Galapagos has initiated a Phase I Proof-of-Mechanism trial to evaluate GLPG0492 for the treatment of cachexia and Duchenne muscular dystrophy.
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The trial aims to evaluate the tolerability, pharmacokinetics (PK) and safety of GLPG0492 on muscle function in healthy volunteers.
Earlier, in a Phase I study in healthy volunteers, GLPG0492 demonstrated good safety and a PK profile which supports once- daily oral dosing.
Galapagos Development SVP Piet Wigerinck said this is the third time this year they initiate a clinical study designed to give insight into the potential clinical benefits of a candidate drug.
"We aim to finalize this study by the end of 2011 before further evaluating the compound in a patient population," Wigerinck said.
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