Purpose

This study will collect tumor specimens with correlated clinical and demographic data from patients who are undergoing a biopsy or similar procedure to obtain tumor tissue as a normal course of their medical management or diagnostic work-up for suspected or confirmed cancer.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  1. Able and willing to provide informed consent for participation 2. Age ≥18 years at time of consent. 3. Have a suspected or confirmed cancer diagnosis that is to be evaluated by means of a biopsy. 4. Subjects who are newly diagnosed or have suspected cancer must be treatment-naïve at the time of biopsy. All other subjects should have the biopsy performed before starting their next line of treatment.

Exclusion Criteria

  1. Have a known auto-immune disease or prior condition (prior organ transplant, chronic kidney or liver disease) that renders them ineligible for immunotherapy (IO) treatment. 2. Severely immunocompromised person(s). Examples include patients on immunosuppressants, HIV positive patients on antiretrovirals, post transplantation patients. 3. Pregnant person(s).

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Study Population Adults aged 18 years or older, who are able and willing to provide written informed consent, have a suspected or confirmed cancer diagnosis and will be undergoing a biopsy or similar procedure to obtain tumor tissue as a normal course of their medical management or diagnostic work-up.
  • Procedure: Biopsy
    Subjects must be clinically able, at investigator discretion, to undergo additional biopsy passes during their biopsy. Biopsy specimen(s) will be obtained during a standard of care (SOC) procedure. If a subject receives a subsequent SOC biopsy for clinical diagnosis purposes, additional sample(s) may be collected and sent to the Sponsor.

Recruiting Locations

Mercy Hospital - FTS
Fort Smith, Arkansas 72903
Contact:
Billy Cater
479-314-5089
billy.cater@mercy.net

Frederick Health Hospital
Frederick, Maryland 21702
Contact:
Ingrid Halvorson
301-662-8477
ihalvorson@frederick.health

Mercy Hospital - SPG
Springfield, Missouri 65804
Contact:
Hanna Dulier, RN. BSN
4178203891
hanna.dulier@mercy.net

Mercy Hospital - South
St Louis, Missouri 63128
Contact:
Danielle Werle, RN, BSN
3145256042
danielle.werle@mercy.net

Mercy Hospital -STL
St Louis, Missouri 63141
Contact:
Alesia Bell
(314) 251-4400
alesia.bell@mercy.net

Mercy Hospital - OKC
Oklahoma City, Oklahoma 73120
Contact:
Trisha Stubhar
405-751-4343
trisha.stubhar@mercy.net

JPS Health Network
Forth Worth, Texas 76104
Contact:
April Bell, MS, CCRC, ACRP-PM
817-702-8254
ABell01@jpshealth.org

More Details

Status
Recruiting
Sponsor
Elephas

Study Contact

Detailed Description

Elephas is researching mechanisms of cutting, sorting and imaging tumors that leave the 3D tumor microenvironment (TME), including its immune cells, intact. This allows qualitative and semi-quantitative identification and characterization of the ex vivo response to exposure of potential immunotherapy. The ex vivo response data will then be compared to the clinical real world response data to inform development efforts. This study will collect tumor specimens from patients with suspected or confirmed cancer. These specimens, along with clinical data and genomic data obtained as part of a patient's standard of care, will be used to perform this research.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.