Questa pagina è stata tradotta automaticamente e l'accuratezza della traduzione non è garantita. Si prega di fare riferimento al Versione inglese per un testo di partenza.

Uno studio con tovorafenib (DAY101) come opzione terapeutica per l'istiocitosi a cellule di Langerhans progressiva, recidivante o refrattaria

29 ottobre 2026 aggiornato da: National Cancer Institute (NCI)

Studio di fase 2 su tovorafenib (DAY101) nell'istiocitosi a cellule di Langerhans recidivante e refrattaria

This phase II trial tests the safety, side effects, best dose and activity of tovorafenib (DAY101) in treating patients with Langerhans cell histiocytosis that is growing, spreading, or getting worse (progressive), has come back (relapsed) after previous treatment, or does not respond to therapy (refractory). Langerhans cell histiocytosis is a type of disease that occurs when the body makes too many immature Langerhans cells (a type of white blood cell). When these cells build up, they can form tumors in certain tissues and organs including bones, skin, lungs and pituitary gland and can damage them. This tumor is more common in children and young adults. DAY101 may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Using DAY101 may be effective in treating patients with relapsed or refractory Langerhans cell histiocytosis.

Panoramica dello studio

Stato

Reclutamento

Condizioni

Intervento / Trattamento

Descrizione dettagliata

PRIMARY OBJECTIVE:

I. To determine overall response rate (ORR) for children and young adults with relapsed or refractory BRAFV600E positive (cohort 1) and BRAFV600E negative (cohort 2) Langerhans cell histiocytosis (LCH) treated with tovorafenib (DAY101) after 2 cycles and must be maintained 4 weeks later.

SECONDARY OBJECTIVES:

I. To determine nature and severity of adverse events in patients treated with tovorafenib (DAY101) for relapsed or refractory LCH.

II. To describe event-free survival (EFS) at 1 year in children and young adults with relapsed and refractory LCH treated with tovorafenib (DAY 101) for up to 1 year.

III. To determine durability of response in children and young adults with relapsed or refractory LCH treated with tovorafenib (DAY101) following cessation of therapy in patients with complete response (CR) at 1 year.

IV. To describe progression-free (and relapse-free) survival (PFS) and overall survival (OS) in children and young adults with relapsed or refractory LCH treated with tovorafenib (DAY101) for up to 1 year.

EXPLORATORY OBJECTIVES:

I. To determine potential role of pathogenic tumor mutation in response to tovorafenib (DAY101), and to evaluate changes in bone marrow and peripheral blood cell populations carrying pathogenic mutations in response to tovorafenib (DAY101) therapy.

Ia. To define somatic mutations in LCH lesion biopsies; Ib. To determine impact of tovorafenib (DAY101) on bone marrow and blood BRAFV600E+ mononuclear cells; Ic. To determine impact of tovorafenib (DAY101) on cerebral spinal fluid and disease response; Id. To determine the performance of standardized immunohistochemical analysis of LCH lesion biopsies.

II. To compare performance of LCH-specific response criteria to Response Evaluation Criteria in Solid Tumors (RECIST) criteria.

III. To describe the pharmacokinetics of tovorafenib (DAY101) when administered to pediatric and young adult patients with relapse or refractory LCH.

OUTLINE: This is a dose escalation study of tovorafenib followed by a phase II trial.

Patients receive tovorafenib orally (PO) once weekly (QW) on days 1, 8, 15, and 22 of each cycle. Cycles repeat every 28 days for 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo multi-gated acquisition (MUGA) or echocardiography (ECHO) scans, and fludeoxyglucose F-18 (FDG)-positron emission tomography (PET) or computed tomography (CT) throughout the trial, and collection of blood and urine samples on study. Patients with suspicion of bone marrow and/or central nervous system involvement will also undergo bone marrow biopsy and aspiration and lumbar puncture on study and during follow up.

After completion of study treatment, patients are followed up at 28 days, months 3, 6, 9, and 12, and then at 2 years post cycle 12.

Tipo di studio

Interventistico

Iscrizione (Stimato)

