๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-03-11

Study of Furmonertinib in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Activating, Including Uncommon, Epidermal Growth Factor Receptor (EGFR) or Human Epidermal Growth Factor Receptor 2 (HER2) Mutations (NCT05364073)

A Phase 1b Dose Escalation and Dose Expansion Study Evaluating the Safety, Pharmacokinetics, and Antitumor Activity of Furmonertinib in Patients With Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With Activating Epidermal Growth Factor Receptor (EGFR) or Human Epidermal Growth Factor Receptor 2 (HER2) Mutations

๐Ÿ”ต Active, Not Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: ArriVent BioPharma, Inc.

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

This is a Phase 1b, open-label, multi-center, dose-escalation and dose expansion study designed to evaluate the safety, pharmacokinetics (PK), and preliminary antitumor activity of furmonertinib in patients with advanced or metastatic non-small cell lung cancer (NSCLC) with activating, including uncommon, Epidermal Growth Factor Receptor (EGFR) or Human Epidermal Growth Factor Receptor 2 (HER2) mutations. Patients will be enrolled into one of 2 stages: Stage 1 (Dose Escalation and Backfill Cohorts) and Stage 2 (Dose Expansion).

Who can join: Review the eligibility criteria below.

Location: ArriVent Investigative Site โ€” Prescott, Arizona

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (42 Sites)

Showing the first 25 of 42 sites.

  • ArriVent Investigative Site โ€” Prescott, Arizona
  • ArriVent Investigative Site โ€” Sacramento, California
  • ArriVent Investigative Site โ€” Whittier, California
  • ArriVent Investigative Site โ€” Celebration, Florida
  • ArriVent Investigative Site โ€” Detroit, Michigan
  • ArriVent Investigative Site โ€” Houston, Texas
  • ArriVent Investigative Site โ€” Fairfax, Virginia
  • ArriVent Investigative Site โ€” Blacktown, New South Wales
  • ArriVent Investigative Site โ€” St Leonards, New South Wales
  • ArriVent Investigative Site โ€” Heidelberg, Victoria
  • Arrivent Investigative Site โ€” Edmonton,
  • Arrivent Investigative Site โ€” Toronto,
  • Allist Investigative Site โ€” Hefei, Anhui
  • Allist Investigative Site โ€” Beijing, Beijing Municipality
  • Allist Investigative Site โ€” Chaoyang, Beijing Municipality
  • Allist Investigative Site โ€” Chongqing, Chongqing Municipality
  • Allist Investigative Site โ€” Harbin, Heilongjiang
  • Allist Investigative Site โ€” Zhengzhou, Henan
  • Allist Investigative Site โ€” Zhengzhou, Henan
  • Allist Investigative Site โ€” Wuhan, Hubei
  • Allist Investigative Site โ€” Xuzhou, Jiangsu
  • Allist Investigative Site โ€” Nanchang, Jianxi
  • Allist Investigative Site โ€” Changchun, Jilin
  • Allist Investigative Site โ€” Jinan, Shandong
  • Allist Investigative Site โ€” Jinan, Shandong

๐Ÿ’ฐ 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 ยง 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.

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  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.
๐Ÿ›๏ธ View Official NIH Record โ†—