Study of IBI3020 Treatment in Participants With Late-Stage Solid Tumors (NCT06963281)
A Phase 1, Multicenter, Open-label Study of IBI3020 Treatment in Participants With Unresectable, Locally Advanced or Metastatic Solid Tumors
๐ฉบ Plain-English Summary (8th-Grade Level)
The main purpose of this study is to evaluate the safety and tolerability of IBI3020 and to determine the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RP2D) of IBI3020.
Who can join: Review the eligibility criteria below.
Location: Mayo Clinic - Arizona โ Pheonix, Arizona
Age range: 18 Years to 75 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (9 Sites)
- Mayo Clinic - Arizona โ Pheonix, Arizona
- Mayo Clinic - Florida โ Jacksonville, Florida
- Mayo Clinic - Rochester โ Rochester, Minnesota
- Montefiore Cancer Center โ New York, New York
- NEXT Houston โ Houston, Texas
- NEXT Dallas โ Irving, Texas
- The sixth affiliated hospital, Sun Yat-sen University โ Guangzhou, Guangdong
- Shandong Cancer Hospital โ Jinan, Shandong
- Shanxi Cancer Hospital โ Taiyuan, Shanxi
๐ Contact the Study Coordinator
Phone: 051269566088
Email: suhua.dong@innoventbio.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ 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.
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- Study of the Effect of Rifampicin on the Pharmacokinetics (PK) of Multiple Doses of Cediranib in Patients With Solid Tumours โ Edmonton, Alberta
- Study of Anti-CEACAM5 ADC M9140 in Participants With Advanced Solid Tumors (PROCEADE PanTumor) โ Santa Monica, California
- A Safety and Efficacy Extension Study of Pertuzumab in Patients With Solid Tumors Previously Enrolled in a Hoffmann-La Roche-Sponsored Pertuzumab Clinical Trial โ Porto Alegre, Rio Grande do Sul
- Safety, Tolerability, and Immunogenicity of mRNA-4157 Alone and in Combination in Participants With Solid Tumors โ Los Angeles, California
- Flavored, Oral Irinotecan VAL-413 (Orotecanยฎ) Given With Temozolomide for Treatment of Recurrent Pediatric Solid Tumors โ Phoenix, Arizona
Explore by condition: All Solid Tumors clinical trials
๐ก 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.