Recruiting at 174 sites Phase 1, Phase 2 Acute Lymphoblastic Leukemia

Acute Lymphoblastic Leukemia study: Biospecimen Collection

Official title The Pediatric Acute Leukemia (PedAL) Screening Trial - A Study to Test Bone Marrow and Blood in Children With Leukemia That Has Come Back After Treatment or Is Difficult to Treat - A Leukemia & Lymphoma Society and Children's Oncology Group Study

ClinicalTrials.gov ID: NCT04726241

What this study is testing

What it's testing
This study is testing whether checking bone marrow and blood can help decide the best treatment for children whose leukemia has come back or is difficult to treat.
Who it's for
You may be able to join if you are a child, teen, or young adult with leukemia that has returned after treatment or is hard to treat.
What's involved
You will give a small blood sample and a bone‑marrow sample. The doctors will use the results to see if you qualify for other studies.
Time commitment
The study involves a few visits for sample collection over a short period.
  • Phase 2: a mid-size study of how well it works

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages up to 22

You may be able to join if

  • Patients must be less than 22 years of age at the time of study enrollment
  • Patient has known or suspected relapsed/refractory (including primary refractory) AML as defined in protocol
  • This includes isolated myeloid sarcoma
  • Patient has known or suspected relapsed/refractory (including primary refractory) myeloid leukemia of Down syndrome (ML-DS)
  • Second or greater B-ALL medullary relapse, excluding KMT2Ar
See the full eligibility criteria
Who can join
  • Patients must be less than 22 years of age at the time of study enrollment
  • Patient has known or suspected relapsed/refractory (including primary refractory) AML as defined in protocol
  • This includes isolated myeloid sarcoma
  • Patient has known or suspected relapsed/refractory (including primary refractory) myeloid leukemia of Down syndrome (ML-DS)
  • Second or greater B-ALL medullary relapse, excluding KMT2Ar
  • Any first or greater B-ALL medullary relapse involving KMT2Ar
  • Any first or greater T-ALL medullary relapse with or without KMT2Ar
  • Patient has known or suspected relapsed/refractory (including primary refractory) mixed phenotype acute leukemia (MPAL) as defined in protocol
  • Patient has known or suspected de novo or relapsed/refractory (including primary refractory) treatment-related AML (t-AML)
  • Patient has known or suspected de novo or relapsed/refractory (including primary refractory) myelodysplastic syndrome (MDS) or treatment-related myelodysplastic syndrome (t-MDS)
  • Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse.
  • Patient has known or suspected de novo or relapsed/refractory (including primary refractory) juvenile myelomonocytic leukemia (JMML)
  • Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse.
  • All patients and/or their parents or legal guardians must sign a written informed consent
  • All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met

The study team makes the final eligibility decision.

Where it is enrolling

  • Birmingham, Alabama, United States
  • Mobile, Alabama, United States
  • Anchorage, Alaska, United States
  • Mesa, Arizona, United States
  • Phoenix, Arizona, United States
  • Tucson, Arizona, United States
  • Little Rock, Arkansas, United States
  • Downey, California, United States
  • Loma Linda, California, United States
  • Long Beach, California, United States
  • Los Angeles, California, United States
  • Madera, California, United States
  • Oakland, California, United States
  • Orange, California, United States
  • Palo Alto, California, United States
  • San Francisco, California, United States
  • Aurora, Colorado, United States
  • Denver, Colorado, United States
  • Hartford, Connecticut, United States
  • New Haven, Connecticut, United States

+ 130 more site(s).

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, up to 22 years. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Birmingham, Alabama, United States; Mobile, Alabama, United States; Anchorage, Alaska, United States; Mesa, Arizona, United States; Phoenix, Arizona, United States; Tucson, Arizona, United States and 144 more locations. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.