Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.

58 recruiting in this ClinicalTrials.gov snapshot · reviewed 2026-08-17

Lymphoma clinical trials, in English

Lymphoma trials split by Hodgkin versus non-Hodgkin, and further by B-cell or T-cell subtype. CAR-T and bispecific antibody studies usually require a measured disease status and a washout from prior treatment. We list recruiting registry cards only. Sourced from ClinicalTrials.gov. Not a recommendation to join any study.

How to read this list

Each headline is a rewrite of registry fields (phase, intervention, condition). Open the NCT link before you call a site. Eligibility is decided by the study team, not by this page. See how to find a trial and eligibility explained.

Phases in this snapshot: Not a traditional drug phase (20) · Phase 2 (16) · Phase 1 (9) · Phase 1 / Phase 2 (6) · Phase 3 (6) · Phase 2 / Phase 3 (1)

Cities that appear on these records

  • Las Vegas, Nevada · 36
  • Chicago, Illinois · 22
  • St Louis, Missouri · 22
  • Des Moines, Iowa · 20
  • Portland, Oregon · 20
  • Bethesda, Maryland · 18
  • Columbus, Ohio · 17
  • Milwaukee, Wisconsin · 16

Browse by US state · city hubs

Intervention hubs that overlap this snapshot: CAR-T therapy · Nivolumab · Ofatumumab · Pembrolizumab

RecruitingNot a traditional drug phaseBethesda, Maryland
Natural History Study of Monoclonal B Cell Lymphocytosis (MBL), Chronic Lymphocytic Leukemia/Small Lymphocy…

Background The development of new technologies now allow scientists to investigate the molecular basis and clinical manifestations of monoclonal B cell lymphocytosis (MBL), chronic lymphocytic leukemia(CLL)/small lymphocytic lymphoma (SLL), lymphoplasmacytic lymphoma (LPL)/Waldenstrom macroglobulinemia (WM), and splenic marginal zone lymphoma (SMZL). Applying these methods in a natural history study can help identify processes involved in disease progression, and possibly lead to the discovery or validation of treatment targets.

NCT00923507 · Official ClinicalTrials.gov record · National Heart, Lung, and Blood Institute (NHLBI)

RecruitingNot a traditional drug phaseSioux Falls, South Dakota
Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

The Coordination of Rare Diseases at Sanford (CoRDS) is an international patient registry that serves as a centralized resource for rare disease research. Individuals affected by rare diseases, undiagnosed conditions, and disorders of unknown prevalence may voluntarily contribute health information to support natural history studies, participant recruitment, and other research efforts.

NCT01793168 · Official ClinicalTrials.gov record · Sanford Health

RecruitingPhase 2Houston, Texas
Phase 2: testing Blinatumomab for B Acute Lymphoblastic Leukemia

This phase II trial studies how well blinatumomab, inotuzumab ozogamicin, and combination chemotherapy work as frontline therapy in treating patients with B acute lymphoblastic leukemia. Immunotherapy with monoclonal antibodies, such as blinatumomab, may induce changes in the body's immune system and may interfere with the ability of tumor cells to grow and spread.

NCT02877303 · Official ClinicalTrials.gov record · M.D. Anderson Cancer Center

RecruitingPhase 2Houston, Texas
Phase 2: testing Bortezomib for Recurrent Acute Lymphoblastic Leukemia

This phase II trial studies the side effects and how well combination chemotherapy works in treating patients with acute lymphoblastic leukemia, lymphoblastic lymphoma, Burkitt lymphoma/leukemia, or double-hit lymphoma/leukemia that has come back or does not respond to treatment. Drugs used in chemotherapy, such as clofarabine, etoposide, cyclophosphamide, vincristine sulfate liposome, dexamethasone and bortezomib, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.

NCT03136146 · Official ClinicalTrials.gov record · M.D. Anderson Cancer Center

RecruitingNot a traditional drug phaseAnchorage, Alaska
Not a traditional drug phase: Questionnaire Administration for Acute Lymphoblastic Leukemia

This study collects blood and tissue samples from patients with cancer and without cancer to evaluate tests for early cancer detection. Collecting and storing samples of blood and tissue from patients with and without cancer to study in the laboratory may help researchers develop tests for the early detection of cancers.

