Clinical Trials Logo

Clinical Trial Summary

This is a multi-center, randomized, blinded, placebo controlled study to evaluate the safety of GSK1278863 and its acute and short-term (e.g. 14d) effects on calf muscle endurance and walking ability in subjects with PAD and symptomatic claudication.


Clinical Trial Description

This is a multi-center, randomized, blinded, placebo controlled study to evaluate the safety of GSK1278863 and its acute and short-term (e.g. 14d) effects on calf muscle endurance and walking ability in subjects with PAD and symptomatic claudication. Functional assessments will be performed following a single high dose (300mg), a single low dose (15mg), and following 14 days of low dose treatment (15mg q.d.). The objectives of this study are to: 1) Evaluate the safety and tolerability of GSK1278863 administered as a single dose and as sub-chronic low dosing (i.e. 14 days) in subjects with peripheral artery disease; 2) To demonstrate the potential pharmacodynamic effect of GSK1278863 on functional measures of calf muscle endurance and fatigability and timed walking distance following a single high or low dose and after 14 days of multiple low dose administration in subjects with claudication-limited peripheral artery disease. In this hypothesis-generating study, multiple assessments of ambulatory and skeletal muscle function will be made during standardized tests of claudication-limited exercise performance, and 3). Characterize the relationship, if any, between the doses and plasma concentrations of GSK1278863 and the pharmacodynamic effects. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02135848
Study type Interventional
Source GlaxoSmithKline
Contact
Status Completed
Phase Phase 2
Start date October 15, 2010
Completion date November 1, 2011

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05783700 - Identification of Biomarkers for the Study of the Diabetic Foot and Evolution.
Recruiting NCT00542646 - Pilot Study to Evaluate the Safety and Preliminary Efficacy of the Peritec Peritoneal Lined Stent and Delivery System Phase 0
Completed NCT05710653 - Inter-individual Physiological Response to a Training and Detraining Period in Cardiometabolic Risk Factors Subjects N/A
Terminated NCT00518284 - Prevention of Restenosis Following Revascularization Phase 2
Completed NCT04585763 - Disrupt PAD+ Study With the Shockwave Medical M5+ Peripheral IVL System N/A
Not yet recruiting NCT05843929 - Prevalence of the Appearance of Diabetic Ulcers in Patients With 3D Insole and LSCI. N/A
Recruiting NCT05860764 - Vascular Amputee Physical Performance Qualitative (VAmPP-Q) Study
Recruiting NCT05720156 - Immunomodulatory Effects of PCSK9 Inhibition
Completed NCT04146493 - Heparin-Binding Protein and Heparins