Topic: Phase 1/2 Study of LOXO-195 in Patients With Previously Treated NTRK F

Phase 1/2 Study of LOXO-195 in Patients With Previously Treated NTRK Fusions or Non-fusion NTRK Cancers

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https://clinicaltrials.gov/ct2/show/NCT03215511

This is a Phase 1/2, multi-center, open-label study designed to evaluate the safety and efficacy of LOXO-195 when administered orally to patients with NTRK fusion cancers treated with prior TRK inhibition or non-fusion NTRK altered cancers regardless of prior kinase inhibitor treatment.

Condition    Intervention    Phase
Carcinoma, Non-Small-Cell Lung
Thyroid Neoplasms
Sarcoma
Colorectal Neoplasms
Salivary Gland Neoplasms
Biliary Tract Neoplasms
Brain Neoplasm, Primary
Breast Ductal Carcinoma NOS
Melanoma
Solid Tumors Cancer of Unknown Primary
Glioblastoma
Bile Duct Neoplasms
Astrocytoma
Head and Neck Squamous Cell Carcinoma
Pontine Glioma
Pancreatic Neoplasms
Ovarian Neoplasms
Carcinoma, Renal Cell
Cholangiocarcinoma
Skin Carcinoma
Carcinoma, Bronchogenic
Bronchial Neoplasms
Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms, Nerve Tissue
Nevi and Melanomas
Intestinal Neoplasms
Thyroid Cancer
GIST
Malignant Peripheral Nerve Sheath Tumors
Breast Secretory Carcinoma
Uterine Neoplasms
Drug: LOXO-195
Phase 1
Phase 2

Access to an investigational treatment associated with this study is available outside the clinical trial.   More info ...

Study Type:    Interventional
Study Design:    Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Treatment
Official Title:    A Phase 1/ 2 Study of the TRK Inhibitor LOXO 195 in Adult Subjects With NTRK Fusion (Previously Treated) or Non-Fusion NTRK Altered Cancers

Resource links provided by NLM:

Genetics Home Reference related topics: lung cancer
Genetic and Rare Diseases Information Center resources: Glioblastoma Ovarian Cancer Neurofibroma Malignant Peripheral Nerve Sheath Tumor Neurofibrosarcoma Secretory Breast Carcinoma Soft Tissue Sarcoma Glioma Neurofibromatosis Schwannoma Carcinoid Tumor Neuroepithelioma Fibrosarcoma Oral Cancer
U.S. FDA Resources

Further study details as provided by Loxo Oncology, Inc.:

Primary Outcome Measures:
Maximum Tolerated Dose (MTD) [ Time Frame: The first 28 days of treatment (Cycle 1) ]
For Phase 1

Recommended dose for further study [ Time Frame: The first 28 days of treatment (Cycle 1) and every cycle (28 days) for approximately 12 months (or earlier if the patient discontinues from the study) ]
For Phase 1

Best overall response of confirmed PR or CR by independent radiology review in NTRK fusion cancer patients previously treated with TRK inhibitor who have progressed [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2


Secondary Outcome Measures:
Incidence of AEs [ Time Frame: From the time of informed consent, for approximately 24 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
For Phase 1 and Phase 2

Severity of AEs [ Time Frame: From the time of informed consent, for approximately 24 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
For Phase 1 and Phase 2

Duration of AEs [ Time Frame: From the time of informed consent, for approximately 24 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
For Phase 1 and Phase 2

Changes in clinical laboratory results compared to baseline [ Time Frame: For approximately 24 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
For Phase 1 and Phase 2

Changes in vital signs compared to baseline [ Time Frame: For approximately 24 months (or earlier if the patient discontinues from the study), and through Safety Follow-up (28 days after the last dose) ]
For Phase 1 and Phase 2

Best overall response of confirmed PR or CR by independent radiology review in NTRK fusion cancer patients previously treated with TRK inhibitor [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 1

Best overall response of confirmed CR or PR as determined by treating investigators using RECIST v1.1 in patients with non-fusion NTRK altered cancers or RANO in patients with primary CNS malignancies. [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 1

Best overall response of confirmed PR or CR using RECIST v1.1 or RANO criteria as appropriate in patients with non-fusion NTRK altered cancers who have demonstration of progression following or during receipt of previous anticancer therapy [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2

Best overall response of confirmed PR or CR using RECIST v1.1 or RANO criteria as appropriate in patients with documented NTRK alterations, including TRK fusions, who discontinued previous anticancer therapy including TRK inhibitors due to intolerance [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2

Duration or response (DOR) for patients with best overall response of confirmed CR or PR by an independent radiology review committee [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2

Duration or response (DOR) for patients with best overall response of confirmed CR or PR by the treating Investigator [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2

Progression-free survival (PFS) [ Time Frame: Approximately every 8 weeks for one year, then every 12 weeks while on treatment, and every 12 weeks after the last dose (for up to 2 years) in patients who have not progressed ]
For Phase 2

