regulatory considerations for mcm development: strategies ... · nda review cycle was 6 months....
TRANSCRIPT
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October 29-30, 2018 | Grand Hyatt • Washington, D.C.
Regulatory Considerations for MCM Development: Strategies and Challenges
Tremel Faison, MS, BARDA/RQAMelissa Willens, MS, BARDA/RQAJeremiah Wille, DSC, BARDA/RQA,
Paul Roney, PhD, BARDA/RQAAndrea Powell, PhD, FDA/CDER/CTECS
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2Saving Lives. Protecting Americans.
• Expedited Programs• Priority Review Voucher• Development under Animal Rule
Agenda
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3Saving Lives. Protecting Americans.
Expedited Programs
CENTER FAST TRACKBREAKTHROUGH
THERAPY/DESIGNATION
ACCELERATED APPROVAL PRIORITY REVIEW
Center Biologics Evaluation & Research
Center for Drug Evaluation & Research
Center for Device & Radiological Health
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4Saving Lives. Protecting Americans.
Expedited Programs - Drugs and Biologics
• Priority Review• Accelerated
Approval
IND NDA/BLA
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5Saving Lives. Protecting Americans.
Fast Track
QUALIFYING CRITERIA
• Intend to treat a serious condition AND nonclinical or clinical data demonstrate the potential to address unmet medical need OR
• Designated as a qualified infectious disease product (QIDP)
BENEFITS/FEATURES:
• Expedite development and review• Rolling review
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6Saving Lives. Protecting Americans.
Breakthrough Therapy
QUALIFYING CRITERIA
• Intend to treat a serious condition, AND
• Preliminary clinical evidence indicates that the drug may demonstrate substantial improvement over available therapy on one or more clinically significant endpoints
BENEFITS/FEATURES:
• Intensive guidance on efficient drug development
• Organizational commitment• Rolling review
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7Saving Lives. Protecting Americans.
Accelerated Approval
QUALIFYING CRITERIA
• Treat a serious condition AND, • Provide meaningful advantage over
available therapies AND • Demonstrate effect on surrogate endpoint
that is reasonably likely to predict clinical benefit or on a clinical endpoint that can be measured earlier than irreversible morbidity or mortality (IMM) that is reasonably likely to predict an effect on IMM or other clinical benefit
BENEFITS/FEATURES:
• Based on an effect on surrogate endpoint or intermediate clinical endpoint that is reasonably likely to predict drug’s clinical benefit
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8Saving Lives. Protecting Americans.
Priority Review
QUALIFYING CRITERIA
• To treat a serious condition AND, if approved, would provide a significant improvement in safety or effectiveness OR
• To propose a labeling change pursuant to a report on a pediatric study under 505A OR (supplements only)
• Designated as a qualified infectious disease product OR
• Submitted with a priority review voucher
BENEFITS/FEATURES:
• Shorter review clock: 6 months versus 10 months compared with standard review
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9Saving Lives. Protecting Americans.
• Xerava (eravacycline) cIAI are serious life threatening infections requiring
new antibiotics, QIDP designation was requested QIDP granted Granted Fast track designation NDA Review cycle was 6 months
Qualified Infectious Disease Product Granted for Tetraphase
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10Saving Lives. Protecting Americans.
Breakthrough Device Program
QUALIFYING CRITERIA
• Provide for more effective treatment• Represent breakthrough technology• No approved or cleared alternative exists• Offer significant advantages over existing
approved or cleared alternatives• Availability is in the best interest of
patients• Must be requested anytime prior to the
submission of marketing application
BENEFITS/FEATURES:
• Sprint discussions, Data Development Plans, Clinical Protocol Agreement, regular status updates
• FDA response is within 60 days
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11Saving Lives. Protecting Americans.
• Spectral MD: DeepView for burn imaging
• Breakthrough Device program suggested by FDA More effective treatment Best interest of patients
• Request submitted and designation granted in less then 30 calendar days Currently working on DDP Have regular updates with FDA
Breakthrough Request Designation
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12Saving Lives. Protecting Americans.
Priority Review Voucher
QUALIFYING CRITERIA
May be granted upon approval of a • Medical countermeasure, • Pediatric rare disease therapeutic,• Eligible tropical disease therapeutic• Indication is to prevent or treat a
PHEMCE identified CBRN threat
• Therapeutic is eligible for priority review• Therapeutic is not previously approved• Only 1 PRV/application
BENEFITS/FEATURES:
• Entitles the holder to have priority review on a NDA/BLA Application
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13Saving Lives. Protecting Americans.
• Ticovirimat treats human smallpox disease
Smallpox is on the PHEMCE list of Material Threats
NDA review cycle was 5 months• Priority review granted• First approval for ticovirimat• Priority Review Voucher awarded
Priority Review Voucher Granted to SIGA
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Placeholder for Andrea Powell(FDA speaker)
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15Saving Lives. Protecting Americans.
Resources for Industry
Expedited Programs for
Serious Conditions –Drugs and BiologicsMay 2014
Material Threat Medical
Countermeasure Priority Review
VouchersJuly 2018
Product Development
Under the Animal Rule
Oct 2015
Breakthrough Devices Program
Draft Oct 2017
Guidance for Industry Guidance for Industry &
FDA
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16Saving Lives. Protecting Americans.