48

Fase

  • Fase 2

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

  • Australia
    • New South Wales
      • Hunter Regional Mail Centre, New South Wales, Australia, 2310
        • Reclutamento
        • John Hunter Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: (02) 4985 5180
        • Investigatore principale:
          • Kristy McCarthy
      • Randwick, New South Wales, Australia, 2031
        • Reclutamento
        • Sydney Children's Hospital
        • Investigatore principale:
          • Draga Barbaric
        • Contatto:
          • Site Public Contact
          • Numero di telefono: (02) 9382-1721
    • Queensland
      • South Brisbane, Queensland, Australia, 4101
        • Reclutamento
        • Queensland Children's Hospital
        • Investigatore principale:
          • Steven A. Foresto
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 61 7 3068 1111
    • Victoria
      • Parkville, Victoria, Australia, 3052
        • Reclutamento
        • Royal Children's Hospital
        • Investigatore principale:
          • Martin A. Campbell
        • Contatto:
    • Western Australia
      • Perth, Western Australia, Australia, 6009
  • Canada
      • Québec, Canada, G1V 4G2
        • Reclutamento
        • CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL)
        • Investigatore principale:
          • Bruno Michon
        • Contatto:
    • Alberta
      • Edmonton, Alberta, Canada, T6G 2B7
        • Reclutamento
        • University of Alberta Hospital
        • Contatto:
        • Investigatore principale:
          • Sarah J. McKillop
    • British Columbia
      • Vancouver, British Columbia, Canada, V6H 3V4
        • Reclutamento
        • British Columbia Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 6477 604-875-2345
        • Investigatore principale:
          • Rebecca J. Deyell
    • Nova Scotia
      • Halifax, Nova Scotia, Canada, B3K 6R8
        • Reclutamento
        • IWK Health Centre
        • Contatto:
        • Investigatore principale:
          • Chelsea Ash
    • Ontario
      • Hamilton, Ontario, Canada, L8N 3Z5
        • Sospeso
        • McMaster Children's Hospital at Hamilton Health Sciences
      • London, Ontario, Canada, N6A 5W9
        • Reclutamento
        • Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 519-685-8306
        • Investigatore principale:
          • Shayna M. Zelcer
      • Toronto, Ontario, Canada, M5G 1X8
        • Reclutamento
        • Hospital for Sick Children
        • Contatto:
        • Investigatore principale:
          • Oussama A. Abla
    • Quebec
      • Montreal, Quebec, Canada, H3H 1P3
        • Reclutamento
        • The Montreal Children's Hospital of the MUHC
        • Contatto:
        • Investigatore principale:
          • Stephanie Mourad
      • Montreal, Quebec, Canada, H3T 1C5
        • Reclutamento
        • Centre Hospitalier Universitaire Sainte-Justine
        • Investigatore principale:
          • Monia Marzouki
        • Contatto:
      • Sherbrooke, Quebec, Canada, J1H 5N4
        • Reclutamento
        • Centre Hospitalier Universitaire de Sherbrooke-Fleurimont
        • Contatto:
        • Investigatore principale:
          • Stephanie Vairy
  • Stati Uniti
    • Alabama
      • Birmingham, Alabama, Stati Uniti, 35233
        • Reclutamento
        • Children's Hospital of Alabama
        • Contatto:
        • Investigatore principale:
          • Matthew A. Kutny
    • Arkansas
      • Little Rock, Arkansas, Stati Uniti, 72202-3591
        • Reclutamento
        • Arkansas Children's Hospital
        • Investigatore principale:
          • Michael W. Bishop
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 501-364-7373
    • California
      • Downey, California, Stati Uniti, 90242
        • Reclutamento
        • Kaiser Permanente Downey Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 626-564-3455
        • Investigatore principale:
          • Robert M. Cooper
      • Loma Linda, California, Stati Uniti, 92354
        • Reclutamento
        • Loma Linda University Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 909-558-4050
        • Investigatore principale:
          • Albert Kheradpour
      • Long Beach, California, Stati Uniti, 90806
        • Reclutamento
        • Miller Children's and Women's Hospital Long Beach
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 562-933-5600
        • Investigatore principale:
          • Jacqueline N. Casillas
      • Los Angeles, California, Stati Uniti, 90027
        • Reclutamento
        • Children's Hospital Los Angeles
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 323-361-4110
        • Investigatore principale:
          • Rebecca S. Parker
      • Madera, California, Stati Uniti, 93636
        • Attivo, non reclutante
        • Valley Children's Hospital
      • Oakland, California, Stati Uniti, 94611
        • Reclutamento
        • Kaiser Permanente-Oakland
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 877-642-4691
          • Email: Kpoct@kp.org
        • Investigatore principale:
          • Aarati V. Rao
      • Oakland, California, Stati Uniti, 94609
        • Reclutamento
        • UCSF Benioff Children's Hospital Oakland
        • Investigatore principale:
          • Jennifer G. Michlitsch
        • Contatto:
      • Orange, California, Stati Uniti, 92868
        • Reclutamento
        • Children's Hospital of Orange County
        • Contatto:
        • Investigatore principale:
          • Elyssa M. Rubin
      • Palo Alto, California, Stati Uniti, 94304
        • Reclutamento
        • Lucile Packard Children's Hospital Stanford University
        • Contatto:
        • Investigatore principale:
          • Jay Michael S. Balagtas
      • San Francisco, California, Stati Uniti, 94158
        • Reclutamento
        • UCSF Medical Center-Mission Bay
        • Contatto:
        • Investigatore principale:
          • Natalie L. Wu
    • Colorado
      • Aurora, Colorado, Stati Uniti, 80045
        • Reclutamento
        • Children's Hospital Colorado
        • Contatto:
        • Investigatore principale:
          • Timothy P. Garrington
      • Denver, Colorado, Stati Uniti, 80218
        • Reclutamento
        • Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center
        • Contatto:
        • Investigatore principale:
          • Florence Choo
    • Connecticut
      • Hartford, Connecticut, Stati Uniti, 06106
        • Reclutamento
        • Connecticut Children's Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 860-545-9981
        • Investigatore principale:
          • Michael S. Isakoff
      • New Haven, Connecticut, Stati Uniti, 06520
        • Reclutamento
        • Yale University