NCT05334069 · Official ClinicalTrials.gov record · Alliance for Clinical Trials in Oncology

RecruitingNot a traditional drug phaseDuarte, California
cfDNA Assay Prospective Observational Validation for Early Cancer Detection and Minimal Residual Disease

This is an watch-and-measure (no experimental treatment required) case-control study to train and validate a genome-wide methylome enrichment platform to detect multiple cancer types and to differentiate amongst cancer types. The cancers included in this study are brain, breast, bladder, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatobiliary, leukemia, lung, lymphoma, multiple myeloma, ovarian, pancreatic, prostate, renal, sarcoma, and thyroid.

NCT05366881 · Official ClinicalTrials.gov record · Adela, Inc

RecruitingPhase 2Birmingham, Alabama
Phase 2: testing Azacitidine for Acute Myeloid Leukemia

This phase II MyeloMATCH treatment trial tests whether the standard approach of cytarabine and daunorubicin in comparison to the following experimental regimens works to shrink cancer in patients with high risk acute myeloid leukemia (AML): 1) daunorubicin and cytarabine liposome alone; 2) cytarabine and daunorubicin with venetoclax; 3) azacitidine and venetoclax; 4) daunorubicin and cytarabine liposome and venetoclax. "High-risk" refers to traits that have been known to make the AML harder to treat.

NCT05554406 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)

RecruitingPhase 3Birmingham, Alabama
Phase 3: testing Bleomycin Sulfate for Lugano Classification Limited Stage Hodgkin Lymphoma AJCC v8

This phase III trial compares the effect of adding immunotherapy (brentuximab vedotin and nivolumab) to standard treatment (chemotherapy with or without radiation) to the standard treatment alone in improving survival in patients with stage I and II classical Hodgkin lymphoma. Brentuximab vedotin is in a class of medications called antibody-drug conjugates.

NCT05675410 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)

RecruitingPhase 2Jacksonville, Florida
Phase 2: Clinical Encounter for Advanced Anal Carcinoma

This clinical trial studies the effect of cancer directed therapy given at-home versus in the clinic for patients with cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Currently most drug-related cancer care is conducted in infusion centers or specialty hospitals, where patients spend many hours a day isolated from family, friends, and familiar surroundings.

NCT05969860 · Official ClinicalTrials.gov record · Mayo Clinic

RecruitingNot a traditional drug phaseAnn Arbor, Michigan
Not a traditional drug phase: Fatigue Reduction Diet for Lymphoma

In this study the investigators are proposing to measure the how well it works, sustainability, and mechanisms of 3 months of individualized counseling of the FRD delivered by registered dietitians, over 8 sessions by phone/video conferencing on fatigue, quality of life, and associated symptoms in persistently fatigued lymphoma cancer survivors compared to 3 months of individualized counseling of the attention control (matched for time and frequency of interactions with the FRD) the General Health Curriculum (GHC). The investigators will randomize and follow 68 lymphoma cancer survivors; accounting for a \~10% drop out rate to achieve a target of 60 patients that will complete the study.

NCT06047626 · Official ClinicalTrials.gov record · University of Michigan Rogel Cancer Center

RecruitingNot a traditional drug phasePalo Alto, California
Patient-Reported Outcomes and Quality of Life in Adult and Pediatric Patients With Nodular Lymphocyte-Predo…

There is a pressing need to measure patient-reported symptoms in patients of all ages diagnosed with nodular lymphocyte-predominant Hodgkin lymphoma (NLPHL). This study aims to measure longitudinal symptom burden and treatment tolerability utilizing validated patient-reported outcomes (PROs) instruments.

NCT06098430 · Official ClinicalTrials.gov record · St. Jude Children's Research Hospital

RecruitingNot a traditional drug phaseFairbanks, Alaska
Not a traditional drug phase: Non-interventional Study for Breast Carcinoma

This is a multi-site clinical study enrolling 2000 newly diagnosed patients with breast, colorectal, melanoma, non-Hodgkin lymphoma, or non-small cell lung cancer, who are planning to receive one or more systemic cancer directed therapies with chemotherapy and/or (immune checkpoint inhibitors) ICIs.

