Blood Sample Collection to Evaluate Biomarkers in Subjects With Untreated Hematologic Malignancies



Status:Recruiting
Conditions:Blood Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:3/27/2019
Start Date:December 7, 2018
End Date:February 14, 2020
Contact:Alexandra Massoud
Email:amassoud@exactsciences.com
Phone:608-957-5652

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The primary objective of this study is to obtain de-identified, clinically characterized,
whole blood specimens to evaluate biomarkers associated with cancer for diagnostic assay
development.

Subjects will have been recently diagnosed with an untreated hematologic malignancy. Subjects
will have a blood sample collected at enrollment and provide medical history prior to
initiation of treatment. There will be no further follow-up.

Inclusion Criteria:

- Subject is male or female ≥ 18 years of age.

- Subject has an untreated hematologic malignancy.

- Subject understands the study procedures and is able to provide informed consent to
participate in the study and authorization for release of relevant protected health
information to the study Investigator.

Exclusion Criteria:

- Any previous cancer diagnosis within the past 5 years (with the exceptions of basal
cell or squamous cell skin cancers).

- Chemotherapy and/or radiation therapy within 5 years prior to enrollment/sample
collection.

- Any treatment for the primary malignancy. Subject may not have started neo-adjuvant
chemotherapy, neo-adjuvant radiation therapy, immunotherapy or other treatment prior
to blood sample collection.

- Less than 3 days between fine needle aspiration (FNA) of target pathology and blood
collection.

- Less than 7 days between biopsy (other than FNA) of target pathology and blood
collection.

- IV contrast (e.g. CT and MRI) within 1 day [or 24 hours] of blood collection.

- Individual has a condition the Investigator believes would interfere with his or her
ability to provide informed consent, comply with the study protocol, which might
confound the interpretation of the study results or put the person at undue risk.
We found this trial at
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Edgewood, Kentucky 41017
Principal Investigator: Brooke Phillips
Phone: 859-301-4726
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Greenbrae, California 94904
Principal Investigator: Peter Eisenberg
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Laguna Hills, California 92653
Principal Investigator: Kenneth Deck
Phone: 949-680-3490
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8901 Carti Way
Little Rock, Arkansas 72205
Principal Investigator: Kamal Patel
Phone: 501-906-3012
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Oceanside, California 92056
Principal Investigator: Himani Singh
Phone: 760-758-5770
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Ogden, Utah 84405
Principal Investigator: Carl Gray
Phone: 801-689-3909
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2776 Enterprise Rd # 100
Orange City, Florida 32763
Principal Investigator: Santosh Nair, MD
Phone: 407-353-1915
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Pinehurst, North Carolina 28374
Principal Investigator: Charles Kuzma
Phone: 910-715-7903
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353 Fairmont Blvd
Rapid City, South Dakota 57701
(605) 719-1000
Principal Investigator: Kathryn Arrambide
Phone: 605-755-2370
Rapid City Regional Hospital Regional Health is an integrated health care system of more than...
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Skokie, Illinois 60076
Principal Investigator: Ira Oliff
Phone: 224-534-7580
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Stamford, Connecticut 06904
Principal Investigator: Salvatore Del Prete
Phone: 203-276-8449
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Wenatchee, Washington 98801
Principal Investigator: Lindsay Overton
Phone: 509-665-5800
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