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A Study of 2141-V11 in Combination With Standard Treatments in People With Prostate Cancer

NCT06347705

This study is recruiting at 7 US sites in 2 states, according to its ClinicalTrials.gov record last updated .

Summary

The purpose of this study is to see whether combining 2141-V11 with various standard treatments is an effective treatment approach for prostate cancer. 2141-V11 works by activating the immune system to find and kill cancer cells. Researchers will look at whether this treatment approach is able to completely get rid of cancer in participants, and they will check for the presence of minimal residual disease (MRD) in participants. MRD is a small number of cancer cells that can be detected in the body after treatment.

Shortened from the sponsor's brief summary. View official record on ClinicalTrials.gov

Conditions studied

  • Prostate Cancer

Eligibility basics and study details

Study type
Interventional
Phase
Phase 2
Ages
18 years and older
Sex
Male
Healthy volunteers
Not accepted
Sponsor
Memorial Sloan Kettering Cancer Center
Last updated on ClinicalTrials.gov
April 16, 2026

These are the basic criteria only. The full inclusion and exclusion criteria are on the official record, and the study team decides who can take part.

US recruiting sites

New Jersey · 3

  • Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities) · Basking Ridge, NJ
  • Memorial Sloan Kettering Monmouth (Limited protocol activities) · Middletown, NJ
  • Memorial Sloan Kettering Bergen (Limited Protocol Activities) · Montvale, NJ

New York · 4

  • Memorial Sloan Kettering Suffolk-Commack (Limited protocol activity) · Commack, NY
  • Memorial Sloan Kettering Westchester (Limited Protocol Activities) · Harrison, NY
  • Memorial Sloan Kettering Cancer Center (All protocol activites) · New York, NY
  • Memorial Sloan Kettering Nassau (Limited Protocol Activites) · Rockville Centre, NY

Source: ClinicalTrials.gov, data processed . Recruiting US sites filtered by distance and site status; summaries shortened.