Phase 2 Lymphoma Trial, Recruiting NCT05827549 Sponsor: Ho Joon Im Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT05827549
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 were 1 year old or younger, or older than 22 years old, at the time their leukemia came back (confirm with trial site, as this age range is unusual — it may mean between 1 and 22 years old)
  • People who have been diagnosed with a specific type of blood cancer called acute lymphoblastic leukemia (ALL), either the B-cell type (B-ALL) or T-cell type (T-ALL)
  • People whose leukemia has come back for the first time, and where the relapse involves the bone marrow (relapse in other parts of the body at the same time is also acceptable)
  • People who have never had a bone marrow or stem cell transplant from a donor
  • People who have never been treated with a drug called blinatumomab before
  • People whose kidneys are working well enough, based on a blood test result that falls within acceptable ranges for their age and sex
  • People whose liver is working well enough, based on a specific blood test result being below a certain level
  • People whose heart is working well enough, as shown by a heart scan (echocardiogram)
  • People who are well enough to carry out daily activities, as measured by a standard health scoring tool appropriate for their age
  • People with a life expectancy of at least one year
  • People who are expected to be able to follow all study procedures and requirements, in the opinion of the study doctor
  • People (or their guardians) who have signed a consent form before any study procedures begin

Who may not be able to join:

  • People with a type of leukemia called Burkitt leukemia/lymphoma or mature B-cell leukemia
  • People whose leukemia has a specific genetic marker called Philadelphia chromosome positive (Ph+)
  • People with B-cell leukemia whose cancer cells do not carry a protein called CD19, as detected by a laboratory test — the trial site would not be able to administer blinatumomab in these cases
  • People whose leukemia came back within one month of finishing an initial treatment course using the same four-drug combination used in this study
  • People with a type of leukemia that has mixed features (called mixed phenotype leukemia)
  • People who have certain inherited genetic conditions, including Down syndrome, Bloom syndrome, ataxia-telangiectasia, Fanconi anemia, Kostmann syndrome, Shwachman syndrome, or other bone marrow failure syndromes
  • People who are known to have HIV
  • Female patients who are pregnant, or who cannot confirm they are not pregnant (confirmed through a urine test, medical history, or evidence of infertility or menopause)
  • People currently taking part in another clinical trial involving an experimental drug
  • People with unstable health conditions that could put them at risk or affect their ability to follow the study requirements
  • People with serious nervous system or brain conditions, such as uncontrolled seizures, paralysis, speech difficulties, a history of severe brain injury, certain brain diseases, psychosis, or significant movement or coordination problems
  • People with a known allergy or serious reaction to any of the drugs used in this study: Idarubicin, Etoposide, Ifosfamide, Cytarabine, Vincristine, Mercaptopurine, or Blinatumomab

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: Ho Joon Im, Asan Medical Center

Phone: +82-10-6231-1573

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
Ho Joon Im
Registry
ClinicalTrials.gov
Start date
4 April 2024
Est. completion
31 December 2032

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Safety/Efficacy

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