Study Of Entrectinib (Rxdx-101) in Children and Adolescents With Locally Advanced Or Metastatic Solid Or Primary CNS Tumors And/Or Who Have No Satisfactory Treatment Options

Running, not enrolling · Phase 1/Phase 2

Conditions studied: Solid Tumors, CNS Tumors

In brief

This is an open-label, Phase 1/2 multicenter dose escalation study in pediatric patients with relapsed or refractory extracranial solid tumors (Phase 1), with additional expansion cohorts (Phase 2) in patients with primary brain tumors harboring NTRK1/2/3 or ROS1 gene fusions, and extracranial solid tumors harboring NTRK1/2/3 or ROS1 gene fusions.

Key facts

Study ID

NCT02650401

Run by

Hoffmann-La Roche

People needed

69

Starts

2016-05-03

Expected to finish

2026-06-30

Last updated by the study team

2026-06-23

Who can join

Age: any, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Disease status:
• Phase 1 portion (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1
• Phase 2 portion:
• Part B: Participants must have measurable or evaluable disease, as defined by RANO
• Part C (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1 ± Curie Scale
• Part D: Participants must have measurable or evaluable disease, as defined by RECIST v1.1
• Part E (closed): Participants must have measurable or evaluable disease, as defined by RECIST v1.1 ± Curie Scale or RANO
• Tumor type:
• Phase 1 portion:
• Part A: Relapsed or refractory extracranial solid tumors
• Phase 2 portion
• Part B: Primary brain tumors with NTRK1/2/3 or ROS1 gene fusions; gene fusions are defined as those predicted to translate into a fusion protein with a functional TRKA/B/C or ROS1 kinase domain, without a concomitant second oncodriver as determined by a nucleic acid-based diagnostic testing method
• Part D: Extracranial solid tumors (including NB) with NTRK1/2/3 or ROS1 gene fusions; gene fusions are defined as those predicted to translate into a fusion protein with a functional TRKA/B/C or ROS1 kinase domain, without a concomitant second oncodriver as determined by a nucleic acid-based diagnostic testing method
• Histologic/molecular diagnosis of malignancy at diagnosis or the time of relapse
• Archival tumor tissue from diagnosis or, preferably, at relapse
• Performance status: Lansky or Karnofsky score ≥ 60% and minimum life expectancy of at least 4 weeks
• Prior therapy: Participants must have a disease that is locally advanced, metastatic, or where surgical resection is likely to result in severe morbidity, and who have no satisfactory treatment options for solid tumors and primary CNS tumors that are neurotrophic tyrosine receptor kinase (NTRK) or ROS1 fusion-positive
• Participants must have recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, or radiotherapy prior to enrollment
• Adequate organ and neurologic function
• Females of childbearing potential must have a negative serum pregnancy test during screening and be neither breastfeeding nor intending to become pregnant during study participation. Agreement to remain abstinent or use use combined contraceptive methods prior to study entry, for the duration of study participation and in the following 90 days after discontinuation of study treatment.
• For male participants with a female partner of childbearing potential or a pregnant female partner: Agreement to remain abstinent or use a condom during the treatment period and for at least 3 months after the last dose of study drug

You may not qualify if…

• Receiving other experimental therapy
• Known congenital long QT syndrome
• History of recent (3 months) symptomatic congestive heart failure or ejection fraction ≤50% at screening
• Known active infections
• Familial or personal history of congenital bone disorders, bone metabolism alterations or osteopenia
• Receiving Enzyme Inducing Antiepileptic Drugs (EIAEDs) within 14 days of first dose.
• Prior treatment with approved or investigational TRK or ROS1 inhibitors
• Known hypersensitivity to entrectinib or any of the other excipients of the investigational medicinal product
• Patients with NB with bone marrow space-only disease
• Incomplete recovery from acute effects of any surgery prior to treatment.
• Active gastrointestinal disease or other malabsorption syndromes that would impact drug absorption.
• Other severe acute or chronic medical or psychiatric condition or lab abnormality that may increase the risk associated with study participation, drug administration or may interfere with the interpretation of study results.

Where it is running

• University of California San Diego — La Jolla, California, United States
• UCSF Benioff Children's Hospital — San Francisco, California, United States
• Children's Hospital Colorado — Aurora, Colorado, United States
• Egleston Children's Hospital at Emory University Atlanta — Atlanta, Georgia, United States
• University of Chicago — Chicago, Illinois, United States
• Johns Hopkins University — Baltimore, Maryland, United States
• Dana Farber Cancer Institute — Boston, Massachusetts, United States
• Washington University,St. Louis Children's Hospital — St Louis, Missouri, United States
• Memorial Sloan Kettering Cancer Center — New York, New York, United States
• Nationwide Children's Hospital — Columbus, Ohio, United States
• Oregon Health & Science Uni — Portland, Oregon, United States
• Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
• St. Jude Children'S Research Hospital — Memphis, Tennessee, United States
• Texas Children's Cancer and Hematology Center — Houston, Texas, United States
• Primary Children's Hospital — Salt Lake City, Utah, United States
• The Hospital for Sick Children — Toronto, Ontario, Canada
• Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine — Shanghai, Shanghai Municipality, China
• Beijing Children's Hospital, Capital Medical University — Beijing, China
• Centre Leon Berard — Lyon, France
• Hôpital de la Timone, Oncologie Pédiatrique — Marseille, France
• Universitaetsklinikum Heidelberg — Heidelberg, Baden-Wurttemberg, Germany
• Hong Kong Children's Hospital — Hong Kong, Hong Kong
• Fondazione IRCCS Istituto Nazionale dei Tumori — Milan, Lombardy, Italy
• Hospital Infantil Universitario Nino Jesus — Madrid, Spain
• Royal Marsden Hospital (Sutton) — London, United Kingdom

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.