Bengaluru-based Biocon has added Rs 21,000 crore in market value over the past couple of years, its stock jumping 230 per cent to Rs 512 a share on Monday. Well in contrast to the 22 per cent drop in the Nifty pharma index. As the US government takes steps to bring down drug prices, stocks of Indian pharmaceutical suppliers dropped. For instance, Sun Pharmaceutical lost 30.5 per cent in this period, wiping away Rs 56,000 crore in market value for investors.Investors' love for Biocon, the biosimilars maker, has not come easily. For, developing a copycat version of biologic drugs is far more expensive and takes much longer than developing a generic version of chemical drugs. Biocon was for long a laggard in the Indian pharma pack. A five-year analysis of Indian pharma stocks showed it grew 61 per cent in the first three years, much below the 98 per cent achieved by the Nifty Pharma.Analysts estimate the cost of developing a generic drug rarely exceeds $5 million (Rs 32 crore) or takes ..
The stock surged 14% to Rs 510, also its all-time high on the BSE in early morning trade on back of heavy volumes.
Kiran Mazumdar Shaw is the chairperson and managing director of Biocon , the company which recently received US Food and Drug Administrator's approval for its anti cancer drug Trastuzumab
A biosimilar is a copy of an innovator biologic drug and is made of living cells
May start monetising its biosimilars by FY19, 30-40% jump in profit likely
At present, Biocon sells branded formulations, including biologics and biosimilars, in India and the UAE
The stock surged 7% to Rs 420 on the BSE in early morning deal, trading close to its 52-week high of Rs 424 touched on July 19, 2017 in intra-day trade
Weak Q2 results led to downward revision of estimates
The stock moved higher by 5.5% to Rs 363 on BSE in noon deal after the company said the USFDA has issued a Complete Response Letter (CRL) for proposed Biosimilar Pegfilgrastim.
Biotechnology firm Biocon today said the US health regulator has issued complete response letter (CRL) for proposed biosimilar Pegfilgrastim, indicated for use in the treatment of cancer. The company, however said it does not expect this CRL to impact the commercial launch timing of biosimilar Pegfilgrastim in the US. This product is a part of the biosimilars portfolio being developed jointly by Biocon and Mylan. "The U.S. Food and Drug Administration has issued a complete response letter (CRL) for Mylan's Biologics License Application (BLA) for MYL-1401H, a proposed biosimilar pegfilgrastim," Biocon said in a regulatory filing. It further said: "The CRL relates to the pending update of the BLA with certain CMC data from facility requalification activities post recent plant modifications. The CRL did not raise any questions on biosimilarity, pharmacokinetic/ pharmacodynamic data, clinical data or immunogenicity". "We do not expect this CRL to impact the commercial ..
The stock was up 5.3% to Rs 353 on BSE in early morning trade.
Biocon's Malaysia facility was inspected by the European Medicines Agency (EMA) in April 2017
In past one month, the stock was down 21% against 2% decline in Sensex.
The stock soared 8.88% to settle at Rs 399.20 on BSE
The stock surged 10% to Rs 404 on BSE in early morning trade on back of heavy volumes.
It touched an intraday high of Rs 360 and an intraday low of Rs 340
French regulator's observations about the formulation facilities will delay product launches
Kiran Mazumdar Shaw, chairman and managing director of Biocon says that India's largest Biopharma company will take remedial measures at its drug product facility within a quarter and ask the French medical regulator to inspect its facility again to get certified for good manufacturing practice (GMP). Biocon has filed for regulatory approvals to market its biosimilars - Trastuzumab and Pegfilgrastim, in the highly regulated European market with the European Medicines Agency (EMA). French National Agency for Medicines and Health Products Safety or ANSM conducted the mandatory site inspections on behalf of EMA as part of its pre approval procedures. "There are no data integrity issues and no product quality issues. The concerns that they have expressed, we are taking remedial measures in short time, within a quarter and as soon as we are ready, we will ask them for a re-inspection," said Shaw. "There will be no material impact"ANSM had conducted audits in March and approved GMP ...
Welcoming Mazumdar-Shaw, Deepika said mental health is an area that requires sustained effort
The stock hit three-month low of Rs 984 on BSE in intra-day trade