drugset / Trial / NCT03733990

A Study to Evaluate Safety, Tolerability and Preliminary Efficacy of FP-1305 in Cancer Patients (MATINS)

NCT03733990

Phase 1/2 Completed 216 enrolled Faron Pharmaceuticals Ltd
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a first in human study to identify whether FP-1305 is suitable to use in humans. The previous pre-clinical studies have demonstrated that FP-1305 binds to a receptor known as CLEVER-1. CLEVER-1 has been shown to support tumour growth. No significant adverse events were witnessed in primates and the dose used will be 300 fold lower than the dose provided to primates which showed no toxicity. The patients with advanced melanoma, uveal melanoma, cholangiocarcinoma, gallbladder cancer, ER+ breast, gastric, ovarian, pancreatic, colorectal, liver or anaplastic thyroid cancer who have exhausted all licenced therapeutic options will die due to their disease. Based on the investigator's existing data CLEVER-1 is expressed in these tumour types. Inhibition of CLEVER-1 with FP-1305 may have an anti-tumour effect in these patients.

Timeline

Start
2018-12-03
Primary completion
2023-09-06
Completion
2023-10-31

Drugs

EvaluationDrugModalityDoseRoute
Subject bexmarilimab Monoclonal antibody 0.1 mg/kg
Subject bexmarilimab Monoclonal antibody 0.3 mg/kg
Subject bexmarilimab Monoclonal antibody 1 mg/kg
Subject bexmarilimab Monoclonal antibody 3 mg/kg
Subject bexmarilimab Monoclonal antibody 10 mg/kg
Subject bexmarilimab Monoclonal antibody 30 mg/kg

Indications