A Study Evaluating the Safety, Efficacy, and Pharmacokinetics of Mosunetuzumab and a Combined Regimen of Mosunetuzumab and Venetoclax in Participants With Relapsed or Refractory Chronic Lymphocytic Leukemia
Tafasitamab, Acalabrutinib, and Obinutuzumab for the Treatment of Previously Untreated Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
A Phase 1 Study of UB-VV111 With and Without Rapamycin in Relapsed/Refractory CD19+ B-cell Malignancies
CMV-MVA Triplex Vaccination in HLA-Matched Related Stem Cell Donors for the Prevention of CMV Infection in Patients Undergoing Hematopoietic Stem Cell Transplant
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A Vaccine (CMV-MVA Triplex Vaccine) for the Enhancement of CMV-Specific Immunity and the Prevention of CMV Viremia in Patients Undergoing Haploidentical Hematopoietic Stem Cell Transplant
A Study of Emavusertib + An Approved Bruton Tyrosine Kinase Inhibitor (BTKi) in Participants With Chronic Lymphocytic Leukemia (CLL) and Other B-cell Malignancies
Surovatamig as Consolidation Therapy in Participants With Chronic Lymphocytic Leukaemia or Small Lymphocytic Lymphoma With Unmutated Immunoglobulin Heavy Chain Variable (IGHV)
Expanded/Activated Gamma Delta T-cell Infusion Following Hematopoietic Stem Cell Transplantation and Post-transplant Cyclophosphamide
Phase II Study Assessing the Efficacy and Toxicity of Olverembatinib Monotherapy in Patients With Chronic Myeloid Leukemia in Chronic Phase After Failing One Prior Therapy With a Second Generation Tyrosine Kinase Inhibitor or Asciminib
Intensity Modulated Total Marrow Irradiation in Fully Human Leukocyte Antigen (HLA)-Matched and Partially-HLA Mismatched Allogeneic Transplantation Patients With High-Risk Acute Myeloid Leukemia (AML), Chronic Myeloid Leukemia (CML), and Myelodysplastic Syndrome (MDS)
A Study of Rebecsinib for Patients With Relapsed/Refractory Secondary Acute Myeloid Leukemia or High Risk Myelofibrosis
SYNERGY-AI: Artificial Intelligence Based Precision Oncology Clinical Trial Matching and Registry
What is chronic lymphocytic leukemia?
Chronic lymphocytic leukemia, or CLL, is a slow growing cancer of B lymphocytes that build up in the blood, bone marrow, and lymph nodes. Most people are diagnosed around age 70, often with no symptoms; when symptoms come, they include tiredness, swollen lymph nodes, frequent infections, night sweats, and weight loss. Small lymphocytic lymphoma is the same disease when the cells sit mainly in lymph nodes, so it is studied in the same trials.
When treatment is needed, it is now mostly targeted pills: BTK inhibitors taken continuously, or venetoclax based combinations taken for a fixed time. CAR T cell therapy was approved for CLL in 2024 for people whose disease has stopped responding to both. Genetic features such as TP53 mutation, deletion 17p, and IGHV status strongly predict how CLL behaves and which trials fit. Other leukemias are on our leukemia clinical trials page.
Types of CLL clinical trials
Early treatment trials. Whether treating high risk CLL before symptoms improves outcomes compared with watch and wait.
Fixed duration trials. Combinations of BTK and BCL2 inhibitors taken for a set time, aiming for long remissions without ongoing treatment.
Next generation drug trials. New BTK and BCL2 inhibitors, including for disease that stopped responding to earlier drugs.
Immunotherapy trials. Bispecific antibodies and CAR T cells used as consolidation or at relapse; see CAR T cell therapy.
Trials for older adults. Large cooperative group studies built for people 65 and older, the majority of patients.
Measurable residual disease studies. Sensitive tests that help decide when treatment can safely stop.
Who can participate in CLL clinical trials?
Trials sort people by whether they have been treated. Untreated trials enroll people who have never had therapy, either because treatment is now needed or, in early treatment studies, because they have high risk genetics but no symptoms yet. Relapsed trials specify prior drugs, often whether a BTK inhibitor or venetoclax has already been used. Most require genetic results such as TP53, deletion 17p, and IGHV, adequate organ function, and the ability to manage daily activities, and many are designed for people 65 and older. Eligibility always varies by study.
How CLL is staged, and why it matters for trials
Rai and Binet stages. Based on blood counts and how many lymph node areas are involved; higher stages usually mean treatment is needed.
Whether treatment is indicated. Symptoms, falling blood counts, or a rapidly rising lymphocyte count; untreated trials usually require one of these.
Genetic risk. TP53 mutation or deletion 17p and unmutated IGHV mean higher risk and often different trials.
Treatment history. Treatment naive or relapsed, and which drug classes have been used.
How to enroll in a CLL clinical trial
Identify your trial. Use the filters and match "treatment naive" or "relapsed" and any genetic feature to your situation.
Select your preferred location. Enter your city or state; cooperative group trials run at hundreds of sites, including community practices.
Explore study details. Click "Learn More" for prior treatment rules, genetic requirements, and the visit schedule.
Complete the health profile. Click "Get started" to begin the 5-step application. Have ready your stage and whether treatment has been recommended, your genetic results, and any prior CLL treatments.
Submit the application. A clinical trial coordinator reviews it and contacts you. Nothing is decided until informed consent, and participation is voluntary at every step.