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Clinical Trial Summary

The purpose of the study is to assess the safety and tolerability of RXC007 when given for 12 weeks (84 days), alone and in combination with nintedanib or pirfenidone.


Clinical Trial Description

The purpose of this study is to investigate the study drug RXC007. The main objectives of this study are as follows: - To determine the safety and tolerability (degree to which side effects of a drug can be tolerated) of RXC007 when it is administered as twice daily doses over a period of up to 12 weeks (84 days). - To investigate the concentration of RXC007 (how much drug is in your blood), how this changes over a period of time and to evaluate whether there are differences in the concentration between different dose strengths of RXC007. - To investigate the effect of RXC007 on the body (known as pharmacodynamics) by analysing the levels of certain biomarkers in the body and to assess the effect of RXC007 on markers associated with Idiopathic Pulmonary Fibrosis (IPF). Biomarkers are markers within the body such as a molecule or compound made by cells in the body, which can be measured and used to identify a particular disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05570058
Study type Interventional
Source Redx Pharma Plc
Contact Helen Timmis, MD
Phone +44 01625 469900
Email h.timmis@redxpharma.com
Status Recruiting
Phase Phase 2
Start date September 8, 2022
Completion date June 2024

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