Both recombinant products are expected to become commercially available by 2008-2009. |
The first product developed under license from Liposis, a UK-based company, aims to reduce the frequency with which CRF patients are injected with poly ethylene glycol (PEG) . Currently, the drug has to be injected twice a week. SII's drug will reduce the frequency to once in two weeks. |
"We are developing a drug with a longer half life, using a novel method. It is much better than what is available in the market," said Umesh Shaligram, director, production,Serum Institute. |
Shaligram said that the new drug, which is being developed from a known molecule, will be non-toxic and will have higher level efficiency than PEG. |
It has been proved that continued use of PEG for 2-3 decades can cause renal toxicity. The new drug is bio-degradable, added Shaligram. |
Once developed, the drug will be sold under a co-owned IPR (intellectual property rights) with Liposis. |
The worldwide market for CRF drugs is estimated at $ 6 billion a year. It is currently undergoing animal trials and is slated to go for human trials in a year. SII is considering a commercial release around 2009-2010. |
Serum Institute is also working on a drug to combat the side effects of chemotherapy and increase the count of white blood cells in cancer patients. The process being used is similar to the interferon-based drugs used for Hepatitis-C, said Shaligram. |
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