At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Rilvegostomig (drug), Pembrolizumab (drug), Carboplatin (drug), Paclitaxel (drug)
- How long the study runs
- Study runs about 68 months (dates as stated)
- About the drug or intervention
- Rilvegostomig — drug: Administered intravenously (IV) on Day 1 of each 21-day cycle · Pembrolizumab — drug: Administered intravenously (IV) on Day 1 of each 21-day cycle · Carboplatin — drug: Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles · Paclitaxel — drug: Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles · Nab-paclitaxel — drug: Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 1,160
- Started
- 2024-11-18
- Last checked
- 2026-09
Plain English Summary
What is this study?
- • Testing a new treatment for non-small cell lung cancer
- • Phase3 - 1,160 participants
- • 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 locally advanced or metastatic squamous non-small cell lung cancer (mNSCLC) whose tumors express programmed death-ligand 1 (PD-L1)
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with non-small cell lung cancer
Where?
- • Aberdeen - Research Site
- • Cambridge - Research Site
- • Edinburgh - Research Site
- • Exeter - Research Site
- • +6 more UK sites
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
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 locally advanced or metastatic squamous non-small cell lung cancer (mNSCLC) whose tumors express programmed death-ligand 1 (PD-L1).
More detail
This is a Phase III, two-arm, randomized, double-blind, global, multicenter study assessing the efficacy and safety of rilvegostomig compared to pembrolizumab, both in combination with platinum-based doublet chemotherapy, as a first-line (1L) treatment for patients with squamous locally advanced or metastatic non-small cell lung cancer (mNSCLC) whose tumors express PD-L1 (tumor cells (TC) ≥ 1%).
How this trial compares with your answers
Answer 2 more questions to improve match
What we know so far
Still need:
- • Tell us your age for better matching
- • Tell us your sex for better matching
Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
Biomarkers mentioned
Treatment history
Treatments you must have had:
- ✓ short axis ≥ 15 mm) with CT or MRI and is suitable for accurate repeated measurements
What the study is looking for
- ✓Histologically or cytologically documented squamous NSCLC.
- ✓Stage III B/C or IV mNSCLC (based on the American Joint Committee on Cancer Edition 8) not amenable to curative...
- ✓Provision of acceptable tumor sample to confirm tumor PD-L1 expression TC ≥ 1%.
- ✓Adequate organ and bone marrow function.
Who cannot take part
- ✗Presence of small cell and neuroendocrine histology components.
- ✗Any prior systemic, non-curative therapy received for NSCLC.
- ✗Any prior treatment with an anti-PD-1 or anti-PD-L1 agent.
- ✗Any prior exposure to an anti-TIGIT therapy or any other anticancer therapy targeting immune-regulatory receptors or...
- ✗Active or prior documented autoimmune or inflammatory disorders requiring chronic systemic treatment with the use of...
See the full criteria
Where Is This Study? (10 UK sites)
Research Site
Aberdeen AB25 2ZN, United Kingdom
Research Site
Cambridge CB2 0QQ, United Kingdom
Research Site
Edinburgh EH4 2XU, United Kingdom
Research Site
Exeter EX2 5DW, United Kingdom
Research Site
Greater London SW3 6JJ, United Kingdom
Research Site
London EC1A 7BE, United Kingdom
Research Site
London SE1 9RT, United Kingdom
Research Site
Manchester M20 4BX, United Kingdom
Research Site
Newcastle upon Tyne NE7 7AF, United Kingdom
Research Site
Preston PR2 9HT, United Kingdom
How to Get in Touch
AstraZeneca Clinical Study Information Center
Sponsor contactCONTACT
