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Phase III Study of Nazartinib (EGF816) Versus Erlotinib/Gefitinib in First-line Locally Advanced / Metastatic NSCLC With EGFR Activating Mutations

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ClinicalTrials.gov Identifier: NCT03529084
Recruitment Status : Withdrawn (Decision by Sponsor not to continue with the trial.)
First Posted : May 18, 2018
Last Update Posted : November 22, 2019
Sponsor:
Information provided by (Responsible Party):
Novartis ( Novartis Pharmaceuticals )

Brief Summary:
This is a phase III, open label, randomized controlled multi-center global study designed to evaluate the safety and efficacy of single agent nazartinib (EGF816) compared with investigator's choice (erlotinib or gefitinib) in patients with locally advanced or metastatic NSCLC who are treatment naïve and whose tumors harbor EGFR activating mutations (L858R or ex19del).

Condition or disease Intervention/treatment Phase
Carcinoma, Non-small Cell Lung Drug: EFG816 Drug: erlotinib or gefitinib Phase 3

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 0 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Masking Description: blinded independent review committee for primary endpoint of PFS
Primary Purpose: Treatment
Official Title: A Randomized, Open-label, Phase III Study of Single Agent Nazartinib Versus Investigator's Choice (Erlotinib or Gefitinib) as First-Line Treatment in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer Harboring EGFR Activating Mutations
Estimated Study Start Date : July 24, 2018
Estimated Primary Completion Date : August 13, 2020
Estimated Study Completion Date : June 3, 2024

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: EGF816
Investigational treatment arm of EGF816 (nazartinib).
Drug: EFG816
It will be administered orally daily.
Other Name: nazartinib

Active Comparator: Investigator's Choice
Investigator's Choice (erlotinib or gefitinib).
Drug: erlotinib or gefitinib

Investigator's choice between erlotinib or gefitinib. These will be locally sourced.

Erlotinib will be administered orally daily. Gefitinib will be administered orally daily.





Primary Outcome Measures :
  1. Progression Free Survival (PFS) by Blinded independent review committee (BIRC) [ Time Frame: Approximately 3 years ]
    PFS using central BIRC assessment according to RECIST 1.1, is defined as the time from the date of randomization to the date of the first documented progression (as assessed by BIRC per RECIST 1.1) or death due to any cause, whichever occurs first.


Secondary Outcome Measures :
  1. Overall Survival [ Time Frame: Approximately 6 years ]
    Overall survival is defined as the time from date of randomization to date of death due to any cause.

  2. PFS by investigator [ Time Frame: Approximately 3 years ]
    PFS by Investigator assessment according to RECIST 1.1, is defined as the time from the date of randomization to the date of the first documented progression (as assessed by Investigator per RECIST 1.1) or death due to any cause, whichever occurs first.

  3. PFS after next-line of treatment (PFS2) using investigator assessment according to RECIST 1.1 [ Time Frame: Approximately 4 years ]
    PFS after next-line of treatment (PFS2) using investigator assessment according to RECIST 1.1 is defined as time from date of randomization to the first documented disease progression (clinical or radiologic) as per investigator assessment on next-line therapy or death from any cause, whichever occurs first.

  4. Time to progression in Central Nervous System (CNS) per central neuro-radiologist BIRC [ Time Frame: Approximately 3 years ]
    Time to progression in CNS, defined as time from date of randomization to the date of first documented progression of brain metastases as assessed by central neuro-radiologist BIRC per modified RECIST 1.1 for patients with at least one non-measurable and/or measurable lesion in the brain at baseline.

  5. Overall response rate (ORR) by central BIRC [ Time Frame: Approximately 3 years ]
    ORR in accordance with RECIST 1.1. ORR is defined as the percentage of participants with best overall response (BOR) of complete response (CR) or partial response (PR)

  6. Duration of response (DOR) by central BIRC [ Time Frame: Approximately 3 years ]
    DOR is defined as the time from date of first documented response (CR and PR) to the date of the first documented progression or death due to underlying cancer, whichever occurs first.

  7. Disease control rate (DCR) by central BIRC [ Time Frame: Approximately 3 years ]
    DCR is defined as the percentage of participants with BOR of CR, PR, or stable disease (SD).

  8. Time to response (TTR) by central BIRC [ Time Frame: Approximately 3 years ]
    TTR is defined as the time from the date of randomization to the first documented response CR or PR.

  9. CNS ORR per central neuro-radiologist BIRC [ Time Frame: Approximately 3 years ]
    CNS ORR in patients with brain metastases who have measurable disease in the brain at baseline review per modified RECIST 1.1

  10. CNS DoR per central neuro-radiologist BIRC [ Time Frame: Approximately 3 years ]
    CNS DoR in patients with brain metastases who have measurable disease in the brain at baseline per modified RECIST 1.1

  11. Charactise Plasma PK (Cmax) of EGF816 [ Time Frame: Day 1 of Cycles 1 to 6 inclusive (21 day cycle) ]
    Peak plasma concentration (Cmax) of EGF816 and its metabolite (LMI258)

  12. Charactise Plasma PK (AUC) of EGF816 [ Time Frame: Day 1 of Cycles 1 to 6 inclusive (21 day cycle) ]
    Area under the plasma concentration versus time curve (AUC) of EGF816 and its metabolite (LMI258)

  13. Charactise Plasma PK (t1/2) of EGF816 [ Time Frame: Day 1 of Cycles 1 to 6 inclusive (21 day cycle) ]
    Elimination half life (t1/2) of EGF816 and its metabolite (LMI258)

  14. Patient Reported Outcome: Health Related Quality of Life (HRQoL) as measured by QLQ-C30 Questionnaire [ Time Frame: Approximately 4 years ]
    HRQoL as measured by European Organization for Research and Treatment of Cancer (EORTC) QLQ-C30 quality of life score

  15. Patient Reported Outcome: Health Related Quality of Life (HRQoL) as measured by QLQ-LC13 Questionnaire [ Time Frame: Approximately 4 years ]
    HRQoL as measured by European Organization for Research and Treatment of Cancer (EORTC) QLQ-LC13 quality of life score

  16. Patient Reported Outcome: Health Related Quality of Life (HRQoL) as measured by EuroQoL-5 Dimension-5 (EQ-5D-5L) Questionnaire [ Time Frame: Approximately 4 years ]
    Global health status/quality of life score of the EQ-5D-5L



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

Inclusion Criteria:

  • Written informed consent obtained prior to any screening procedures.
  • Histologically documented locally advanced or metastatic, stage IIIB/ IIIC or stage IV NSCLC with documented EGFR activating mutation (L858R or ex19del)
  • Provision of a tumor tissue sample to allow for retrospective analysis of EGFR mutation status
  • No prior treatment with any systemic antineoplastic therapy in the advanced setting
  • Recovered from all toxicities related to prior treatment
  • Presence of at least one measurable lesion according to RECIST 1.1
  • Eastern Cooperative Oncology Group (ECOG) performance ≤1
  • Meet the following laboratory values at the screening visit:

    • Absolute Neutrophil Count ≥1.5 x 109/L
    • Platelets ≥75 x 109/L
    • Hemoglobin (Hgb) ≥9 g/dL
    • Creatinine Clearance ≥ 45 mL/min using Cockcroft-Gault formula
    • Total bilirubin ≤1.5 x ULN
    • Aspartate transaminase (AST) ≤ 3.0 x ULN, except for patients with liver metastasis, who may only be included if AST ≤5.0 x ULN
    • Alanine transaminase (ALT) ≤ 3.0 x ULN, except for patients with liver metastasis, who may only be included if ALT ≤5.0 x ULN

Exclusion Criteria:

  • Prior treatment with EGFR-TKI.
  • Known T790M positive mutation. Any other known EGFR activating mutations other than L858R or ex19del. Patients whose tumors harbor other EGFR mutations concurrent with L858R or ex19del EGFR mutations are eligible.
  • Symptomatic brain metastases
  • History of interstitial lung disease or interstitial pneumonitis
  • Any medical condition that would, in the investigator's judgment, the patient's in the study due to safety concerns, compliance with clinical study procedures or interpretation of study results
  • Presence or history of a malignant disease other than NSCLC that has been diagnosed and/or required therapy within the past 3 years..
  • Presence of clinically significant ophthalmologic abnormalities
  • Bullous and exfoliative skin disorders of any grade
  • Presence or history of microangiopathic hemolytic anemia with thrombocytopenia.
  • Known history of testing positive for human immunodeficiency virus (HIV) infection
  • Cardiac or cardiac repolarization abnormality
  • Major surgery: ≤4 weeks to starting study treatment or who have not recovered from side effects of such procedure.
  • Unable or unwilling to swallow tablets or capsules
  • Female patients who are either pregnant or nursing
  • Women of child bearing potential who refuse or are not able to use a highly effective method of contraception as defined in the study protocol.
  • Sexually active males unless they use a condom during intercourse while taking drug and for 3 months after the last dose of study treatment.

Other protocol-defined inclusion/exclusion criteria may apply


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): NCT03529084


Sponsors and Collaborators
Novartis Pharmaceuticals
Investigators
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Study Director: Novartis Pharmaceuticals Novartis Pharmaceuticals
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Responsible Party: Novartis Pharmaceuticals
ClinicalTrials.gov Identifier: NCT03529084    
Other Study ID Numbers: CEGF816A2302
2017-003998-34 ( EudraCT Number )
First Posted: May 18, 2018    Key Record Dates
Last Update Posted: November 22, 2019
Last Verified: November 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Undecided
Plan Description:

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent expert panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data is currently available according to the process described on www.clinicalstudydatarequest.com.


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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 Novartis ( Novartis Pharmaceuticals ):
Non small cell lung cancer
NSCLC
EGFR mutation
EGF816
nazartinib
erlotinib
gefitinib
Additional relevant MeSH terms:
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Carcinoma, Non-Small-Cell Lung
Carcinoma, Bronchogenic
Bronchial Neoplasms
Lung Neoplasms
Respiratory Tract Neoplasms
Thoracic Neoplasms
Neoplasms by Site
Neoplasms
Lung Diseases
Respiratory Tract Diseases
Erlotinib Hydrochloride
Gefitinib
Antineoplastic Agents
Protein Kinase Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action