Study to Assess the Feasibility of Stopping Prostate Cancer Treatment Early in Elderly Patients
Launched by UNIVERSITY OF CHICAGO · Feb 12, 2025
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at whether elderly men with prostate cancer can safely stop their hormone treatment earlier than usual. The treatment being studied is called LHRH agonist therapy, which helps lower testosterone levels that can fuel prostate cancer growth. Researchers believe that after being on this treatment for a long time, many older patients may no longer need it because their testosterone levels have become very low and stable. Throughout the study, participants will have their testosterone levels checked regularly to monitor their health.
To participate in this study, men must be at least 70 years old and have been receiving LHRH agonist therapy for more than three years. They should also have a low baseline testosterone level and be able to understand and agree to the study requirements. Importantly, this trial is not yet recruiting participants, but it aims to provide valuable insights into the treatment needs of older men with prostate cancer. If you or someone you know fits these criteria, this study could offer a chance to explore the possibility of reducing or stopping treatment safely.
Gender
MALE
Eligibility criteria
- Inclusion Criteria:
- • Prostate cancer with \>3 years of LHRH agonist therapy.
- • Age ≥70 years.
- • ECOG performance status ≤2
- • Baseline testosterone of \< 20 ng/ml
- • No prior chemotherapy or Lu-PSMA (unless survival predictions are favorable).
- • Ability to understand and sign informed consent.
- Exclusion Criteria:
- • none
About University Of Chicago
The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
Chicago, Illinois, United States
Patients applied
Trial Officials
Nabiel Mir, MD
Study Chair
University of Chicago
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported