๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2025-12-08

JZP898 Intravenous Infusion as Monotherapy and Combination With Pembrolizumab in Adults With Advanced/Metastatic Solid Tumors (NCT06108050)

A Phase 1, First-in-human, Open-label, Multicenter Study of JZP898 as Monotherapy and in Combination With Pembrolizumab in Participants With Advanced or Metastatic Solid Tumors

๐ŸŸข Recruiting Phase1 ๐Ÿ’Š Investigational Drug / Biologic Sponsor: Jazz Pharmaceuticals

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

This Phase 1 first-in-human study will investigate the safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary antitumor activity of JZP898 monotherapy as well as JZP898 in combination with pembrolizumab in adult participants with advanced or metastatic solid tumors.

Who can join: Review the eligibility criteria below.

Location: California Cancer Associates for Research and Excellence โ€” Encinitas, California

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 (10 Sites)

  • California Cancer Associates for Research and Excellence โ€” Encinitas, California
  • California Cancer Associates for Research and Excellence โ€” Fresno, California
  • Sarah Cannon Research Institute at HealthONE โ€” Denver, Colorado
  • Florida Cancer Specialists โ€” Orlando, Florida
  • Duke University Medical Center - Duke Cancer Institute โ€” Durham, North Carolina
  • Sidney Kimmel Cancer Center at Thomas Jefferson University Hospital โ€” Philadelphia, Pennsylvania
  • SCRI Oncology Partners โ€” Nashville, Tennessee
  • Texas Oncology - Baylor Charles A Sammons Cancer Center โ€” Dallas, Texas
  • The University of Texas MD Anderson Cancer Center โ€” Houston, Texas
  • Virginia Cancer Specialists โ€” Fairfax, Virginia

๐Ÿ“ž Contact the Study Coordinator

Phone: (215) 832-3750

Email: ClinicalTrialDisclosure@JazzPharma.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.

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†—