Lymphoma Trial, Recruiting NCT06610344 Sponsor: Abramson Cancer Center at Penn Medicine Condition: Lymphoma
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Lymphoma Trial, Recruiting

NCT06610344
Recruiting Not Applicable

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 aged 18 years or older
  • People who have been diagnosed with a type of blood cancer called large B-cell lymphoma (LBCL), confirmed by a laboratory test
  • People whose doctor has planned treatment for them using one of two specific CAR-T cell therapies (Yescarta or Kymriah), which are commercially available
  • People whose organs are functioning well enough, and who are physically well enough (as judged by the treating doctor), to receive standard CAR-T treatment
  • People who are not already enrolled in another clinical trial for "bridging therapy" (a treatment given before CAR-T)
  • People who have had a PET/CT scan, CT scan, or MRI showing at least one measurable area of disease, taken before the cell collection process (leukapheresis) for CAR-T manufacturing
  • People whose side effects from previous treatments have settled to a level the treating doctor considers acceptable for trial participation
  • People who are able to give informed consent and are willing to follow all study procedures for the full duration of the study

Who may not be able to join:

  • People who are pregnant or breastfeeding
  • People with a known allergy to energy drinks
  • People with a history of inflammatory bowel disease
  • People with type 1 diabetes, or who require insulin
  • People with chronic kidney disease where kidney function (eGFR) is below 30 mL/min/1.73m²
  • People who have a second, separate cancer for which they are currently receiving treatment, or which would make it difficult for doctors to assess how the lymphoma is responding to treatment

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 27 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Elise Chong, MD, Abramson Cancer Center at the University of Pennsylvania

Phone: 215-615-4312

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
Not Applicable
Sponsor
Abramson Cancer Center at Penn Medicine
Registry
ClinicalTrials.gov
Start date
7 January 2025
Est. completion
15 September 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety and tolerability

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: 27 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