Recruiting
Phase 1

JUR-003

Sponsor:

Juri Biosciences, Inc.

Code:

NCT07824349

Conditions

Metastatic Castration Resistant Prostate Cancer

Oligometastatic Prostate Cancer (OMPC)

Metastatic Hormone Sensitive Prostate Cancer

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Interventions

JUR-003

Study Details

Brief summary:

JUR-003-ONC-101 is a first-in-human Phase 1a/1b open-label, multicenter study to evaluate the safety, tolerability, PK, pharmacodynamics, and preliminary anti-tumor activity of JUR-003 in patients with prostate cancer. This study is divided into 2 parts: Phase-1a Dose Escalation (Part 1), and Phase-1b Dose Expansion (Part 2). In each part, patients who meet specific eligibility criteria will be enrolled.

Conditions

Metastatic Castration Resistant Prostate Cancer

Oligometastatic Prostate Cancer (OMPC)

Metastatic Hormone Sensitive Prostate Cancer

Study ID

NCT07824349

Start date

Sep, 2026

Status verified date

Jul, 2026

Completion date

Jun, 2030

Anticipated

Primary completion date

Jun, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: Male

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Must be ≥18 years of age at the time the informed consent form (ICF) is signed.
  • Has a histologically or cytologically confirmed adenocarcinoma of the prostate.
  • Has either of the following:

1. Measurable disease per RECIST v1.1 (with PCWG3 modifications)
2. Evaluable disease per PCWG4, as assessed by the local site Investigator/radiology
3. For Part 2.1B (omPC expansion) only: PSMA-avid disease on PSMA-PET, defined as lesion(s) demonstrating uptake above blood pool (PSMA score ≥1) and assessed by the Investigator as consistent with metastatic prostate cancer, in the setting of biochemical recurrence (PSA ≥0.2 ng/mL).

Exclusion Criteria:

  • Has a diagnosis of immunodeficiency.
  • Has had a prior stem cell, bone marrow, or organ transplant.
  • Has a known history of human immunodeficiency virus (HIV) infection.
  • Has active or chronic hepatitis B virus (HBV), or hepatitis C virus (HCV) infection.
  • Has an active autoimmune disease (non-immunotherapy induced conditions) that has required systemic treatment in the past 2 years (ie, with use of disease modifying agents, corticosteroids, or immunosuppressive drugs).
  • Has a history of (noninfectious) pneumonitis that required steroids or current active organizing pneumonitis/interstitial lung disease.
  • Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Individuals with previously treated CNS metastases may participate in JUR-003 monotherapy cohorts (Parts 1.1, 2.1, and 1.3 where applicable) provided they are radiologically stable (ie, without evidence of progression for at least 2 weeks by repeat imaging \[note that the repeat imaging should be performed during study Screening\]), clinically stable, and without requirement of steroid treatment for at least 14 days prior to first dose of study drug.
  • Has untreated spinal cord compression. Individuals must be neurologically stable off steroids for at least 4 weeks prior to first dose of study drug.
  • Has a history of a previous secondary malignancy within 3 years of Screening (except basal cell or squamous cell carcinoma of the skin or carcinoma in situ treated with curative therapy or other localized, low-grade tumors deemed cured, or whose natural history does not have the potential to interfere with the safety or efficacy assessments of the current study and not treated with systemic anticancer therapy \[except hormonal therapy\]).
  • Has a known psychiatric or substance abuse disorder that would interfere with the individuals' ability to cooperate with the requirements of the study.
  • Has a history of venous thromboembolic events (eg, pulmonary embolism) within 1 month prior to the first dose of JUR-003. Uncomplicated (Grade ≤2) deep vein thrombosis is not considered exclusionary.

Study Design

Enrollment

210 participants

Anticipated

Allocation

Non randomized

Intervention Model

Sequential

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Part 1 (Dose Escalation)

Participants will receive JUR-003 to determine the recommended dose for expansion (RDE) regimen.

experimental: Part 2 (Dose Expansion)

Participants will receive JUR-003 at the RDE as determined in Part 1 of the study to confirm the safety and anti-tumor activity.

Interventions

JUR-003

JUR-003 will be administered intravenously.

Primary outcome measure

  • Safety and Tolerability [ Time Frame: 2 years ]
  • Determine Recommended Dose for Expansion [ Time Frame: 1 year ]
  • Characterize Pharmacokinetics [ Time Frame: 2 years ]

Central Contacts and Locations

Central contacts

Locations

START Midwest

Recruiting

Grand Rapids, Michigan, United States, 49546

START New York

Recruiting

Lake Success, New York, United States, 11042

More Information

Sponsor

Juri Biosciences, Inc.

Last update posted

Sep 22, 2026

Last verified

Jul, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-24. This information was provided to ClinicalTrials.gov by Juri Biosciences, Inc. on 2026-09-22. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.