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Clinical trialNCT02453282Active, not recruitingPhase 3Interventional

Phase III Open Label First Line Therapy Study of MEDI 4736 (Durvalumab) With or Without Tremelimumab Versus SOC in Non Small-Cell Lung Cancer (NSCLC)

SponsorAstraZenecaEnrollment1,118Non-Small-Cell Lung Carcinoma NSCLC
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This is a randomized, open-label, multi-center, global, Phase III study to determine the efficacy and safety of MEDI4736 + tremelimumab combination therapy and MEDI4736 monotherapy versus platinum-based SoC chemotherapy in the first-line treatment of patients with epidermal growth factor receptor (EGFR) and anaplastic lymphoma kinase (ALK) wild-type locally advanced or metastatic NSCLC

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

196 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

Australia
  • Research Site

    Box Hill, Australia

  • Research Site

    Gosford, Australia

  • Research Site

    Kogarah, Australia

  • Research Site

    Melbourne, Australia

  • Research Site

    Port Macquarie, Australia

  • Research Site

    Southport, Australia

  • Research Site

    St Leonards, Australia

Belgium
  • Research Site

    Brussels, Belgium

  • Research Site

    Charleroi, Belgium

  • Research Site

    Duffel, Belgium

  • Research Site

    Leuven, Belgium

  • Research Site

    Liège, Belgium

Canada
  • Research Site

    Greater Sudbury, Ontario, Canada

  • Research Site

    Kingston, Ontario, Canada

  • Research Site

    Newmarket, Ontario, Canada

  • Research Site

    Oshawa, Ontario, Canada

  • Research Site

    Saint Catherines, Ontario, Canada

  • Research Site

    Sault Ste. Marie, Ontario, Canada

  • Research Site

    Toronto, Ontario, Canada

  • Research Site

    Regina, Saskatchewan, Canada

  • Research Site

    Saskatoon, Saskatchewan, Canada

France
  • Research Site

    Bordeaux, France

  • Research Site

    Brest, France

  • Research Site

    Créteil, France

  • Research Site

    Lille, France

  • Research Site

    Lyon, France

  • Research Site

    Marseille, France

Germany
  • Research Site

    Aachen, Germany

  • Research Site

    Bad Berka, Germany

  • Research Site

    Berlin, Germany

  • Research Site

    Berlin, Germany

  • Research Site

    Freiburg im Breisgau, Germany

  • Research Site

    Gauting, Germany

  • Research Site

    Hamburg, Germany

  • Research Site

    Heidelberg, Germany

  • Research Site

    Hemer, Germany

  • Research Site

    Homburg/Saar, Germany

  • Research Site

    Immenhausen, Germany

  • Research Site

    Löwenstein, Germany

  • Research Site

    Lübeck, Germany

156 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

Gemcitabine + CarboplatinGemcitabine + CisplatinMEDI4736MEDI4736+TremelimumabPaclitaxel + CarboplatinPemetrexed + CarboplatinPemetrexed + CisplatinTremelimumab →
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
21 Jul 2015
Primary completion
4 Oct 2018
Completion
31 Dec 2026
Last update posted
6 Aug 2026
Registered enrollment
1,118
Registry id
NCT02453282

Cross-registrations

EU-CTR / CTIS (EudraCT)2015-001279-39

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.