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A Study to Test the Effect of the Drug Larotrectinib in Adults and Children With NTRK-fusion Positive Solid Tumors (NAVIGATE)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02576431
Recruitment Status : Recruiting
First Posted : October 15, 2015
Last Update Posted : October 20, 2020
Sponsor:
Information provided by (Responsible Party):
Bayer

Brief Summary:
This research study is done to test how well different types of cancer respond to the drug called larotrectinib. The cancer must have a change in a particular gene (NTRK1, NTRK2 or NTRK3). Larotrectinib is a drug that blocks the actions of these NTRK genes in cancer cells and can therefore be used to treat cancer.

Condition or disease Intervention/treatment Phase
Solid Tumors Harboring NTRK Fusion Drug: BAY2757556 (Larotrectinib, Vitrakvi) Phase 2

Expanded Access : An investigational treatment associated with this study has been approved for sale to the public.   More info ...

Detailed Description:

The primary objective of this study is to investigate the efficacy of larotrectinib for the treatment of advanced solid tumors harboring a fusion of neurotrophic tyrosine receptor kinase (NTRK) of types 1-3 in children and adults.

Secondary objectives comprise the efficacy and safety of larotrectinib in different NTRK-tumor types.

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Study Type : Interventional
Estimated Enrollment : 203 participants
Allocation: Non-Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 2 Basket Study of the Oral TRK Inhibitor Larotrectinib in Subjects With NTRK Fusion-positive Tumors
Actual Study Start Date : September 30, 2015
Estimated Primary Completion Date : August 15, 2023
Estimated Study Completion Date : September 30, 2025

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Arm 1_NSCLC
Patients with solid non-small cell lung cancer (NSCLC) harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 2_Thyroid
Patients with solid thyroid tumors harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 3_Sarcoma
Patients with soft-tissue sarcoma harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 4_Colorectal
Patients with solid colorectal tumors harboring NTRK fusions
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 5_Salivary
Patients with solid salivary tumors harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 6_Biliary
Patients with solid biliary tumors harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 7_Primary CNS
Patients with solid tumors in the primary central nervous system (CNS) harboring NTRK fusions (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 8_Other tumors
Patients with e.g. kidney cancer, squamous cell cancer of head or neck or ovarian solid tumors harboring NTRK fusions
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 9_Solid tumors without confirmed NTRK fusion
Patients eligible for arms 1 to 8, but with documented NTRK fusion from a laboratory where CLIA or equivalent certification cannot be confirmed by the sponsor at the time of consent (arm closed)
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 10_Lung cancer
Patients with lung cancer harboring NTRK fusions
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 11_Melanoma
Patients with melanoma harboring NTRK fusions
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101

Experimental: Arm 12_Breast cancer
Patient with non-secretory breast cancer harboring NTRK fusions
Drug: BAY2757556 (Larotrectinib, Vitrakvi)
Larotrectinib will be administered orally as capsule or liquid solution at a dose of 100 mg twice daily in continuing 28-days cycles.
Other Name: LOXO-101




Primary Outcome Measures :
  1. Best overall response rate by IRC [ Time Frame: Up to 120 months ]
    Proportion of subjects with either complete response or partial response as determined by an independent radiology committee (IRC) using RECIST or RANO criteria.


Secondary Outcome Measures :
  1. Best overall response rate by investigator [ Time Frame: Up to 120 months ]
    Proportion of subjects with either complete response or partial response as determined by the treating investigator using RECIST or RANO criteria.

  2. Duration of response (DOR) by IRC [ Time Frame: Up to 120 months ]
    Duration of response is the number of months from the start of confirmed complete response or partial response to disease progression or death. Complete response, partial response and disease progression are assessed by an independent radiology committee (IRC).

  3. Duration of response (DOR) by investigator [ Time Frame: Up to 120 months ]

    Duration of response is the number of months from the start of confirmed complete response or partial response to disease progression or death.

    Complete response, partial response and disease progression are assessed by the treating investigator.


  4. Clinical benefit rate (CBR) [ Time Frame: Up to 120 months ]
    Proportion of subjects with best overall response of complete response, partial response or stable disease lasting 16 or more weeks following the initiation of larotrectinib.

  5. Progression-free survival (PFS) after Larotrectinib [ Time Frame: Up to 120 months ]
    Number of months from initiation of larotrectinib to either disease progression or death due to any cause.

