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Spots Global Cancer Trial Database for REGN2810 in Pediatric Patients With Relapsed, Refractory Solid, or Central Nervous System (CNS) Tumors and Safety and Efficacy of REGN2810 in Combination With Radiotherapy in Pediatric Patients With Newly Diagnosed or Recurrent Glioma

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Trial Identification

Brief Title: REGN2810 in Pediatric Patients With Relapsed, Refractory Solid, or Central Nervous System (CNS) Tumors and Safety and Efficacy of REGN2810 in Combination With Radiotherapy in Pediatric Patients With Newly Diagnosed or Recurrent Glioma

Official Title: A Safety and Pharmacokinetic Study of Single Agent REGN2810 in Pediatric Patients With Relapsed or Refractory Solid or Central Nervous System (CNS) Tumors and a Safety and Efficacy Trial of REGN2810 in Combination With Radiotherapy in Pediatric Patients With Newly Diagnosed Diffuse Intrinsic Pontine Glioma, Newly Diagnosed High-Grade Glioma, or Recurrent High-Grade Glioma

Study ID: NCT03690869

Study Description

Brief Summary: Phase 1: * To confirm the safety and anticipated recommended phase 2 dose (RP2D) of REGN2810 (cemiplimab) for children with recurrent or refractory solid or Central Nervous System (CNS) tumors * To characterize the pharmacokinetics (PK) of REGN2810 given in children with recurrent or refractory solid or CNS tumors Phase 2 (Efficacy Phase): * To confirm the safety and anticipated RP2D of REGN2810 to be given concomitantly with conventionally fractionated or hypofractionated radiation among patients with newly diagnosed diffuse intrinsic pontine glioma (DIPG) * To confirm the safety and anticipated RP2D of REGN2810 given concomitantly with conventionally fractionated or hypofractionated radiation among patients with newly diagnosed high-grade glioma (HGG) * To confirm the safety and anticipated RP2D of REGN2810 given concomitantly with re-irradiation in patients with recurrent HGG * To assess PK of REGN2810 in pediatric patients with newly diagnosed DIPG, newly diagnosed HGG, or recurrent HGG when given in combination with radiation * To assess anti-tumor activity of REGN2810 in combination with radiation in improving overall survival at 12 months (OS12) among patients with newly diagnosed DIPG * To assess anti-tumor activity of REGN2810 in combination with radiation in improving progression-free survival at 12 months (PFS12) among patients with newly diagnosed HGG * To assess anti-tumor activity of REGN2810 in combination with radiation in improving overall survival at OS12 among patients with recurrent HGG

Detailed Description:

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Children's Hospital Los Angeles (CHLA), Los Angeles, California, United States

Rady Children's Hospital, San Diego, California, United States

UCSF Benioff Children's Hospital, San Francisco, California, United States

Children's National Health System (Children's National Medical Center), Washington, District of Columbia, United States

University of Florida- Neurosurgery, Gainesville, Florida, United States

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, United States

Johns Hopkins - Pediatric Oncology, Baltimore, Maryland, United States

Massachusetts General Hospital, Boston, Massachusetts, United States

Dana Farber Cancer Institute/ Boston Children's Hospital, Boston, Massachusetts, United States

C. S. Mott/University of Michigan, Ann Arbor, Michigan, United States

Children's Hospitals and Clinics of Minnesota, Minneapolis, Minnesota, United States

University of Minnesota / Masonic Cancer Center, Minneapolis, Minnesota, United States

Washington University School of Medicine, Saint Louis, Missouri, United States

Nationwide Children's Hospital, Columbus, Ohio, United States

Oregon Health & Science University (OHSU) - Doernbecher Children's Hospital, Portland, Oregon, United States

The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States

St. Jude Children's Research Hospital, Memphis, Tennessee, United States

Texas Children's Cancer & Hematology Centers Baylor College of Medicine, Houston, Texas, United States

University of Utah, Salt Lake City, Utah, United States

Seattle Children's Hospital, Seattle, Washington, United States

Contact Details

Name: Clinical Trial Management

Affiliation: Regeneron Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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