Lymphoproliferative Disorder

7

Review clinical trials related to Lymphoproliferative Disorder. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Nivolumab in Epstein-Barr Virus (EBV)-Positive Lymphoproliferative Disorders and EBV-Positive Non-HodgkinLymphomas

Background: The drug Nivolumab has been approved to treat some cancers. Researchers want to see if it can slow the growth of other cancers. They want to study its effects on cancers that may have not responded to chemotherapy or other treatments. Objectives: To see if Nivolumab slows the growth of some types of cancer or stops them from getting worse. To test the safety of the drug. Eligibility: People 12 and older who have Epstein-Barr Virus (EBV)-positive lymphoproliferative disorders or EBV-positive non-Hodgkin lymphomas with no standard therapy Design: Participants will be screened with: Medical history Physical exam Blood and urine tests CAT scan of the chest, abdomen, and pelvis Tumor and bone marrow biopsies (sample taken) Magnetic resonance imaging scan of the brain Lumbar puncture (also known as spinal tap) Positron emission tomography/computed tomography scan with a radioactive tracer Every 2 weeks, participants will get Nivolumab by vein over about 1 hour. They will also have: Physical exam Blood and pregnancy tests Review of side effects and medications During the study, participants will repeat most of the screening tests. They may also have other biopsies. After stopping treatment, participants will have a visit every 3 months for 1 year. Then they will have a visit every 6 months for years 2-5, and then once a year. They will have a physical exam and blood tests. ...

Participants needed: 40
Trial details
Phase: Phase 2Age: 12+Biological sex: AllType: InterventionalSponsor: National Cancer Institute (NCI)Updated: Jul 2, 2026Locations: 1
Eligibility criteria

Subjects must have histologically or cytologically confirmed EBV-positive LPD or... [+33]

Subjects who are receiving any other investigational agents. [+14]

Status: Recruiting

Registry of Older Patients With Cancer

RATIONALE: Gathering information about older patients with cancer may help the study of cancer in the future. PURPOSE: This research study is gathering information from older patients with cancer into a registry.

Participants needed: 3,000
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: UNC Lineberger Comprehensive Cancer CenterUpdated: Jun 29, 2026Locations: 7
Eligibility criteria

Patients must have an appointment at the North Carolina Cancer Hospital and agre... [+2]

Status: Recruiting

Project: Every Child for Younger Patients With Cancer

This study gathers health information for the Project: Every Child for younger patients with cancer. Gathering health information over time from younger patients with cancer may help doctors find better methods of treatment and on-going care.

Participants needed: 75,000
Trial details
Age: Up to 25Biological sex: AllType: ObservationalSponsor: Children's Oncology GroupUpdated: May 5, 2026Locations: 278
Eligibility criteria

Enrollment must occur within 6 months of initial disease presentation OR within... [+17]

Status: Recruiting

Acalabrutinib and Obinutuzumab for the Treatment of Previously Untreated Follicular Lymphoma or Other Indolent Non-Hodgkin Lymphomas

This phase II trial studies the effect of acalabrutinib and obinutuzumab in treating patients with follicular lymphoma or other indolent non-Hodgkin lymphoma for which the patient has not received treatment in the past (previously untreated). Acalabrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Immunotherapy with obinutuzumab may induce changes in body's immune system and may interfere with the ability of cancer cells to grow and spread. Giving acalabrutinib and obinutuzumab may kill more cancer cells.

Participants needed: 49
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Emory UniversityUpdated: Feb 9, 2026Locations: 1
Eligibility criteria

Men and women >= 18 years of age [+13]

The presence or history of histologically transformed or co-existing high-grade... [+24]

Status: Recruiting

Understanding the Mechanisms of Clonal and Non-clonal Cytopenia Following CAR-T Therapy for Multiple Myeloma or CD19+ Lymphoproliferative Disorder (LPD)

This clinical trial evaluates the impact of preexisting and therapy-emergent germline and somatic variants on cytopenia in patients with multiple myeloma or CD19 positive lymphoproliferative disorder (LPD) following chimeric antigen receptor T-cell (CAR-T) therapy. The most common adverse event after CAR-T therapy is lower than normal blood cells (cytopenia) and up to one third of patients experience cytopenia that last longer than 30 days post-infusion. Germline and somatic variants are changes in genes found using cancer genomic tests. Cancer genetic/genomic testing is a series of tests that find specific changes in cancer cells or in blood deoxyribonucleic acid. Identifying gene mutations may help identify the risk of cytopenia in patients with multiple myeloma or CD19 positive LPD following CAR-T therapy.

Participants needed: 82
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Mayo ClinicUpdated: Jan 8, 2026Locations: 7
Eligibility criteria

Age ≥ 18 years [+6]

Ineligible for CAR-T therapy [+1]

Status: Recruiting

Tissue, Blood, and Body Fluid Sample Collection From Patients With Hematologic Cancer

RATIONALE: Collecting and storing samples of tissue, blood, and body fluid from patients with cancer to study in the laboratory may help the study of cancer in the future. PURPOSE: This research study is collecting and storing blood and tissue samples from patients being evaluated for hematologic cancer.

Participants needed: 15,000
Trial details
Age: 18-120Biological sex: AllType: ObservationalSponsor: UNC Lineberger Comprehensive Cancer CenterUpdated: Oct 27, 2025Locations: 1
Eligibility criteria

Acute myeloid leukemia [+14]

Status: Recruiting

3'-Deoxy-3'-[18F] Fluorothymidine PET Imaging in Patients With Cancer

RATIONALE: Diagnostic procedures, such as 3'-deoxy-3'-\[18F\] fluorothymidine (FLT) PET imaging, may help find and diagnose cancer. It may also help doctors predict a patient's response to treatment and help plan the best treatment. PURPOSE: This phase I trial is studying FLT PET imaging in patients with cancer.

Trial details
Age: 18-120Biological sex: AllType: InterventionalSponsor: Barbara Ann Karmanos Cancer InstituteUpdated: Jul 8, 2025Locations: 1
Eligibility criteria

Histologically confirmed solid tumor or hematologic malignancy [+7]