Prospective Collection of Whole Blood From Active Non-Small Cell Lung Cancer Patients for Supplemental Research

Description

The study objective is to collect biospecimen samples (e.g., whole blood) from participants diagnosed with active lung cancer to investigate the immune response to develop treatments and therapies.

Conditions

Non Small Cell Lung Cancer

Study Overview

Study Details

Study overview

The study objective is to collect biospecimen samples (e.g., whole blood) from participants diagnosed with active lung cancer to investigate the immune response to develop treatments and therapies.

Prospective Collection of Whole Blood From Active Non-Small Cell Lung Cancer Patients for Supplemental Research

Prospective Collection of Whole Blood From Active Non-Small Cell Lung Cancer Patients for Supplemental Research

Condition
Non Small Cell Lung Cancer
Intervention / Treatment

-

Contacts and Locations

Waltham

Sanguine Biosciences, Waltham, Massachusetts, United States, 02451

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Participants willing and able to provide written informed consent
  • * Participants are willing and able to provide appropriate photo identification
  • * Participant's age 18 - 100 years old
  • * Participants diagnosed with active non-small cell lung cancer (Adenocarcinoma or Squamous Cell only. All stages are acceptable.)
  • * Participants must have associated tissue biomarker data (EFGR and MET mutations) in their medical records
  • * Participants who are pregnant or nursing
  • * Participants with a known history of HIV, hepatitis, or other infectious diseases
  • * Participants who have taken an investigational product in the last 30 days
  • * Participants who have experienced excess blood loss, including blood donation defined as 250 mL in the last month or 500 mL in the previous two months
  • * Participants currently enrolled in a clinical trial
  • * Participants currently in remission

Ages Eligible for Study

18 Years to 100 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Sanguine Biosciences,

Study Record Dates

2024-03-31