Case Study of Prior Knowledge: Development and ... · Case Study of Prior Knowledge: Development...
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Case Study of Prior Knowledge: Development and Implementation of a Binding Assay to Assess the Potency of Synagis® (palivizumab)
Mark A. Schenerman, Ph.D.CASSS CMC Strategy Forum – Japan December, 2017
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Outline• What is prior knowledge?• Mechanism and epidemiology of RSV
disease• What is Synagis® and how does it
prevent RSV disease?• Potency assay assessment• Use of the F protein binding ELISA• How can prior knowledge be used for
”next generation” products?
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What is Prior Knowledge?
Overall Knowledge
Published literature
Non-clinical
information
Clinical information
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Influence of Prior Knowledge
Sponsor’s clinical
experience
Published clinical experience
Sponsor’s pre-clinical experience
Published pre-clinical experience
Published literature*
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Mostinfluential
Leastinfluential *for example, manufacturing/QC publication from
another company
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Credibility Index
Peer-reviewed published
papers
QA-reviewed company reports
Witnessed lab notebooks
Trade journal articles*
5*not peer-reviewed
Mostcredible
Leastcredible
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Respiratory Syncytial Virus (RSV)• Isolated in 1956• Orthopneumovirus family (ssRNA viruses)• Most important viral agent of serious
respiratory tract disease in the pediatric population
• No fully effective anti-viral therapy or approved vaccine
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Orthopneumovirus Structure
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RSV Life Cycle
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Mab Binding to F Protein Antigen
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WHO meeting on RSV in High Risk Infants (2016) https://www.google.com/url?sa=t&rct=j&q=&esrc=s&source=web&cd=3&cad=rja&uact=8&ved=0ahUKEwjp0I3I0sfWAhWD4SYKHVhoAgYQFggxMAI&url=http%3A%2F%2Fwww.health.gov.on.ca%2Fen%2Fpro%2Fprograms%2Fdrugs%2Ffunded_drug%2Ffund_respiratory.aspx&usg=AFQjCNFaRMvg1nUc5nV_QUIJgnBc4CMM1g
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RSV Prophylaxis• Anti-viral therapies and vaccines are not
currently an effective option for infants at risk of infection
• Passive immunotherapy using intravenous immune globulins has proven to be safe and effective (RespiGam®)
• Passive immunotherapy using monoclonal antibody (Synagis®--palivizumab) at a reduced dose has proven to be safe and effective
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Synagis® (palivizumab)
• Humanized monoclonal antibody (MAb)
• Launched September 1998
• Prevention of serious lower respiratory tract disease caused by RSV in high risk infants
• 300,000+ infants annually in U.S.
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Why is Synagis® Important?
• RSV is the most common cause of lower respiratory infections in infants and children worldwide (estimated 3.4 million episodes of severe RSV infection resulting in hospital admission)
• Each year in the United States, more than 90,000 infants are hospitalized with RSV disease
• There are approximately 325,000 infants at high risk of acquiring severe RSV disease in the U.S.
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Assays for Potency
• Microneutralization• F protein binding ELISA• Fusion inhibition• Cotton rat prophylaxis
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Binding Assay Used for Potency Test?• Mechanism of action is well-established* (preclinical)• Development of animal models, cell culture based
assays, and binding assays (preclinical)• Accelerated stability studies show parallel or
comparable results (preclinical)• Clinical data shows no significant adverse events
(clinical)• Parallel real-time stability data shows no adverse
trends (clinical)• Continue monitoring animal models/bioassays as a
characterization test (marketed product)
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*Collins, PL, Chanock, RM, and Murphy, BR. (2001) in Fields VirologyVolume 1, 4th edition, Lippincott, Williams, and Wilkins, Philadelphia, pp. 1443-1485.
