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Home / Malaria News / New Drug Synriam Approved to Treat Malaria in India

New Drug Synriam Approved to Treat Malaria in India

July 6, 2012 By Malaria.com Leave a Comment

A new drug to treat malaria, Synriam, was launched in India by Ranbaxy Laboratories Limited. The drug will provide additional options for malaria treatment as  traditional drugs become increasingly ineffective against the deadly malarial parasite because of acquired resistance to available medications.

Taken as a tablet once a day for three days, Synriam may be more effective, cheaper, and have fewer side effects and does not have to be taken with food, according to the University of Nebraska Medical Center (UNMC). From 2000 to 2010, Jonathan Vennerstrom, Ph.D., a professor at the UNMC College of Pharmacy, led an international team that created the drug compound that led to the development of Synriam. Developed by Ranbaxy Pharmaceuticals Limited, the medication now is approved for treatment in adults in India. The company also is working to create a children’s formula and make the drug available in Africa, Asia and South America.

“With more than 200 million cases of malaria each year, the potential impact this drug could have on saving and improving lives worldwide is significant,” Dr. Vennerstrom said. “That’s been our goal and now we are at the finish line.

Tim Wells, MMV’s chief scientific officer, said the completion of a phase III study in Indian adults and the approval of the combination by the Indian regulators was a major milestone. “We look forward to more data from patients in Africa and from studies with children, since this is where the vast majority of the disease is,” he said.

Courtney Fletcher, Pharm.D., dean of the UNMC College of Pharmacy, said another benefit of arterolane, the key component in the new drug invented by Dr. Vennerstrom, is it’s a synthetic. “This is an importance advance in antimalaria drugs. Since it’s a synthetic drug, it doesn’t depend on the availability of a natural plant source like some other antimalarials, which also makes it less expensive.”

Dr. Vennerstrom and his team also have developed a second drug candidate that might be even more superior than the first. It currently is being tested in phase II clinical trials by MMV in Bangkok, Thailand.

“This drug candidate seems to stay in the body longer, and therefore it may be possible to use a single dose instead of three doses,” Dr. Vennerstrom said. “We all forget to take our medications from time to time, so compliance becomes much easier when you have a single-dose drug.”

As a child of missionary parents working in Ethiopia, Dr. Vennerstrom took medications to prevent malaria.

Dr. Vennerstrom and his team received more than $12 million in grants from Medicines for Malaria Venture (MMV), a non-profit organization in Geneva, Switzerland. He has been studying malaria for more than 25 years. The research team included scientists at the Swiss Tropical and Public Health Institute in Switzerland and Monash University in Australia. MMV receives about 60 percent of its funding from the Bill and Melinda Gates Foundation.

“We were very fortunate to receive the support for our project from MMV,” he said. “It is always unpredictable whether or not a drug candidate will be successful.”

Source: University of Nebraska Medical Center (UNMC)

Filed Under: Malaria News Tagged With: arterolane, Courtney Fletcher, Jonathan Vennerstrom, Malaria Treatment, Medicines for Malaria Venture (MMV), Ranbaxy, Tim Wells, University of Nebraska Medical Center (UNMC)

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