Type | Subsidiary |
---|---|
Industry | Pharmaceuticals & Biotherapeutics |
Founded | 1995 |
Fate | Acquired by Vertex Pharmaceuticals |
Aurora Biosciences was a biotechnology company founded in 1995 in San Diego to commercialize fluorescence assays based on Roger Y. Tsien's discoveries concerning green fluorescent protein and its uses in basic research - work for which Tsien eventually won the 2008 Nobel Prize in chemistry along with two other chemists.
Aurora was formed at a time when established pharmaceutical companies were seeking to harness the fruits of the Human Genome Project, which had overwhelmed them with potential drug targets, and the explosion of new research tools enabled by biotechnology, as well as revolutions in chemistry that allowed many more, and many more kinds, of potential drugs to be made.
In 2000, as the investment climate turned against platform companies, Aurora started to work on its own drug discovery programs. It struck a deal with the Cystic Fibrosis Foundation under which CFF invested $30 million in Aurora, with the promise of further investment based on success, in exchange for Aurora agreeing to discover and develop new drugs to treat cystic fibrosis. [1] This was one of the first examples of venture philanthropy. Aurora was acquired by Vertex Pharmaceuticals in 2001, [2] but the arrangement with CFF continued and resulted in the discovery of ivacaftor in 2005 and the approval of that drug in 2012.[ citation needed ]
Aurora Biosciences was founded in 1995 in San Diego to commercialize fluorescence assays based on Roger Y. Tsien's discoveries concerning green fluorescent protein and its uses in basic research, work for which he eventually won the 2008 Nobel Prize in chemistry along with two other chemists. [3] [4] [5] Aurora was incorporated in California in May 1995 and was reincorporated in Delaware in January 1996. [6] Tsien co-founded the company with two colleagues from the faculty of University of California, San Diego, Charles Zuker and Michael Geoffrey, and a venture capitalist, Kevin J. Kinsella of Avalon Ventures. The first business people they brought on were Tim Rink, who became Chairman and CEO, and Frank Craig to lead assay R&D and Harry Stylli to drive sales in the assay business. [7] [8]
Aurora received its first round of funding of $13.6 million in March 1996 [7] and was able to raise $40 million in its IPO in 1997 on the NASDAQ exchange, [6] [9] even though it held the offering just after a bull run, when the markets had somewhat soured on biotechnology IPOs. [9] [10]
Aurora's business was focused on providing assay development services to companies trying to discover drugs, and to develop and sell new high-throughput screening (HTS) equipment and assays to use on the equipment. [11] They were leaders in the effort to increase throughput and lower the cost of screening that took the field from screening 800 compounds a week in 1986 to being able to screen 100,000 compounds in a day, or "ultra HTS". [3] [12] [13] The business model of providing discovery services based on a "platform technology" was typical in the late 1990s, as established pharmaceutical companies were seeking to harness rapid advances in biotechnology, and small biotech companies making those advances useful proliferated. [14] [15]
Besides deploying its know-how in use of GFP as a reporter gene, scientists at Aurora invented CCF2, a dye combining fluorescein and 7-hydroxycoumarin that creates a fluorescent signal when cleaved by beta-lactamase; this allowed beta-lactamase to be used as a reporter gene. The BLA system has become widely used in research labs. [16] [17] Aurora also sold proprietary stable cell lines containing its reporters for use in assays conducted with its equipment, and was unusual among its peers for requiring milestones and royalty payments on drugs brought to market that were discovered using its cell lines. [18]
By 2000 its customers included Becton Dickinson, Bristol-Myers Squibb, Eli Lilly, Roche, Genentech, Glaxo Wellcome, Merck, the National Cancer Institute, Pfizer, Pharmacia, Warner-Lambert, and Wyeth Ayerst, [19] and it was recognized as the industry leader in assay development and high-throughput screening services. [20] [21]
In 2000 Aurora changed its business model to focus on discovering and developing new drugs itself, rather than providing services to help others do so, as part of the general trend in the biotechnology industry away from discovery platforms and toward product-focused companies, which occurred as the hype over the "genomic revolution" waned. [15] [22] [23] In that year it received a $30 million investment from Cystic Fibrosis Foundation to identify and develop up to three drug candidates to treat cystic fibrosis; this transaction was one of the first examples of venture philanthropy. [24] [25] [26] That funding eventually grew to $150 million and led to the discovery of ivacaftor in 2005 and contributed to the eventual FDA approval of that drug in 2012. [27]
