Study of Oral RXDX-101 in Adult Patients With Locally Advanced or Metastatic Cancer Targeting NTRK1, NTRK2, NTRK3, ROS1, or ALK Molecular Alterations.

  • Cancer
  • Solid Tumors
Please note that the recruitment status of the trial at your site may differ from the overall study status because some study sites may recruit earlier than others.
Trial Status:

Completed

This trial runs in
Cities
  • Aurora
  • Boston
  • Houston
  • Nashville
  • New York
  • Orange
  • San Francisco
  • Sarasota
  • Seoul
  • Washington
Trial Identifier:

NCT02097810 GO40784 RXDX-101-01

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      The source of the below information is public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc.. It has been summarised and edited into simpler language. For more information about this clinical trial see the For Expert tab on the specific ForPatients page or follow these links to https://clinicaltrials.gov and/or https://euclinicaltrials.eu and/or https://www.isrctn.com.

      The below information is taken directly from public registry websites such as ClinicalTrials.gov, EuClinicalTrials.eu, ISRCTN.com, etc., and has not been edited.

      Results Disclaimer

      Trial Summary

      Entrectinib (RXDX-101) is an orally available inhibitor of the tyrosine kinases TrkA (coded by the gene NTRK1), TrkB (coded by the gene NTRK2), TrkC (coded by the gene NTRK3), ROS1 (coded by the gene ROS1), and ALK (coded by the gene ALK). Molecular alterations to one or more of these targets are present in several different tumor types, including non-small cell lung cancer (NSCLC), colorectal cancer (CRC), prostate cancer, papillary thyroid cancer, pancreatic cancer, and neuroblastoma. Patients with locally advanced or metastatic cancer with a detectable molecular alteration in targets of interest may be eligible for enrollment. Phase 1 will assess safety and tolerability of entrectinib via standard dose escalation scheme and determine the recommended Phase 2 dose. Safety and efficacy will be assessed in the dose expansion portion of the study.

      Hoffmann-La Roche Sponsor
      Phase 1 Phase
      NCT02097810,RXDX-101-01,GO40784 Trial Identifier
      Entrectinib Treatments
      Locally Advanced Solid Tumors, Metastatic Solid Tumors Condition
      Official Title

      A Phase 1, Multicenter, Open-Label Study of Oral Entrectinib (RXDX-101) in Adult Patients With Locally Advanced or Metastatic Cancer Confirmed to be Positive for NTRK1, NTRK2, NTRK3, ROS1, or ALK Molecular Alterations

      Eligibility criteria

      All Gender
      ≥18 Years Age
      No Healthy Volunteers
      Inclusion Criteria
      • Histologically or cytologically confirmed diagnosis of locally advanced or metastatic solid tumors that have a NTRK1, NTRK2, NTRK3, ROS1, or ALK molecular alteration.
      • Measurable disease according to RECIST version 1.1.
      • Prior cancer therapy is allowed, including crizotinib, ceritinib, and investigational drugs.
      • Prior radiotherapy is allowed
      • Patients with controlled asymptomatic central nervous system involvement are allowed.
      • Resolution of all acute toxic effects (excluding alopecia) of any prior anti-cancer therapy to National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) Version 4.03 Grade less than or equal to 1.
      • Eastern Cooperative Oncology Group (ECOG) performance status (PS) ≤ 2.
      • Adult patients age 18 years or older.
      • Life expectancy of at least 3 months.
      Exclusion Criteria
      • Current participation in another therapeutic clinical trial.
      • Prior treatment with entrectinib.
      • History of prolonged QTc interval (e.g., repeated demonstration of a QTc interval > 450 milliseconds).
      • History of additional risk factors for torsade de pointes (e.g., family history of long QT syndrome).
      • Known active infections (bacterial, fungal, viral including HIV positivity).
      • Gastrointestinal disease (e.g., Crohn's disease, ulcerative colitis, or short gut syndrome) or other malabsorption syndromes that would impact on drug absorption.
      • Known interstitial lung disease, interstitial fibrosis, or history of tyrosine kinase inhibitor-induced pneumonitis.
      • Peripheral neuropathy ≥ Grade 2.

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