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NCT05656573RecruitingPhase 1

CART-PSMA Cells for Advanced Prostate Cancer

Phase I Study of CART-PSMA Cells in Patients With Advanced Prostate Cancer

Source: ClinicalTrials.gov · Last updated 15 Nov 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This is a single center, open-label phase 1 study to assess the safety and feasibility of PSMA-specific CAR modified autologous T cells (CART-PSMA cells) in patients with advanced prostate cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
20 (estimated)
First submitted
1 Dec 2022
Start date
1 Mar 2023
Primary completion date
1 Dec 2025
Lead sponsor
Nova Therapeutics LLC
NCT number
NCT05656573

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 20
  • From 1 Mar 2023 to the primary completion date, 1 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients who are already undergoing other clinical drug trials or other gene therapy or cell therapy.
  • Patients who are being treated with immunosuppressive agents or systemic steroids (other than inhalation therapy).

Other illness

  • Patients with other malignant tumors or major diseases.
  • Patients with uncontrolled active infection.
  • Patients with active hepatitis B or hepatitis C infection.
  • Patients with human immunodeficiency virus (HIV) infection.
  • Patients with various types of serious heart disease or a history of severe cerebrovascular disease.
  • Patients with congenital immune deficiency diseases or bone marrow deficiency diseases.
  • Patients with active autoimmune disease, including connective tissue disease, uveitis, inflammatory bowel disease, or multiple sclerosis; or a history of severe (as judged by the physician-investigator) autoimmune disease requiring prolonged immunosuppressive therapy.
  • Patients with active medical condition that, in the opinion of the physician-investigator, would substantially increase the risk of uncontrollable CRS (cytokine release syndrome) or CAR Neurotoxicity.

Who the study is looking for

  • All participants must have the ability to understand and the willingness to sign a written informed consent.
  • Histologic confirmation of prostate cancer.
  • Tumor expressing PSMA as demonstrated by immunohistochemistry analysis or other methods.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 - 2.
  • Under general air conditions, blood oxygen saturation \>90%.
  • Adequate liver function, specifically alanine aminotransferase (ALT) \< 3 times of upper limit of normal (ULN), aspartate transferase (AST)\< 3 times of ULN, serum bilirubin and alkaline phosphatase \< 2 times of ULN.
  • Adequate renal function, specifically serum creatinine \< 2.0 mg/dl.
  • Adequate cardiac function, specifically left ventricular ejection fraction (LVEF)≥50%.
  • Hemoglobin concentration ≥80g/L.
  • The side effects brought by the latest treatment should be recovered, and the latest chemotherapy should be at least 7 days before; At least three t½ have passed since the latest immunotherapy.

Age in the registry: 35 years to 85 years · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chinese PLA General Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.