Menu
Peptide Database
Results
No peptides found
Featured

Use search to browse all 100+ peptides

Triptorelin

Decapeptyl, Trelstar, Gonapeptyl, Pamorelin

Quick Stats
Studies 178
Trials 100
Active Not Recruiting EARLY PHASE1 INTERVENTIONAL NCT03511196

Intermittent Androgen Deprivation Therapy for Stage IV Castration Sensitive Prostate Cancer

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Adaptive Androgen Deprivation Therapy (ADT) plus Standard of Care. The purpose of this study is to develop adaptive therapy for high risk metastatic castration sensitive prostate cancer (mCSPC).

Detailed Description

Investigators proposed this pilot feasibility study to use prostate specific antigen (PSA) response and testosterone level to guide the treatment with androgen deprivation therapy (ADT) \[Leuprolide, Goserelin, and Triptorelin are the most commonly used GnRH agonists for ADT\] and/or abiraterone plus prednisone. Adaptive therapy is a program of chemotherapy where the type and dosage of drug changes in an attempt to kill more of the cancer. Abiraterone acetate with prednisone is a standard of care treatment for mCRPC (metastatic castration resistant prostate cancer). It works by interrupting the male hormone (androgen) making process in the testes, adrenal glands, and tumors. This helps to prevent the growth of tumors that need these hormones to grow.

Interventions

Name: Adaptive Androgen Deprivation Therapy (ADT)
Type: DRUG
Description: ADT with Leuprolide, Goserelin, or Triptorelin, as GnRH agonist, every 4 weeks as outlined in study arm description.
Name: Abiraterone
Type: DRUG
Description: Prednisone 5 mg once a day with food.
Name: Prednisone
Type: DRUG
Description: Abiraterone 1000 mg daily with empty stomach.

Primary Outcomes

Measure: Rate of Participant Retention
TimeFrame: 12 months from participant's first dose of ADT
Description: Percentage of participants who remain on study at month 12. The study will be terminated early if 2 or more of the first 6 enrolled subjects discontinued study due to cancer progression within a year of study enrollment.

Trial Information

NCT ID

NCT03511196

Status

Active Not Recruiting

Study Type

INTERVENTIONAL

Phases

EARLY PHASE1

Sponsor

H. Lee Moffitt Cancer Center and Research Institute

Last Updated

December 15, 2025