Biowaivers and Harmonization Guidelines for Class...
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• Barbara M. Davit, Merck & Co., Inc.
• 3rd FDA/PQRI Conference on Advancing Product Quality
• March 22, 2017
Biowaivers and Harmonization Guidelines for Class I and 3 Drugs:
Biowaiver Case Studies
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I am an employee and shareholder of Merck & Co., Inc.
The comments presented are my own and not intended to represent those of Merck & Co., Inc.
Disclaimer
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Introduction – initiating BCS evaluation
Navigating regulatory guidelines
Case studies
Summary and conclusions
Agenda
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Introduction – initiating BCS evaluation
Navigating regulatory guidelines
Case studies
Summary and conclusions
Agenda
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Drug teams determine BCS classification of all preclinical candidate (PCC) drugs
Presently, drug teams do not evaluate BDDCS
Initiating BCS classification
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Class I
High solubility
High intestinal permeability
Class II
Low solubility
High intestinal permeability
Class III
High solubility
Low intestinal permeability
Class IV
Low solubility
Low intestinal permeability
BCS classification – cont’d
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Early in development, in vitro solubility and in
vitro permeability studies are conducted to
obtain preliminary BCS classification
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A two-staged approach
A preliminary classification is undertaken based on predicted clinical efficacious dose
In vitro solubility studies are conducted
Permeability is assessed in vitro – LLC-PK1 cells
BCS classification guides further development
BCS classification processes
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• Consider conducting pivotal permeability studies
• Conduct multimedia in vitro dissolution studies
• Consider BCS biowaiver application(s) Class I
• Conduct in vitro dissolution studies
• If weak base with pH-sensitive solubility, may consider developing enabled formulation Class II
• Consider conducting pivotal permeability studies
• Conduct multimedia in vitro dissolution studies
• Consider BCS biowaiver application(s) Class III
• Conduct in vitro dissolution studies
• If weak base with pH-sensitive solubility, may consider developing enabled formulation Class IV
Impact of BCS classification in further drug development
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Conducted later in development, if – Clinical dose established
– Likely to Initiate Phase III File for marketing approval in US and/or EU
Preclinical options – Caco-2 cells; rat intestinal perfusion
Clinical options – Oral bioavailability; mass balance
Pivotal in vitro permeability studies
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Introduction – initiating BCS evaluation
Navigating regulatory guidelines
Case studies
Summary and conclusions
Agenda
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BCS application US-FDA EMA
BCS Class I biowaivers
permitted Yes Yes
BCS Class III biowaivers
permitted No Yes
BCS biowaivers permitted
for pharmaceutical
alternatives (e.g., capsule
v tablet)
No Yes
Criteria for high in vivo
permeability ≥ 90% oral bioavailability ≥ 85% oral bioavailability
pH range for in vitro
solubility studies pH 1 – 7.5 pH 1.2 – 6.8
Paddle speed for
dissolution studies 50 rpm; no exceptions
50 rpm; will consider 75
rpm with justification
Differences between US, EMA BCS biowaiver criteria until 2015
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Can request a BCS biowaiver for
pharmaceutical alternatives
BCS Class III biowaivers may be granted if criteria
are met
In vivo evidence of high permeability demonstrated by oral BA of ≥ 85%
pH range for in vitro solubility
studies is now 1.2 to 6.8
Paddle speed of 75 rpm may be acceptable with
justification
Changes to FDA criteria for BCS biowaivers implemented in 2015
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BCS application US-FDA EMA
Strength for
solubility studies Highest strength
Highest single
therapeutic dose
Method for
determining high
intestinal
permeability
In vitro and
preclinical methods
acceptable
Only a clinical
absolute BA or
mass balance
study
In vitro dissolution
testing for BCS
classification
500 mL media 900 mL media
Some major differences between US, EMA BCS biowaiver criteria
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Introduction – initiating BCS evaluation
Navigating regulatory guidelines
Case studies
Summary and conclusions
Agenda
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Drug approved worldwide
Absolute BA = 87% (as per labeling)
Designated as Class III under original FDA BCS guidance posted in 2000
Will seek Class I designation from FDA, as per 2015 draft guidance criteria – Investigating development of Drug A in an
immediate-release (IR) fixed-dose combination doublet with a second Class I drug
Drug A
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Drug is highly soluble
Initially developed as an IR capsule; changed formulation to an IR tablet; both rapidly dissolving
High intestinal permeability shown in vitro
FDA rejected BCS biowaiver request in support of change from capsule to tablet
Drug B
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May resubmit BCS biowaiver request to FDA, considering revisions in 2015 draft guidance
Under draft guidance, sponsors may request BCS biowaiver for capsule v tablet BA comparison
Drug B (cont’d)
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Drug is highly soluble, and tablets are rapidly dissolving
Stability study results necessitated change to a different API morphic form during Phase III
BCS Class I biowaiver designation will be requested from both US-FDA and EMA
Conducted an in vitro permeability study with Caco-2 cells, and an in vivo clinical mass balance study showing > 85% absorption
Drug C
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In vitro permeability study results will be used to support BCS Class I biowaiver request for US-FDA filing
In vivo mass balance study results will be used to support BCS Class I biowaiver request for EMA filing
US-FDA and EMA requirements for showing high permeability not harmonized
Fortunately, both in vitro and clinical studies were conducted
Drug C (con’t)
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Introduction – initiating BCS evaluation
Navigating regulatory guidelines
Case studies
Summary and conclusions
Agenda
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Preliminary BCS classification can be conducted early to guide drug development
Pivotal studies to confirm BCS Class I or III are conducted later in development
Attempts to harmonize US-FDA and EMA BCS guidance benefit worldwide filings
Challenges still exist due to several differences between US and EMA criteria for Class I/III designation
Summary and conclusions
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Jean-Michel Cardot
Paul Fackler
Dave Storey
Henry Wu
Acknowledgements
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