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Clinical Trial ● Currently Recruiting Phase III NCT05899608

Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients

Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients — Recruiting • Phase III • Oncology • NCT05899608.

📅 30 Apr 2026 ⏱ 2 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase III
NCT ID
NCT05899608
Sponsor
Summit Therapeutics
Start
2023-10-26
ClinicaliQ Trial Snapshot
  • Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients — Recruiting • Phase III • Oncology • NCT05899608.
  • Treatment Being Tested: Ivonescimab (a dual TIGIT/PD-L1 pathway inhibitor) combined with chemotherapy compared to pembrolizumab (PD-L1 inhibitor) combined with chemotherapy as first-line therapy for metastatic NSCLC, with primary endpoints of overall survival and progression-free survival.
  • Patient Eligibility: Adults with previously untreated metastatic non-small cell lung cancer suitable for first-line chemotherapy; the study is multiregional and randomised in a double-blind design, suggesting inclusion of diverse patient populations across different geographical settings.
Use This Page For
  • Quick orientation before opening the registry record.
  • Checking recruitment status, phase and sponsor at a glance.
  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

This is a Phase 3 Randomized, double-blind, Multiregional Study of Ivonescimab Combined with Chemotherapy Versus Pembrolizumab Combined with Chemotherapy for the First-line Treatment of Metastatic Non-small Cell Lung Cancer. The primary endpoint is overall survival and progression free survival assessed by investigator. The key secondary endpoints include response and safety.

Eligibility Snapshot
  • : * Age ≥ 18 years old at the time of enrollment * Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1 * Expected life expectancy ≥ 3 months * Metastatic (Stage IV) NSCLC * Histologically or cytologically confirmed squamous or non-squamous NSCLC * Recorded measurement of the Tumor Proportion Score (TPS) or Tumor Cells (TC) for PD-L1 expression, irrespective of the PD-L1 expression, prior to randomization * At least one measurable noncerebral lesion according to RECIST 1.1 * No prior systemic treatment for metastatic NSCLC

Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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