Prostatectomy Clinical Trials

Clinical trials related to Prostatectomy Procedure

IIT2023-10-Posadas-PC-Net : A Platform Study of Epigenetic Therapy Before Prostatectomy in Men With Prostate Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

This is an open-label, non-randomized, exploratory platform protocol designed to assess the safety and antitumor activity of epigenetic therapies in participants with localized prostate cancer who are undergoing radical prostatectomy. The epigenetic therapy is intended to increase the sensitivity of the underlying tumor to the patient's immune system. The platform study will evaluate safety, biomarkers, and clinical activity of an epigenetic therapy. The particular details relevant to each module within this platform study will be provided as appendices to the core protocol.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Men electing to undergo radical prostatectomy with preoperative tissue available.

• Age ≥18 years

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1

• Adequate organ function defined by:

‣ AST and ALT \< 2.5 x ULN

⁃ Total bilirubin \< 1.5 x ULN

⁃ Platelets \> 90 x 1000/μL

⁃ Hemoglobin (Hgb) \> 8.5 g/dL

⁃ Serum Creatinine (Cr) \<1.5 x ULN or eGFR \> 30 mL/min

• People with partners of childbearing potential in circumstances that may result in the pregnancy, must have had a successful vasectomy (with medically confirmed lack of sperm that are alive) OR must either practice complete abstinence or agree to use adequate contraception (latex or synthetic condom during sexual contact with a female of childbearing potential) from the start of study treatment until 3 months following last dose of study intervention. Subjects should not donate sperm on study, during interruptions in treatment and for 3 months following completion of study drug treatment.

• Written informed consent obtained from subject and ability for subject to comply with the requirements of the study.

Locations
United States
California
Cedars-Sinai Cancer at SOCC
RECRUITING
Los Angeles
Contact Information
Primary
Clinical Trial Navigator
cancer.trial.info@cshs.org
3104232133
Time Frame
Start Date: 2026-04
Estimated Completion Date: 2029-10
Participants
Target number of participants: 20
Treatments
Experimental: Neoadjuvant Epigenetic Therapy
Related Therapeutic Areas
Sponsors
Leads: Edwin Posadas, MD

This content was sourced from clinicaltrials.gov

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