Detroit-based Ash Stevens, Inc. (ASI) has nearly a half-century of experience in the development and manufacture of active pharmaceutical ingredients, but it’s in the area of cancer APIs where it specializes. ASI was founded in 1962 to provide chemical research to the U.S. government and has a longstanding relationship with the National Cancer Institute.
ASI also recently made the news as a key member of the fledgling Michigan CMC Alliance, a consortium of contract service providers that have banded together to leverage their collective facilities and intellectual capital.
We spoke with ASI’s Jim Hamby, Director of Business Development, to get an insider’s view of the challenge of making APIs for oncology products, and on the new alliance.
PhM: What are the key considerations in the developing and manufacturing APIs for cancer drugs? What are the distinct challenges from the contract provider’s perspective?
(Click to enlarge image) Barrier isolation systems in ASI’s Riverview, Michigan facility.
J.H.: There are several important aspects unique to cancer drug development. The drugs are often targeted to unmet medical needs for life-threatening conditions so the timelines are often accelerated. That means that the same amount of work to support a successful CMC section of an NDA needs to be completed in a much shorter period of time. This mandates a very tight, flawlessly managed regulatory program.
Cancer agents also tend to be classified as “potent”. In reality, this is a euphemism for toxic compounds. A developer/manufacturer therefore needs systems and proper engineering controls to ensure that those involved in the synthesis remain safe. We have a major commitment to barrier isolation systems for this purpose. These isolation systems provide the highest level of worker and environmental safety.
PhM: What is the acceptable percentage of impurity for API of small molecule cancer drugs in GMP production?
J.H.: The level of impurity is predicated on data obtained from the acute toxicology study. For early stage development, levels as high as 3% to 5% may be “qualified” based on the tox study. Even though these levels may be acceptable, FDA may question levels that high. Levels in the range of 0.5% to 1.0% are not unusual for “qualified” impurities in early stages of development.
For some impurities, for example, Residual Solvents or Heavy Metals, Guidance documents or compendial references (sp. USP) specify generally accepted levels. Higher levels can be justified, however, due to the small administered dose.
PhM: Is it necessary to analyze the identity of impurity material?
J.H.: In early phases of development, it is not necessary to identify the structure of an impurity. It is permissible to call such an impurity “Unknown A with HPLC RRT = x”. Using this nomenclature in the tox lot and subsequent GMP lots for early phases would be acceptable. The structure of all impurities greater than 0.1% should be known prior to filing an NDA.
PhM: Do different products require a separate contained facility for API synthesis, GMP batch and packaging?
J.H.: The compounds would not require separate facilities. Ash Stevens has suitable production laboratories and potent compound handling facilities for synthesis of such materials.
[pullquote]The facilities are designated as “multi-use” meaning they may be used for synthesis of different products ... but only one such product could be synthesized in the area at any one time.
Ash Stevens develops, and suitably validates, cleaning procedures and cleaning verification analytical methods so that the facilities may be cleaned and demonstrated to be clean after use. This is an important part of our service, where each client relies upon the other to support programs to ensure that cross-contamination is mitigated.
PhM: Tell us more about the Michigan CMC Alliance — how did it come about? Was there a model for this?
J.H.: The Alliance, an informal arrangement of people looking to support each other, was formed as large pharmaceutical companies in Michigan began to contract. This afforded smart, entrepreneurial people the opportunities to use their expertise, gained through many years working in big pharma, to start their own businesses working with emerging pharmaceutical companies to develop novel therapies.
Michigan CMC Alliance’s purpose is to support the growth and success of life science companies. The Michigan CMC Alliance provides CMC resources and expert strategies for drug development, as well as education on the complexities of the CMC development process. In so doing, the emerging company doesn’t have to build a deep bench internally, which is a costly endeavor.
PhM: What does Ash Stevens get out of the alliance?
J.H.: We have the opportunity to work with a broad group of professionals with expertise throughout the entire CMC world, not just our own area of expertise, which is API.
(Click to enlarge image) A pilot scale reactor bay located in a down draft suite with a 100L Hastelloy vessel.
PhM: How will the alliance ensure seamless, consistent service to clients with so many partners involved?
J.H.: One of the most useful assets that we have is that many in the Alliance have previously worked together and have developed a good working relationship. We are also geographically close, facilitating easy face-to-face meetings and rapid communication.
Contracting News and Notes
In case you missed it, GlaxoSmithKline and Pfizer will partner and create a new company devoted to HIV medicines. The two companies will blend GSK’s portfolio of HIV drugs on the market with the more promising candidates that Pfizer has in development.
DSM Pharmaceutical Products will take over production of drugs made at Shire’s Owings Mills, Md., site as that facility prepares to close.
Injectable manufacturer APP Pharmaceuticals has hired 50 employees recently laid off from the neighboring Astellas Pharma facility in Grand Island, N.Y., and has taken over some of the facilities for office and laboratory needs as it expands. “We have finished hiring Astellas employees but are actively hiring for open manufacturing positions,” company spokeswoman Debra Lynn Ross said recently.
APP, based in Schaumburg, Ill., expected to take possession of the Astellas plant, which became available when Astellas decided to return production of its Protopic dermatology ointment to its Toyama, Japan site.
Biotech contract research and manufacturer Leinco Technologies is moving from St. Louis to Florida. The communities of Jupiter and Palm Beach Gardens have loaned Leinco $350,000 for capital investment and relocation. Leinco wants to be part of the biotech cluster that includes the Scripps Research Institute and Max Planck Institute.
Patheon has expanded its Toronto facility, adding 10,000 square feet of GMP space dedicated to oral contraceptive production — including capabilities for dispensing, granulation, compression, film coating and primary packaging. The new space will use abatement technology to eliminate solvent emissions aimed at meeting future Canadian environmental standards.
Germany’s Rottendorf Pharma has expanded its contract development activities to formulation, validation, clinical batch production and updating of files.
Symyx Technologies has launched the Symyx Contract Development and Manufacturing Organization (CDMO) to expand its services to help biopharma companies with formulation development, and preclinical and cGMP fill/finish manufacturing. The company, known for its lab notebooks as well, recently signed an agreement with Thermo Fisher to couple the notebooks and software with Thermo’s LIMS systems.
Oracle Corp. has agreed to buy Relsys International, a provider of drug safety and risk management software and analytics solutions.
Golden State Medical Supply (GSMS) has partnered with IBM to offer electronic pedigree compliance services to pharmaceutical manufacturers seeking a “quick and proven” means of complying with California and global pedigree requirements.
Siemens Energy & Automation will work with drug packager Aylward Enterprises on the design of Aylward’s new ACT 9000 Series Bottle Filler. Aylward is looking to increase the accuracy of tablet measurements tenfold, it says.
A new Web site, goBalto.com, has launched to provide a Web 2.0 means of researching and rating pharma contract service providers.