Bengaluru, India: July 25, 2012 
             
            Commenting on the results, Chairman and  Managing Director Kiran Mazumdar-Shaw stated, "I am pleased to report that we have seen strong performances across all our  business verticals and this reflects the success of our segmented business  model. I draw attention to our R&D investments that have increased 75% YoY this  quarter. This increase arises from the enhanced spend on clinical development, that  is integral to delivering long-term sustainable growth. On the licensing front,  we are in discussions for several advancing research programs. We are hopeful  that many of these will be realized going forward. This will endorse our  R&D-led value creation strategy. We believe that the changing dynamics in  global healthcare are providing a number of exciting opportunities which are  well-aligned with our business strategy of delivering affordable products for  chronic therapies. I believe we will continue to make good progress through the  rest of the year.” 
          Highlights: 
          
            - Q1 FY13 financials reflect strong  performance across business verticals:
 
            
              - Biopharma Business grew 23% YoY on  traction in all segments.
 
              - Branded Formulations robust 52% YoY growth  led by Oncology, Diabetology and Comprehensive Care.
 
              - Research Services (Syngene and  Clinigene) grew 40% YoY.
 
             
            - EBITDA and PAT margins at 23% and 13%  respectively. EBITDA and PAT margins largely impacted by increased R&D  spend.
 
            - Global Phase I trial for biosimilar  Glargine completed successfully.
 
            - Itolizumab: 52-week results from  Phase III trial in Psoriasis confirm achievement of primary endpoint and  multiple secondary endpoints.
 
            - Inauguration of Abbott Nutrition  R&D Center, a state-of-the-art nutrition R&D hub in Biocon Park.
 
           
          Business Performance and Outlook (Vertical-wise) 
             
            Biopharma: Small Molecules & Biosimilars 
            The biopharma business built on the growth momentum  from the previous quarters, with robust sales in Statins and increased traction  in the Insulins and other biopharma portfolios. 
          Our Fidaxomicin commercialization partner, Optimer Pharma,  has introduced the product in Europe with the first phase rolled out in select  East European nations.  
          The global phase I study for  biosimilar Insulin Glargine has been successfully completed with positive Pharmaco-Kinetic (PK) and Pharmaco-Dynamic (PD) data. The trial  met all its primary and secondary endpoints to unequivocally establish PK-PD  equivalence between our biosimilar Insulin Glargine and innovator product  
            (Lantus®).  
   
            Expressing satisfaction at the outcome of this study, Dr.  Abhijit Barve, President R&D, Biocon Limited said, “These successful results pave  the way for biosimilar drug approvals for Biocon across the globe.”  
          Branded Formulations  
            Our  branded formulations vertical posted a robust YoY growth of 52% propelled by  our Oncology, Diabetology and Comprehensive Care divisions. INSUPenTM,  our insulin pen, launched in November 2011 has garnered accolades from  doctors and patients alike for its thoughtful design and usability. The patient  care model spanning across the pen’s features and the on-call/on-field support  have also been well received. 
          This  quarter was also marked by the launch of Xortib® and Genexor® in Oncology and  Matabac® in the Comprehensive Care division. 
          Novel Molecules 
            Biocon  continues to make excellent progress on its various novel assets. We continue  our engagement with potential partners for our licensable assets: IN-105 and  Itolizumab. The 52-week data from the Phase III trial in Psoriasis confirms the  achievement of primary endpoint and multiple secondary endpoints. We intend to  file for regulatory approval and marketing authorization for the treatment of  Psoriasis, for this molecule in the Indian market shortly. 
          Research Services (Syngene and  Clinigene) 
            The first quarter of FY13  witnessed sustained impetus in our research services arm which grew 40% YoY. Commenting  on this performance, Peter Bains, Director, Syngene  International, said,"  Syngene and Clinigene started the year well, with particularly strong  performances in biology and custom synthesis". The highlight of  the quarter was the inauguration of the Abbott Nutrition Research &  Development (ANRD) center. ANRD is committed to developing products for  maternal and child nutrition & diabetes care, attuned to the needs of the  Indian sub-continent. A dedicated team of over 50 scientists will be working at  this centre. 
          About Biocon 
            Biocon Limited (BSE  code: 532523, NSE Id: BIOCON, ISIN Id: INE376G01013) is India's premier biotechnology company with  a strategic focus on biopharmaceuticals and research services. Established in 1978 by Dr.  Kiran Mazumdar-Shaw, the Group is an integrated, innovation-driven healthcare  enterprise with offerings that  traverse the entire drug development value chain. Balancing its novel  molecule research pipeline with a diversified product portfolio, Biocon  delivers affordable solutions to partners and customers in over 70 countries  across the globe. Many of these products have USFDA and EMA acceptance. Stellar  products from Biocon's stable include the world's first Pichia-based recombinant human Insulin, INSUGEN® and glargine,  BASALOG® coupled with a state of  the art insulin pen device, INSUPen® and India's first indigenously produced monoclonal  antibody BioMAb-EGFR®. 
  archive.biocon.com 
   
  Disclaimer 
Certain statements in  this release concerning our future growth prospects are forward-looking  statements, which are subject to a number of risks, uncertainties and  assumptions that could cause actual results to differ materially from those  contemplated in such forward-looking statements. Important factors that could  cause actual results to differ materially from our expectations include,  amongst others general economic and business conditions in India, our ability  to successfully implement our strategy, our research and development efforts,  our growth and expansion plans and technological changes, changes in the value  of the Rupee and other currency changes, changes in the Indian and  international interest rates, change in laws and regulations that apply to the  Indian and global biotechnology and pharmaceuticals industries, increasing  competition in and the conditions of the Indian biotechnology and  pharmaceuticals industries, changes in political conditions in India and  changes in the foreign exchange control regulations in India. Neither our  company, our directors, nor any of our affiliates, have any obligation to  update or otherwise revise any statements reflecting circumstances arising  after this date or to reflect the occurrence of underlying events, even if the  underlying assumptions do not come to fruition. 
 
 
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