        • Contatto:
        • Investigatore principale:
          • Farzana Pashankar
    • Delaware
      • Wilmington, Delaware, Stati Uniti, 19803
        • Reclutamento
        • Alfred I duPont Hospital for Children
        • Contatto:
        • Investigatore principale:
          • Vibhuti Agarwal
    • District of Columbia
      • Washington D.C., District of Columbia, Stati Uniti, 20010
        • Reclutamento
        • Children's National Medical Center
        • Investigatore principale:
          • Jeffrey S. Dome
        • Contatto:
    • Florida
      • Fort Myers, Florida, Stati Uniti, 33908
        • Reclutamento
        • Golisano Children's Hospital of Southwest Florida
        • Contatto:
        • Investigatore principale:
          • Emad K. Salman
      • Gainesville, Florida, Stati Uniti, 32610
        • Reclutamento
        • UF Health Cancer Institute - Gainesville
        • Investigatore principale:
          • Brian Stover
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 352-273-8010
      • Hollywood, Florida, Stati Uniti, 33021
        • Reclutamento
        • Memorial Regional Hospital/Joe DiMaggio Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 954-265-1847
          • Email: OHR@mhs.net
        • Investigatore principale:
          • Iftikhar Hanif
      • Jacksonville, Florida, Stati Uniti, 32207
        • Reclutamento
        • Nemours Children's Clinic-Jacksonville
        • Contatto:
        • Investigatore principale:
          • Vibhuti Agarwal
      • Miami, Florida, Stati Uniti, 33155
        • Reclutamento
        • Nicklaus Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 888-624-2778
        • Investigatore principale:
          • Ziad A. Khatib
      • Miami, Florida, Stati Uniti, 33136
        • Sospeso
        • University of Miami Miller School of Medicine-Sylvester Cancer Center
      • Orlando, Florida, Stati Uniti, 32806
        • Reclutamento
        • Arnold Palmer Hospital for Children
        • Contatto:
        • Investigatore principale:
          • Zhongbo Hu
      • Orlando, Florida, Stati Uniti, 32827
        • Reclutamento
        • Nemours Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Vibhuti Agarwal
      • Pensacola, Florida, Stati Uniti, 32504
      • St. Petersburg, Florida, Stati Uniti, 33701
        • Reclutamento
        • Johns Hopkins All Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Jennifer B. Dean
      • Tampa, Florida, Stati Uniti, 33607
        • Reclutamento
        • Saint Joseph's Hospital/Children's Hospital-Tampa
        • Contatto:
        • Investigatore principale:
          • Don E. Eslin
    • Georgia
      • Atlanta, Georgia, Stati Uniti, 30329
        • Reclutamento
        • Children's Healthcare of Atlanta - Arthur M Blank Hospital
        • Investigatore principale:
          • Kathryn S. Sutton
        • Contatto:
      • Savannah, Georgia, Stati Uniti, 31404
        • Reclutamento
        • Memorial Health University Medical Center
        • Contatto:
        • Investigatore principale:
          • James N. Yarnall
    • Hawaii
      • Honolulu, Hawaii, Stati Uniti, 96826
        • Reclutamento
        • Kapiolani Medical Center for Women and Children
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 808-983-6090
        • Investigatore principale:
          • Wade T. Kyono
    • Illinois
      • Chicago, Illinois, Stati Uniti, 60611
        • Reclutamento
        • Lurie Children's Hospital-Chicago
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 773-880-4562
        • Investigatore principale:
          • Joanna L. Weinstein
      • Chicago, Illinois, Stati Uniti, 60637
        • Reclutamento
        • University of Chicago Comprehensive Cancer Center
        • Contatto:
        • Investigatore principale:
          • Perry C. Morocco
      • Peoria, Illinois, Stati Uniti, 61637
    • Indiana
      • Indianapolis, Indiana, Stati Uniti, 46202
        • Reclutamento
        • Riley Hospital for Children
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 800-248-1199
        • Investigatore principale:
          • Jennifer A. Belsky
    • Iowa
      • Des Moines, Iowa, Stati Uniti, 50309
        • Reclutamento
        • Blank Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Samantha L. Mallory
      • Iowa City, Iowa, Stati Uniti, 52242
        • Reclutamento
        • University of Iowa/Holden Comprehensive Cancer Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 800-237-1225
        • Investigatore principale:
          • Andrew P. Groves
    • Kentucky
      • Lexington, Kentucky, Stati Uniti, 40536
        • Reclutamento
        • University of Kentucky/Markey Cancer Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 859-257-3379
        • Investigatore principale:
          • James T. Badgett
    • Louisiana
      • New Orleans, Louisiana, Stati Uniti, 70118
        • Reclutamento
        • Children's Hospital New Orleans
        • Investigatore principale:
          • Maria C. Velez-Yanguas
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 504-894-5377
      • New Orleans, Louisiana, Stati Uniti, 70121
        • Reclutamento
        • Ochsner Medical Center Jefferson
        • Contatto:
        • Investigatore principale:
          • Craig Lotterman
    • Maryland
      • Baltimore, Maryland, Stati Uniti, 21287
        • Reclutamento
        • Johns Hopkins University/Sidney Kimmel Cancer Center
        • Contatto:
        • Investigatore principale:
          • Elias Zambidis
      • Baltimore, Maryland, Stati Uniti, 21215
        • Reclutamento
        • Sinai Hospital of Baltimore
        • Investigatore principale:
          • Jason M. Fixler
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 410-601-9083
    • Michigan
      • East Lansing, Michigan, Stati Uniti, 48823
        • Sospeso
        • Michigan State University
      • Grand Rapids, Michigan, Stati Uniti, 49503
        • Reclutamento
        • Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Kathleen Y. Butler
      • Kalamazoo, Michigan, Stati Uniti, 49007
        • Reclutamento
        • Bronson Methodist Hospital
        • Contatto:
        • Investigatore principale:
          • Kathleen Y. Butler
    • Minnesota
      • Minneapolis, Minnesota, Stati Uniti, 55404
        • Reclutamento
        • Children's Hospitals and Clinics of Minnesota - Minneapolis
        • Investigatore principale:
          • Michael K. Richards
        • Contatto:
      • Minneapolis, Minnesota, Stati Uniti, 55455
        • Attivo, non reclutante
        • University of Minnesota/Masonic Cancer Center
    • Mississippi
      • Jackson, Mississippi, Stati Uniti, 39216
        • Reclutamento
        • University of Mississippi Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 601-815-6700
