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Sputum Labeling Utilizing Synthetic Meso-Tetra (4-Carboxyphenyl) Porphine (TCPP) for Detection of Lung Cancer

Primary Purpose

Lung Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
CyPath®
Sponsored by
bioAffinity Technologies Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Lung Cancer focused on measuring Lung Cancer, Porphyrin, Fluorescence, Diagnostic, Sputum Cytology, Early Detection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Participants who have never smoked nor have known lung diseases

Exclusion Criteria:

  • Severe obstructive lung disease
  • Angina with minimal exertion
  • Pregnancy
  • Have or have had cancer other than lung cancer
  • Worked in the mining Industry

Sites / Locations

  • Radiology Associates of Albuquerque (RAA)

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

CyPath® Assay of Deep-Lung Sputum Sample

Arm Description

Deep-lung sputum was obtained from healthy individuals who had no known lung disease, was labeled with TCPP and evaluated to detect red fluorescent [ie, cancer] cells (RFCs) from deep-lung sputum samples.

Outcomes

Primary Outcome Measures

Number of Red Fluorescent [i.e., Cancer] Cells (RFCs) in Sputum From Healthy Participants
The presence or absence of red fluorescent (RFCs) cancer cells was evaluated in sputum samples from healthy individuals labeled with CyPath®. Testing for the study was performed at one study center to collect sputum samples from healthy individuals who have no known lung disease. Comparison of sputum specimens from one cohort of Participants who are healthy with two additional cohorts of Participants, including individuals at high risk for lung cancer and individuals diagnosed with lung cancer, that has already been completed.

Secondary Outcome Measures

Full Information

First Posted
March 4, 2015
Last Updated
June 16, 2015
Sponsor
bioAffinity Technologies Inc.
Collaborators
Radiology Associates of Albuquerque
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1. Study Identification

Unique Protocol Identification Number
NCT02388074
Brief Title
Sputum Labeling Utilizing Synthetic Meso-Tetra (4-Carboxyphenyl) Porphine (TCPP) for Detection of Lung Cancer
Official Title
Sputum Labeling Utilizing Synthetic Meso Tetra (4-Carboxyphenyl) Porphine (TCPP) for Detection of Lung Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
bioAffinity Technologies Inc.
Collaborators
Radiology Associates of Albuquerque

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a single center study to assess the efficacy of CyPath® Early Detection Lung Cancer Assay to detect lung cancer cells from deep lung sputum.
Detailed Description
Meso Tetra (4-Carboxyphenyl) Porphine (TCPP) is a porphyrin that can label cancer cells by reacting to the increased number of low-density lipoproteins coating the surface of cancer cells and the porous nature of the cancer cell membrane, causing the cell to fluoresce under specific wavelengths of light. The primary objective of this clinical trial is to determine the the presence or absence of red fluorescent [ie, cancer] cells (RFCs) from deep-lung sputum samples using the CyPath® Early Lung Cancer Detection Assay from one cohort of Participants who are healthy. The results from this trial will be compared with two additional cohorts of Participants including individuals at high risk for lung cancer and individuals diagnosed with lung cancer. Collection of the sputum samples from high-risk individuals and lung cancer patients is complete (NCT00894127). Participants who satisfy the inclusion/exclusion criteria will be enrolled into the study and assigned to the healthy cohort. The sputum samples will be collected at the study site or at the Participant's home after explanation of the collection procedure by study staff. Samples will be identified with an identification number blinding the sample identity. Each subject's sputum specimen will be processed onto 13 microscope slides at the University of Texas Health Science Center of San Antonio (UTHSCSA) Laboratory. The UTHSCSA laboratory will process each sputum sample onto slides using the ThinPrep T2000 processor for use in the CyPath® Early Lung Cancer Detection Assay. Twelve slides from each sputum sample will be labeled with CyPath®. One slide will be used to preform PAP staining for the presence of macrophages. Macrophages are an indication that the sputum sample is from deep within the lungs. A cytopathologist will review the slide and record results on a specimen adequacy form. bioAffinity researchers who will be blinded as to the Participant's identity will perform the CyPath® labeling and scoring of the slides. The study results of the healthy cohort will be used for comparison with the results of a closed study in which the sputum from individuals at high risk of lung cancer and individuals diagnosed with lung cancer was compared. Findings of the CyPath® assay will not be used in the diagnosis or treatment of Participants.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Cancer
Keywords
Lung Cancer, Porphyrin, Fluorescence, Diagnostic, Sputum Cytology, Early Detection

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Investigator
Allocation
N/A
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CyPath® Assay of Deep-Lung Sputum Sample
Arm Type
Experimental
Arm Description
Deep-lung sputum was obtained from healthy individuals who had no known lung disease, was labeled with TCPP and evaluated to detect red fluorescent [ie, cancer] cells (RFCs) from deep-lung sputum samples.
Intervention Type
Device
Intervention Name(s)
CyPath®
Intervention Description
CyPath® diagnostic assay for the early detection of lung cancer using sputum
Primary Outcome Measure Information:
Title
Number of Red Fluorescent [i.e., Cancer] Cells (RFCs) in Sputum From Healthy Participants
Description
The presence or absence of red fluorescent (RFCs) cancer cells was evaluated in sputum samples from healthy individuals labeled with CyPath®. Testing for the study was performed at one study center to collect sputum samples from healthy individuals who have no known lung disease. Comparison of sputum specimens from one cohort of Participants who are healthy with two additional cohorts of Participants, including individuals at high risk for lung cancer and individuals diagnosed with lung cancer, that has already been completed.
Time Frame
2 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participants who have never smoked nor have known lung diseases Exclusion Criteria: Severe obstructive lung disease Angina with minimal exertion Pregnancy Have or have had cancer other than lung cancer Worked in the mining Industry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lara Patriquin, MD
Organizational Affiliation
Radiology Associates of Albuquerque
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radiology Associates of Albuquerque (RAA)
City
Albuquerque
State/Province
New Mexico
ZIP/Postal Code
87109
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Sputum Labeling Utilizing Synthetic Meso-Tetra (4-Carboxyphenyl) Porphine (TCPP) for Detection of Lung Cancer

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