Phase 2 Lymphoma Trial, Recruiting NCT06043323 Sponsor: M.D. Anderson Cancer Center Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06043323
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:

  • Adults aged 18 or older
  • People who have been diagnosed with follicular lymphoma (a type of slow-growing blood cancer), Grade 1 to 3A, confirmed by a tissue biopsy — people with a history of this lymphoma transforming into a faster-growing type may also be considered at the doctor's discretion
  • People whose follicular lymphoma has come back or stopped responding to at least 2 previous rounds of treatment
  • People who are reasonably well and able to carry out daily activities (as measured by a standard medical scale called ECOG, scored 0–2)
  • People whose kidneys, liver, blood, and lungs are functioning well enough to be considered suitable for CAR-T cell therapy (confirm with trial site for specific values)
  • People who have at least one area of lymphoma that can be measured on a scan (CT or MRI) or physical exam, at least 1 cm in size
  • People who have previously had radiation therapy, provided it has not already reached the maximum safe dose for surrounding healthy tissue
  • Women who could potentially become pregnant must have a negative pregnancy test within one week before radiation treatment planning
  • People who are able to understand the trial and are willing to sign a consent form

Who may not be able to join:

  • People who have had another type of cancer (other than B-cell lymphoma) in the past 3 years that has required active treatment such as surgery, radiation, or systemic therapy — skin cancers that are not melanoma are generally excluded from this restriction
  • Women who are currently pregnant
  • Women who are breastfeeding and are not willing to stop before the chemotherapy preparation phase and for 12 months after receiving the CAR-T cell treatment
  • People who urgently need additional chemotherapy or a drug called rituximab in the period between the cell collection step and the CAR-T cell infusion (steroids may still be permitted)
  • People for whom additional radiation therapy would exceed the safe limits for surrounding healthy organs
  • People who have had a severe, immediate allergic reaction to a group of antibiotics called aminoglycosides
  • People who have an active, uncontrolled fungal, bacterial, or viral infection that requires intravenous (drip) antibiotics — some milder infections that are responding to treatment may still be permitted (confirm with trial site)

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 28 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

Principal Investigator: Susan Wu, MD, M.D. Anderson Cancer Center

Phone: (281) 630-7607

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
Registry
ClinicalTrials.gov
Start date
8 January 2024
Est. completion
1 September 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of Adverse Events, Graded According to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version (v) 5.0

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: 28 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