Phase 2 Lymphoma Trial, Recruiting NCT06308588 Sponsor: M.D. Anderson Cancer Center Condition: Lymphoma
Back to Lymphoma

Phase 2 Lymphoma Trial, Recruiting

NCT06308588
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 who have been diagnosed with Philadelphia chromosome-positive acute lymphoblastic leukaemia (Ph+ ALL) that has not been treated before, or has had only minimal prior treatment (no more than one or two courses of chemotherapy), and where the leukaemia is still detectable at low levels in the blood or bone marrow.
  • People aged 12 or older who have Ph+ ALL that has come back or has not responded to previous treatment, or who have a related condition called lymphoid blast phase CML that has been previously treated.
  • People who are well enough to carry out basic daily activities, as measured by standard medical scales (confirm with trial site for exact score requirements).
  • People who weigh at least 40 kg.
  • People whose liver is working well enough, based on blood test results (unless any abnormal results are thought to be caused by the leukaemia itself).
  • People whose kidneys are working well enough, based on a standard kidney function measurement.
  • People whose pancreas is working well enough, based on blood test results.
  • People whose heart is functioning adequately, as assessed by a doctor.
  • Women who could become pregnant must have a negative pregnancy test before joining the trial.
  • People who are willing to use reliable contraception before, during, and for four months after taking part in the trial.
  • People who are willing and able to give written informed consent to participate.

Who may not be able to join:

  • People who have a serious active infection that is not being controlled by antibiotics taken by mouth or through a drip.
  • People who have another active cancer (other than certain common skin cancers) that a doctor believes is likely to reduce life expectancy to less than one year.
  • People who have severe heart failure (Grade III–V as defined by standard heart failure criteria).
  • People whose heart's electrical activity shows a prolonged interval on an ECG recording (above a certain measurement), unless this is corrected by treatment and approved by a heart specialist.
  • People who have a significant history of certain brain or nervous system conditions, such as epilepsy, stroke, dementia, Parkinson's disease, or psychosis (note: leukaemia that has spread to the brain does not automatically exclude someone — confirm with trial site).
  • People who have received an experimental anti-leukaemia treatment or chemotherapy within the seven days before joining the trial, unless they have fully recovered from side effects, or unless their disease is rapidly worsening in a life-threatening way.
  • Women who are pregnant or breastfeeding.
  • Men enrolled in the trial are expected to understand the risks to any partner who could become pregnant and to use effective contraception.

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 19 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: Nicholas Short, MD, M.D. Anderson Cancer Center

Phone: (713) 563-4485

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
5 August 2024
Est. completion
1 May 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety and adverse events (AEs)

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: 19 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