NCT06418204 · Official ClinicalTrials.gov record · Wake Forest University Health Sciences

RecruitingPhase 2Tucson, Arizona
Phase 2: testing Ibrutinib for High Grade B-Cell Lymphoma With MYC and BCL6 Rearrangements

This phase II trial tests how well venetoclax, ibrutinib, prednisone, obinutuzumab, and Revlimid® (ViPOR) works in treating patients with CD10 negative diffuse large B-cell lymphoma (DLBCL) and high-grade lymphoma with MYC and BCL2 rearrangements that has come back after a period of improvement (relapsed) and/or that has not responded to previous treatment (refractory). Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors.

NCT06649812 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)

RecruitingPhase 2Anchorage, Alaska
Phase 2: testing Obinutuzumab for Relapsed or Refractory Aggressive B-Cell Non-Hodgkins Lymphoma

This Phase II trial evaluates the optimization of the cytokine release syndrome (CRS) profile for glofitamab in combination with gemcitabine and oxaliplatin (Glofit-GemOx) followed by glofitamab this drug alone treatment regimen (Cohort A), and for glofitamab this drug alone (Cohort B) in participants with relapsed or refractory aggressive B-cell Non-Hodgkin's lymphoma. The study utilizes an optimized steroid premedication regimen and monitoring schedule specifically designed to enable the administration of the treatment regimen in an outpatient setting.

NCT06806033 · Official ClinicalTrials.gov record · Hoffmann-La Roche

RecruitingPhase 2Duarte, California
Phase 2: testing Glofitamab for Recurrent Mantle Cell Lymphoma

This phase II trial tests the safety and side effects of glofitamab and obinutuzumab and how well they work in treating patients with mantle cell lymphoma that has come back after a period of improvement (relapsed) or that has not responded to previous treatment (refractory) after receiving CD19-directed chimeric antigen receptor (CAR) T-cell therapy. CAR T-cell therapy is a form of immunotherapy where the immune system cell, T-cell, is changed to attack cancer cells.

NCT07003295 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)

RecruitingNot a traditional drug phaseNijmegen, Gelderland
SKIN Disease Profiling by an Exploratory, pRospective, Biomarker Study in dermatoloGY Practice (SKINERGY)

The goal of this watch-and-measure (no experimental treatment required) study is to comprehensively profile six immune-mediated inflammatory diseases, including atopic dermatitis (AD), plaque psoriasis (PSO), hidradenitis suppurativa (HS), cutaneous T-cell lymphoma subtype mycosis fungoides (MF), chronic spontaneous urticaria (CSU), and cutaneous lupus erythematosus (CLE) in daily practice. Data will be compared with data from healthy volunteers.

NCT07021495 · Official ClinicalTrials.gov record · Leiden University Medical Center

RecruitingNot a traditional drug phaseBirmingham, Alabama
Not a traditional drug phase: Bone Marrow Transplant with Ossium's HPC, Marrow (bone marrow recovered from deceased organ and tissue donors) for Bone Marrow Transplant (BMT)

Ossium recognizes that not all patients who could benefit from Ossium's HPC, Marrow can access the PRESERVE trial for logistical or eligibility reasons. The HOPE program is expanded access program to serve these patients by providing our bone marrow product

NCT07145411 · Official ClinicalTrials.gov record · Ossium Health, Inc.

RecruitingPhase 1Kunming, Yunnan
Phase 1: testing Invivo CAR-T for B-Acute Lymphoblastic Leukemia

This study is an investigator-initiated single center, single arm clinical study with a target population of patients with relapsed or refractory malignant hematological tumors. It is an early exploratory clinical study of the safety, tolerability and initial how well it works in the treatment of relapsed or refractory malignant hematological tumors.

NCT07239323 · Official ClinicalTrials.gov record · Chongqing Precision Biotech Co., Ltd

RecruitingPhase 1Duarte, California
Phase 1: testing Cyclophosphamide for Follicular Helper T-Cell Lymphoma

This phase I trial tests the safety, side effects and best dose of ruxolitinib in combination with cyclophosphamide, doxorubicin, vincristine, prednisone (CHOP) chemotherapy and how well the combination works in treating patients with untreated nodal T-follicular helper (TFH) cell lymphoma. Ruxolitinib phosphate blocks a protein called janus kinase, which may help keep abnormal blood cells or cancer cells from growing.

