Phase 2 Lymphoma Trial, Recruiting NCT07015242 Sponsor: Juno Therapeutics, Inc., a Bristol-Myers Squibb Company Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07015242
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:

  • People who are 18 years of age or older at the time of signing the consent form.
  • People who have been diagnosed with primary central nervous system (CNS) lymphoma — a type of lymphoma that starts in the brain or spinal cord — confirmed by a tissue test before the study screening.
  • People whose doctor has determined they are not suitable for a stem cell transplant, either because they are aged 65 or older, or because they have a health comorbidity score of 3 or higher (a measure of other health conditions — confirm with trial site).
  • People whose doctor considers them suitable to receive a treatment regimen based on a chemotherapy drug called high-dose methotrexate.
  • People who have already received between 4 and 6 doses of high-dose methotrexate-based treatment for their CNS lymphoma before joining the trial, with no other prior cancer treatments for this condition (steroid use for symptom control may be permitted under certain conditions — confirm with trial site).
  • People whose CNS lymphoma has responded to prior high-dose methotrexate treatment, meaning scans show the lymphoma has either completely disappeared or mostly gone.
  • People with a functional ability score of 0, 1, or 2 on a standard medical scale — meaning they are fully active or able to carry out light activity (confirm with trial site).
  • People of childbearing potential who have a negative pregnancy test within 24 hours before starting the study treatment.

Who may not be able to join:

  • People whose CNS lymphoma has spread from a lymphoma elsewhere in the body (secondary CNS lymphoma).
  • People whose lymphoma is located only in the eye, only in the fluid around the brain and spinal cord, or whose CNS lymphoma has come back or stopped responding to treatment.
  • People with a significant medical condition or abnormal lab results that a doctor considers would make participation too risky.
  • People who have had another type of cancer that has not been in remission for at least 2 years.
  • People who have previously received CAR T-cell therapy or any other gene therapy that involves editing the human genome.
  • People with a current or past diagnosis of HIV.
  • People with currently active hepatitis B or hepatitis C infection.
  • People with an active autoimmune disease that requires treatment with immune-suppressing medications.
  • People who have previously had an allogeneic (donor) stem cell transplant or a solid organ transplant and require immune-suppressing medications as a result.
  • Additional criteria set out in the study protocol may also apply (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 21 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: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

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
Juno Therapeutics, Inc., a Bristol-Myers Squibb Company
Registry
ClinicalTrials.gov
Start date
6 November 2025
Est. completion
9 January 2028

Where this trial is recruiting

🇫🇷 France 🇩🇪 Germany 🇺🇸 United States

Primary endpoints

Progression-free Survival (PFS)

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: 21 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