        • Investigatore principale:
          • Amanda Strobel
    • Missouri
      • St Louis, Missouri, Stati Uniti, 63110
        • Reclutamento
        • Washington University School of Medicine
        • Contatto:
        • Investigatore principale:
          • Bryan A. Sisk
      • St Louis, Missouri, Stati Uniti, 63141
        • Reclutamento
        • Mercy Hospital Saint Louis
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 314-251-7066
        • Investigatore principale:
          • Robin D. Hanson
      • St Louis, Missouri, Stati Uniti, 63104
        • Reclutamento
        • Cardinal Glennon Children's Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 314-268-4000
        • Investigatore principale:
          • William S. Ferguson
    • Nebraska
      • Omaha, Nebraska, Stati Uniti, 68114
        • Reclutamento
        • Children's Hospital and Medical Center of Omaha
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 402-955-3949
        • Investigatore principale:
          • Jill C. Beck
      • Omaha, Nebraska, Stati Uniti, 68198
        • Reclutamento
        • University of Nebraska Medical Center
        • Contatto:
        • Investigatore principale:
          • Jill C. Beck
    • Nevada
      • Las Vegas, Nevada, Stati Uniti, 89135
        • Reclutamento
        • Alliance for Childhood Diseases/Cure 4 the Kids Foundation
        • Contatto:
        • Investigatore principale:
          • Joseph L. Lasky
      • Las Vegas, Nevada, Stati Uniti, 89144
        • Reclutamento
        • Summerlin Hospital Medical Center
        • Contatto:
        • Investigatore principale:
          • Joseph L. Lasky
    • New Jersey
      • Hackensack, New Jersey, Stati Uniti, 07601
        • Reclutamento
        • Hackensack University Medical Center
        • Investigatore principale:
          • Katharine Offer
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 551-996-2897
      • Morristown, New Jersey, Stati Uniti, 07960
        • Reclutamento
        • Morristown Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 973-971-5900
        • Investigatore principale:
          • Kathryn L. Laurie
      • New Brunswick, New Jersey, Stati Uniti, 08903
        • Reclutamento
        • Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital
        • Investigatore principale:
          • Marissa Botwinick
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 732-235-8675
      • Paterson, New Jersey, Stati Uniti, 07503
        • Reclutamento
        • Saint Joseph's Regional Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 973-754-2207
          • Email: HallL@sjhmc.org
        • Investigatore principale:
          • Alissa Kahn
    • New York
      • Albany, New York, Stati Uniti, 12208
        • Reclutamento
        • Albany Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 518-262-5513
        • Investigatore principale:
          • Lauren R. Weintraub
      • Brooklyn, New York, Stati Uniti, 11219
        • Reclutamento
        • Maimonides Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 718-765-2500
        • Investigatore principale:
          • Mahmut Y. Celiker
      • New Hyde Park, New York, Stati Uniti, 11040
        • Reclutamento
        • The Steven and Alexandra Cohen Children's Medical Center of New York
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 718-470-3460
        • Investigatore principale:
          • Julie I. Krystal
      • New York, New York, Stati Uniti, 10032
        • Reclutamento
        • NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
        • Investigatore principale:
          • Nobuko Hijiya
        • Contatto:
      • New York, New York, Stati Uniti, 10065
        • Reclutamento
        • Memorial Sloan Kettering Cancer Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 212-639-7592
        • Investigatore principale:
          • Christopher J. Forlenza
      • New York, New York, Stati Uniti, 10016
        • Reclutamento
        • Laura and Isaac Perlmutter Cancer Center at NYU Langone
        • Investigatore principale:
          • Elizabeth A. Raetz
        • Contatto:
      • New York, New York, Stati Uniti, 10029
        • Reclutamento
        • Mount Sinai Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 212-824-7309
          • Email: CCTO@mssm.edu
        • Investigatore principale:
          • Pamela R. Merola
      • New York, New York, Stati Uniti, 10065
        • Reclutamento
        • NYP/Weill Cornell Medical Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 212-746-1848
        • Investigatore principale:
          • Nitya Gulati
      • Syracuse, New York, Stati Uniti, 13210
        • Reclutamento
        • State University of New York Upstate Medical University
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 315-464-5476
        • Investigatore principale:
          • Melanie A. Comito
      • The Bronx, New York, Stati Uniti, 10467
        • Reclutamento
        • Montefiore Medical Center - Moses Campus
        • Contatto:
        • Investigatore principale:
          • Alice Lee
      • Valhalla, New York, Stati Uniti, 10595
        • Attivo, non reclutante
        • New York Medical College
    • North Carolina
      • Asheville, North Carolina, Stati Uniti, 28801
      • Durham, North Carolina, Stati Uniti, 27710
        • Reclutamento
        • Duke University Medical Center
        • Investigatore principale:
          • Jessica M. Sun
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 888-275-3853
      • Greenville, North Carolina, Stati Uniti, 27834
        • Reclutamento
        • East Carolina University
        • Contatto:
        • Investigatore principale:
          • Andrea R. Whitfield
      • Winston-Salem, North Carolina, Stati Uniti, 27157
        • Reclutamento
        • Wake Forest University Health Sciences
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 336-713-6771
        • Investigatore principale:
          • Sarah Supples
    • Ohio
      • Cleveland, Ohio, Stati Uniti, 44106
        • Reclutamento
        • Rainbow Babies and Childrens Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 216-844-5437
        • Investigatore principale:
          • Duncan S. Stearns
      • Columbus, Ohio, Stati Uniti, 43205
        • Reclutamento
        • Nationwide Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Mark A. Ranalli
      • Dayton, Ohio, Stati Uniti, 45404
        • Reclutamento
        • Dayton Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 800-228-4055
        • Investigatore principale:
          • Jordan M. Wright
    • Oklahoma
      • Oklahoma City, Oklahoma, Stati Uniti, 73104
        • Reclutamento
