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Week of Aug. 30, 2010: Company and People Notes: Lonza Acquires Vivante; PPD Appoints VP of Quality Management; And More.
AMRI Burlington (Burlington, MA), formerly Hyaluron and now a subsidiary of AMRI, received a Warning Letter from the US Food and Drug Administration for violations of good manufacturing practices. Among the violations listed in the letter are: failure to thoroughly investigate batch failures, including the presence of particulate contaminants in products, and a lack of procedures to avoid microbiological contamination of sterile products. AMRI acquired Hyaluron in June 2010, and the business now operates as AMRI Burlington.
CMC Biologics (Copenhagen), a contract manufacturing organization, completed a new disposable manufacturing facility at its Seattle, Washington, site. The multipurpose, single-use facility will allow for early-phase clinical manufacture of a range of biopharmaceuticals, including monoclonal antibodies and other mammalian cell culture-based recombinant proteins. The facility contains a 100 L and two 500 L single-use bioreactors and disposable mixers.
Catalent Pharma Solutions (Somerset, NJ), a provider of solutions for the global pharmaceutical industry, worked with BioAlliance Pharma (Paris) on the development, approval, and launch of miconazole 50 mg buccal tablets for the local treatment of oropharyngeal candidiasis. The product, which has been on the market in Europe since 2007 under the name Loramyc, was approved in April 2010 by FDA and has been launched in the US under the trade name Oravig by Strativa Pharmaceuticals, a division of Par Pharmaceuticals (Woodcliff Lake, NJ).
In a separate announcement, Catalent said it entered into a clinical-supply-services agreement to support Sunesis’ (South San Francisco, CA) Phase III VALOR trial of vosaroxin, a drug to treat cancer, in first relapse or primary refractory acute myeloid leukemia (AML). Catalent will provide services in labeling and kitting of the clinical-trial materials to be used in the trial and will provide supply-chain support to clinical sites. The clinical packaging and logistics will be handled in Catalent’s Philadelphia, Pennsylvania, and Schorndorf, Germany, facilities.
IBA (Ion Beam Applications, Louvain-la-Neuve, Belgium) entered into an agreement with Bayer Schering Pharma (Berlin) for chemical-process development and clinical-trial doses supply of Florbetaben, a molecular-imaging compound in development for the detection of Alzheimer’s disease pathology. Under the terms of the agreement, IBA will manufacture and supply Bayer with doses of the compound Florbetaben for clinical trials. Under the terms of the agreement, IBA will receive several million euros of milestone payments and fees depending on the amount of required doses for the clinical trials.
Lonza (Basel) acquired Vivante GMP Solutions (Houston, TX), a custom manufacturing organization focused on viral-based therapeutics. As a result, Vivante’s employees have joined Lonza and will operate as Lonza’s Viral-based Therapeutics Business.
Meda (Solna, Sweden), a specialty pharmaceutical company, agreed to acquire Alaven (Marietta, GA), also a specialty pharmaceutical company. Closing of the transaction is subject to regulatory approval, and the companies expect the acquisition to be completed by early October.
Novartis (Basel) completed its purchase of the eye-care company Alcon’s stock from Nestlé, resulting in 77% ownership of Alcon. Novartis completed the acquisition of the remaining 52% of Alcon shares owned by Nestlé for a total of $28.3 billion.
Ricerca Biosciences (Concord, OH), a contract research organization, completed the purification of an active pharmaceutical ingredient (API) under current good manufacturing practices (CGMP) controls. The process involved chiral separation of a single API from three chiral isomers. More than 800 g of material was processed to produce 525 g of the desired isomer with > 99.7% chiral purity and > 99% achiral purity. With the current configuration of the Prep HPLC system, Ricerca can process up to 1–2 kg of material under CGMP controls, and the system is expandable to 6–8 kg capacity. It includes an automated fraction collection system to assist in the purification process.
Stirling Pharma (Sydney, Australia) is on schedule to open its manufacturing plant in Cape Breton, Canada, in September. The plant will manufacture acetaminophen.
Xcelience (Tampa, FL), a contract research organization, and IriSys (San Diego), a contract services organization, entered into a business alliance agreement to advance the ability to streamline access to CMC and regulatory services for North American pharmaceutical and biotechnology companies.
Bionor Pharma (Oslo) appointed Henrik Lund as its CEO. Lund, who previously worked at AstraZeneca (London), took over the position from Trond Syvertsen.
Pharmaceutical company Celgene (Summit, NJ) appointed Jacqualyn A. Fouse senior vice-president and CFO, effective Sept. 27, 2010. Fouse will report to Robert J. Hugin, CEO of Celgene.
Frank Baldino, Jr., chairman and CEO of Cephalon (Frazer, PA), a biopharmaceutical company, took a temporary medical leave of absence. During Baldino's absence, J. Kevin Buchi, the company's COO, will assume Baldino's responsibilities. Before assuming the newly created role of COO earlier this year, Buchi served as the company's CFO for 14 years.
PPD (Wilmington, NC), a contract research organization, named Neil McCullough vice-president of quality-management systems. McCullough previously worked at Pfizer (New York).
Verenium (Cambridge, MA), a biotechnology company, appointed Kevin Bracken vice-president of manufacturing. Bracken will report to Janet Roemer, president and COO of Verenium's enzymes business.
XenoPort (Santa Clara, CA), a biopharmaceutical company, announced that President William J. Rieflin has been elected to the XenoPort board of directors, effective Sept. 17, 2010, and will resign as president of XenoPort to accept a position as CEO of a private biotechnology company. He will continue to serve as a consultant to XenoPort during a transition period.