Safety and Efficacy of OTL78

Sponsor: Clinton Bahler

Sponsor score: 0

ClinicalTrials ID:NCT07725523

This open-label trial evaluates OTL78, a PSMA-targeted fluorescent dye, in up to 45 male participants with confirmed prostate cancer undergoing prostatectomy and lymph node dissection. Eligibility includes age 18+, specific cancer criteria, and consent. Participants receive 0.06 mg/kg zopocianine 1-7 days pre-surgery for enhanced cancer tissue visualization using NIR imaging.

Patient Parameters

Program Overview

This is a trial to assess the accuracy of an imaging agent, PSMA targeted fluorescent dye OTL78 (zopocianine), in combination with Near InfraRed (NIR) fluorescent imaging, to improve the detection of malignant (growing in an uncontrolled way) tissue in adult patients undergoing standard of care prostatectomy and lymph node dissection for biopsy confirmed prostate cancer. This trial is intended to confirm results from previous Phase 2 dose finding studies and to support the dose selection for subsequent Phase 3 development.

Description

Prostate cancer (PCa) is the second leading cause of cancer-related death behind lung cancer. Prostate cells express Prostate Specific Membrane Antigen (PSMA), which is overexpressed in PCa cells in over 90% of patients. On Target has developed a PSMA-targeted agent, the drug product OTL78, that fluoresces under NIR illumination to help with the identification of prostate cancer tissue during resection surgery that has extended beyond the capsule of the prostate into adjacent fossa/surgical bed tissue and lymph nodes before wound closure. Intra-operative identification of cancer tissue using real-time imaging modalities that could improve tumor identification, demarcation and lymph node involvement may provide a very useful tool to reduce the frequency of residual cancer and increase complete removal of locally involved lymph nodes.

This study is an open label trial of an imaging agent, PSMA targeted fluorescent dye (zopocianine, OTL78), in up to 45 participants with biopsy confirmed PCa who have been scheduled to undergo a laparoscopic radical prostatectomy with pelvic lymph node dissection in order to confirm the optimal dose and administration-to-surgery interval of the drug in visualizing cancerous tissue during a standard of care radical prostatectomy.

Eligibility Criteria

Inclusion Criteria

  1. Provision of signed and dated informed consent and HIPAA form

  2. Male participants 18 years of age and older

  3. Known primary prostate cancer and any one of the following:

    1. Grade group 3-5;
    2. Suspected extra-prostatic extension (EPE) or seminal vesicle invasion (SVI);
    3. Suspected lymph node metastasis (clinical stage cN1) by magnetic resonance imaging or by Prostate Specific Membrane Antigen positron emission tomography

  4. Planned to undergo a standard of care robotic prostatectomy and lymph node dissection

  5. Ability to understand the requirements of the study and agree to abide by the study restrictions and to return for the required assessments

  6. Agree to use a medically acceptable method of birth control (e.g., spermicide in conjunction with a barrier such as a condom) or sexual abstinence for the duration of the study, including through final study visit (6 weeks) after the dose of study drug. Sperm donation is prohibited during the study and for 3 months after the dose of study drug. Female partners must use hormonal or barrier contraception unless postmenopausal or abstinent.

  7. Participant scheduled to have or has had a PSMA-PET Scan for surgical treatment planning within 12 months of surgery.

Exclusion Criteria

  1. The surgeon plans to perform an extraperitoneal approach

  2. History of anaphylactic reactions to products containing indocyanine green

  3. History of allergy to any of the components of ZOPOCIANINE:

    1. 2-[3-(1,3-dicarboxypropyl)ureido] pentanedioic acid (DUPA)
    2. Polyethylene glycol-dipeptide linker
    3. Chlorodye

  4. Impaired renal or hepatic function:

    1. Renal: creatinine clearance (eGFR) < 50 mL/min
    2. Hepatic: total bilirubin > 2 × upper limit of normal or ALT/AST > 3 × upper limit of normal.

  5. Participant with QTc interval ≥ 470 msec per electrocardiogram (ECG) at screening calculated via the Bazett formula.

  6. Significant acute or chronic medical, neurologic, or illness in the participant that, in the judgment of the Principal Investigator, could compromise participant safety, limit the ability to complete the study, and/or compromise the objectives of the study.

Locations

FACILITYZIPCITYSTATE
Indiana University Health North Hospital46032CarmelIndiana
Indiana University School of Medicine46202IndianapolisIndiana

Get This Program In Your Inbox

You can sign up and apply your patients for this program.