Protocol Details

Screening Protocol for Clinical Trial Eligibility

This study is currently recruiting participants.

Summary | Eligibility | Citations | Contacts

Summary

Number

001863-C

Sponsoring Institute

National Cancer Institute (NCI)

Recruitment Detail

Type: Participants currently recruited/enrolled
Gender: Male & Female
Min Age: 18 Years
Max Age: 120 Years

Referral Letter Required

No

Population Exclusion(s)

Children;
Pregnant Women;
Neonates

Keywords

Chimeric antigen receptors (CAR-T);
Tumor infiltrating lymphocyte (TIL);
Cellular Therapy;
Gene Therapy

Recruitment Keyword(s)

None

Condition(s)

Immunotherapy;
Human Papillomavirus

Investigational Drug(s)

None

Investigational Device(s)

None

Intervention(s)

None

Supporting Site

National Cancer Institute

Background:

Immunotherapy is a type of treatment that helps a person s own immune system to fight cancer. Some tumor cells produce high levels of specific antigens. Antigens are proteins or other substances that provoke an immune response. Immunotherapy involves collecting a person s own immune cells, such as white blood cells; these cells are then changed to be better at targeting the antigens on their cancer cells. To test new immunotherapies, researchers want to find people with cancer that has specific antigens and other characteristics.

Objective:

To screen people who might be eligible for clinical trials to treat cancer with immunotherapy. These trials will be held at the NIH or at Rutgers Cancer Institute of New Jersey.

Eligibility:

People aged 18 years or older who have cancer. The cancer must be eligible for immunotherapy trials.

Design:

Participants' medical records will be reviewed. This review will include results of blood tests; imaging scans; photographs or videos; and reports on tissue samples.

Participants may have the following samples collected for testing:

Blood. About 3 tablespoons of blood will be drawn from a vein in the arm. The blood will be tested to find the participant s tissue type.

Tumor tissue. If a recent one is not available, a new tissue sample may be taken from the participant s tumor. The tissue will be tested for the presence of specific antigens. The tumor tissue sample may also be tested for certain genes or other molecules.

Eligibility

ELIGIBILITY:

-Age >= 18 years of age.

-Ability and willingness of subject to provide informed consent.

-Biopsy proven or suspected malignant disease.


Citations:

Not Provided

Contacts:

Principal Investigator

Referral Contact

For more information:

Stacey L. Doran, M.D.
National Cancer Institute (NCI)
NIHBC 10 - CLINICAL CENTER BG RM 8D44A
10 CENTER DR
BETHESDA MD 20892
(240) 447-5352
stacey.doran@nih.gov
Laura A. Parsons-Wandell, R.N.
National Cancer Institute (NCI)
National Institutes of Health
Building 10
Room 4-3140
10 Center Drive
Bethesda, Maryland 20892
(240) 858-7480
laura.parsons-wandell@nih.gov
NCI Referral Office
National Institute of Health Clinical Center (CC), 9000 Rockville Pike, Bethesda, Maryland 20892, United States: NCI Clinical Trials Referral Office
(888) 624-1937
ncimo_referrals@mail.nih.gov

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