Strides announces WHO pre-qualification for Artemether+Lumifantrine

Strides Arcolab announced the World Health Organization (WHO) pre-qualification of its anti-malarial product Artemether + Lumifantrine (AL) tablets. AL constitutes over 80 per cent of Artemesinin Combination Therapy (ACT) procured under Global Fund and other similar programmes. The benefits of ACTs are their high efficacy, fast action and reduced likelihood of resistance developing. WHO currently advises that all malaria cases should be treated with ACT.

Over 300 million new malaria cases were reported in Africa alone in 2011. It is estimated that only about 10 per cent of the actual incidence gets reported. ACT procurement plan for 2013 is estimated to be in the region of $450 million.

Commenting on the development, Manish Gupta, Chief Executive Officer-Pharma, Strides Arcolab stated, “This approval is another initiative by Strides to make high quality, affordable medicines available in the African sub-continent and other middle-income countries and compliments our basket of products in the anti-HIV/AIDS and anti-TB therapies for these markets.”

With this approval, Strides becomes the only player to provide complete treatment portfolio in the major diseases of HIV, TB and malaria, which continue to plaque the low and middle-income countries.

The product will be manufactured at the US-FDA approved and WHO pre-qualified facility in Bangalore. The supplies of the product will commence immediately.

EP News Bureau Mumbai

Comments (0)
Add Comment