Leukaemia Trial, Recruiting NCT07602088 Sponsor: Janssen Research & Development, LLC Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT07602088
Recruiting Not Applicable

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 have been diagnosed with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) and whose condition has reached a point where treatment is needed, based on international medical guidelines from 2018.
  • People for whom a doctor has already decided — before and separately from this study — to start a specific combination treatment using two medicines called ibrutinib and venetoclax, used together for a set period of time.
  • People who are willing to sign a consent form that allows the trial site to verify their medical records, in line with local rules.
  • People who are able to read, understand, and fill in questionnaires about their health and wellbeing in their local language throughout the study.

Who may not be able to join:

  • People who have previously received any treatment for CLL or SLL.
  • People who have taken part in a trial involving an experimental medicine, vaccine, or invasive experimental medical device within the 30 days before the study begins or before the first data collection point.
  • People who are currently enrolled in, or plan to join, another clinical trial that involves an active medical intervention (participation in observational studies or registries not run by Janssen may be permitted — confirm with trial site).
  • People for whom there are any restrictions or limitations under the currently approved prescribing guidelines for ibrutinib or venetoclax in Romania that would prevent treatment with this combination.

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 20 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Janssen Research & Development, LLC Clinical Trial, Janssen Research & Development, LLC

Phone: 844-434-4210

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
18 May 2026
Est. completion
30 January 2029

Where this trial is recruiting

🇷🇴 Romania

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: 20 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