A Study of IBI363 in Subjects with Advanced Solid Malignancies (NCT06281678)
A Phase 2, Open-label, Multicenter Study of IBI363 (PD1-IL2m) in Subjects with Advanced Solid Malignancies
🩺 Plain-English Summary (8th-Grade Level)
This is a Phase 2, open-label, multicenter study designed to evaluate the efficacy, safety and tolerability of IBI363 (study drug) in subjects with advanced, refractory solid malignancies.
Who can join: Review the eligibility criteria below.
Location: University of California, San Francisco (UCSF) — San Francisco, 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 (9 Sites)
- University of California, San Francisco (UCSF) — San Francisco, California
- Ocala Oncology Center — Ocala, Florida
- BRCR Medical Center — Plantation, Florida
- University of Kansas Medical Center (KUMC) — Fairway, Kansas
- Michigan Hematology & Oncology Consultants - MedOnc Dearborn — Dearborn, Michigan
- Michigan Hematology & Oncology Consultants - MedOnc Troy — Troy, Michigan
- MD Anderson Cancer Center-University of Texas — Houston, Texas
- Oncology Consultants P.A. — Houston, Texas
- Fred Hutchinson Cancer Center — Seattle, Washington
📞 Contact the Study Coordinator
Phone: (832) 207-5244
Email: amanda.guo@innoventbio.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.