        • University of Oklahoma Health Sciences Center
        • Contatto:
        • Investigatore principale:
          • Rene Y. McNall-Knapp
    • Oregon
      • Portland, Oregon, Stati Uniti, 97239
        • Reclutamento
        • Oregon Health and Science University
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 503-494-1080
          • Email: trials@ohsu.edu
        • Investigatore principale:
          • Katrina Winsnes
    • Pennsylvania
      • Danville, Pennsylvania, Stati Uniti, 17822
        • Reclutamento
        • Geisinger Medical Center
        • Investigatore principale:
          • Jagadeesh Ramdas
        • Contatto:
      • Philadelphia, Pennsylvania, Stati Uniti, 19104
        • Reclutamento
        • Children's Hospital of Philadelphia
        • Investigatore principale:
          • Michael D. Hogarty
        • Contatto:
      • Philadelphia, Pennsylvania, Stati Uniti, 19134
        • Reclutamento
        • Saint Christopher's Hospital for Children
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 215-427-8991
        • Investigatore principale:
          • Gregory E. Halligan
      • Pittsburgh, Pennsylvania, Stati Uniti, 15224
        • Reclutamento
        • Children's Hospital of Pittsburgh of UPMC
        • Contatto:
        • Investigatore principale:
          • Julia E. Segal
    • South Carolina
      • Columbia, South Carolina, Stati Uniti, 29203
        • Reclutamento
        • Prisma Health Richland Hospital
        • Investigatore principale:
          • Stuart L. Cramer
        • Contatto:
      • Greenville, South Carolina, Stati Uniti, 29605
        • Reclutamento
        • BI-LO Charities Children's Cancer Center
        • Investigatore principale:
          • Aniket Saha
        • Contatto:
    • South Dakota
      • Sioux Falls, South Dakota, Stati Uniti, 57117-5134
        • Reclutamento
        • Sanford USD Medical Center - Sioux Falls
        • Contatto:
        • Investigatore principale:
          • Jordan Fritch-Hanson
    • Tennessee
      • Knoxville, Tennessee, Stati Uniti, 37916
        • Reclutamento
        • East Tennessee Childrens Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 865-541-8266
        • Investigatore principale:
          • Susan E. Spiller
      • Nashville, Tennessee, Stati Uniti, 37232
        • Reclutamento
        • Vanderbilt University/Ingram Cancer Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 800-811-8480
        • Investigatore principale:
          • Devang J. Pastakia
      • Nashville, Tennessee, Stati Uniti, 37203
        • Reclutamento
        • The Children's Hospital at TriStar Centennial
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 615-342-1919
        • Investigatore principale:
          • Clinton M. Carroll
    • Texas
      • Austin, Texas, Stati Uniti, 78723
        • Reclutamento
        • Dell Children's Medical Center of Central Texas
        • Contatto:
        • Investigatore principale:
          • Shannon M. Cohn
      • Dallas, Texas, Stati Uniti, 75390
        • Reclutamento
        • UT Southwestern/Simmons Cancer Center-Dallas
        • Contatto:
        • Investigatore principale:
          • Erin B. Butler
      • El Paso, Texas, Stati Uniti, 79905
        • Reclutamento
        • El Paso Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Benjamin Carcamo
      • Houston, Texas, Stati Uniti, 77030
        • Reclutamento
        • Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 713-798-1354
          • Email: burton@bcm.edu
        • Investigatore principale:
          • Olive S. Eckstein
      • Houston, Texas, Stati Uniti, 77030
        • Reclutamento
        • UT MD Anderson Cancer Center
        • Contatto:
        • Investigatore principale:
          • Najat C. Daw
      • San Antonio, Texas, Stati Uniti, 78207
        • Reclutamento
        • Children's Hospital of San Antonio
        • Contatto:
        • Investigatore principale:
          • Julie Voeller
      • San Antonio, Texas, Stati Uniti, 78229
        • Reclutamento
        • University of Texas Health Science Center at San Antonio
        • Contatto:
        • Investigatore principale:
          • Allison C. Grimes
      • San Antonio, Texas, Stati Uniti, 78229
        • Reclutamento
        • Methodist Children's Hospital of South Texas
        • Contatto:
        • Investigatore principale:
          • Jose M. Esquilin
      • Temple, Texas, Stati Uniti, 76508
        • Reclutamento
        • Scott and White Memorial Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 254-724-5407
        • Investigatore principale:
          • Nicholas W. McGregor
    • Utah
      • Salt Lake City, Utah, Stati Uniti, 84113
        • Reclutamento
        • Primary Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 801-585-5270
        • Investigatore principale:
          • Taumoha Ghosh
    • Virginia
      • Charlottesville, Virginia, Stati Uniti, 22908
        • Reclutamento
        • University of Virginia Cancer Center
        • Contatto:
        • Investigatore principale:
          • Brian C. Belyea
      • Norfolk, Virginia, Stati Uniti, 23507
        • Reclutamento
        • Children's Hospital of The King's Daughters
        • Contatto:
        • Investigatore principale:
          • Melissa S. Mark
      • Richmond, Virginia, Stati Uniti, 23298
        • Reclutamento
        • VCU Massey Comprehensive Cancer Center
        • Investigatore principale:
          • Nadirah El-Amin
        • Contatto:
    • Washington
      • Seattle, Washington, Stati Uniti, 98105
        • Reclutamento
        • Seattle Children's Hospital
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 866-987-2000
        • Investigatore principale:
          • Sarah E. Leary
      • Spokane, Washington, Stati Uniti, 99204
        • Reclutamento
        • Providence Sacred Heart Medical Center and Children's Hospital
        • Contatto:
        • Investigatore principale:
          • Judy L. Felgenhauer
    • West Virginia
      • Charleston, West Virginia, Stati Uniti, 25304
        • Reclutamento
        • Vandalia Health/CAMC Institute for Academic Medicine
        • Investigatore principale:
          • Mohamad H. Badawi
        • Contatto:
    • Wisconsin
      • Green Bay, Wisconsin, Stati Uniti, 54301
        • Reclutamento
        • Saint Vincent Hospital Cancer Center Green Bay
        • Investigatore principale:
          • Catherine A. Long
        • Contatto:
      • Milwaukee, Wisconsin, Stati Uniti, 53226
        • Reclutamento
        • Children's Hospital of Wisconsin
        • Investigatore principale:
          • Peter H. Shaw
        • Contatto:
          • Site Public Contact
          • Numero di telefono: 414-955-4727
          • Email: MACCCTO@mcw.edu

