Regulatory Roundup for Week of November 12, 2012 - Pharmaceutical Technology

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Regulatory Roundup for Week of November 12, 2012

ePT--the Electronic Newsletter of Pharmaceutical Technology

Encouraging Orphan Drugs
by Jill Wechsler

Pharmaceutical companies, scientists, and regulators are championing the development of new treatments for rare diseases as key to spurring biomedical discovery. Experts at an October conference on rare diseases sponsored by the National Organization for Rare Disorders and the Drug Information Association discussed FDASIA provisions that expand FDA staff, guidance, and public outreach to support orphan drug research and approval. John Jenkins, director of the Center for Drug Evaluation and Research (CDER) Office of New Drugs, outlined additional FDASIA policies that provide assistance to sponsors of “breakthrough therapies,” expand accelerated approval of drugs to treat life-threatening conditions, and special incentives for developing treatments for rare pediatric conditions.

Beyond FDA, the National Center for Advancing Translational Sciences at the National Institutes of Health is supporting development of therapeutics for rare and neglected diseases through its drug “repurposing” program plus collaborative research projects. Venture capitalists, moreover, eye more flexible clinical research requirements for orphan drugs as a way for biopharmaceutical companies to gain regulatory approval more quickly and efficiently.

FDA Updates

FDA has provided information on its Enhanced Communication Team created in response to PDUFA V and FDA’s promotion of innovation through interactive communication between the agency and sponsors during drug development.

The following industry guidance documents have been released by FDA:

Generic drug-user fee notice, October 2012: manufacturers will pay approximately $17,500 for FDA’s Office of Generic Drugs to process a backlogged abbreviated new drug application (ANDA). The first manufacturer to reference a drug master file will pay a one-time fee of $21,340. Filing an ANDA will cost $51,520 at time of submission, and about half that amount for a prior approval supplement. Facility fees are due from FDA by mid-January and will be higher for foreign manufacturers.

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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
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Reducing drug shortages
27%
Breakthrough designations
9%
Protecting the supply chain
41%
Expedited reviews of drug submissions
9%
More stakeholder involvement
14%
View Results
Jim Miller Outsourcing Outlook Jim Miller Health Systems Raise the Bar on Reimbursing New Drugs
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerThe Mainstreaming of Continuous Flow API Synthesis
Jill Wechsler Regulatory Watch Jill Wechsler Industry Seeks Clearer Standards for Track and Trace
Siegfried Schmitt Ask the Expert Siegfried SchmittData Integrity
Sandoz Wins Biosimilar Filing Race
NIH Translational Research Partnership Yields Promising Therapy
Clusters set to benefit from improved funding climate but IP rights are even more critical
Supplier Audit Program Marks Progress
FDA, Drug Companies Struggle with Compassionate Use Requests
Source: ePT--the Electronic Newsletter of Pharmaceutical Technology,
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