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OncoMatch/Clinical Trials/NCT02584244

Feasibility of the LUM Imaging System for Detection of Gastrointestinal Cancers

Is NCT02584244 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including LUM015 and LUM 2.6 Imaging Device for colorectal cancer.

Phase 1/2RecruitingLumicell, Inc.NCT02584244Data as of Jun 2026

Treatment: LUM015 · LUM 2.6 Imaging DeviceThe overall goal of this feasibility study is to assess the initial safety and efficacy of LUM015 in ex vivo far-red imaging of colorectal, pancreatic, and esophageal cancers (adenocarcinoma) using the LUM Imaging System.

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Extracted eligibility criteria

Treatments studied

Other

LUM015LUM 2.6 Imaging Device

Cancer type

Colorectal Cancer

Pancreatic Cancer

Esophageal Carcinoma

Gastric Cancer

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: investigational drug

Subjects who have taken an investigational drug within 30 days of enrollment

Lab requirements

Blood counts

Leukocytes >= 3,000/mcL; Absolute neutrophil count >= 1,500/mcL; Platelets >= 100,000/mcL

Kidney function

Creatinine within normal institutional limits or creatinine clearance >= 60 mL/min/1.73 m2 for subjects with creatinine levels above institutional normal

Liver function

total bilirubin within normal institutional limits (except in cases of malignant biliary obstruction); AST (SGOT)/ALT (SGPT) <= 2.5 X institutional upper limit of normal (<= 5 x ULN in cases of malignant biliary obstruction)

Cardiac function

QTc interval <= 480ms

Subjects must have normal organ and marrow function as defined below: Leukocytes >= 3,000/mcL; Absolute neutrophil count >= 1,500/mcL; Platelets >= 100,000/mcL; total bilirubin within normal institutional limits (except in cases of malignant biliary obstruction); AST (SGOT)/ALT (SGPT) <= 2.5 X institutional upper limit of normal (<= 5 x ULN in cases of malignant biliary obstruction); Creatinine within normal institutional limits or creatinine clearance >= 60 mL/min/1.73 m2 for subjects with creatinine levels above institutional normal. Subjects with QTc interval > 480ms [excluded].

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Massachusetts General Hospital · Boston, Massachusetts

Showing up to 5 US sites.

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Frequently asked questions

Is NCT02584244 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior investigational drug disqualifies patients from enrollment.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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