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RecruitingProstate Cancer

Study of STM-416p Administered to Patients Undergoing Radical Prostatectomy

Eligible age

18+ yrs

Accepts

Men

Locations

2 states

Healthy volunteers

No

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About this study

A Study of STM-416p Administered Intraoperatively to Patients Undergoing Radical Prostatectomy

Sponsor: SURGE Therapeutics

You may qualify if…

  • 1. Males aged 18 years or older at time of informed consent.
  • 2. Have a histologically confirmed diagnosis of prostate cancer, and are scheduled to undergo radical prostatectomy within 28 days of screening.
  • 3. Grade Group 2-5.
  • 4. Eastern Cooperative Oncology Group (ECOG) Performance Status ≤2 at Screening.
  • 5. Have adequate organ and bone marrow function at screening.
  • 6. Able to understand and be willing to sign an Institutional Review Board/Ethics Committee-approved written informed consent document

You may not qualify if…

  • 1. Have an invasive malignancy, other than the disease under study.
  • 2. Anticipated to require the use of a drain after radical prostatectomy.
  • 3. Received any other anticancer therapy (e.g., including but not limited to chemotherapy, biologic therapy, immunotherapy, targeted therapy, endocrine therapy, radiation therapy, intravesical therapy ) within 28 days.
  • 4. History of allergic reactions attributed to compounds of similar chemical or biologic composition as those used in the STM-416p formulation including poloxamer 407 and sodium hyaluronate.
  • 5. History of allogeneic organ transplant.
  • 6. History of primary immunodeficiency.
  • 7. QTc interval \>470 msec at Screening.

Where it's recruiting

Arizona

Tucson

Florida

Gainesville

Source: ClinicalTrials.gov · NCT06450106 · last updated 2026-02-19

Study of STM-416p Administered to Patients Undergoing Radical Prostate · TrialPath