Phase 2 Lymphoma Trial, Recruiting NCT06792825 Sponsor: Masonic Cancer Center, University of Minnesota Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06792825
Recruiting Phase 2

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:

  • You have been diagnosed with marginal zone lymphoma, confirmed by a tissue biopsy
  • You have been diagnosed with follicular lymphoma (CD20-positive, stage 1, 2, or 3a), confirmed by a tissue biopsy
  • You have not yet received any systemic (whole-body) treatment for your lymphoma
  • Your lymphoma requires treatment because of one or more of the following: a large tumor mass (over 7cm), or three or more affected sites each larger than 3cm
  • You have symptoms such as unexplained fever, night sweats, or losing more than 10% of your body weight in the past 6 months
  • Your lymphoma is causing other symptoms or putting pressure on vital organs (such as the kidneys, eyes, or digestive system), or causing fluid build-up around organs
  • You have follicular lymphoma with a high number of cancer cells circulating in your blood, or your lymphoma is rated high-risk based on a specific scoring system called FLIPI2 (confirm with trial site)
  • Your heart, lungs, and other organs are functioning well enough, based on tests done recently before joining the study
  • You are willing and able to use reliable contraception (two forms at once) during treatment and for 12 months after your last dose, or to abstain completely from sex during that time
  • You are able to take blood-thinning or anti-clotting medication while on the study drug lenalidomide
  • You are able to give written consent to participate voluntarily

Who may not be able to join:

  • You currently have or test positive for an active hepatitis B infection, or have certain markers in your blood indicating past hepatitis B exposure with detectable virus
  • You have chronic hepatitis C or an active hepatitis C infection currently being treated with antiviral medication
  • You are HIV positive or have an active HIV infection
  • You have previously used the drug lenalidomide
  • You have had another type of cancer in the past, unless you have been cancer-free for 5 or more years
  • You have significant nerve damage or nerve-related symptoms (such as numbness or pain) that are at a moderate or severe level
  • You have another serious illness that is not well controlled
  • You currently have an active infection requiring treatment, or have received a live vaccine within the past 14 days
  • Your lymphoma has spread to your brain or spinal cord, or has done so in the past
  • You are not willing to take blood-thinning or anti-clotting medication as required by the study
  • You have had a blood clot in an artery within the past year, or a serious blood clot in a vein (confirm severity level with trial site)
  • You are pregnant or breastfeeding, as the study drugs are known to be harmful to unborn babies — women who could become pregnant must have two negative pregnancy tests before starting treatment and agree to regular pregnancy testing throughout the study

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 22 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 612-624-9452

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

Status
Recruiting
Phase
Phase 2
Sponsor
Masonic Cancer Center, University of Minnesota
Registry
ClinicalTrials.gov
Start date
7 August 2025
Est. completion
8 July 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Complete response (CR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov