj) of Follitropin Alfa

InterventionalRandomizedopen55 enrolledStarted 2025-07Completion 2025-121 site · United StatesEMD Serono Research & Development Institute, Inc.

SELECT: A Phase II Adjuvant Trial Evaluating the Impact of Omitting Chemotherapy Based on Patient's Selection for Moderate to High-Anatomical Risk, Low-Genomic Risk, ER-Positive, HER2- Negative Breast Cancer With a Combination Regimen of Ribociclib and Optimized Endocrine Therapy

NCT06953882·Phase 2
Recruiting

Primary endpoint: Discontinuation rate of ribociclib in patients with resected moderate to high-anatomical risk, low-genomic risk, ER-positive, HER2-negative breast cancer

InterventionalRandomizedopen140 targetStarted 2025-07Completion 2030-091 site · United StatesYale University

MC230502 Dynamic Investigator Initiated Enterprise (DIVINE) in Prostate Cancer

NCT06378866·Phase 2·KYNB
Recruiting

Primary endpoint: Modified radiographic progression-free survival (mrPFS) (Groups A & B)

InterventionalRandomizedopen532 targetStarted 2024-06Completion 2029-053 sites · United StatesMayo Clinic

A Phase IIIb Study to Characterize the Efficacy and Safety of Adjuvant Ribociclib Plus Endocrine Therapy in a Close-to-clinical Practice Patient Population With HR+ HER2- Early Breast Cancer (Adjuvant WIDER)

NCT05827081·Phase 3·NVS
Recruiting

Primary endpoint: Invasive Breast Cancer Free Survival (iBCFS) rate at 3 years

Interventionalopen1,400 targetStarted 2024-02Completion 2030-0950 sites · United StatesNovartis Pharmaceuticals

A Phase 2 Trial of (Z)-Endoxifen + Goserelin as Neoadjuvant Treatment for Premenopausal Women With ER+, HER2-, Breast Cancer

NCT05607004·Phase 2·ATOS
Active, not recruiting

Primary endpoint: PK Cohort - (Z)-endoxifen steady-state plasma concentrations

Interventionalopen87 targetStarted 2023-02Completion 2027-0414 sites · United StatesAtossa Therapeutics, Inc.

Real World Evidence Study on Metastatic Prostate Cancer Patient Characteristics, Treatment Patterns and Outcomes in the Pirkanmaa Hospital District in Finland

Completed

Primary endpoint: Body Mass Index (BMI)

Observational1,083 enrolledStarted 2023-02Completion 2024-041 site · FinlandPfizer

A Post-trial Access Roll-over Study to Allow Access to Ribociclib (LEE011) for Patients Who Are on Ribociclib Treatment in Novartis-sponsored Study

NCT05161195·Phase 4·NVS
Active, not recruiting

Primary endpoint: Percentage of participants with treatment-emergent adverse events (AES)

Interventionalopen134 targetStarted 2022-07Completion 2030-0850 sites · Argentina, Brazil, China, Costa Rica…Novartis Pharmaceuticals

Parallel Phase III Randomized Trials of Genomic-Risk Stratified Unfavorable Intermediate Risk Prostate Cancer: De-Intensification and Intensification Clinical Trial Evaluation (GUIDANCE)

NCT05050084·Phase 3·CGON
Active, not recruiting

Primary endpoint: Distant metastasis (DM) (De-intensification study)

InterventionalRandomizedopen2,050 targetStarted 2021-12Completion 2026-1150 sites · United StatesNRG Oncology