Eli Lilly has outlined its growth strategy at its annual meeting with the investment community; chief among the company?s goals are plans to launch two new drugs per year beginning in 2013 and a strategy to increase its position in emerging markets.
Eli Lilly has outlined its growth strategy at its annual meeting with the investment community; chief among the company’s goals are plans to launch two new drugs per year beginning in 2013 and a strategy to increase its position in emerging markets.
“In 2009, Lilly has once again exhibited strong performance in a tough environment, and we've continued with a series of actions aimed at speeding innovation to patients and delivering greater value to our customers," said John C. Lechleiter, Lilly's President and CEO, in a company press statement. "Through these actions and more, we are transforming Lilly to compete and to win in an ever-more demanding and challenging environment. We see a divergence of strategies among our peers to deal with these challenges, including the wave of consolidation this year. Many companies are seeking to lower risk by reducing their focus on innovative medicines. This is not our path. Our strategy is to create value by accelerating the flow of innovative new medicines that provide improved outcomes for individual patients.”
The company plans to have at least 10 molecules in Phase III clinical development by the end of 2011 and hopes to launch two new drugs per year beginning in 2013, according to comments by Steve M. Paul, executive Vice President of Science and Technology, and President of Lilly Research Laboratories, in the company press release. He pointed to efforts by the company to accelerate drug discovery and development to help meet these goals. These include its phenotypic drug-discovery programme, risk-sharing collaborations, the early-stage work of its Chorus team (a global network of internal and external partners in drug development) and its new Development Center of Excellence.
Eli Lilly currently has 60 new molecules in development, including 25 in Phases II and III, according to Paul. He added that biotechnology-based molecules now represent more than one-third of the company’s clinical pipeline. Lilly further strengthened its position in biologics through the acquisition of the biopharmaceutical company ImClone Systems (NY, USA) in 2008.
Lilly recently refocused its operations around five business units: oncology, diabetes, established markets, emerging markets, and animal health, and part of the company’s growth strategy is to enhance its position in seven key emerging markets: Brazil, Russia, India, China, Mexico, South Korea and Turkey, with its top priority being China. These seven markets accounted for 9% of the company’s revenues in the first nine months of 2009. In the first 9 months of 2009, the company’s sales in China increased 20%, and Lilly doubled the size of its affiliate in China from 1100 to 2200 employees. The company is currently building a second insulin-manufacturing plant in Suzhou. In 2008, Lilly’s sales in China were more than $200 million.
Lilly has a three-pronged strategy to increase its growth in emerging markets. First, it says it will seek to maximize core assets, which includes both patented and postpatent drugs, and will seek to accelerate new product launches and to capitalize on longer product life cycles in select countries, including China. Secondly, it wants to add select non-Lilly drugs to build upon its core therapeutic focus, particularly in diabetes, oncology, and neuroscience, which could include product acquisitions and copromotion and comarketing agreements. And thirdly, the company wants to establish local alliances in select countries where the company’s current infrastructure is not well-suited to capture growth.
Offering a long-term outlook for its overall performance, the company expects to achieve annual revenues of at least $20 billion between 2012 and 2014.
Why is the PDA Pharmaceutical Microbiology Conference the Hottest Ticket in the Industry?
October 10th 2024Get a glimpse of the power and popularity behind the PDA Pharmaceutical Microbiology Conference from two planning committee members, Julia Marre, PhD (Associate Director, Scientific and Regulatory Affairs at Pocket Naloxone Corp) and Dawn Watson (Executive Director, Global Micro Quality and Sterility Assurance at Merck). This candid conversation reveals why this industry event is so influential…and always sold out! The speakers discuss what makes the PDA Pharmaceutical Microbiology Conference so vital to industry professionals, as well as how to become a part of this dynamic professional community.
Navigating Annex 1 for Early Phase Sterile Fill Finish in Clinical Supplies
November 21st 2024Stay compliant with Annex 1 for early phase sterile fill finish processes. Discover how to implement robust contamination control strategies, integrate isolator technology, and conduct integrity testing to meet stringent European Union standards. The guide provides a comprehensive look at key elements such as PUPSIT, critical zone controls, and monitoring and training for aseptic processes.
Your Ultimate Guide for CMC Testing Support for Gene and Cell Therapy
November 21st 2024Explore the complexities of gene and cell therapy development with our comprehensive guide to Chemistry, Manufacturing, and Controls (CMC) testing. Learn how our expertise ensures the safety, potency, and quality of advanced therapies, supporting your journey from product development through regulatory approval.