30 closest matches · ranked by relevance
Neuroblastoma
Primary: Overall Response Rate [Complete Response + Very Good Partial Response + Partial Response (CR + VGPR + PR)] — 42 Participants
Neuroblastoma
Primary: Overall Responses — 3; 18; 12; 1 Participants
Neuroblastoma · Medulloblastoma
Primary: Number of Participants With Related Adverse Events as a Measure of Safety and Tolerability — 45 Participants
Neuroblastoma
Primary: Percentage of Participants That Are Able to Meet Feasibility Parameters. — 100 percentage of participants
Recurrent Neuroblastoma
Primary: Number of Patients With Unacceptable Dose Limiting Toxicities (DLTs) — 1; 2; 9; 18 participants
Neuroblastoma
Primary: Overall Response - Complete Response (CR), Very Good Partial Response (VGPR) and Partial Response (PR) — 5; 3 participants
Neuroblastoma
Primary: Number of Responders (Response Rate) — 0; 5; 13; 18 participants
Disseminated Neuroblastoma · Recurrent Neuroblastoma
Primary: Median Time to Progression as Assessed by Response Evaluation Criteria in Solid Tumors — 45; 42 days
Neuroblastoma · Medulloblastoma · Relapse
Primary: Number of Participants With Adverse Events as a Measure of Safety and Tolerability — 14 participants
Neuroblastoma
Primary: Number of Participants With Dose-limiting Toxicity as a Measure of Tolerability — 0; 0 participants with DLT
Neuroblastoma
Primary: Response (Complete Response, Very Good Partial Response, and Partial Response) at 60-days Post Stem Cell Infusion — 4; 3 participants
Neuroblastoma
Primary: Maximum Tolerated Dose — 18.6 mCi/kg
Neuroblastoma
Primary: Number of Participants With Immediate and Short Term Toxicity of Infusion Over 8 Weeks — 0; 0; 3 Participants
Recurrent B-Cell Childhood Acute Lymphoblastic Leukemia · Recurrent Childhood B-Lymphoblastic Lymphoma
Primary: 3-year Overall Survival Rate of Patients With Relapsed ALL — 94.4; 55.5; 72.63 percentage of participants — p=0.035
Ganglioneuroblastoma · Recurrent Neuroblastoma
Primary: Percentage of Randomized Patients Who Are Responders — 5.6; 52.9 Percentage of patients
Neuroblastoma
Primary: MTD/RP2D Determination Cohort A — 0; 0; 0 Participants
High Risk Neuroblastoma
Primary: Percentage of Patients Who Experienced a Significant (CTC Grade 3-5) Nonhematologic Toxicity of Interest (Pain, Hypotension, Allergic Reactions, Capillary Leak Syndrome…
Central Nervous System Tumor, Pediatric · Neuroblastoma
Primary: Therapy Completion Rate — .40 proportion of participants
Neuroblastoma
Primary: Overall Survival (OS) Rates — 99.4; 93.5; 88.4 percentage of participants
Neuroblastoma
Primary: Objective Tumor Response After One Course of Therapy — 5; 5; 11 Participants
Ganglioneuroblastoma · Stage 1 Neuroblastoma · Stage 2 Neuroblastoma
Primary: The Tolerability of BuMel Regimen — 9 participants
Pleuropulmonary Blastoma · Recurrent Malignant Peripheral Nerve Sheath Tumor · Recurrent Neuroblastoma
Primary: Objective Response by Response Evaluation Criteria in Solid Tumors Version 1.1 — 0.00; 6.25; 0.00; 0.00 Percent of participants
High Risk Neuroblastoma · Recurrent Neuroblastoma · Recurrent Osteosarcoma
Primary: Percent (95% CI) of Participants With Grade 3 or Higher Adverse Events (Dose Finding Cohort) — 71.4; 100 percentage of participants
Neuroblastoma Recurrent
Primary: Number of Participants With Adverse Events as a Measure of Safety and Tolerability — 2; 1; 3 Participants
Ganglioneuroblastoma · Localized Resectable Neuroblastoma · Localized Unresectable Neuroblastoma
Primary: Percentage of MIBG Avid Patients Treated With Meta-iodobenxylguanide (MIBG) Labeled With Iodine-131 — 86.8 Percentage of participants
Neuroblastoma
Primary: Assess the Activity of High-dose 3F8/GM-CSF
Neuroblastoma
Primary: Number of Participants With Adverse Events as a Measure of Safety and Tolerability — 2; 4; 0; 5 participants
Adenocarcinoma · Neoplasms
Primary: Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs): Part 1 — 4; 5; 3; 7 participants
Neuroblastoma
Primary: Assess the Impact of High-dose 3F8/GM-CSF on Relapse-free Survival
Neuroblastoma
Primary: MTD/RP2D Determination A1 — 0; 0; 0; 0 Participants