Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Recruiting Phase 3

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

NCT06692738 · tracked via the Priya Life Science Spain tracker
Phase
Phase 3
Started
2024-11-18
Last updated
2026-09-18

Condition(s) studied

Non-small Cell Lung Cancer

Investigational drug(s) / intervention(s)

Rilvegostomig →Pembrolizumab →Carboplatin →Paclitaxel →Nab-paclitaxel →

Rilvegostomig: Administered intravenously (IV) on Day 1 of each 21-day cycle

Pembrolizumab: Administered intravenously (IV) on Day 1 of each 21-day cycle

Carboplatin: Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles

Paclitaxel: Administered intravenously (IV) on Day 1 of each 21-day cycle up to 4 cycles

Nab-paclitaxel: Administered intravenously (IV) on Days 1, 8, and 15 of each 21-day cycle up to 4 cycles

Study summary

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).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * 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 treatment. * Absence of documented tumor genomic mutation results from tests conducted as part of standard local practice in any actionable driver oncogenes for which there are locally approved and available targeted 1L therapies. * Provision of acceptable tumor sample to confirm tumor PD-L1 expression TC ≥ 1%. * At least one lesion not previously irradiated that qualifies as a RECIST 1.1 TL at baseline and can be accurately measured at baseline as ≥ 10 mm in the longest diameter (except lymph nodes, which must have short axis ≥ 15 mm) with CT or MRI and is suitable for accurate repeated measurements. * Adequate organ and bone marrow function. Exclusion Criteria: * Presence of small cell and neuroendocrine histology components. * Brain metastases unless asymptomatic, stable, and not requiring steroids or anticonvulsants for at least 7 days prior to randomization. A minimum of 2 weeks must have elapsed between the end of local therapy (brain radiotherapy or surgery) and randomization. Participants must have recovered from the acute toxic effect of radiotherapy (eg, dizziness and signs of increased intracranial pressure) or surgery prior to randomization. * 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 mechanisms. * History of another primary malignancy except for malignancy treated with curative intent with no known active disease ≥ 2 years before the first dose of study intervention and of low potential risk for recurrence. * Active or prior documented autoimmune or inflammatory disorders requiring chronic systemic treatment with the use of disease-modifying agents or other immunosuppressive drugs. * Active primary immunodeficiency/active infectious disease(s). * Active tuberculosis infection.

Primary outcome measure(s)

  • Overall survival (OS) — Up to approximately 6 years
    OS is defined as the time from randomization until the date of death due to any cause.
  • Progression-free survival (PFS) — Up to approximately 6 years
    PFS is defined as the time from randomization until radiological progression per Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST 1.1) or death due to any cause (in the absence of progression).

Trial sites (328)

FacilityCityRegionStatus
Research Site Tucson Arizona Recruiting
Research Site Springdale Arkansas Recruiting
Research Site Anaheim California Recruiting
Research Site Beverly Hills California Recruiting
Research Site Loma Linda California Recruiting
Research Site Los Alamitos California Recruiting
Research Site Redlands California Recruiting
Research Site San Francisco California Recruiting
Research Site Walnut Creek California Recruiting
Research Site West Haven Connecticut Recruiting
Research Site Newark Delaware Recruiting
Research Site Bay Pines Florida Recruiting
Research Site Fort Lauderdale Florida Recruiting
Research Site Gainesville Florida Recruiting
Research Site Gainesville Florida Withdrawn
Research Site Jacksonville Florida Recruiting
Research Site Athens Georgia Recruiting
Research Site Atlanta Georgia Withdrawn
Research Site Savannah Georgia Not Yet Recruiting
Research Site Boise Idaho Recruiting
Research Site Chicago Illinois Recruiting
Research Site Decatur Illinois Recruiting
Research Site Hinsdale Illinois Recruiting
Research Site Quincy Illinois Recruiting
Research Site Rockford Illinois Withdrawn
Research Site Fort Wayne Indiana Not Yet Recruiting
Research Site Waterloo Iowa Recruiting
Research Site Lexington Kentucky Recruiting
Research Site Lexington Kentucky Withdrawn
Research Site Louisville Kentucky Recruiting
Research Site Louisville Kentucky Recruiting
Research Site Alexandria Louisiana Withdrawn
Research Site Baton Rouge Louisiana Recruiting
Research Site Covington Louisiana Withdrawn
Research Site Shreveport Louisiana Recruiting
Research Site Shreveport Louisiana Recruiting
Research Site Scarborough Maine Recruiting
Research Site Baltimore Maryland Completed
Research Site Bethesda Maryland Recruiting
Research Site Bethesda Maryland Not Yet Recruiting

+ 288 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06692738 on ClinicalTrials.gov ↗ ← All trials in Spain