Lymphoma Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with follicular lymphoma (a type of slow-growing blood cancer), grades 1, 2, or 3a, confirmed by lab testing at the NCI
- People whose disease can be seen and measured on CT or PET scans — this includes scans taken at any point since diagnosis, not only the most recent one
- People who have enough tissue available from their original diagnosis biopsy (if the biopsy was taken more than 12 months ago or enough tissue is not available, a repeat biopsy may optionally be done; the trial's lead doctor makes the final decision on this)
- People aged 18 or older
- People who are generally well enough to carry out daily activities, as measured by standard medical scoring (confirm with trial site)
Who may not be able to join:
- People who have previously had a more aggressive form of lymphoma called diffuse large B-cell lymphoma, or whose lymphoma has transformed into a more aggressive type
- People who have already received systemic treatment (such as chemotherapy, biological therapy, or monoclonal antibody therapy) for lymphoma — though prior radiation therapy is permitted; people treated for a different cancer (not lymphoma) may still be considered if that treatment ended at least 3 years before their follicular lymphoma diagnosis and there is no sign of that other cancer returning
- People who are HIV-positive
- People who have another cancer currently requiring active treatment
- People with another serious, life-threatening illness unrelated to lymphoma
- People who are not able to give their own informed consent to take part
- People who are currently pregnant (if a participant becomes pregnant during the study, invasive procedures would be paused to avoid risk to the unborn baby)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Rahul Lakhotia, M.D., National Cancer Institute (NCI)
Phone: (240) 760-6050
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Characteristics of treatment received (e.g., type, response, etc.) and molecular biology (e.g., pathology, histologic transformation) will be described; Time to initiation of first-line systemic treatment (TTT1), defined as the number of days from study enrollment until the date of initiation of first-line systemic treatment
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.