Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

En studie med tovorafenib (DAY101) som et behandlingsalternativ for progressiv, residiverende eller refraktær Langerhans-cellehistiocytose

29. oktober 2026 oppdatert av: National Cancer Institute (NCI)

Fase 2-studie av Tovorafenib (DAY101) i residiverende og refraktær Langerhans-cellehistiocytose

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.

Studieoversikt

Status

Rekruttering

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

48

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

5 måneder til 22 år (Barn, Voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
Fremgangsmåte: Bone Marrow Biopsy

Undergo bone marrow biopsy

Andre navn:
  • Biopsi av benmarg
  • Biopsi, benmarg
Fremgangsmåte: Computed Tomography

Undergo CT

Andre navn:
  • CT
  • KATT
  • CAT-skanning
  • Beregnet aksial tomografi
  • Datastyrt aksialtomografi
  • Datastyrt tomografi
  • CT skann
  • tomografi
  • Datastyrt aksial tomografi (prosedyre)
  • Datastyrt tomografi (CT) skanning
  • Diagnostisk CAT -skanning
  • Diagnostisk CAT -skannertype
Fremgangsmåte: Echocardiography Test

Undergo ECHO

Andre navn:
  • Ekkokardiografi
  • EC
Fremgangsmåte: Multigated Acquisition Scan

Undergo MUGA

Andre navn:
  • Skanning av blodbasseng
  • Likevektsradionuklidangiografi
  • Gated Blood Pool Imaging
  • MUGA
  • Radionuklid ventrikulografi
  • RNVG
  • SYMA-skanning
  • Synchronized Multigated Acquisition Scanning
  • MUGA Scan
  • Multi-Gated Acquisition Scan
  • Radionuklid ventrikulogramskanning
  • Gated Heart Pool Scan
  • RNV Scan
Fremgangsmåte: Bone Marrow Aspiration

Undergo bone marrow aspiration

Fremgangsmåte: Lumbar Puncture

Undergo lumbar puncture

Andre navn:
  • LP
  • Spinal Tap
Fremgangsmåte: Biospecimen Collection

Undergo collection of blood and urine samples

Andre navn:
  • Biologisk prøvesamling
  • Bioprøve samlet
  • Prøvesamling
Fremgangsmåte: FDG-Positron Emission Tomography and Computed Tomography Scan

Undergo FDG-PET imaging

Andre navn:
  • FDG PET/CT
Legemiddel: Tovorafenib

Given PO

Andre navn:
  • TAK-580
  • MLN2480
  • BIIB-024
  • DAG 101
  • DAG-101
  • MLN-2480
  • pan-RAF kinasehemmer DAY101
  • TAK580
  • Ojemda
  • BIIB 024
  • BIIB024
  • MLN 2480
  • TAK 580

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Frequency of dose limiting toxicity (dose finding phase)
Tidsramme: Up to 28 days

Will be analyzed descriptively.
Up to 28 days
Overall response rate (phase II)
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Event free survival rate
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percent peripheral blood mononuclear cells with mutated allele
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

National Cancer Institute (NCI)

Etterforskere

  • Hovedetterforsker: Carl E Allen, Children's Oncology Group

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

28. mars 2024

Primær fullføring (Antatt)

30. september 2028

Studiet fullført (Antatt)

30. september 2028

Datoer for studieregistrering

Først innsendt

21. april 2023

Først innsendt som oppfylte QC-kriteriene

21. april 2023

Først lagt ut (Faktiske)

25. april 2023

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

30. oktober 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

29. oktober 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • NCI-2022-06282
  • U10CA180886 (U.S. NIH-stipend/kontrakt)
  • ANHL2121 (Annen identifikator: CTEP)
  • NCI-2022-06282 (Registeridentifikator: CTRP (Clinical Trial Reporting Program))
  • ANHL2121 (Annen identifikator: Children's Oncology Group)

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

JA

IPD-planbeskrivelse

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.

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere