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Phase 3 N=664 Randomized Quadruple-blind Treatment

MYL-1402O Compared With Avastin®, in Patients With Stage IV nsNSCLC

NSCLC Stage IV

Enrolled (actual)
664
Serious AEs
17.2%
Results posted
Feb 2021
Primary outcome: Primary: Primary Efficacy Analysis of Overall Response Rate ( ORR) of MYL-1402O as Compared to Avastin — 140; 144; 197; 190 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Bevacizumab as MYL-1402O (Biological); Bevacizumab as Avastin (Biological)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Mylan Pharmaceuticals Inc
Primary completion
Jun 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Primary Efficacy Analysis of Overall Response Rate ( ORR) of MYL-1402O as Compared to Avastin
140; 144; 197; 190

Summary

Assess the Efficacy and Safety of MYL-1402O Compared with Avastin®, in the First-line Treatment of Patients with Stage IV Non-Squamous Non-Small Cell Lung Cancer

Eligibility Criteria

Key Inclusion Criteria

  • Written and signed informed consent
  • Male or female at least 18 years of age with documented imaging diagnosis of Stage IV unresectable, recurrent or metastatic nsNSCLC with at least one measurable lesion as defined by RECIST 1.1
  • Documented histologic or cytologic diagnosis of advanced nsNSCLC with negative or unknown sensitizing epidermal growth factor receptor (EGFR) mutation, and negative or unknown echinoderm microtubule-associated protein like 4 anaplastic lymphoma kinase (EML4 ALK) rearrangement.
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • Has not received any prior systemic therapy for first-line treatment of advanced lung cancer, except adjuvant chemotherapy, and remained disease-free for at least 12 months from time of surgery, and at least 6 months from last dose of chemotherapy.
  • Treated and stable brain metastasis.

Key Exclusion Criteria

  • Documented squamous NSCLC or small cell type or large cell neuroendocrine histology
  • History of significant hemoptysis, central tumors with proximity to large vessels and tumor with cavitation
  • Received prior treatment with paclitaxel, bevacizumab or anthracycline or had known hypersensitivity to any of these components.
  • Recent significant cardiac condition or vascular event or inadequately controlled hypertension.
  • On anticoagulant therapy not considered stable
  • Risk of hemorrhage in the central nervous system
  • Recent history of surgery, nonhealing wound, active ulcer, or untreated bone fracture.
  • History of gastrointestinal fistula, perforation, or abscess.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04633564). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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