🏛️ Verified NIH Record • Updated 2025-06-29

FIH Trial of VERT-002 in Patients With Locally Advanced or Metastatic Solid Tumors With MET Alterations (NCT06669117)

A First-In-Human (FIH) Phase I/II Open-label, Multicentre, Dose Escalation and Expansion Trial of VERT-002 in Patients With Locally Advanced or Metastatic Solid Tumors Including Non-small Cell Lung Cancer (NSCLC) Harboring Mesenchymal-Epithelial Transition (MET) Alterations

🟢 Recruiting Phase1 / Phase2 💊 Investigational Drug / Biologic Sponsor: Pierre Fabre Medicament

🩺 Plain-English Summary (8th-Grade Level)

The goal of this clinical trial is to investigate the safety, the activity of VERT-002 (PFL-002), and the optimal safe dose to be used, in participants with solid tumors including non-small cell lung cancer.

Who can join: Review the eligibility criteria below.

Location: Georgetown Lombardi Comprehensive Cancer Center — Washington D.C., District of Columbia

Age range: 18 Years

🧪 Interventions in This Study

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria ↗

📍 All Participating Trial Locations (19 Sites)

  • Georgetown Lombardi Comprehensive Cancer Center — Washington D.C., District of Columbia
  • Gabrail Cancer Research Center — Canton, Ohio
  • Sarah Cannon Research Institute Oncology Partners — Nashville, Tennessee
  • Institut Jules Bordet — Anderlecht,
  • APHP de Marseille - Hôpital Nord — Marseille,
  • Institut de Cancerologie de Ouest (ICO) - Saint-Herblain — Saint-Herblain,
  • Institut Universitaire du Cancer de Toulouse - Oncopole — Toulouse,
  • Gustave Roussy — Villejuif,
  • Universitaet zu Koeln - Centrum fuer Integrierte Onkologie (CIO) — Cologne,
  • Universitätsklinikum Carl Gustav Carus Dresden — Dresden,
  • Azienda Ospedaliero - Universitaria San Luigi Gonzaga — Orbassano,
  • Nederlands Kanker Instituut - Antoni van Leeuwenhoek Ziekenhuis — Amsterdam,
  • Yonsei University College of Medicine — Seoul,
  • Asan Medical Center (AMC) — Seoul,
  • Hospital Universitario 12 de Octubre — Madrid,
  • Hospital Universitario La Paz — Madrid,
  • National Taiwan University Hospital — Taipei,
  • Taipei Medical University Hospital — Taipei,
  • Taipei Veterans General Hospital — Taipei,

📞 Contact the Study Coordinator

Phone: +33 684 66 43 48

Email: yuhua.wang@pierre-fabre.com

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Solid Tumor clinical trials

💡 How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
🏛️ View Official NIH Record ↗