  6. Overall survival time [ Time Frame: Up to 120 months ]
    Number of months from the initiation of larotrectinib to the date of death due to any cause.

  7. Progression-free survival (PFS) after past cancer therapy [ Time Frame: Up to 120 months ]
    Number of months from initiation of the line of therapy preceding larotrectinib to either disease progression or death due to any cause.

  8. Number of subjects with adverse events [ Time Frame: Up to 120 months ]
  9. Number of subjects with serious adverse events [ Time Frame: Up to 120 months ]
  10. Number of subjects with treatment-related adverse events [ Time Frame: Up to 120 months ]
  11. Severity of adverse events [ Time Frame: Up to 120 months ]
  12. Severity of serious adverse events [ Time Frame: Up to 120 months ]
  13. Severity of treatment-related adverse events [ Time Frame: Up to 120 months ]
  14. Duration of adverse events [ Time Frame: Up to 120 months ]
  15. Duration of serious adverse events [ Time Frame: Up to 120 months ]
  16. Duration of treatment-related adverse events [ Time Frame: Up to 120 months ]
  17. Number of subjects with safety-relevant changes in clinical parameters or vital signs after drug administration [ Time Frame: Up to 120 months ]
  18. Severity of safety-relevant changes in clinical parameters or vital signs after drug administration [ Time Frame: Up to 120 months ]
  19. Proportion of subjects that has any tumor regression as a best response [ Time Frame: Up to 120 months ]
  20. Concordance coefficient [ Time Frame: Up to 120 months ]
    Describes the concordance of prior molecular profiling that detected an NTRK fusion within the subject's tumor and a diagnostic test being evaluated by the sponsor



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   12 Years and older   (Child, Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Locally-advanced or metastatic malignancy with an NTRK1, NTRK2, or NTRK3 gene fusion identified through molecular assays
  • Subjects must have received prior standard therapy appropriate for their tumor type and stage of disease, or in the opinion of the investigator, would be unlikely to tolerate or derive clinically meaningful benefit from appropriate standard of care therapy
  • Subjects must have at least one measurable lesion as defined by RECIST v1.1

Exclusion Criteria:

  • Prior progression while receiving approved or investigational tyrosine kinase inhibitors targeting TRK. Subjects who received less than 28 days of treatment and discontinued because of intolerance or toxicity are eligible.
  • Symptomatic or unstable brain metastases. (Note: Subjects with asymptomatic brain metastases are eligible to participate in the study.) Subjects with primary CNS tumors are eligible.
  • Active uncontrolled systemic bacterial, viral, or fungal infection, unstable cardiovascular disease, or other systemic disease that would limit compliance with study procedures.
  • Pregnancy or lactation.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02576431


Contacts
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Contact: Bayer Clinical Trials Contact (+)1-888-84 22937 clinical-trials-contact@bayer.com

Locations
Show Show 121 study locations
Sponsors and Collaborators
Bayer
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Bayer
ClinicalTrials.gov Identifier: NCT02576431    
Other Study ID Numbers: 20289
LOXO-TRK-15002 ( Other Identifier: Loxo Oncology, Inc )
2015-003582-28 ( EudraCT Number )
First Posted: October 15, 2015    Key Record Dates
Last Update Posted: October 20, 2020
Last Verified: October 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description:

Availability of this study's data will be determined according to Bayer's commitment to the EFPIA/PhRMA "Principles for responsible clinical trial data sharing". This pertains to scope, timepoint and process of data access.

As such, Bayer commits to sharing upon request from qualified researchers patient-level clinical trial data, study-level clinical trial data, and protocols from clinical trials in patients for medicines and indications approved in the US and EU as necessary for conducting legitimate research. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.

Interested researchers can use www.clinicalstudydatarequest.com to request access to anonymized patient-level data and supporting documents from clinical studies to conduct research. Information on the Bayer criteria for listing studies and other relevant information is provided in the Study sponsors section of the portal.


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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Bayer:
Non-small cell lung cancer
Thyroid cancer
Colorectal cancer
Salivary gland cancer
Biliary cancer
Central nervous system (CNS) Tumor
Breast cancer
Sarcoma
Melanoma
Neurotrophic tyrosine receptor kinase (NTRK)
NTRK1
NTRK2
NTRK3
Fusion Positive
TRK fusion
TRKA
TRKB
TRKC
ETV6
Additional relevant MeSH terms:
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Neoplasms