Phase 2 Lymphoma Trial, Recruiting NCT06635330 Sponsor: Kara Yakhteh Tajhiz Azma Company Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06635330
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:

  • Children and teenagers between 2 and 18 years old who have a type of blood cancer called B-cell acute lymphoblastic leukaemia (B-ALL) that has come back or stopped responding to treatment, and whose cancer cells carry a marker called CD19
  • The cancer must be present in the bone marrow at the time of joining
  • The person must be well enough to go through a blood-filtering procedure called apheresis, which collects certain cells from the blood
  • A life expectancy of more than 12 weeks
  • A general health and ability-to-function score above 50% as measured by standard medical scales used for children and adults (confirm with trial site)
  • At least 7 days must have passed since the last chemotherapy treatment and the last use of steroid medications
  • The patient and/or their guardian must provide informed consent to participate
  • A suitable donor for a stem cell transplant must already be available

Who may not be able to join:

  • People who have another active cancer in addition to the B-ALL being studied
  • People who have a type of tumour formed by leukaemia cells outside the bone marrow (called a chloroma), signs of leukaemia affecting the brain or spinal cord on an MRI scan, or significant neurological symptoms
  • People with any disorder affecting the brain or nervous system
  • People with an active condition called graft-versus-host disease (GVHD), where previously transplanted cells are attacking the body
  • People who have received radiation therapy within the last 14 days
  • People who have previously received treatments that targeted CD19 or CD20 markers on cancer cells
  • People who have received donor lymphocyte injections or any other cell-based therapy within the last 30 days
  • People with a serious active infection at the time of joining
  • People with significant problems affecting the function of major organs such as the heart, liver, or kidneys

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

Phone: +989124779968

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
Kara Yakhteh Tajhiz Azma Company
Registry
ClinicalTrials.gov
Start date
20 May 2024
Est. completion
22 September 2026

Where this trial is recruiting

Iran

Primary endpoints

Percentage of patients with overall remission rate (ORR) of complete response (CR) or complete remission with incomplete blood count recovery (CRi); Overall survival; Incidence of cytokine release syndrome: grade 3 and 4; Incidence of Immune effector cell-associated neurotoxicity syndrome (ICANS): grade 3 and 4; Event-free survival

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