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Mechanism of Action• Binding to the F protein (specific neutralizing
epitope) on the surface of the virion• Glycosylation of the antibody plays no
significant role• Complement plays no significant role• Molar equivalent of Fab has comparable
binding• Fc region plays no significant role in potency
of antibody
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Effects of DeglycosylationSample Description
F protein ELISA (% of Reference Standard)
Microneutralization (ED50 of sample/ED50 of Ref. Std.)
PNGase treated Ref. Std.*
93% 0.76
Reference Standard Control
95% 1.13
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*Reference Standard lot was digested with PNGase (8 Units of enzyme per mg of Synagis) for 22 hours at 37°C. The control digestion was performed under identical conditions without enzyme. The completeness of digestion was monitored by observing a shift in molecular weight of the heavy chain on SDS-PAGE and CGE.
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Effect of Complement
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• Complement has no effect on neutralization
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Accelerated Stability
• F protein ELISA and microneutralizationshowed parallel trends (no significant decline)
• HPSEC showed significant decrease• Potency assays may not be as sensitive
an indicator of stability as biochemical tests
• Rate of decline for assays is product-and assay-specific
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Accelerated Stability of Synagis®
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• Neither assay showed significant change during accelerated stability
Red bars indicate 95% confidence intervals.
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Real-time vs. Accelerated Stability
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60
70
80
90
100
110
120
130
140
0 10 20 30 40 50
Months of storage
% o
f Ref
. Std
.
HPSEC (2-8C)HPSEC (40C)ELISA (2-8C)ELISA (40C)
• HPSEC showed significant change during accelerated stability but ELISA did not
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Similar Clinical Results Between Lots
• Multiple lots (> 12) from different scales made at different locations showed comparable animal and human PK results
• Real-time stability data on multiple lots showed no significant differences
• If clinical lots showed differences, these would need to be discussed with the regulatory authorities because binding alone might not be detecting the changes
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Cotton Rat Prophylaxis
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• No difference in potency in animals using different batches
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Human PK
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3 MG/KG MEAN SERUM LEVELS
1
10
100
0.0
0
0.2
5
0.5
0
1.0
0
4.0
0
8.0
0
12.0
0
1.0
0
2.0
0
3.0
0
4.0
0
5.0
0
7.0
0
14.0
0
21.0
0
30.0
0
37.0
0
60.0
0
HOURS DAYS
TIME
SE
RU
M L
EV
EL (
MC
G/M
L
3 mg/kg IM 15 mg/kg IV
• No difference in human PK, regardless of dose or method of administration
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Validation Comparisons
Parameter ELISA Microneut.Repeatability < 10% CV < 20% CVLinearity > 0.990 > 0.970Selectivity Specific for
SynagisSpecific for Synagis
Intermediate precision
< 20% CV < 30% CV
Robustness < 20% CV < 30% CV
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Conclusions• Synagis® potency assay developed based on
understanding of the mechanism, effectiveness of passive immunotherapy, and parallel stability data
• All results suggested that Fc function played no significant role in product potency
• Microneutralization and F protein binding ELISA behaved the same during accelerated and real-time stability testing over multiple lots
• F protein binding ELISA could be used for potency testing
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Application of Prior Knowledge to New Products
• Understanding of mechanism of action (MoA) can enable faster development of next generation products– Must demonstrate same MoA in new product
• Simplified control strategy may be achieved sooner, if product is in the same class (e.g., monoclonal antibody)
• For antibodies that have more complex mechanisms of action, using binding assays as the sole measure of potency may not be suitable
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Acknowledgements (MedImmune)
• Bob Strouse, Sheau-Chiann Wang, Tony DeFusco, and Fadi Hakki (Analytical Dev.)
