Phase 2 Lymphoma Trial, Recruiting NCT05848687 Sponsor: Tanja Andrea Gruber Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05848687
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:

  • The patient must be 365 days old or younger at the time of diagnosis.
  • The patient must have a newly diagnosed blood cancer called acute lymphoblastic leukemia (ALL) or acute undifferentiated leukemia, where the cancer cells test positive for a protein called CD19.
  • Patients with a mixed type of acute leukemia may be eligible, provided the cancer cells test positive for CD19.
  • Patients with a specific type of mature B-cell ALL that has a particular gene change called a KMT2A rearrangement may be eligible.
  • Prior treatment must have been very limited — only small amounts of certain medicines (hydroxyurea for 72 hours or less, steroids for one week or less, cytarabine for 72 hours or less), at most one dose of vincristine, and at most one intrathecal (spinal) chemotherapy dose.
  • A parent or legal guardian must be willing and able to provide written informed consent following all required guidelines.

Who may not be able to join:

  • Patients who have received treatments beyond the very limited prior therapy described above.
  • Patients with mature B-cell ALL that does not have the KMT2A gene rearrangement.
  • Patients whose cancer is a type called AML (acute myelogenous leukemia) or T-cell ALL.
  • Patients who have Down syndrome.
  • Patients whose parent or legal guardian is unable or unwilling to provide written informed consent.

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 7 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: Tanja A Gruber, MD, PhD, Stanford University

Phone: 650 723 5535

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
Tanja Andrea Gruber
Registry
ClinicalTrials.gov
Start date
3 November 2023
Est. completion
1 December 2028

Where this trial is recruiting

🇨🇦 Canada 🇺🇸 United States

Primary endpoints

Minimal Residual Disease

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: 7 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