Phase 2 Lymphoma Trial, Recruiting NCT07024706 Sponsor: AstraZeneca Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07024706
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 a type of blood cancer called CLL (Chronic Lymphocytic Leukaemia) or SLL (Small Lymphocytic Lymphoma), confirmed using standard 2018 diagnostic guidelines.
  • People who previously received a first course of treatment combining two specific types of targeted therapy drugs (a BTK inhibitor and a BCL2 inhibitor, with or without a third drug called obinutuzumab), where that treatment was given for a fixed period of time, the cancer responded well (at least a partial response), and at least 2 years have passed since that treatment ended.
  • People for whom certain genetic test results are available or can be obtained before the trial begins, covering three specific markers related to the cancer's biology (IGHV mutation status, deletion of chromosome 17p, and TP53 mutation status).
  • People whose general physical health and ability to carry out daily activities falls within an acceptable range, as measured by a standard medical scale (ECOG score of 0, 1, or 2).
  • People whose liver, kidneys, and bone marrow are functioning at an adequate level.

Who may not be able to join:

  • People with other significant health conditions that, in the treating doctor's opinion, would make participation unsuitable.
  • People with serious heart or stroke-related conditions.
  • People who are currently bleeding, or who have a history of bleeding disorders (such as haemophilia or von Willebrand disease).
  • People with moderate to severe liver cirrhosis (classified as Child-Pugh B or C).
  • People who have a history of another cancer, either in the past or currently.
  • People who are HIV positive.
  • People who have a history of a serious brain condition called Progressive Multifocal Leukoencephalopathy (PML) (confirm with trial site).
  • People with a currently active Hepatitis B or Hepatitis C infection.
  • People who have been taking steroid medications above a certain dose (more than 20 mg) in the week before the first trial treatment dose.
  • People who have previously had a severe allergic reaction to any of the medications used in this trial.
  • People who need to take certain medications that strongly interact with a liver enzyme called CYP3A4, as these can affect how trial drugs work in the body (confirm specific medications with trial site).
  • People who are taking blood-thinning medications such as warfarin or similar drugs from the same class.
  • People who have had a major surgical procedure within 30 days before the first trial treatment dose.

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 6 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

Phone: 1-877-240-9479

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
Registry
ClinicalTrials.gov
Start date
4 June 2026
Est. completion
1 May 2029

Where this trial is recruiting

🇦🇹 Austria 🇧🇷 Brazil 🇨🇿 Czechia 🇮🇪 Ireland 🇮🇹 Italy 🇵🇱 Poland 🇪🇸 Spain 🇺🇸 United States

Primary endpoints

Overall Response Rate (ORR)

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: 6 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