Follicular lymphoma is a slow-growing blood cancer that starts in white blood cells called B cells. It's the second most common type of non-Hodgkin lymphoma. Many people live for years with the disease, which can be managed with cycles of treatment and observation rather than continuous therapy.
What's actually going on in research
Trials are testing combinations of targeted drugs that avoid traditional chemotherapy, newer antibody drugs that last longer in the body, CAR T-cell therapy for relapsed disease, and bispecific antibodies that redirect the immune system. Researchers are also studying whether early treatment changes outcomes compared to watchful waiting for low-burden disease.
Bispecific antibodies
These engineered proteins connect a patient's own T cells directly to lymphoma cells, forcing an immune attack. Several are now FDA-approved for relapsed follicular lymphoma, with trials testing them earlier in treatment.
CAR T-cell therapy
Axicabtagene ciloleucel and tisagenlecleucel are approved for follicular lymphoma that has returned after two or more treatments. Studies are testing whether using CAR T earlier, or in combination with other drugs, improves long-term outcomes.
Chemotherapy-free regimens
Combinations of drugs like lenalidomide, rituximab, and BTK inhibitors are being tested as first-line treatment. If successful, they could spare patients the side effects of chemotherapy while controlling the disease.
What to know before you search
Eligibility typically depends on disease stage, number of prior treatments, whether the lymphoma is causing symptoms, and sometimes genetic features of the tumor cells.
What types of trials are currently open
- Treatment trials — Testing new drug combinations, often comparing chemotherapy-free regimens to standard approaches for newly diagnosed disease.
- Relapsed disease trials — Testing CAR T-cell therapy, bispecific antibodies, and novel targeted drugs for lymphoma that has returned after prior treatment.
- Maintenance therapy trials — Testing whether drugs given after initial treatment can delay the lymphoma's return.
- Watchful waiting studies — Following people with low-burden disease to understand when treatment becomes necessary and what predicts progression.
- Biomarker studies — Analyzing tumor samples and blood tests to identify which patients are likely to respond to specific treatments or have more aggressive disease.
Recently added Follicular Lymphoma trials
Take a single dose of an experimental drug to test liver processing
Moderate Hepatic Impairment Study Phase This phase employs a multicenter, open-label, parallel-group, single-dose study design.Two cohorts are established in this phase: Cohort A: Subjects with moderate hepatic impairment Cohort B: Subjects with normal hepatic function A total of 8 subjects of either gender will be enrolled in each cohort. Enrolled subjects will be admitted to the Phase I clinical research unit on Day -1 and fasted for at least 10 hours. On Day 1, subjects will receive a single oral dose of 20 mg HS-10506 tablets in a fasted state. Water intake is prohibited within 1 hour before and after dosing (excluding water used for drug administration). Food intake is restricted for at least 4 hours post-dose. All study medications will be administered with approximately 240 mL of water. Subjects with normal hepatic function (Cohort B) serve as the matched control group for subjects with moderate hepatic impairment (Cohort A), and shall meet the following matching criteria: The mean body mass index (BMI) of Cohort B is within ±10% of the mean BMI of Cohort A. The mean age of Cohort B is within ±3 years of the mean age of Cohort A. The number of male and female subjects in Cohort B is consistent with that in Cohort A for each gender. Mild Hepatic Impairment Study Phase Based on the results of the moderate hepatic impairment study phase, the sponsor and principal investigator will jointly determine whether to conduct a study to evaluate the effect of mild hepatic impairment. The phase design and procedures of the mild hepatic impairment are consistent with those of the moderate hepatic impairment. Subjects with normal hepatic function (Cohort D) serve as the matched control group for subjects with mild hepatic impairment (Cohort C), and shall meet the following matching criteria: The mean BMI of Cohort D is within ±10% of the mean BMI of Cohort C. The mean age of Cohort D is within ±3 years of the mean age of Cohort C. The number of male and female subjects in Cohort D is consistent with that in Cohort C for each gender.
Track your recovery after spinal fusion surgery for one year
This study is setup to be able to gather information on the safety and performance of the Fortilink-TS Ti cage of Paradigm Spine GmbH, up to one-year after the surgery. The device is intended to be used in intervertebral fusion surgery. Around 50 participants will participate in this study in 2 hospitals. The Fortilink-TS Ti cage is meant to be placed in the lower back, to treat degenerative disc disease with up to grade I spondylolisthesis. The study will involve data gathering based on routine care. The study will only entail collection of data (medical history prior to the surgery, data from the surgery and data in the follow up after one year). Fortilink-TS Ti cages are not new, but have been on the market since 2020. The clinical study is performed to actively gather data on the use of this product in the intended group of patients, to monitor its safety and performance. The treatment and follow-up provided in this study does not differ from the standard of care; meaning that participants in the study will receive the same treatment and follow the same follow-up visits and assessments as patients undergoing the same procedure outside of the study.
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