NCT07278856 · Official ClinicalTrials.gov record · City of Hope Medical Center

RecruitingPhase 3Skokie, Illinois
Phase 3: testing Rocbrutinib for CLL / SLL

This is a Phase 3, randomly assigned, open-label, multicenter study comparing rocbrutinib (LP-168) versus pirtobrutinib in adult participants with relapsed or refractory chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who have previously received a covalent Bruton's tyrosine kinase inhibitor (cBTKi). Approximately 306 you would be randomly assigned 1:1 to receive rocbrutinib 200 mg orally once daily or pirtobrutinib 200 mg orally once daily, administered continuously in 28-day cycles until disease progression, unacceptable toxicity, withdrawal of consent, or other discontinuation criteria are met.

NCT07342478 · Official ClinicalTrials.gov record · Newave Pharmaceutical Inc

RecruitingPhase 3Shanghai, Shanghai Municipality
Phase 3: testing HMPL-760 for Relapsed/Refractory Diffuse Large B-Cell Lymphoma

This is a Phase III randomly assigned, neither you nor the study doctors know who gets the real treatment, positive controlled study to measure the how well it works, safety, and pharmacokinetics of HMPL-760 in combination with R-GemOx versus dummy treatment (placebo) in combination with R-GemOx in patients with R/R DLBCL.

NCT07409428 · Official ClinicalTrials.gov record · Hutchmed

RecruitingPhase 1Rockville, Maryland
Phase 1: testing Cyclophosphamide for AIDS-Related Diffuse Large B-cell Lymphoma

This phase I trial studies the safety and side effects of glofitamab plus a chemoimmunotherapy regimen called R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) in treating patients newly-diagnosed with HIV-associated large B-cell lymphoma. Glofitamab is a bispecific monoclonal antibody, which can bind to two different antigens that are expressed by cancer cells (CD3 and CD20) at the same time.

NCT07649304 · Official ClinicalTrials.gov record · National Cancer Institute (NCI)

RecruitingPhase 2Beijing, Beijing Municipality
Phase 2: testing Zanubrutinib for Primary Central Nervous System Lymphoma (PCNSL)

This is a prospective, single-arm, phase II clinical study evaluating the how well it works and safety of Zanubrutinib (a BTK inhibitor) plus Lenalidomide (an immunomodulatory drug) in frail elderly patients with newly diagnosed primary central nervous system lymphoma (PCNSL). The study plans to enroll 33 patients who are aged ≥ 70 years and classified as frail, a population for whom standard first-line treatment regimens, high-dose methotrexate-based chemotherapy, may be "unfit".

NCT07839247 · Official ClinicalTrials.gov record · Xiaohui Ren

RecruitingNot a traditional drug phaseBeijing, Beijing Municipality
Not a traditional drug phase: testing High-dose methotrexate-based therapy for Primary Central Nervous System Lymphoma (PCNSL)

This project aims to establish and prospectively register a longitudinal, multimodal biobank for primary central nervous system lymphoma (PCNSL). The study will primarily enroll patients undergoing needle biopsy or surgical resection of lesions involving the brain, spinal cord, or meninges, with a pathological diagnosis of central nervous system lymphoma.

NCT07842835 · Official ClinicalTrials.gov record · Xiaohui Ren

FAQ: Lymphoma trials

How do I find recruiting Lymphoma clinical trials?

This hub lists 58 recruiting Lymphoma studies from a ClinicalTrials.gov snapshot, rewritten in plain English. Each card links to its NCT record. You can also search the official registry for “lymphoma” at https://clinicaltrials.gov/search?cond=lymphoma.

What does a Lymphoma trial page on PlainTrials include?

A phase explainer, a plain-English summary grounded in the brief summary, inclusion/exclusion extracted from the public eligibility block, sponsor name, and any central contact the sponsor published. It is not a match to a trial.

Where are Lymphoma studies located in this snapshot?

Sites that appear on these records include Las Vegas, Nevada; Chicago, Illinois; St Louis, Missouri; Des Moines, Iowa; Portland, Oregon. A city on a record is not a guarantee that the site is taking new patients this week — call the NCT contact.

Can PlainTrials tell me if I qualify for a Lymphoma study?

No. Eligibility is decided by the study team using the protocol, labs, and consent. Our “who it is for” list is a readable extract of public inclusion text only.

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