T-Cell Leukemia/Lymphoma Biorepository

U
Utpal Dave, MD

Primary Investigator

Enrolling By Invitation
100 years and younger
All
Phase N/A
1 Location

Brief description of study

What is the purpose of this study?
The purpose of this study is to collect and store specimens for future research related to T-Cell lymphoma and leukemia diagnosis and treatment.

THIS STUDY IS ENROLLING BY INVITATION ONLY - Consistent with most oncology trials, patients are not actively “recruited,” but are screened by their physician for appropriate clinical trial(s) at the time of their routine clinic visit. Occasionally, a patient may be a self-referral or physician referral, but are still screened for appropriate clinical trials at the time of their routine clinic visit. PI and staff may send copies of relevant consent forms to these patients to look over prior to actually consenting or enrolling them. This may take place at the patient's visit at which the consent is presented or the patient's next visit to the outpatient hematology/oncology clinic.

Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:
IU Clinical Trials Office 
Phone: (317) 278-5632

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: T-Cell lymphoma,leukemia
  • Age: - 100 Years
  • Gender: All

Inclusion Criteria
  • Patients with confirmed, suspected, or relapsed diagnosis of T-cell leukemia or lymphoma who require as part of standard medical care the performance of phlebotomy, lymph node or skin biopsy, bone marrow aspirate, apheresis, or splenectomy.  
  • Patients who have had these procedures in the past with a confirmed diagnosis may donate archived samples.
Exclusion Criteria
  • Concurrent disease or condition that would make the patient inappropriate for study participation, or any serious medical or psychiatric disorder that would interfere with the subject’s safety or rendering of informed consent.

Updated on 01 Aug 2024. Study ID: 1704971405, IUSCC-0608
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