ALL, Childhood

5

Review clinical trials related to ALL, Childhood. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Healthy Weight Intervention Families During ALL Treatment: NOURISH-ALL

The purpose of this study is to conduct a single arm pilot of the NOURISH-ALL (Nourishing Our Understanding of Role modeling to Improve Support and Health in Acute Lymphoblastic Leukemia) intervention focused on three components of participant engagement. This is a single arm intervention study that involves participation in a 6-session family intervention and three time points of multimethod data collection. The primary outcome is participant engagement, measured as recruitment, retention, and intended dose received. This study will be conducted over 5 years in three phases: * Aim 1a: Adapting the NOURISH-ALL Intervention for Families of Youth with ALL (Year 1) * Aim 1b: Iteratively Refining the NOURISH-ALL Intervention (Year 2) * Aim 2: Pilot Single-Arm Trial of NOURISH-ALL Focused on Participant Engagement (Years 3-5)

Participants needed: 46
Trial details
Age: 2-12Biological sex: AllType: ObservationalSponsor: University of Kansas Medical CenterUpdated: Jul 2, 2026Locations: 2
Eligibility criteria

Children ages 2-12 years old and their primary caregiver ages 18-90 [+7]

Primary oncology provider identifies safety concerns regarding the child's parti...

Status: Recruiting

Ruxolitinib and Chemotherapy in Adolescents and Young Adults With Ph-like Acute Lymphoblastic Leukemia

This study will test if adding ruxolitinib to standard multi-drug chemotherapy regimen will be safe and tolerated in adolescents and young adults with newly diagnosed Ph-like acute lymphoblastic leukemia (ALL).

Participants needed: 15
Trial details
Phase: Phase 1Age: 18-39Biological sex: AllType: InterventionalSponsor: University of ChicagoUpdated: Jun 29, 2026Locations: 2
Eligibility criteria

Newly diagnosed de novo B-precursor acute lymphoblastic leukemia (ALL) as determ... [+17]

Patients who are receiving any other investigational agent. [+8]

Status: Recruiting

Childhood Cancer Survivors' Affective Response to Exercise

The primary objective of this study is to assess the feasibility of administering the Personalized Single-Category Implicit Association Test (PSC-IAT) to young adult survivors of childhood cancer. Participants will perform a total of three trials of a cognitive task before and after their scheduled SJLIFE cardiovascular stress testing. Participants will then be asked to participate in a qualitative interview about the cognitive task tool and body sensations and emotions experienced during exercise.

Participants needed: 125
Trial details
Age: 18-39Biological sex: AllType: ObservationalSponsor: St. Jude Children's Research HospitalUpdated: Apr 23, 2026Locations: 1
Eligibility criteria

Participants enrolled in St. Jude Lifetime Cohort (SJLIFE) aged 18-39 years at c... [+4]

Individuals who cannot speak, read, and/or understand English. [+3]

Status: Recruiting

CAR T-cell Therapy Directed to CD70 for Pediatric Patients With Hematological Malignancies

The study participant has one of the following blood cancers: acute myelogenous leukemia (AML)/myelodysplastic syndrome (MDS), acute lymphoblastic leukemia (B-ALL, T-ALL) or Lymphoma. Your cancer has been difficult to treat (refractory) or has come back after treatment (relapse). Primary Objective To determine the safety and maximum tolerated dose of intravenous infusions of escalating doses of CD70-CAR T cells in patients (≤21 years) with recurrent/refractory CD70+ hematological malignancies after lymphodepleting chemotherapy. Secondary Objectives To evaluate the antileukemic activity of CD70-CAR T cells. We will determine the anti- leukemic activity of the CD70-CAR T cells in the bone marrow and in the treatment of extramedullary disease.

Participants needed: 18
Trial details
Phase: Phase 1Age: Up to 21Biological sex: AllType: InterventionalSponsor: St. Jude Children's Research HospitalUpdated: Jan 23, 2026Locations: 1
Eligibility criteria

Relapsed disease that is CD70 positive [+7]

Known primary immunodeficiency [+6]

Status: Recruiting

Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia

A five-year prospective observational cohort study. The study is focused on observing the relation between static germline variants and therapeutic response in Indian children with acute lymphoblastic leukemia (ALL). The project is an International multicenter setup. This collaborative research project between Switzerland and India includes one main center in Geneva that has conceptualized, designed, received grants for the study and two investigating centers in India (Puducherry and New-Delhi) involved in study design, patient care and recruitment for this specific study. All the participants for the study will be recruited form these two centers in India, and no patient recruitment is planned at main center i.e. Geneva. The study will be conducted in two phases. The first aims to investigate genetic predisposition (static germline variants) to early chemotherapy treatment related toxicities (TRTs). The second aims to investigate somatic genetic markers associated with the efficacy of steroid treatment among patients undergoing the standardized IciCLe-ALL-14 treatment protocol. A total of 500 children with ALL will be recruited to investigate primary objective of the study i.e. TRT, and a subset of 250 patients will be included to investigate another research question i.e. response to steroid therapy.

Participants needed: 556
Trial details
Age: 1-18Biological sex: AllType: ObservationalSponsor: University of Geneva, SwitzerlandUpdated: Jan 15, 2026Locations: 2
Eligibility criteria

Age > 1 year old and ≤18 years old at enrolment [+5]

Previously tretaed patients [+2]