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Clinical Trials/NCT01519804
NCT01519804
Completed
Phase 2

A Randomized, Phase II, Multicenter, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy and Safety of Onartuzumab (Metmab) in Combination With Paclitaxel + Cisplatin or Carboplatin as First-Line Treatment for Patients With Stage IIIb (T4 Disease) or IV Squamous Non-Small Cell Lung Cancer (NSCLC)

Genentech, Inc.0 sites108 target enrollmentApril 2012

Overview

Phase
Phase 2
Intervention
cisplatin/carboplatin
Conditions
Non-Squamous Non-Small Cell Lung Cancer
Sponsor
Genentech, Inc.
Enrollment
108
Primary Endpoint
Progression-free survival (tumor assessments according to RECIST criteria)
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This multicenter, randomized, double-blind, placebo-controlled study will evaluate the efficacy and safety of onartuzumab (MetMAb) in combination with paclitaxel plus platinum in patients with incurable Stage IIIB or Stage IV squamous non-small cell lung cancer (NSCLC). Patients will be randomized to receive either onartuzumab (MetMAb) 15 mg/kg iv or placebo on Day 1 of each 21-day cycle in combination with 4 cycles of paclitaxel 200 mg/m2 iv and platinum (carboplatin/cisplatin) iv on Day 1 of each 21-day cycle. Patients who have not progressed after 4 cycles will continue with either onartuzumab (MetMAb) or placebo as maintenance therapy until disease progression or unacceptable toxicity occurs.

Registry
clinicaltrials.gov
Start Date
April 2012
End Date
September 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients, \>/= 18 years of age
  • Histologically or cytologically confirmed Stage III B or Stage IV squamous non-small cell lung cancer (NSCLC)
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1
  • No prior chemotherapy for squamous NSCLC
  • Adequate tissue for central IHC assay of Met receptor, and EGFR testing if EGFR status is unknown
  • Radiographic evidence of disease

Exclusion Criteria

  • Prior systemic treatment for Stage IIIB or IV squamous NSCLC
  • NSCLC with histology classified as adenocarcinoma, large cell, mixed adenosquamous, or NSCLC not otherwise specified (NOS)
  • Prior exposure to experimental treatment targeting either the HGF or Met pathway
  • Patients with tumors confirmed to have EGFR-activating mutations who are suitable for anti-EGFR therapy (e.g. gefitinib or erlotinib), as determined by the investigator
  • Uncontrolled brain metastases and treatment by neurosurgical resection or brain biopsy within 4 weeks prior to Day 1 of Cycle 1
  • History of another malignancy in the previous 3 years except for prior history of in situ cancer or basal or squamous cell skin cancer
  • Pregnant or lactating women
  • Uncontrolled diabetes
  • Impaired bone marrow, liver or renal function as defined by protocol
  • Significant history of cardiovascular disease

Arms & Interventions

MetMAb+paclitaxel+platinum

Intervention: cisplatin/carboplatin

MetMAb+paclitaxel+platinum

Intervention: onartuzumab

MetMAb+paclitaxel+platinum

Intervention: paclitaxel

Placebo+paclitaxel+platinum

Intervention: Placebo

Placebo+paclitaxel+platinum

Intervention: cisplatin/carboplatin

Placebo+paclitaxel+platinum

Intervention: paclitaxel

Outcomes

Primary Outcomes

Progression-free survival (tumor assessments according to RECIST criteria)

Time Frame: up to approximately 32 months

Progression-free survival: Subgroup of patients with Met diagnostic-positive squamous NSCLC

Time Frame: up to approximately 32 months

Secondary Outcomes

  • Overall survival(up to approximately 32 months)
  • Overall response rate (tumor assessments according to RECIST criteria)(up to approximately 32 months)
  • Duration of response (time from first documented objective response to disease progression)(up to approximately 32 months)
  • Disease control rate (rate of partial response plus complete response plus stable disease for at least 6 weeks)(up to approximately 32 months)
  • Serum levels of anti-therapeutic antibodies (MetMAb ATAs)(Pre-dose Day 1 of Cycles 1, 2 and 4)
  • Safety: Incidence of adverse events(up to approximately 32 months)
  • Pharmacokinetics: serum concentration (Cmin/Cmax)(Pre- and post-dose on Day 1 of Cycles 1, 2 and 4 and up to 2 years)
  • Plasma concentrations of paclitaxel/platinum(Pre- and post-dose on Day 1 of Cycles 1 and 4)

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