• Gail Folena-Wasserman (Development)• Julie Lanahan (QC)• Dave Pfarr (Research)• Julia Goldstein (Regulatory)• Franco Piazza (Clinical)• Filip Dubovsky (Clinical)
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Johns Hopkins University (JHU) proposal to study correlation between quality data and
immunogenicity
• Mark Schenerman, Ph.D.President, CMC Biotech-MAS Consulting
Confidential information30 June 2017
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CONFIDENTIAL – DO NOT DISTRIBUTE
Monoclonal dimer levels have no significant
correlation with patient immunogenicity
Hypothesis
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Principle Investigator
Caleb Alexander,Associate Professor
John Hopkins UniversityBloomberg School of Public Health
Departmental Affiliations•Epidemiology (Primary)
•Division: Cardiovascular Disease and Clinical Epidemiology•School of Medicine (Joint)
Center & Institute Affiliations•Center for Drug Safety and Effectiveness•Center for Health Services and Outcomes Research•Center for Mental Health and Addiction Policy Research•Center of Excellence in Regulatory Science and Innovation (CERSI)
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• Assemble product quality (dimer levels) and clinical safety
(immunogenicity) data on monoclonal antibodies to either
prove or disprove the hypothesis (see mock database slide)
–Data includes different monoclonal antibodies that are
IgG1, IgG2, or IgG4 isotypes and have been evaluated in
the clinic (Phase 2-3)
• Database is owned by JHU (or CERSI)
• Solicit other monoclonal manufacturers to contribute data
• Sponsors would anonymize the data (lot numbers) so it
could be publically studied for trends
How will the study be done?
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• Proprietary information will be protected by JHU
• Only JHU will know the identities of the companies that participate;
sponsors must give permission to be named in public presentations
• Database will eventually have a public-facing view so that other global
epidemiologists can analyze the data
Data compilation by JHU
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• JHU epidemiologists at the Bloomberg School of Public Health will
analyze the data for trends in safety (immunogenicity)
• Through the collaborative interaction with industry sponsors, various
sub-set analyses may be performed based on patient population,
indication, and Ig subtype.
• Findings will be published in a high impact journal (e.g., Nature)
Data analysis by JHU Epidemiologist (Caleb Alexander)
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• Builds industry collaboration with a world renowned epidemiology
group at JHU
• JHU group lends credibility to the study; makes subsequent
publication more impactful
• JHU group is part of joint FDA/JHU foundation (CERSI) that is
dedicated to product safety monitoring
• Delivers on the challenge presented by regulators to analyze and
correlate quality and safety data
Benefits of the Study
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• New safety signal identified through the study; would need to be
reported to regulators
Risks
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• Opens the opportunity for discussion with regulators whether dimer
could be considered less risk (non-CQA)
• May enable greater manufacturing flexibility, while maintaining
appropriate control of all aggregates
• Science-driven approach to challenging the Health Authority
stereotype that “all aggregates are a high risk of immunogenicity”
Possible outcomes 1
Hypothesis is proven
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• Maintains current state
• All aggregates considered to be the highest immunogenicity risk
• No change to current approach to process development or product
control
Possible outcomes 2
Hypothesis is disproven
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• Maintains current state
• All aggregates considered to be the highest immunogenicity risk
• No change to current approach to process development or product
control
Possible outcomes 3
No clear conclusion
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What is the Center for Regulatory Science & Innovation (CERSI)?
• FDA's Centers of Excellence in Regulatory Science and Innovation (CERSIs) are collaborations between FDA and academic institutions to advance regulatory science through innovative research, education, and scientific exchanges. Evolving areas of science are promising new approaches to improving our health while demanding new ways to evaluate the safety and effectiveness of the products FDA regulates. FDA’s Strategic Plan for Advancing Regulatory Science describes how FDA is harnessing these new technologies in collaboration with academia, industry, and other governmental agencies to develop the tools, standards, and approaches required to assess the safety, efficacy, quality, and performance of innovative products.
• CERSI centers: –University of Maryland–Georgetown University–University of California at San Francisco (UCSF) in a joint effort with Stanford University
(UCSF-Stanford)–Johns Hopkins University–Yale University in joint effort with Mayo Clinic
• https://www.fda.gov/ScienceResearch/SpecialTopics/RegulatoryScience/ucm301667.htm