A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Clinical Activity of GSK5733584 for Injection in Subjects With Advanced Solid Tumors
GlaxoSmithKline
Summary
The goal of this study is to assess the safety and tolerability of GSK5733584. The study will also see how the levels of GSK5733584 change over time at different dose amount.
Eligibility
- Age range
- 18+ years
- Sex
- All
- Healthy volunteers
- No
Inclusion Criteria: * Males or females aged 18 years or older (≥18 years). * Participants with pathologically confirmed advanced solid tumor (who have failed or are intolerant to standard of care). * PROC cohort 1. Histologically documented, advanced (metastatic and/or unresectable) high-grade serous/endometrioid ovarian, primary peritoneal, or fallopian tube cancer. 2. Must have received or are intolerant to 1 but no more than 3 lines of prior systemic therapy. 3. Platinum-resistant disease, defined as progression or relapse within 6 months after the completion of platinum-based thera…
Interventions
- DrugGSK5733584
GSK5733584 will be administered
Locations (47)
- GSK Investigational SiteLake Mary, Florida
- GSK Investigational SiteFairway, Kansas
- GSK Investigational SiteBoston, Massachusetts
- GSK Investigational SiteBoston, Massachusetts
- GSK Investigational SiteDetroit, Michigan
- GSK Investigational SiteGrand Rapids, Michigan