Adcirca (tadalafil) is an oral inhibitor of phosphodiesterase type 5 (PDE5), the enzyme responsible for the degradation of cyclic guanosine monophosphate (cGMP). Pulmonary hypertension is the result of upregulation of PDE5 gene expression, causing vasoconstriction in the lung. Inhibition of PDE5 by tadalafil increases the concentrations of cGMP resulting in elaxation of pulmonary vascular smooth muscle cells and vasodilation of the pulmonary vascular bed.
Adcirca is specifically indicated for the treatment of pulmonary arterial hypertension (WHO Group I) to improve exercise ability.
Adcirca is supplied as a 20 mg tablet for oral administration. The recommended initial dose of the drug is 40 mg (two 20 mg tablets) taken once daily with or without food. Dividing the dose (40 mg) over the course of the day is not recommended.
FDA approval of Adcirca for pulmonary hypertension was based on a randomized, double-blind, 16 week placebo-controlled study in 405 subjects (mean age 54 years), 341 of whom completed the study. The subjects were randomly assigned to 1 of 5 treatment groups (tadalafil 2.5, 10, 20, 40 mg, or placebo). The primary efficacy endpoint was the change from baseline at week 16 in 6-MWD. The mean baseline 6-minute walk distance (6-MWD) was 343 meters. In the Adcirca 40 mg treatment group, the placebo-adjusted mean change increase in 6-MWD was 33 meters (p=0.0004). The improvement in 6-MWD was apparent at 8 weeks of treatment and then maintained at week 12 and week 16. There was less clinical worsening (defined as death, lung transplantation, atrial septostomy, hospitalization because of worsening PAH, initiation of new PAH therapy or worsening WHO functional class) in the Adcirca 40 mg group compared to the placebo group and the groups that used lower doses of Adcirca.
A long-term extension study was conducted in 357 subjects from the placebo-controlled study. Of these, 311 subjects were treated with tadalafil for at least 6 months and 182 for 1 year (median exposure 356 days; range 2 days to 415 days). The survival rate in the extension study was 96.5 per 100 patient years.
Adverse events associated with the use of Adcirca may include, but are not limited to, the following:
Adverse reactions identified during post-approval use of tadalafil:
Adcirca (tadalafil) is an oral inhibitor of phosphodiesterase type 5 (PDE5), the enzyme responsible for the degradation of cyclic guanosine monophosphate (cGMP). Pulmonary arterial hypertension is associated with impaired release of nitric oxide by the vascular endothelium and consequent reduction of cGMP concentrations in the pulmonary vascular smooth muscle. PDE5 is the predominant phosphodiesterase in the pulmonary vasculature. Inhibition of PDE5 by tadalafil increases the concentrations of cGMP resulting in elaxation of pulmonary vascular smooth muscle cells and vasodilation of the pulmonary vascular bed.
For additional information regarding Adcirca or pulmonary arterial hypertension, please visit the Adcirca web page.
The Adcirca (tadalafil) drug information shown above is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.