Phase 2 Leukaemia Trial, Recruiting NCT07221500 Sponsor: Nurix Therapeutics, Inc. Condition: Leukaemia
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Phase 2 Leukaemia Trial, Recruiting

NCT07221500
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:

  • You must be 18 years of age or older
  • You must have been diagnosed with a type of blood cancer called CLL or SLL that has come back or stopped responding to treatment, confirmed using standard diagnostic guidelines
  • You must be well enough to carry out basic daily activities, based on a standard health rating scale scored 0 to 2 (confirm with trial site)
  • You must have previously received three specific types of cancer treatments: two different types of BTK inhibitor drugs and one BCL-2 inhibitor drug, either given separately or together as part of your treatment history
  • If you have SLL, your disease must be measurable on a scan or imaging
  • Your liver, kidneys, and bone marrow must be functioning well enough to take part
  • You must be willing to sign a consent form showing you understand what the study involves and agree to take part

Who may not be able to join:

  • You may not be eligible if you have or are suspected to have a related blood condition called prolymphocytic leukemia or Richter's transformation
  • You must not have received another experimental or cancer-fighting treatment within a certain number of days before starting the trial (confirm exact timeframe with trial site)
  • You must not have received antibody-based cancer therapy within 4 weeks before the first dose
  • You must not have had limited radiation therapy to a small area within 7 days, or wider-field radiation therapy within 28 days, before starting the trial
  • You must not have been taking high-dose steroid tablets (more than 20mg of prednisone or similar) within the 7 days before starting the trial, unless used for a scan preparation
  • You must not have taken immune-suppressing medications (other than steroids) within the 60 days before starting the trial
  • You must not have previously been treated with a specific type of drug called a BTK degrader
  • You must not have had CAR T-cell therapy or a stem cell transplant within the 90 days before joining the trial
  • You must not have had a blood clot, stroke, or bleeding in the brain within the 6 months before starting the trial

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 23 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: Nurix Study Director, Nurix Therapeutics, Inc.

Phone: 415-417-3418

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
Nurix Therapeutics, Inc.
Registry
ClinicalTrials.gov
Start date
15 October 2025
Est. completion
1 January 2028

Where this trial is recruiting

🇫🇷 France 🇮🇹 Italy 🇵🇱 Poland 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Objective response rate without partial response with lymphocytosis (PR-L) as determined by an Independent Review Committee (IRC)

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: 23 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