๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-03-27

Study to Evaluate IMP9064 as a Monotherapy or in Combination in Patients With Advanced Solid Tumors (NCT05269316)

A First-in-human, Phase 1/2, Open-label, Multi-center, Dose-escalation and Dose-expansion Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Anti-tumor Activity of the ATR Inhibitor IMP9064 Monotherapy and in Combination With PARP Inhibitor Senaparib in Patients With Advanced Solid Tumors

๐ŸŸข Recruiting Phase1 / Phase2 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Impact Therapeutics, Inc.

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

This is a Phase 1/2, multicenter, open-label study to evaluate the safety and efficacy of IMP9064 as monotherapy or in combination with PARP inhibitor Senaparib in patients with advanced solid tumors

Who can join: Review the eligibility criteria below.

Location: Hackensack University Medical Center PARTNER โ€” Hackensack, New Jersey

Age range: 18 Years

๐Ÿงช Interventions in This Study

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 (8 Sites)

  • Hackensack University Medical Center PARTNER โ€” Hackensack, New Jersey
  • Mount Sinai โ€” New York, New York
  • Greenville Hospital System University Medical Center (ITOR) โ€” Greenville, South Carolina
  • Mary Crowley Cancer Research Centers โ€” Dallas, Texas
  • Blacktown Hospital โ€” Blacktown, New South Wales
  • Linear Clinical Research Limited โ€” Nedlands,
  • Beijing Cancer Hospital โ€” Beijing, Beijing Municipality
  • National Taiwan University Hospital โ€” Taipei,

๐Ÿ“ž Contact the Study Coordinator

Phone: +86-021-68411121

Email: xiangna.chen@impacttherapeutics.com

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

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.

Explore by condition: All Solid Tumor clinical trials

๐Ÿ’ก 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.
๐Ÿ›๏ธ View Official NIH Record โ†—