1438-0012 DAREON-Lung-1

  • Research type

    Research Study

  • Full title

    DAREON®-Lung-1: A Phase III multi-center, open-label, randomised trial of intravenous obrixtamig in combination with atezolizumab, carboplatin, and etoposide vs. atezolizumab,carboplatin, and etoposide as first-line treatment in patients with extensive-stage small cell lung cancer

  • IRAS ID

    1013157

  • Contact name

    Medical Information

  • Contact email

    medinfo.bra@boehringer-ingelheim.com

  • Sponsor organisation

    Boehringer Ingelheim Limited

  • Research summary

    This study is open to adults with advanced small cell lung cancer (SCLC). The purpose of this study is to find out if a study medicine called obrixtamig plus standard treatment (atezolizumab, carboplatin, and etoposide) improves survival when compared to standard treatment alone. Obrixtamig is an antibody-like molecule that may help the immune system fight cancer. Another purpose of the study is to test a medical device being developed to measure levels of the tumour marker DLL3.
    Participants are put into 2 groups randomly, which means by chance. One group receives obrixtamig and standard treatment. The other group receives standard treatment without obrixtamig. All treatments are given as infusions into a vein.
    Participants are in the study for up to 3 years. During this time, they visit the study site regularly. Participants in the group receiving obrixtamig stay overnight at the study site following the first 2 obrixtamig treatments. At the visits, doctors check the size of the tumour(s). The results are compared between the 2 groups to see whether the treatment works. The doctors also regularly check participants’ health and take note of any unwanted effects.

  • REC name

    North East - Tyne & Wear South Research Ethics Committee

  • REC reference

    26/NE/0059

  • Date of REC Opinion

    29 Jun 2026

  • REC opinion

    Further Information Favourable Opinion