Postmarketing Surveillance Study on Atorlip-F (Atorvastatin/Fenofibrate combination)

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18 Mar, 14

PROMISE Trial

Aim

To evaluate the efficacy and safety of ATORLIP F (atorvastatin 10 mg plus micronized fenofibrate 160 mg tablets) under real world conditions in Indian patients with combined hyperlipidemia.

Participating Centers

20 centres across India.

Study Design

  • Open label, non-comparative, practice based study
  • Patients enrolled at the discretion of the treating physician.

Patients

Combined hyperlipidemia

Dosage of Atorlip F

One tablet daily

Study Duration

6 months

Parameters Evaluated

  • Efficacy: Effect on lipids and 10-year risk of myocardial infarction (estimated) by PROCAM risk calculator at 3 months.
  • Safety: Assessed at 3 months and 6 months including effect on liver enzymes.

Results

ATORLIP F resulted in significant reductions in LDL cholesterol by 28.9% (p<0.001).

HDL cholesterol was significantly increased by 11.3% with ATORLIP F (p<0.001). In patients with low HDL(<40 mg/dl)at baseline, ATORLIP F increased HDL by 19.9% (p<0.001).

Non-HDL cholesterol was significantly reduced by 30.9% (p<0.001)

Triglyceride (TG) was significantly reduced by 36.6% (p<0.001)

ATORLIP F significantly reduced TG/HDL ratio, the surrogate marker of small dense LDL by 43.4%. In addition ATORLIP F was associated with attainment of TG/HDL goal <3.8 in 135 patients (46.1%).

ATORLIP F also yielded significant reductions in total cholesterol and other lipid ratios

ATORLIP F significantly reduced the probability of having a myocardial infarction in the next 10 years by 54.3%.

Safety:
  • Total 8 patients experienced adverse events viz., fatigue, nausea, body ache and gastritis, all of which were of mild nature and transient.
  • No patient discontinued therapy due to adverse events
  • None of the patients reported myopathy or rhabdomyolysis with ATORLIP F.
  • There were no clinically significant increase in SGOT and SGPT at 3 months and 6 months after therapy with ATORLIP F. Further none of the patients had an increase greater than 3 times upper limit of the normal for both this enzymes.
  • Tolerability of ATORLIP F was rated excellent or good by the study investigators in 93.5% patients.

Conclusion

  • Thus, Atorlip-F represents an effective and safe therapeutic strategy for the management of combined hyperlipidemia in Indians under real world conditions.
  • Improvements in lipids with Atorlip-F may significantly reduce MI risk.

The Ind Pract 2009;62:75-82