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 5 mesi a 22 anni (Bambino, Adulto)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  • 180 days- < 22 years (at time of study enrollment)

  • Patient must have a body surface area of ≥ 0.3 m^2

  • Patients with progressive, relapsed, or recurrent LCH with measurable disease at study entry

    • Patients must have had histologic verification of LCH (from either original diagnosis or relapse/progression) at the time of study entry

      • Tissue confirmation of relapse is recommended but not required.
      • Pathology report must be submitted for central confirmation of diagnosis within 7 days of enrollment.
      • Formalin-fixed paraffin-embedded (FFPE) blocks or unstained slides (initial diagnosis and/or subsequent biopsies) will be required for retrospective central confirmation of diagnosis and molecular studies
      • Patients with mixed histiocytic disorders (e.g. LCH with juvenile xanthogranuloma) may be included

    • Patients must have measurable disease

    • Patients must have progressive or refractory disease or experience relapse after at least one previous systemic treatment strategy

    • Pathogenic somatic mutation detected in genes encoding tyrosine kinase receptors (CSFR1, ERBB3 or ALK), RAS or RAF (may be from original or subsequent biopsy or peripheral blood/bone marrow aspirate). Clinical mutation reports may include quantitative polymerase chain reaction (PCR) (e.g. BRAFV600E) and/or Sanger or next generation sequencing. Immunohistochemistry (e.g. VE1 antibody for BRAFV600E) alone is not sufficient

  • Participant must be able to take an enteral dose and formulation of medication. Study medication is only available as an oral suspension or tablet, which may be taken by mouth or other enteral route such as nasogastric, jejunostomy, or gastric tube

  • Karnofsky >= 50% for patients > 16 years of age and Lansky >= 50% for patients =< 16 years of age

  • Patients must have a performance status corresponding to Eastern Cooperative Oncology Group (ECOG) scores of 0, 1 or 2. Use Karnofsky for patients > 16 years of age and Lansky for patients =< 16 years of age

  • Myelosuppressive chemotherapy: Patients must not have received within 14 days of entry onto this study

  • Investigational agent or any other anticancer therapy not defined above: Patients must not have received any investigational agent or any other anticancer therapy (including MAPK pathway inhibitor) for at least 14 days prior to planned start of tovorafenib (DAY101)

  • Radiation therapy (RT): Patient must not have received RT within 2 weeks after the last dose fraction of RT

  • Patients must have fully recovered from any prior surgery

  • Patients must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, targeted inhibitor, and/or radiotherapy with toxicities reduced to grade 1 or less (Common Terminology Criteria for Adverse Events [CTCAE] version 5.0)

  • Steroids: =< 0.5 mg/kg/day of prednisone equivalent (maximum 20 mg/day) averaged during the month prior to study enrollment is permissible

  • Strong inducers or inhibitors of CYP2C8 are prohibited for 14 days before the first dose of tovorafenib (DAY101) and from planned administration for the duration of study participation

  • Medications that are breast cancer resistant protein (BCRP) substrates that have a narrow therapeutic index are prohibited for 14 days before the first dose of tovorafenib (DAY101) and for the duration of study participation

  • Peripheral absolute neutrophil count (ANC) >= 750/uL unless secondary to bone marrow involvement, in such cases bone marrow involvement must be documented (must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

  • Platelet count >= 75,000/uL (unsupported/without transfusion within the past 7 days) (must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

  • Patients with marrow disease must have platelet count of >= 75,000/uL (transfusion support allowed) and must not be refractory to platelet transfusions. Bone marrow involvement must be documented

  • Hemoglobin >= 8 g/dL (unsupported/without transfusion within the past 7 days). Patients with marrow disease must have hemoglobin >= 8 g/dL (transfusion support allowed). Bone marrow involvement must be documented

  • Hematopoietic growth factors: At least 14 days after the last dose of a long-acting growth factor (e.g., Neulasta [registered trademark]) or 7 days for short-acting growth factor

  • A serum creatinine based on age/sex as follows (must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

    • Age: 6 months to < 1 year; Maximum Serum Creatinine (mg/dL):= 0.5 mg/dl (male and female)
    • Age: 1 to < 2 years; Maximum Serum Creatinine (mg/dL): = 0.6 mg/dl (male and female)
    • Age: 2 to < 6 years; Maximum Serum Creatinine (mg/dL): = 0.8 mg/dl (male and female)
    • Age: 6 to < 10 years; Maximum Serum Creatinine (mg/dL): = 1.0 mg/dl (male and female)
    • Age: 10 to < 13 years; Maximum Serum Creatinine (mg/dL): = 1.2 mg/dl (male and female)
    • Age: 13 to < 16 years; Maximum Serum Creatinine (mg/dL): = 1.5 mg/dl (male) and 1.4 mg/dl (female)
    • Age: >= 16 years; Maximum Serum Creatinine (mg/dL): = 1.7 mg/dl (male) and 1.4 mg/dl (female)
    • OR- a 24 hour urine creatinine clearance >= 50 mL/min/1.73 m^2
    • OR- a glomerular filtration rate (GFR) >= 50 mL/min/1.73 m^2. GFR must be performed using direct measurement with a nuclear blood sampling method OR direct small molecule clearance method (iothalamate or other molecule per institutional standard)
    • Note: Estimated GFR (eGFR) from serum creatinine, cystatin C or other estimates are not acceptable for determining eligibility

