First-Time-in-Human Study of GSK4381562 in Participants With Advanced Solid Tumors (NCT05277051)
A Phase 1 First-Time-in-Human, Open-Label Study of GSK4381562 Administered as Monotherapy and in Combination With Anticancer Agents in Participants With Selected Advanced Solid Tumors
π©Ί Plain-English Summary (8th-Grade Level)
This is a first time in-human (FTIH) study designed to investigate the safety, tolerability, pharmacokinetics (PK), and immunogenicity of remzistotug in participants with select loco-regionally recurrent solid tumors or metastatic solid tumors where curative or standard treatment options have been exhausted.
Who can join: Review the eligibility criteria below.
Location: GSK Investigational Site β San Francisco, California
Age range: 18 Years
π§ͺ Interventions in This Study
π "Do I Qualify?" β 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria β
π All Participating Trial Locations (26 Sites)
Showing the first 25 of 26 sites.
- GSK Investigational Site β San Francisco, California
- GSK Investigational Site β Charlotte, North Carolina
- GSK Investigational Site β Oklahoma City, Oklahoma
- GSK Investigational Site β Philadelphia, Pennsylvania
- GSK Investigational Site β Dallas, Texas
- GSK Investigational Site β San Antonio, Texas
- GSK Investigational Site β Salt Lake City, Utah
- GSK Investigational Site β Nedlands, Western Australia
- GSK Investigational Site β Ottawa, Ontario
- GSK Investigational Site β Toronto, Ontario
- GSK Investigational Site β Chengdu,
- GSK Investigational Site β Jinan,
- GSK Investigational Site β Shanghai,
- GSK Investigational Site β Wuhan,
- GSK Investigational Site β Dijon,
- GSK Investigational Site β Lille,
- GSK Investigational Site β Chiba,
- GSK Investigational Site β Tokyo,
- GSK Investigational Site β Seoul,
- GSK Investigational Site β Seoul,
- GSK Investigational Site β Barcelona,
- GSK Investigational Site β Madrid,
- GSK Investigational Site β Madrid,
- GSK Investigational Site β MΓ‘laga,
- GSK Investigational Site β Manchester,
π° 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 Β§ 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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π‘ How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.