Phase 2 Lymphoma Trial, Recruiting NCT06919939 Sponsor: University of Miami Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06919939
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 at the time of signing the consent form
  • People who are willing and able to sign a consent form and follow the trial's procedures
  • People diagnosed with certain types of large B-cell lymphoma (a blood cancer) that has come back or stopped responding to treatment, based on specific medical classifications (confirm with trial site)
  • People whose lymphoma has returned 6 or more months after finishing treatment, or whose disease progressed during or within 6 months of completing treatment
  • People who have already received at least one previous treatment for their lymphoma, including treatments containing two specific types of medication (an anti-CD20 antibody and an anthracycline-based therapy)
  • People who have at least one measurable area of lymphoma that meets specific size requirements on scans
  • People with a general health/activity level rating of 0, 1, or 2 on a standard medical scale (meaning they are able to carry out at least some daily activities)
  • People whose blood, liver, and kidney test results fall within acceptable ranges, tested within 6 weeks before starting treatment
  • People who are willing to avoid pregnancy during the trial and for at least 12 months after the last dose of the trial treatment
  • People living with HIV, provided they are stable on HIV medication, have an adequate immune cell count, and have an undetectable level of the virus in their blood
  • People with a life expectancy of at least 12 weeks
  • People taking steroid (glucocorticoid) medication at the time of screening, provided the dose has been reduced to no more than 25 mg per day in the 14 days before the first dose of trial treatment

Who may not be able to join:

  • People whose lymphoma has spread to the brain or spinal cord, or who have lymphoma that started in the central nervous system
  • People who have previously been treated with a type of immune cell therapy called anti-CD19 CAR-T therapy
  • People who have previously received a type of treatment called a bispecific anti-CD20xCD3 antibody
  • People who have previously had a stem cell transplant (either using their own cells or a donor's cells)
  • People with significant lung conditions, such as pulmonary fibrosis or chronic obstructive pulmonary disease (COPD), that affect their ability to be physically active
  • People with significant heart conditions, including unstable chest pain, a heart attack within the past 6 months, or severe heart failure
  • People who are pregnant or breastfeeding
  • People who have not sufficiently recovered from a major surgery before starting the trial
  • People with an ongoing serious infection currently requiring antibiotics, antifungal, or antiviral medication, or who needed intravenous antibiotics for a major infection within 2 weeks of the trial start
  • People who have received a live vaccine within 30 days of starting the trial, or who expect to need one during the trial (note: standard flu shots and approved COVID-19 vaccines are generally permitted — confirm with trial site)
  • People with an active hepatitis B infection (people with certain past hepatitis B markers may still be eligible if a specific blood test is negative — confirm with trial site)
  • People with an active hepatitis C infection (people who test positive for hepatitis C antibodies may still be eligible if a further blood test is negative — confirm with trial site)
  • People with a known active COVID-19 infection at the time of joining (specific testing requirements apply — confirm with trial site)
  • People with severe chronic lung disease or another serious medical condition likely to make tolerating the trial treatment very difficult
  • People with a seizure disorder requiring ongoing treatment who have had a seizure within the past two years
  • People who do not have the capacity to make their own informed decisions

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 16 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: Juan Alderuccio, MD, University of Miami

Phone: 305-243-4372

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
7 January 2026
Est. completion
7 January 2031

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of Participants Experiencing Cytokine Release Syndrome (CRS)-related Toxicity after Epcoritamab Administration; Number of Participants Experiencing Immune Effector Cell Associated Neurotoxicity Syndrome (ICANS)-related Toxicity; Number of Participants Experiencing Neurologic Toxicities Associated with Epcoritamab; Number of Participants Experiencing Fluid Accumulation Associated with Loncastuximab; Number of Participants Experiencing Hepatotoxicity Associated with Loncastuximab

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: 16 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