Feasibility of the LUM Imaging System for Detection of Prostate Cancer

L

Lumicell

Status and phase

Terminated
Phase 2
Phase 1

Conditions

Neoplasm, Residual
Prostate Cancer

Treatments

Combination Product: LUM Imaging System

Study type

Interventional

Funder types

Industry

Identifiers

NCT03441464
CL0005

Details and patient eligibility

About

The primary objective of this feasibility study is to determine if administration of LUM015 will result in positive fluorescence of tumor tissue from ex vivo specimen imaging with the LUM Imaging device from patients undergoing radical prostatectomy for prostate cancer. Both normal tissue and tumor tissue will be imaged and analyzed. The LUM Imaging System is a portable combination product consisting of an imaging device and an imaging agent (LUM015). Patients with an established diagnosis of prostate cancer and who are eligible for radical prostatectomy will be screened. Eligible patients will be enrolled and on the day of their planned surgery, LUM015 will be administered 2-6 hours prior to surgery. Patients will undergo radical prostatectomy 2-6 hours after LUM015 administration. All surgical specimens will be imaged with the LUM imaging device and have routine diagnostic assessment. Patients will be monitored for adverse events from time of injection through the first standard of care post-surgical follow-up visit.

Full description

The primary objective of this feasibility study is to determine if administration of LUM015 will result in positive fluorescence of tumor tissue from ex vivo specimen imaging with the LUM Imaging device from patients undergoing radical prostatectomy for prostate cancer. Both normal tissue and tumor tissue will be imaged and analyzed. The LUM Imaging System is a portable combination product consisting of an imaging device and an imaging agent (LUM015). Patients with an established diagnosis of adenocarcinoma of the prostate and who are eligible for radical prostatectomy will be screened. Patients will be seen by their surgeon in an office visit and undergo routine preoperative testing within 8 weeks of their planned procedure. After obtaining informed consent and confirming eligibility, patients will be enrolled and on the day of their planned surgery, LUM015 will be administered by bolus intravenous injection 2-6 hours prior to surgery. This injection is the only procedure that will be performed on patients outside of their routine care (standard of care). LUM015 will be administered in a single dose between 0.5 -1.5 mg/kg in up to 9 patients. An additional 3 patients will not be injected with LUM015, but their specimens will undergo LUM imaging. Patients will undergo radical prostatectomy 2-6 hours after LUM015 administration. All surgical specimens will be sent to the pathology suite for imaging with the LUM imaging device and routine diagnostic assessment. Imaging will be performed on the resected specimens. Alternatively, specimens can also be imaged in the operating room. Imaged areas showing high fluorescence will be marked with ink to guide pathology evaluation and determine whether the area contains tumor. Samples of imaged areas showing low fluorescence signal will also be evaluated by pathology to determine whether the area only contains normal tissue. Additional resection will not be performed if a positive surgical margin is detected by imaging. Patients are expected to be admitted to the hospital for the surgical procedure and will remain in the hospital post-surgery per standard of care treatment. Laboratory studies will be performed to assess for any imaging agent related adverse events prior to hospital discharge and at the standard of care post-surgical follow-up visit. Patients will be followed through their first standard of care post-surgical visit. Additionally, patients will be monitored for adverse events from time of injection through the first standard of care post-surgical visit. Patients with adverse events that are possibly related to LUM015 will be followed until resolution or stabilization of the adverse event.

Enrollment

9 patients

Sex

Male

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with clinically localized or locally advanced prostate cancer and scheduled for radical prostatectomy
  • Age 40 years or older
  • Able and willing to follow study procedures and instructions
  • Received and signed informed consent form
  • Otherwise healthy except for diagnosis of cancer

Normal organ and marrow function as defined below:

  • Hemoglobin 13.9 - 16.3 g/dL
  • Leukocytes 4500 - 11,000 uL
  • Platelets 150,000 - 450,000 uL
  • Total bilirubin within normal institutional limits
  • AST (SGOT)/ALT (SGPT) within normal institutional limits
  • Creatinine within normal institutional limits or creatinine clearance within normal institutional limits
  • ECOG performance status of 0 or 1

Exclusion criteria

  • Known current substance addiction
  • Have taken an investigational drug within 30 days of enrollment
  • Received methylene blue prior to tissue excision
  • QT Interval > 480ms
  • Have not recovered from an adverse event due to pharmaceutical or diagnostic agent
  • Uncontrolled hypertension defined as persistent systolic blood pressure > 180 mm Hg, or diastolic blood pressure > 100 mm Hg; subjects with known HTN should be under these values while under pharmaceutical therapy
  • History of allergic reaction attributed to drugs containing polyethylene glycol (PEG).
  • History of allergic reaction to any oral or intravenous contrast agents.
  • Uncontrolled intercurrent illness including but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, COPD or asthma requiring hospitalization within the past 12 months, or psychiatric illness/social situations that would limit compliance with study requirements
  • Sexually active subjects unwilling/unable to use medically acceptable forms of contraception during study participation
  • HIV-positive subjects on combination antiretroviral therapy
  • Investigator feels subject's participation is not in the best interest of the subject
  • Previously treated with local or systemic therapies to treat prostate cancer

Trial design

Primary purpose

Device Feasibility

Allocation

Non-Randomized

Interventional model

Sequential Assignment

Masking

None (Open label)

9 participants in 4 patient groups

1st Tier Dose Level
Experimental group
Description:
3 patients administered single dose of LUM015 at 0.5 mg/kg. Imaging with the LUM imaging device will be performed ex vivo on resected tissue.
Treatment:
Combination Product: LUM Imaging System
2nd Tier Dose Leel
Experimental group
Description:
3 patients administered single dose of LUM015 at 1.0 mg/kg. Imaging with the LUM imaging device will be performed ex vivo on resected tissue.
Treatment:
Combination Product: LUM Imaging System
3rd Tier Dose Level
Experimental group
Description:
After evaluation of the fluorescence signal observed with the LUM imaging device in the three other cohorts,the subsequent 3 patients will receive a dose of 0.5-1.5 mg/kg.
Treatment:
Combination Product: LUM Imaging System
Auto-fluorescence
No Intervention group
Description:
No LUM015 injection will be given to three (3) patients to measure baseline tissue fluorescence. The tissue will still be imaged ex-vivo using the LUM Imaging Device

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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