Drug firm Ranbaxy Laboratories has received regulatory nod to launch its indigenously developed anti-malarial drug Synriam in 7 African nations.
The company has received regulatory approval to launch its first New Chemical Entity (NCE) Synriam in seven African countries —— Nigeria, Uganda, Senegal, Cameroon, Guinea, Kenya and Ivory Coast, Ranbaxy Laboratories said in a statement.
The product has already been launched in Uganda and will be made available in other six countries towards the end of January 2015, it added.
The new drug conforms to the recommendations of the World Health Organisation (WHO) for using combination therapy in malaria.
Synriam provides quick relief from most malaria—related symptoms, including fever, and has a high cure rate of over 95 per cent, Ranbaxy said.
The dosage regimen for the product is simple as the patient is required to take just one tablet per day for three days, compared to other medicines where two to four tablets are required to be taken, twice daily, for three or more days, Ranbaxy said.
“Since Synriam has a synthetic source, unlike artemisinin based drugs, production can be scaled up whenever required and a consistent supply can be maintained at a low cost,” it added.
Ranbaxy had commenced the research on the drug in 2003, and received the Drug Controller General of India’s (DCGI) approval in 2011 to manufacture and market it in India.
The product is used for treatment of acute uncomplicated “Plasmodium falciparum malaria” in patients aged 12 years and above, Ranbaxy said.
The company is also conducting Phase III clinical trials for the paediatric formulation of Synriam in paediatric patients suffering from the same problem, it added.
Shares of Ranbaxy Laboratories were today trading at Rs 643.90 per scrip in the afternoon trade on the BSE, up 0.12 per cent from their previous close.