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ACTIVE NOT RECRUITING
NCT04452955
PHASE2

A Study to Assess Safety and Efficacy of PRL3-Zumab in Patients With Solid Tumors

Sponsor: Intra-IMMUSG Pte Ltd

View on ClinicalTrials.gov

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

BIOLOGICAL

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