  • Bilirubin (sum of conjugated + unconjugated) =< 1.5 x upper limit of normal (ULN) for age (must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

  • Alanine aminotransferase (ALT) =< 3 x ULN for age (must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

  • Serum albumin >= 2 g/dl must be performed within 7 days prior to enrollment, must be repeated prior to the start of protocol therapy if > 7 days have elapsed from their most recent prior assessment)

  • For patients with liver disease caused by their histiocytic disorder (as evaluated on radiographic imaging or biopsy): patients may be enrolled with abnormal bilirubin, aspartate aminotransferase (AST), ALT and albumin with documentation of histiocytic liver disease

  • Fractional shortening (FS) of >= 25% or ejection fraction of >= 50%, as determined by echocardiography or multigated acquisition scan (MUGA) within 28 days prior to study enrollment. Depending on institutional standard, either FS or left ventricular ejection fraction (LVEF) is adequate for enrollment if only one value is measured; if both values are measured, then both values must meet criteria above (must be obtained within 28 days prior to enrollment and start of protocol therapy) (repeat if necessary)

  • No evidence of dyspnea at rest, no exercise intolerance, and a pulse oximetry > 94% if there is clinical indication for determination; unless it is due to underlying pulmonary LCH

  • Central Nervous System Function Defined As:

    • Patients with seizure disorder may be enrolled if well controlled
    • Central nervous system (CNS) toxicity =< Grade 2

  • Human immunodeficiency virus (HIV) infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial unless antiretroviral therapy interacts with the metabolism of tovorafenib (DAY101) and cannot safely be changed to antivirals that do not interact with study medication

  • All patients and/or their parent(s) 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.

Exclusion Criteria:

  • LCH arising along with other hematologic malignancy (e.g. mixed LCH with acute lymphoblastic leukemia) or any history of non-histiocytic malignancy

  • Disease scenarios as below will be excluded

    • Skin-limited disease
    • Gastrointestinal (GI) tract involvement only (those that have disease that can be determined by endoscopic biopsies only)
    • LCH-associated neurodegeneration (LCH-ND) without parenchymal lesions or other systemic lesions

  • Patients with activating mutations in MAP2K1 are not eligible for this study due to drug target specificity. Mutation status will be submitted to study team within 7 days of enrollment

  • Refractory nausea and vomiting, malabsorption, or external biliary shunt that would preclude adequate absorption of tovorafenib (DAY101)

  • Uncontrolled systemic bacterial, viral, or fungal infection

  • Major surgical procedure or significant traumatic injury within 14 days prior to study enrollment, or anticipation of need for major surgical procedure during the course of the study. Placement of a vascular access device or minor surgery is permitted within fourteen (14) days of study enrollment (provided that the wound has healed)

  • History of significant bowel resection that would preclude adequate absorption or other significant malabsorptive disease

  • Ophthalmologic considerations: Patients with known significant ophthalmologic conditions or known risk factors for retinal vein occlusion (RVO) or central serous retinopathy (CSR) are not eligible

  • History of solid organ or hematopoietic bone marrow transplantation

  • Clinically significant active cardiovascular disease, or history of myocardial infarction, or deep vein thrombosis/pulmonary embolism within 6 months prior to enrollment, ongoing cardiomyopathy, or current prolonged QT interval > 440 ms based on triplicate electrocardiogram (ECG) average

  • History of Grade >= 2 CNS hemorrhage or history of any CNS hemorrhage within 28 days of study entry

  • History of any drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome or Stevens Johnsons syndrome (SJS) or who are allergic to tovorafenib (DAY101) or any of its components

  • CTCAE version (V.) 5.0 Grade 3 symptomatic creatinine kinase (CPK) elevation (> 5 x ULN)

  • Female patients who are pregnant are ineligible. A pregnancy test is required for female patients of childbearing potential

  • Lactating females who plan to breastfeed their infants are ineligible

  • Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of their study participation are ineligible. Women of childbearing potential must use non-hormonal contraception during tovorafenib treatment and for at least 28 days after the last dose. Men should use effective contraception and must not father a child while taking tovorafenib and for 14 days after the last dose

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: N / A
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Treatment (tovorafenib)

Patients receive tovorafenib PO QW on days 1, 8, 15, and 22 of each cycle. Cycles repeat every 28 days for 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo MUGA or ECHO scans, and FDG-PET or CT throughout the trial, and collection of blood and urine samples on study. Patients with suspicion of bone marrow and/or central nervous system involvement will also undergo bone marrow biopsy and aspiration and lumbar puncture on study and during follow up.
Procedura: Bone Marrow Biopsy

Undergo bone marrow biopsy

Altri nomi:
  • Biopsia del midollo osseo
  • Biopsia, midollo osseo
Procedura: Computed Tomography

Undergo CT

Altri nomi:
  • CT
  • GATTO
  • TAC
  • Tomografia assiale computerizzata
  • Tomografia computerizzata
  • tomografia
  • Tomografia assiale computerizzata (procedura)
  • Scansione tomografia computerizzata (CT).
  • Scansione CAT diagnostica
  • Tipo di servizio di scansione CAT diagnostica
Procedura: Echocardiography Test

