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Clinical Trials/NL-OMON45219
NL-OMON45219CompletedPhase 3

A Phase III, Open-label, Randomised, Multi-centre, International Study of MEDI4736, Given as Monotherapy or in Combination with Tremelimumab, Determined by PD-L1 Expression, Versus Standard of Care in Patients with Locally Advanced or Metastatic Non-Small Cell Lung Cancer (Stage IIIB IV) who Have Received at Least Two Prior Systemic Treatment Regimens Including One Platinum based Chemotherapy Regimen and Do Not Have Known EGFR TK Activating Mutations or ALK Rearrangements (ARCTIC) - D4191C00004 - ARCTIC

Astra Zeneca0 sites18 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
18

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 64 (—)

Inclusion Criteria

  • - At least 18 years of age
  • - Documented evidence of NSCLC (Stage IIIB/ IV disease)
  • - Disease progression or recurrence after both a platinum-baed chemotherapy regimen and at least 1 additional regimen for treatment of NSCLC
  • - World Health Organization (WHO) Performance Status of 0 or 1
  • - Estimated life expectancy more than 12 weeks

Exclusion Criteria

  • - Prior exposure to any anti-PD-1 or anti-PD-L1 antibody
  • - Brain metastases or spinal cord compression unless asymptomatic, treated and stable (not requiring steroids)
  • - Active or prior documented autoimmune disease within the past 2 years
  • - Evidence of severe or uncontrolled systemic disease, including active bleeding diatheses or active infections including acute or chronic hepatitis B, C and HIV
  • - Any unresolved toxicity CTCAE >Grade 2 from previous anti-cancer therapy
  • - Known EGFR TK activating mutations or ALK rearrangements. Patients with EGFR TK inactivating mutations, e.g. exon 20, are eligible
  • - Any prior Grade *3 immune-related adverse event (irAE) while receiving any previous immunotherapy agent, or any unresolved irAE >Grade 1
  • - Active or prior documented inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis)

Investigators

Sponsor
Astra Zeneca

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