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New cell prep method aims to tame transplant complications in kids

NCT ID NCT06393660

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access This study
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study offers a special way to prepare donor stem cells for children and teens under 22 who need a transplant but lack a perfectly matched sibling donor. The method uses the CliniMACS® system to remove certain immune cells, which may help reduce the risk of graft-versus-host disease (a serious complication where donor cells attack the patient's body). The goal is to make the transplant safer and more effective for controlling transplant-related disorders.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

Up to 21 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Recipient Inclusion Criteria: * Age less than 22 years of age * No available genotypically matched related donor (sibling) * Availability of a suitable donor and graft source * Haploidentical related mobilized peripheral blood cells * 9/10 or 10/10 allele matched (HLA-A, -B, -C, -DRB1, -DQB1) volunteer unrelated donor mobilized peripheral blood cells Donor Inclusion Criteria: * Matching as described in the Recipient and Donor Suitability Criteria * Size and vascular access appropriate by center standard for peripheral blood stem cell (PBSC) collection. Donors with inadequate peripheral access will require placement of an apheresis catheter for collection. * Must meet appropriate screening/eligibility requirements: * Haploidentical matched family members: screened by center health screens and found to be eligible. * Unrelated donors: meet suitability criteria to donate PBSC * HIV negative * Not pregnant or lactating * Recipient must not have high-level donor specific anti-HLA antibodies according to institutional practices. * Must agree to donate PBSC * Must give informed consent Recipient Suitability: \- Adequate organ functioning as demonstrated by: * MUGA ≥ 50% or ECHO \>30% * 24-hour Creatinine Clearance or Glofil ≥ 50 ml/min or Serum Creatinine ≤2 times the upper limit of normal * DLCO \> 65% of predicted value. FEV1 \>65% of predicted * AST / ALT ≤ 2.5 and/or Bilirubin ≤ 1.5 times the upper limit of normal * Pregnancy test negative * HIV 1 / 2 (HIV screen) negative with a negative qualitative HIV PCR. * HTLV I negative * RPR or VDRL negative * RVP (Respiratory Viral PCR) with a negative result * Positive hepatitis testing does not make the patient ineligible. Hepatitis results will be evaluated on a case-by-case basis by the transplant physician to determine donor suitability/eligibility. Donor Suitability: \- Allowed Donor Sources * Fully matched sibling donors are not allowed. * Unrelated donors. HLA typing of at least 10 alleles is required. Donor must be matched at 9/10 or 10/10 alleles (HLA-A, -B, -C, -DRB1, -DQB1). Haploidentical matched family members. Minimum match level full haploidentical (at least 5/10; HLA-A, -B, -C, -DRB1, -DQB1 alleles), but use of haploidentical donors with extra matches (e.g., 6, 7, or 8/10) encouraged. * Cord blood is not allowed as a stem cell source on this IDE. Recipient and Donor Exclusion Criteria: * Pregnant or lactating females are ineligible as the risk to unborn children and infants is unknown * Presence of life-threatening, uncontrolled opportunistic infection (fungal, bacterial, or viral infections). Patients with history of fungal disease during induction therapy may proceed if they have a significant response to antifungal therapy with no or minimal evidence of disease remaining by CT evaluation. * HIV or HTLV I/II infection

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Children's Medical Center - Dallas

    AVAILABLE

    Dallas, Texas, 75235, United States

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