In 2000 Aurora acquired PanVera, a contract manufacturing organization that specialized in protein production and that also sold assays, for $86 million in stock. [28]
In 2001, Aurora was acquired by Vertex Pharmaceuticals for $592 million in stock. [29] [30] Vertex wanted access to Aurora's insight into drug targeting of ion channels and G-protein coupled receptors, wanted to apply Aurora's assay expertise to its programs in kinase inhibitors and caspase inhibitors, and wanted access to PanVera's protein production capacities. [31] [32]
In 2003 Vertex sold PanVera to Invitrogen for $95 million in cash and $10 million in assumption of debt and other costs. [33] Later that year Vertex sold Aurora's instrument business to a private equity group, which created Aurora Discovery from it. [34] Aurora Discovery eventually changed its name to Aurora Biotechnologies, and in 2009 was acquired by Nexus Biosystems, which made and sold automated biobank and chemical storage equipment. [35] [36]
Vertex retained Aurora's drug discovery facility and staff in San Diego; ivacaftor was discovered there in 2005. [22] [37]
Chiron Corporation was an American multinational biotechnology firm founded in 1981, based in Emeryville, California, that was acquired by Novartis on April 20, 2006. It had offices and facilities in eighteen countries on five continents. Chiron's business and research was in three main areas: biopharmaceuticals, vaccines, and blood testing. Chiron's vaccines and blood testing units were combined to form Novartis Vaccines and Diagnostics, while Chiron BioPharmaceuticals was integrated into Novartis Pharmaceuticals. In 2014, Novartis completed the sale of its blood transfusion diagnostics unit to Grifols and announced agreements for the sale of its vaccines unit to GlaxoSmithKline.
Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene.
Vertex Pharmaceuticals, Inc. is an American biopharmaceutical company based in Boston, Massachusetts. It was one of the first biotech firms to use an explicit strategy of rational drug design rather than combinatorial chemistry. It maintains headquarters in South Boston, Massachusetts, and three research facilities, in San Diego, California, and Milton Park, near Oxford, England.
Promega Corporation is a Madison, Wisconsin-based manufacturer of enzymes and other products for biotechnology and molecular biology with a portfolio covering the fields of genomics, protein analysis and expression, cellular analysis, drug discovery and genetic identity.
John Mendlein is a biotech executive who has held leadership positions in biotech companies in Boston, San Diego and Toronto.
Hit to lead (H2L) also known as lead generation is a stage in early drug discovery where small molecule hits from a high throughput screen (HTS) are evaluated and undergo limited optimization to identify promising lead compounds. These lead compounds undergo more extensive optimization in a subsequent step of drug discovery called lead optimization (LO). The drug discovery process generally follows the following path that includes a hit to lead stage:
BIOVIA is a software company headquartered in the United States, with representation in Europe and Asia. It provides software for chemical, materials and bioscience research for the pharmaceutical, biotechnology, consumer packaged goods, aerospace, energy and chemical industries.
Drug discovery depends on methods by which many different chemicals are assayed for their activity. These chemicals are stored as physical quantities in a chemical library or libraries which are often assembled from both outside vendors and internal chemical synthesis efforts. These chemical libraries are used in high-throughput screening in the drug discovery hit to lead process.
Venture philanthropy is a type of impact investment that takes concepts and techniques from venture capital finance and business management and applies them to achieving philanthropic goals. The term was first used in 1969 by John D. Rockefeller III to describe an imaginative and risk-taking approach to philanthropy that may be undertaken by charitable organizations.
Roger Yonchien Tsien was an American biochemist. He was a professor of chemistry and biochemistry at the University of California, San Diego and was awarded the Nobel Prize in Chemistry for his discovery and development of the green fluorescent protein, in collaboration with organic chemist Osamu Shimomura and neurobiologist Martin Chalfie. Tsien was also a pioneer of calcium imaging.
