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Contact the study team using the details below to take part. If there are no contact details below please ask your doctor in the first instance.

Contact Information:

AstraZeneca Clinical Study Information Center 1-877-240-9479
information.center@astrazeneca.com


Study Location:

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Be Part of Research - Trial Details - A Global Phase III Study of Rilvegostomig or Pembrolizumab Plus Chemotherapy for First-Line Treatment of Metastatic Squamous Non-small Cell Lung Cancer (NSCLC)

A Global Phase III Study of Rilvegostomig or Pembrolizumab Plus Chemotherapy for First-Line Treatment of Metastatic Squamous Non-small Cell Lung Cancer (NSCLC)

Recruiting

Open to: ALL

Age: 18.0 - N/A

Medical Conditions

Lung Neoplasms
Carcinoma, Non-Small-Cell Lung


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


The purpose of ARTEMIDE-Lung02 is to assess the efficacy and safety of rilvegostomig in combination with platinum-based chemotherapy for the first-line (1L) treatment of patients with metastatic squamous non-small cell lung cancer (mNSCLC) whose tumors express programmed death-ligand 1 (PD-L1).

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Nov 2024 Feb 2029

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : Administered intravenously (IV) on Day 1 of each 21-day cycle

Intervention Arm Group : Arm A;

Intervention Type : DRUG
Intervention Description : Administered intravenously (IV) on Day 1 of each 21-day cycle

Intervention Arm Group : Arm B;

Intervention Type : DRUG
Intervention Description : Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles

Intervention Arm Group : Arm A;Arm B;

Intervention Type : DRUG
Intervention Description : Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles

Intervention Arm Group : Arm A;Arm B;

Intervention Type : DRUG
Intervention Description : Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles

Intervention Arm Group : Arm A;Arm B;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • Research Site
    Preston
    PR2 9HT
  • Research Site
    Cambridge
    CB2 0QQ
  • Research Site
    Manchester
    M20 4BX
  • Research Site
    London
    EC1A 7BE
  • Research Site
    London
    SE1 9RT
  • Research Site
    Edinburgh
    EH4 2XU
  • Research Site
    Aberdeen
    AB25 2ZN
  • Research Site
    Exeter
    EX2 5DW
  • Research Site
    Newcastle upon Tyne
    NE7 7AF
  • Research Site
    Greater London
    SW3 6JJ

AstraZeneca Clinical Study Information Center 1-877-240-9479
information.center@astrazeneca.com



The study is sponsored by AstraZeneca




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Read full details for Trial ID: NCT06692738
Last updated 12 June 2025

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