Overall survival (OS) [ Time Frame: Up to 24 months ]
For Phase 2

Clinical benefit rate (CBR) [ Time Frame: Up to 24 months ]
For Phase 2


Estimated Enrollment:    120
Anticipated Study Start Date:    July 2017
Estimated Study Completion Date:    December 2019
Estimated Primary Completion Date:    August 2019 (Final data collection date for primary outcome measure)
Arms    Assigned Interventions
Experimental: LOXO-195
Phase 1- Dose Escalation and determination of MTD; Multiple dose levels of LOXO-195 to be evaluated Phase 2 - Treatment with LOXO-195 at the recommended dose from Phase 1 identified for further study
Drug: LOXO-195
Oral LOXO-195

Detailed Description:
The trial will be conducted in 2 parts: dose escalation (Phase I ) and dose expansion (Phase 2) . During Phase 1, patients with advanced solid tumors are eligible if the tumor has progressed following or has not adequately responded to standard therapy, or if the patient is intolerant of, or unlikely to benefit from or refuses standard therapy. Prior TRK inhibitor therapy is required for patients harboring an NTRK fusion. During Phase 2, the same patient population as designated for Phase 1 will be treated with the dose of LOXO-195 which has been identified during phase 1 to assess specified endpoints.
  Eligibility

Ages Eligible for Study:      18 Years and older   (Adult, Senior)
Sexes Eligible for Study:      All
Accepts Healthy Volunteers:      No
Criteria
Key Inclusion Criteria:

Advanced solid tumor for which, in the opinion of the Investigator, no other standard or investigational therapy offers greater benefit.
A solid tumor diagnosis in the setting of:

a documented NTRK fusion and a clinical history of relapse following a response to a prior TRK inhibitor
a documented NTRK fusion unresponsive to a prior TRK inhibitor
a documented NTRK fusion and a clinical history of intolerance to a prior TRK inhibitor
a documented NTRK alteration other than a fusion, whether or not treated with a prior TRK inhibitor
Patients will be identified via a CLIA certified (or equivalent) laboratory
Performance Status: Eastern Cooperative Oncology Group (ECOG) score ≤ 3. If enrolled with primary CNS tumor to be assessed by RANO, Karnofsky Performance Status (KPS) ≥ 50%
Life expectancy > 4 weeks
Adequate hematologic, hepatic and renal function.
Patients with stable CNS primary tumor, brain metastases, or treated spinal cord compression are eligible if neurological symptoms and steroid use (if applicable) have been stable for 7 days prior to the first dose of LOXO-195
Ability to receive study drug therapy orally
Key Exclusion Criteria:

Required treatment with certain strong CYP3A4 inhibitors or inducers.
Clinically significant active cardiovascular disease or history of myocardial infarction within 6 months prior to planned start of LOXO-195 or prolongation of the QT interval corrected (QTcF) > 480 msec.
Major surgery within 7 days of enrollment
Uncontrolled systemic bacterial, fungal or viral infection
Untreated/symptomatic leptomeningeal carcinomatosis, spinal cord compression, primary CNS metastases or primary CNS malignancy.
Pregnancy or lactation.
   Contacts and Locations
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, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT03215511

Contacts
Contact: Patient Advocacy    1-855-NTRK-123    clinicaltrials@loxooncology.com   

Locations
United States, New York
Memorial Sloan Kettering Cancer Center    Recruiting
New York, New York, United States, 10065
Sponsors and Collaborators
Loxo Oncology, Inc.
Investigators
Study Director:    Nora Ku, MD    Senior Medical Director, Loxo Oncology
  More Information

Responsible Party:    Loxo Oncology, Inc.
ClinicalTrials.gov Identifier:    NCT03215511     History of Changes
Other Study ID Numbers:    LOXO-EXT-17005
Study First Received:    June 30, 2017
Last Updated:    July 10, 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD:    No

Studies a U.S. FDA-regulated Drug Product:    Yes
Studies a U.S. FDA-regulated Device Product:    No
Keywords provided by Loxo Oncology, Inc.:
NTRK Fusion Positive
LOXO-195
Loxo
TRK
TRK Fusion
NTRK1
NTRK2
NTRK3
TRKA
TRKB
TRKC
NTRK
ETV6
fusion
tumors
CNS tumors
solid tumors
central nervous system tumors
advanced cancer
primary CNS tumor
Advanced CNS tumor
Metastatic CNS tumor
NTRK1 fusion
NTRK2 fusion
NTRK3 fusion
ETV6-NTRK3
ETV6 fusion
Metastatic cancer
Cancer of Unknown Primary Site

Additional relevant MeSH terms:
Carcinoma
Neoplasms
Melanoma
Carcinoma, Squamous Cell
Glioblastoma
Thyroid Diseases
Astrocytoma
Thyroid Neoplasms
Cholangiocarcinoma
Carcinoma, Non-Small-Cell Lung
Colorectal Neoplasms
Head and Neck Neoplasms
Lung Neoplasms
Pancreatic Neoplasms
Ovarian Neoplasms
Brain Neoplasms
Carcinoma, Ductal
Carcinoma, Renal Cell
Nerve Sheath Neoplasms
Neurofibroma
Neurilemmoma
Neurofibrosarcoma
Uterine Neoplasms
Biliary Tract Neoplasms
Thoracic Neoplasms
Intestinal Neoplasms
Respiratory Tract Neoplasms
Bronchial Neoplasms
Carcinoma, Bronchogenic
Bile Duct Neoplasms

ClinicalTrials.gov processed this record on July 13, 2017

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