Light Dosimetry for Photodynamic Therapy With Porfimer Sodium in Treating Participants With Malignant Mesothelioma or Non-Small Cell Lung Cancer With Pleural Disease Undergoing Surgery

NCT03678350 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2026-03-27

No results posted yet for this study

Summary

This phase I trial studies the side effects and how well light dosimetry system works during photodynamic therapy with porfimer sodium in treating participants with malignant mesothelioma , non-small cell lung cancer or any other malignancy with pleural disease undergoing surgery. Light dosimetry measures the amount of laser light given during photodynamic therapy. Photodynamic therapy uses a drug, such as porfimer sodium, that becomes active when it is exposed to light. The activated drug may kill tumor cells. Using light dosimetry for intraoperative photodynamic therapy may help doctors estimate how much light is delivered during photodynamic therapy and decide if the treatment should be stopped or continued.

Conditions

  • Malignant Mesothelioma
  • Non-Small Cell Lung Carcinoma
  • Pleural Disorder

Interventions

DEVICE

Light Dosimetry for Intranoperative Therapy

Undergo IO-PDT

PROCEDURE

Photodynamic Therapy

Undergo IO-PDT

DRUG

Porfimer Sodium

Given IV

Sponsors & Collaborators

  • Lumeda,Inc.

    collaborator UNKNOWN
  • Roswell Park Cancer Institute

    lead OTHER

Principal Investigators

  • Saikrishna Yendamuri · Roswell Park Cancer Institute

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-17
Primary Completion
2023-11-13
Completion
2025-10-09
FDA Drug
Yes
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03678350 on ClinicalTrials.gov