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A Pivotal Phase 2 Trial of Antibody Naxitamab (hu3F8) and Granulocyte-Macrophage Colony Stimulating Factor (GM-CSF) in High-Risk Neuroblastoma Patients With Primary Refractory Disease or Incomplete Response to Salvage Treatment in Bone and/or Bone Marrow

Who is this study for? Patients with Neuroblastoma
What treatments are being studied? GM-CSF + Naxitamab
Status: Active_not_recruiting
Location: See all (20) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

Children and adults diagnosed with high-risk neuroblastoma patients with primary refractory disease or incomplete response to salvage treatment in bone and/or bone marrow will be treated for up to 101 weeks with naxitamab and granulocyte-macrophage colony stimulating factor (GM-CSF). Patients will be followed for up to five years after first dose. Naxitamab, also known as hu3F8 is a humanised monoclonal antibody targeting GD2

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Healthy Volunteers: f
View:

• Diagnosis of neuroblastoma as defined per International Neuroblastoma Response Criteria

• High-risk neuroblastoma patients with either primary refractory disease or incomplete response to salvage treatment (in both cases including stable disease, minor response and partial response) evaluable in bone and/or bone marrow.

• Life expectancy ≥ 6 months

Locations
United States
Indiana
Riley Hospital for Children
Indianapolis
New York
Memorial Sloan Kettering Cancer Center
New York
Other Locations
Canada
The Hospital for Sick Children
Toronto
Denmark
Rigshospitalet
Copenhagen
Germany
University Medical Center Hamburg-Eppendorf
Hamburg
Johannes Gutenberg-Universität
Mainz
University Hospital Regensburg
Regensburg
Hong Kong Special Administrative Region
Hong Kong Children's Hospital
Hong Kong
Queen Mary Hospital
Hong Kong
India
Tata Memorial Centre
Mumbai
Italy
Giannina Gaslini Hospital
Genoa
Fondazione IRCCS Istituto Nazionale dei Tumori
Milan
Ospedale Pediatrico Bambino Gesù
Rome
Spain
Hospital Sant Joan de Déu
Barcelona
Hospital Infantil Universitario Niño Jesús
Madrid
Hospital Universitario Virgen Del Rocío
Seville
Hospital Universitario y Politécnico La Fe
Valencia
United Kingdom
The Royal Glasgow Children's Hospital
Glasgow
Leeds General Infirmary
Leeds
University Hospital Southampton
Southampton
Time Frame
Start Date: 2018-04-03
Completion Date: 2028-04
Participants
Target number of participants: 122
Treatments
Experimental: GM-CSF + Naxitamab
Each investigational cycle is started with 5 days of GM-CSF administered at 250 µg/m2/day in advance of the start of Naxitamab administration. GM-CSF is thereafter administered at 500 µg/m2/day on days 1 to 5. As standard treatment, Naxitamab is administered at 3 mg/kg/day on days 1, 3, and 5 totalling 9 mg/kg per cycle. Treatment cycles are repeated every 4 weeks until CR or PR followed by 5 additional cycles every 4 weeks (±1 week). Subsequent cycles are repeated every 8 weeks (±2 weeks) through 101 weeks from first infusion at the discretion of the investigator. After end of treatment patients will enter a long-term follow up for up to 3 years after end of treatment visit.
Sponsors
Leads: Y-mAbs Therapeutics

This content was sourced from clinicaltrials.gov