Ataluren, sold under the brand name Translarna, is a medication for the treatment of Duchenne muscular dystrophy. It was designed by PTC Therapeutics.
High throughput cell biology is the use of automation equipment with classical cell biology techniques to address biological questions that are otherwise unattainable using conventional methods. It may incorporate techniques from optics, chemistry, biology or image analysis to permit rapid, highly parallel research into how cells function, interact with each other and how pathogens exploit them in disease.
Caliper, A PerkinElmer Company produces products and services for life sciences researchThe firm, founded in 1995, is based in Hopkinton, Massachusetts with direct sales, service and application-support operations in countries around the globe. The firm's products include instruments, software and reagents, laboratory automation tools microfluidics, lab automation & liquid handling, optical imaging technologies, and services for drug discovery & drug development.
Ivacaftor is a drug used to treat cystic fibrosis in people with certain mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, who account for 4–5% cases of cystic fibrosis. It is also included in combination drugs, lumacaftor/ivacaftor and tezacaftor/ivacaftor, which are used to treat people with cystic fibrosis.
Lumacaftor (VX-809) is a pharmaceutical drug that acts as a chaperone during protein folding and increases the number of CFTR proteins that are trafficked to the cell surface. It is available in a single pill with ivacaftor; the combination, lumacaftor/ivacaftor, is used to treat people with cystic fibrosis who are homozygous for the F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, the defective protein that causes the disease. It was developed by Vertex Pharmaceuticals and the combination was approved by the FDA in 2015. As of 2015, lumacaftor had no medical use on its own.
Lumacaftor/ivacaftor, sold under the brand name Orkambi among others, is a combination of lumacaftor and ivacaftor used to treat people with cystic fibrosis who have two copies of the F508del mutation. It is unclear if it is useful in cystic fibrosis due to other causes. It is taken by mouth.
Kevin Donald Lustig is a male American scientist and entrepreneur and founder of three life science companies: the pharmaceutical company Kalypsys in 2001; the online research marketplace Scientist.com in 2007; and the non-profit lab incubator Bio, Tech and Beyond in 2013.
Joshua S. Boger is an organic chemist and the founder of Vertex Pharmaceuticals Incorporated. He is considered a pioneer in the field of structure-based rational drug design. Drugs developed include amprenavir, an HIV protease inhibitor; telaprevir, a protease inhibitor for treatment of hepatitis C; and Kalydeco, for the treatment of cystic fibrosis. In 2003, Vertex was listed as one of forty worldwide Technology Pioneers by the World Economic Forum. As of 2012, Boger became executive chairman of Alkeus Pharmaceuticals.
Jeffrey Leiden, M.D., Ph.D. is the executive chairman of Vertex Pharmaceuticals, a biotechnology company based in Boston, Massachusetts. He was initially appointed to the board of directors of the company in 2009 and was CEO and president from February 2012 to March 2020.
Peter Grootenhuis was a Dutch-American Medicinal Chemist. Grootenhuis was the Project Leader and Co-Inventor of Ivacaftor (VX-770), the first CFTR potentiator FDA approved drug to treat the underlying cause of Cystic Fibrosis (CF) in patients with certain mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene, who account for 4-5% of CF cases. Grootenhuis also led the Vertex team to subsequent discovery of Orkambi, the combination of Ivacaftor and Lumacaftor(VX-809), approved to treat CF in people with two copies of the F508del mutation. Most recently, Grootenhuis's team discovered Tezacaftor (VX-661) and Elexacaftor (VX-445), which in combination with Ivacaftor are the components of Trikafta, a drug approved by the FDA in 2019 to treat CF in more than 90% of CF patients. For Grootenhuis’ contributions to the discovery of these compounds, he was awarded the 2018 IUPAC Richter Prize, the American Chemical Society’s 2013 Heroes of Chemistry Award, and inducted into the American Chemical Society Division of Medicinal Chemistry Hall of Fame. Grootenhuis has contributed to the discovery of over 11 clinical candidates, co-authored more than 100 peer reviewed papers and is inventor of 65 + U.S Patents, and more than 50 EU Patents.