Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT05403385 · ClinicalTrials.gov registry record · Phase 2

Study of Inupadenant (EOS100850) With Chemotherapy as Second Line Treatment for Nonsquamous Non-small Cell Lung Cancer

A Phase 2 study of Metastatic NSCLC - Non-Small Cell Lung Cancer and Locally Advanced NSCLC - Non-Small Cell Lung Cancer, sponsored by iTeos Therapeutics.

Active
Registry status
Phase 2
Development phase
36
Enrollment target
20
Study locations

NCT05403385: Active Phase 2 study of Metastatic NSCLC - Non-Small Cell Lung Cancer and Locally Advanced NSCLC - Non-Small Cell Lung Cancer, sponsored by iTeos Therapeutics.

NCT05403385 is a Phase 2 study of Metastatic NSCLC - Non-Small Cell Lung Cancer and Locally Advanced NSCLC - Non-Small Cell Lung Cancer that is active but no longer recruiting, run by iTeos Therapeutics. The registered enrollment target is 36 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (73% lower). The trial reports 20 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05403385, a Phase 2 study of Metastatic NSCLC - Non-Small Cell Lung Cancer and Locally Advanced NSCLC - Non-Small Cell Lung Cancer, is active but no longer recruiting, sponsored by iTeos Therapeutics.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
36 participants
Enrollment target
20
Study locations

Study Summary

The study will first determine the optimal dose of inupadenant to be given in combination with carboplatin and pemetrexed to patients that progressed after receiving first line anti-PD(L)1 treatment for locally advanced or metastatic non-small cell lung cancer. The efficacy and safety of the combination is then compared to standard of care carboplatin and pemetrexed in the same populations.

Primary Outcome

Incidence of dose-limiting toxicities

Interventions

  • DRUG Carboplatin
  • DRUG Placebo
  • DRUG Pemetrexed
  • DRUG inupadenant

Study Locations (20)

Other

  • Algemeen Ziekenhuis Sint-Lucas - Ghent
  • Jessa Ziekenhuis - Hasselt
  • AZ Delta - Roeselare
  • Vseobecna Fakultni Nemocnice - Prague
  • CHU de Caen - Caen
  • Hopital de la Timone Centre d'Essais Précoces en Cancérologie de Marseille (CEPCM) - Marseille
  • CHU Nantes - Nantes
  • Istituto Nazionale dei Tumori - Milan
  • Gruppo Humanitas - Istituto Clinico Humanitas - Rozzano
  • Centro Oncologico de Galicia - A Coruña
  • Hospital Infanta Cristina (Hospital Universitario de Badajoz) - Badajoz
  • Hospital Universitario Vall d'Hebron - Barcelona
  • Althaia Hospital - Manresa
  • Complejo Hospitalario Universitario de Ourense - Ourense

Arkansas

  • Highlands Oncology Group - Fayetteville

Florida

  • H. Lee Moffitt Cancer Center and Research Institute - Tampa

Ontario

  • William Osler Health System - Brampton

Balearic Islands

  • Hospital Universitari Son Espases - Palma de Mallorca

Pamplona

  • Complejo Hospitalario de Navarra (CHN) - Pamplona

Valencia

  • Hospital Universitari i Politecnic La Fe de Valencia - Valencia

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2022-08-26
Est. Completion 2025-10
Phase Phase 2
iTeos Therapeutics

3 total trials

What the registry record for NCT05403385 still lists

NCT05403385 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (73% lower).

The record links to 2 conditions, with Metastatic NSCLC - Non-Small Cell Lung Cancer appearing as the primary indexed condition, and to 4 interventions - of which Carboplatin is the first listed.

NCT05403385 names 20 study sites across 7 states, led by Other, Arkansas, Florida.

Frequently Asked Questions

What is clinical trial NCT05403385 about?

NCT05403385 is a clinical study titled "Study of Inupadenant (EOS100850) With Chemotherapy as Second Line Treatment for Nonsquamous Non-small Cell Lung Cancer". The study will first determine the optimal dose of inupadenant to be given in combination with carboplatin and pemetrexed to patients that progressed after receiving first line anti-PD(L)1 treatment for locally advanced or metastatic non-small cell lung cancer. The efficacy and safety of the combina...

What is the current status of trial NCT05403385?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 36 participants. The study started on 2022-08-26. Estimated completion is 2025-10.

What conditions does trial NCT05403385 study?

This clinical trial studies the following conditions: Metastatic NSCLC - Non-Small Cell Lung Cancer, Locally Advanced NSCLC - Non-Small Cell Lung Cancer.

What interventions are being tested in trial NCT05403385?

The interventions under investigation include: Carboplatin (DRUG), Placebo (DRUG), Pemetrexed (DRUG), inupadenant (DRUG).

Who is sponsoring clinical trial NCT05403385?

This trial is sponsored by iTeos Therapeutics, which has 3 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05403385 being conducted?

This trial has 20 study locations across Arkansas, Florida, Ontario, Balearic Islands, Pamplona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Metastatic NSCLC - Non-Small Cell Lung Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05403385's enrollment target sits among peer trials

36 1496th of 2000 higher than 477 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00929006 · 36 participants · Early Phase 1

    Acute Progesterone Suppression of Wake vs. Sleep Luteinizing Hormone Pulse Frequency in Pubertal Girls With and Without Hyperandrogenism

  • NCT01891318 · 36 participants · Phase 1

    Neoadjuvant Radiosurgery for Resectable Brain Metastases: Phase I/II Study

  • NCT02291848 · 36 participants · Phase 1

    Tumor-Associated Antigen-Specific Cytotoxic T-Lymphocytes for Multiple Myeloma

  • NCT02366819 · 36 participants · Phase 4

    Genetic Analysis-Guided Irinotecan Hydrochloride Dosing of mFOLFIRINOX in Treating Patients With Locally Advanced Gastroesophageal or Stomach Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05403385, the US trial registry maintained by the National Library of Medicine. NCT05403385 (small enrollment · wide site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.