Undergo ECHO

Altri nomi:
  • Ecocardiografia
  • CE
Procedura: Multigated Acquisition Scan

Undergo MUGA

Altri nomi:
  • Scansione della pozza di sangue
  • Angiografia con radionuclidi di equilibrio
  • Imaging del pool di sangue recintato
  • MUGA
  • Ventricolografia con radionuclidi
  • RNVG
  • Scansione SIMA
  • Scansione di acquisizione multigate sincronizzata
  • Scansione MUGA
  • Scansione di acquisizione multi-gate
  • Scansione del ventricologramma con radionuclidi
  • Scansione del pool cardiaco recintato
  • Scansione RNV
Procedura: Bone Marrow Aspiration

Undergo bone marrow aspiration

Procedura: Lumbar Puncture

Undergo lumbar puncture

Altri nomi:
  • LP
  • Colpetto spinale
Procedura: Biospecimen Collection

Undergo collection of blood and urine samples

Altri nomi:
  • Raccolta di campioni biologici
  • Biocampione raccolto
  • Raccolta di campioni
  • Raccolta campione
Procedura: FDG-Positron Emission Tomography and Computed Tomography Scan

Undergo FDG-PET imaging

Altri nomi:
  • FDG ANIMALE DOMESTICO/TAC
Droga: Tovorafenib

Given PO

Altri nomi:
  • TAK-580
  • MLN2480
  • BIIB-024
  • GIORNO 101
  • GIORNO-101
  • GIORNO101
  • MLN-2480
  • pan-RAF chinasi inibitore DAY101
  • TAK580
  • Ojemda
  • BIIB024
  • 2480 mln
  • TAK 580

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Frequency of dose limiting toxicity (dose finding phase)
Lasso di tempo: Up to 28 days

Will be analyzed descriptively.
Up to 28 days
Overall response rate (phase II)
Lasso di tempo: After 2 cycles of therapy (each cycle is 28 days)

Will be assessed using minimax Simon's two-stage designs in each of the BRAFV600E and non-BRAFV600E cohorts separately. The two arms will not be directly compared. The 95% confidence interval for the overall response rate will be adjusted for the two-stage design.
After 2 cycles of therapy (each cycle is 28 days)

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Event free survival rate
Lasso di tempo: At 1 and 2 years

Will be estimated by the Kaplan-Meier method beginning at study enrollment. Will be evaluated two years after enrollment of the last patient on the trial and estimates at specific timepoints will be presented along with log-log transformed 95% confidence intervals. Events are defined as relapse/progression, second malignant neoplasm, or death.
At 1 and 2 years
Progression free survival rate
Lasso di tempo: Up to 2 years

Will be estimated by the Kaplan-Meier method beginning at study enrollment. Will be evaluated by two years after enrollment of the last patient on the trial and estimates at specific timepoints will be presented along with log-log transformed 95% confidence intervals.
Up to 2 years
Duration of response rate
Lasso di tempo: After 12 months of therapy. From the scan confirming the complete response or partial response (whichever is recorded first), until the first occurrence of recurrent or progressive disease or death (event) or last known status on trial

Response is based on modified Response Evaluation Criteria for Solid Tumors (RECIST)/Positron Emission Tomography Response Criteria in Solid Tumors (PERCIST) consistent with other recent pediatric Langerhans Cell Histiocytosis trials (NCT02670707 and NCT04079179) and adult histiocytosis trials with MAPK inhibitors. Comparison of response assessed via RECIST versus (vs.) PERCIST will be analyzed by displaying two-way tables of the responses with no formal statistical testing.
After 12 months of therapy. From the scan confirming the complete response or partial response (whichever is recorded first), until the first occurrence of recurrent or progressive disease or death (event) or last known status on trial
Overall survival rate
Lasso di tempo: Up to 2 years

Will be estimated by the Kaplan-Meier method beginning at study enrollment. Will be evaluated two years after enrollment of the last patient on the trial and estimates at specific timepoints will be presented along with log-log transformed 95% confidence intervals.
Up to 2 years

Altre misure di risultato

Misura del risultato
Misura Descrizione
Lasso di tempo
Percent peripheral blood mononuclear cells with mutated allele
Lasso di tempo: Up to 2 years

Will be analyzed descriptively using logistic regression with complete response/progressive response vs. stable disease/progressive disease as the response variable.
Up to 2 years

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

National Cancer Institute (NCI)

Investigatori

  • Investigatore principale: Carl E Allen, Children's Oncology Group

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

28 marzo 2024

Completamento primario (Stimato)

30 settembre 2028

Completamento dello studio (Stimato)

30 settembre 2028

Date di iscrizione allo studio

Primo inviato

21 aprile 2023

Primo inviato che soddisfa i criteri di controllo qualità

21 aprile 2023

Primo Inserito (Effettivo)

25 aprile 2023

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 ottobre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

29 ottobre 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Termini MeSH pertinenti aggiuntivi

Altri numeri di identificazione dello studio

  • NCI-2022-06282
  • U10CA180886 (Sovvenzione/contratto NIH degli Stati Uniti)
  • ANHL2121 (Altro identificatore: CTEP)
  • NCI-2022-06282 (Identificatore di registro: CTRP (Clinical Trial Reporting Program))
  • ANHL2121 (Altro identificatore: Children's Oncology Group)

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

SÌ

Descrizione del piano IPD

NCI is committed to sharing data in accordance with NIH policy. For more details on how clinical trial data is shared, access the link to the NIH data sharing policy page.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

Sì

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

Sottoscrivi