A Phase 2 study of the efficacy and safety of PH-797804 taken for 12 weeks in adults with COPD taking a background of salmeterol/fluticasone combination

Mise à jour : Il y a 4 ans
Référence : EUCTR2010-024219-15

Femme et Homme

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Extrait

To evaluate the efficacy and safety/tolerability of 12 weeks administration of PH-797804 in adults with moderate to severe COPD (GOLD stage II/III) on a background of salmeterol xinafoate/fluticasone propionate combination.


Critère d'inclusion

  • Chronic Obstructive Pulmonary Disease (COPD)