Phase 1 Lymphoma Trial, Recruiting NCT05370430 Sponsor: PeproMene Bio, Inc. Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT05370430
Recruiting Phase 1

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 signed an informed consent form (or had a legal representative sign on their behalf)
  • People aged 18 or older who are well enough to carry out basic daily activities (confirmed by a doctor using a standard health scale)
  • People with a confirmed diagnosis of a type of B-cell non-Hodgkin lymphoma (B-NHL), including certain subtypes, who have already received a specified number of prior treatments
  • People whose lymphoma cells have a specific protein marker called BAFF-R on their surface
  • People with a tumor measuring at least 1.5 cm on a CT or PET scan, or with detectable disease in the blood, bone marrow, digestive tract, skin, or spleen
  • People who have previously received CAR T-cell therapy, provided it was at least 3 months before a cell collection procedure and certain levels of those prior CAR T-cells are no longer detected in the blood
  • People whose blood counts meet minimum levels — including white blood cells, platelets, and red blood cell-related measures — with some flexibility if lymphoma is present in the bone marrow
  • People whose liver function test results are within acceptable ranges
  • People whose kidneys are functioning at an adequate level
  • People whose heart is pumping well enough and whose heart rhythm and oxygen levels meet specified thresholds
  • People who test negative for HIV, and who either test negative for hepatitis B and C, or have an undetectable viral load if previously exposed
  • Females of childbearing potential who have a negative pregnancy test and agree to use effective contraception or abstain from sex for at least 3 months after treatment ends

Who may not be able to join:

  • People who have previously received a bone marrow or stem cell transplant from another person (allogeneic transplant)
  • People who received their own stem cells back in a transplant (autologous transplant) fewer than 6 months before the cell collection procedure
  • People currently taking steroid medications or other long-term immune-suppressing drugs
  • People whose lymphoma has spread to the heart
  • People who need immediate treatment due to serious complications caused by their cancer, such as a blocked bowel
  • People with an active autoimmune disease that requires immune-suppressing medication
  • People with a primary immune deficiency condition
  • People with significant heart problems, including severe heart failure (NYHA Class III or IV), certain irregular heart rhythms, a heart attack within the past 6 months, a stroke within the past 6 months, or a serious blood clot within the past 6 months
  • People with certain neurological conditions, including a history of optic neuritis, inflammatory diseases of the brain or nervous system, or a seizure disorder
  • People with a history of another cancer, unless it was fully removed or treated with the intent to cure, or has been in remission for at least 3 years
  • People with an uncontrolled infection or lymphoma that has spread to the brain or spinal cord (active CNS lymphoma)
  • Females who are pregnant or breastfeeding
  • People the trial doctors determine may not be safe to participate, or who may not be able to follow the study procedures

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 20 July 2026
Phase 1: approximately ~10% 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: Elizabeth Budde, MD, City of Hope Medical Center

Phone: 714-599-8077

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 1
Sponsor
PeproMene Bio, Inc.
Registry
ClinicalTrials.gov
Start date
13 June 2022
Est. completion
13 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of adverse events; Maximum Tolerated Dose (MTD)

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: 20 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