for people ages up to 22 years (full criteria)
study started
estimated completion



This is a 5-part, open-label, Phase 1/2 multicenter, dose escalation study in pediatric patients with relapsed refractory solid tumors; 2) primary CNS tumors; 3) neuroblastoma; 4) non-neuroblastoma, extracranial solid tumors with NTRK1/2/3, ROS1 or ALK gene rearrangements; and 5) patients who are otherwise eligible but unable to swallow capsules. The study is designed to explore the safety, maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D), pharmacokinetics, and antitumor activity of entrectinib.

Official Title

A Phase 1/2, Open-Label, Dose-Escalation and Expansion Study Of Entrectinib (Rxdx-101) in Children and Adolescents With No Curative First-Line Treatment Option, Recurrent or Refractory Solid Tumors And Primary Cns Tumors, With or Without Trk, Ros1, or Alk Fusions


Solid Tumors CNS Tumors TRK Tyrosine kinase NTRK NTRK1 NTRK2 NTRK3 ROS1 ALK Pediatric Relapsed Refractory Solid Tumor Metastatic Cancer Gene rearrangement Neuroblastoma Infantile fibrosarcoma Secretory breast cancer Congenital mesoblastic nephroma Pontine glioma Brain tumors Sarcoma Ewing sarcoma Glial tumors Salivary Gland Cancer (MASC) Papillary thyroid cancer Medulloblastoma Wilms tumor (anaplastic) Central Nervous System Neoplasms Neoplasms Entrectinib Extracranial solid tumors harboring NTRK1/2/3, CNS tumors harboring- NTRK1/2/3, ROS1, ALK Expansion: CNS tumors harboring- NTRK1/2/3, ROS1, ALK Expansion: Extracranial solid tumors harboring NTRK1/2/3


You can join if…

Open to people ages up to 22 years

  1. Ability to swallow capsules unless enrolled in Part E
  2. Body surface area (BSA): Subjects must have a body surface area ≥ 0.45 m2 at the time of the study enrollment, unless enrolled in Part E
  3. Disease status: Subjects must have measurable or evaluable disease, by RECIST v1.1 ± Curie Scale Criteria or RANO/RANO-BM
  4. Tumor type:
  5. Part A: Relapsed or refractory extracranial solid tumors and (Phase 1b expansion) relapsed or refractory extracranial solid tumors with molecular alterations, non-gene fusions;
  6. Part B: Relapsed or refractory primary CNS tumors with molecular alterations, including gene fusions, documented by a CLIA-approved lab prior to enrollment;
  7. Part C: Relapsed or refractory neuroblastoma;
  8. Part D: Relapsed or refractory non-neuroblastoma, extracranial solid tumors with NTRK1/2/3, ROS1, or ALK gene fusions documented by a CLIA-approved lab prior to enrollment;
  9. Part E: Any patient unable to swallow capsules who otherwise meet all other eligibility criteria for Part A (expansion) B, C or D
  10. Histologic/molecular diagnosis of malignancy at diagnosis or the time of relapse
  11. Archival tumor tissue from diagnosis or, preferably, at relapse
  12. Age: Male or female from birth to age < 22 years, unless enrolled in Part E
  13. Performance status: Lansky or Karnofsky score ≥ 60% and minimum life expectancy of at least 4 weeks
  14. Patient's cancer must have relapsed after or failed to respond to frontline curative therapy or there must not be other potentially curative treatment options available
  15. . Adequate organ and neurologic function
  16. . Females of child bearing potential must have a negative serum pregnancy test within 14 days prior to entrectinib dosing

You CAN'T join if...

  1. Receiving other experimental therapy
  2. Known congenital long QT syndrome
  3. Known active infections
  4. Receiving Enzyme Inducing Antiepileptic Drugs (EIAEDs) within 14 days of first dose.
  5. Prior treatment with approved or investigational TRK, ROS1, or ALK inhibitors
  6. Patients with NB with bone marrow space-only disease
  7. Incomplete recovery from acute effects of any surgery prior to treatment.
  8. Active gastrointestinal disease or other malabsorption syndromes that would impact drug absorption.
  9. 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.


  • UCSF Benioff Children's Hospital; UCSF Pediatrics Hematology Oncology accepting new patients
    San Francisco California 94158 United States
  • Rady Childrens Hospital accepting new patients
    San Diego California 92123 United States
  • Children'S Hospital of Orange County accepting new patients
    Orange California 92868-3874 United States


accepting new patients
Start Date
Completion Date
Hoffmann-La Roche
Phase 1
Study Type
Last Updated