AZD0901 in Participants With Advanced Solid Tumours Expressing Claudin18.2 (NCT06219941)
A Phase II, Open-label, Multi-centre Study to Evaluate Safety, Tolerability, Efficacy, PK, and Immunogenicity of AZD0901 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Tumours Expressing Claudin 18.2 (CLARITY-PanTumour01)
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to assess the safety, tolerability, efficacy, pharmacokinetics (PK), and immunogenicity of AZD0901 as monotherapy and in combination with anti-cancer agents in participants with locally advanced unresectable or metastatic solid tumours expressing CLDN18.2.
Who can join: Review the eligibility criteria below.
Location: Research Site — Orange, California
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (52 Sites)
Showing the first 25 of 52 sites.
- Research Site — Orange, California
- Research Site — Palo Alto, California
- Research Site — Santa Rosa, California
- Research Site — Louisville, Kentucky
- Research Site — Commack, New York
- Research Site — Providence, Rhode Island
- Research Site — Houston, Texas
- Research Site — Melbourne,
- Research Site — Murdoch,
- Research Site — Randwick,
- Research Site — Kingston, Ontario
- Research Site — Toronto, Ontario
- Research Site — Montreal, Quebec
- Research Site — Sherbrooke, Quebec
- Research Site — Changsha,
- Research Site — Chengdu,
- Research Site — Tbilisi,
- Research Site — Chūōku,
- Research Site — Kashiwa,
- Research Site — Kitaadachi-gun,
- Research Site — Kōtoku,
- Research Site — Nagoya,
- Research Site — Osakasayama-shi,
- Research Site — George Town,
- Research Site — Johor Bahru,
📞 Contact the Study Coordinator
Phone: (877) 240-9479
Email: information.center@astrazeneca.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.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.