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A Study to Assess Safety and Efficacy of PRL3-Zumab in Patients With Solid Tumors
Sponsor: Intra-IMMUSG Pte Ltd
Summary
This is a multi-center, Phase 2, open-label, single dose level study of PRL3-zumab monotherapy in patients with unresectable or metastatic solid tumor.
Official title: An Open Label, Multicenter, Safety and Efficacy Phase 2 Study of PRL3-Zumab in Solid Tumors
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
51
Start Date
2020-12-12
Completion Date
2026-03-01
Last Updated
2025-12-02
Healthy Volunteers
No
Conditions
Interventions
PRL3-zumab
Starting dose of 6 mg/kg will be administered as IV infusion over 60 minutes every 2 weeks (±2 days)
Locations (5)
HonorHealth Research
Scottsdale, Arizona, United States
St. Jude Medical Center
Fullerton, California, United States
The Angeles Clinic
Los Angeles, California, United States
Norton Healthcare
Louisville, Kentucky, United States
Comprehensive Cancer Centers of Nevada
Las Vegas, Nevada, United States