Long-term safety and efficacy of aliskiren and valsartan combination with or without the addition of HCT in patients with hypertension

Curr Med Res Opin. 2010 Dec;26(12):2841-9. doi: 10.1185/03007995.2010.528282. Epub 2010 Nov 9.

Abstract

Objective: To assess the long-term safety and antihypertensive efficacy of aliskiren/valsartan 300/320 mg combination.

Methods: This was a 54-week, multicenter, open-label study (core phase), followed by a 26-week extension phase. Efficacy variables were change in msDBP and msSBP from baseline to endpoint (54-week and 80-week). Safety was assessed by monitoring and recording adverse events (AEs). ClinicalTrials.gov Identifier: NCT00386607 RESULTS: A total of 601 patients (msDBP ≥ 90 and <110 mmHg) entered the 54-week core study. Optional add-on HCT was allowed at week 10 onwards if BP was ≥ 140/90 mmHg at two consecutive visits. Of the 486 patients completed the core study, 180 patients entered the extension phase and received aliskiren/valsartan and add-on HCT (12.5 or 25 mg). Overall the combination of aliskiren/valsartan was well-tolerated and the majority of AEs were mild-to-moderate in severity. The incidence of SAEs was low (core phase: n = 22 [3.7%]; extension phase: n = 4 [2.2%]). Elevated serum potassium (>5.5 mmol/L at any time during the study) was observed in 21 (3.6%) patients. The majority of these elevations were transient and returned to normal in subsequent visits, and the discontinuation rate due to elevated serum potassium was low (0.3% [n = 2]). Decreased serum potassium levels (<3.5 mmol/L at any time during the study) was observed in 26 (4.4%) patients, mainly in patients receiving aliskiren/valsartan/HCT (n = 22; 7.1%). At the 54-week endpoint, a mean BP reduction of 20.5/13.4 mmHg from baseline (baseline BP: 152.9/97.0 mmHg) was observed and 66.9% (n = 398/595) of patients achieved BP control with aliskiren/valsartan with or without HCT. At the end of the extension phase (80-week endpoint), additional reduction in BP was obtained (overall, 28.8/18.3 mmHg) and 86.6% (n = 155/179) of patients achieved BP control with aliskiren/valsartan/HCT. A limitation is the absence of an active comparator group.

Conclusion: Long-term treatment with the combination of aliskiren/valsartan with or without HCT provided clinically meaningful BP reductions and high rates of BP control and was well-tolerated.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Algorithms
  • Amides / administration & dosage*
  • Amides / adverse effects
  • Antihypertensive Agents / administration & dosage
  • Antihypertensive Agents / adverse effects
  • Drug Combinations
  • Drug-Related Side Effects and Adverse Reactions / epidemiology
  • Female
  • Follow-Up Studies
  • Fumarates / administration & dosage*
  • Fumarates / adverse effects
  • Humans
  • Hydrochlorothiazide / administration & dosage*
  • Hydrochlorothiazide / adverse effects
  • Hypertension / drug therapy*
  • Hypertension / epidemiology
  • Incidence
  • Male
  • Middle Aged
  • Tetrazoles / administration & dosage*
  • Tetrazoles / adverse effects
  • Time Factors
  • Treatment Outcome
  • Valine / administration & dosage
  • Valine / adverse effects
  • Valine / analogs & derivatives*
  • Valsartan
  • Young Adult

Substances

  • Amides
  • Antihypertensive Agents
  • Drug Combinations
  • Fumarates
  • Tetrazoles
  • Hydrochlorothiazide
  • aliskiren
  • Valsartan
  • Valine

Associated data

  • ClinicalTrials.gov/NCT00386607