Pharmacovigilance. Building capacity and improving methods peter_arlett.pdf · EPITT (European...
Transcript of Pharmacovigilance. Building capacity and improving methods peter_arlett.pdf · EPITT (European...
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Pharmacovigilance.Building capacity and Building capacity and improving methods
DIA European Regulatory Affairs Forum
An agency of the European Union
Peter ArlettEMA
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In this talk
• EMA is the hub of the European Network
• Eudravigilanceg
• EPiTT
• ENCePP
• Other initiatives• Other initiatives
• IMI Protect
• International work
I t ti b fit d i k• Integrating benefits and risks
• Looking forward
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EMA is the hub of the European NetworkEMA is the hub of the European Networkpp“coordination of the supervision, under practical conditions of use, of medicinal products which have been medicinal products which have been authorised within the Community and the provision of advice on the measures necessary to ensure the
f d ff i f h safe and effective use of these products, in particular by evaluation, coordination of the implementation of pharmacovigilance obligations and pharmacovigilance obligations and the monitoring of such implementation”
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EudraVigilanceg
• EudraVigilance: operational since December 2001
• Provides a data-processing network which interlinks the EMA with all • Provides a data-processing network, which interlinks the EMA with all Member States, the EC and marketing authorisation holders
• Operates between ‘trusted’ (registered) users only
• Supports fully automated, rapid, secure (encrypted), electronic exchange of case reports between registered users
• Provides a common EU pharmacovigilance database accessible to all • Provides a common EU pharmacovigilance database accessible to all Member States (all member states can report to the system and all Member States can analyse the data to conduct safety reviews)
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EudraVigilanceg
• New business rules to improve utility (especially important for SUSARs))
• EudraVigilance Access policy – policy finalised 2010
• Data quality tender – to start 2010
• International standardisation – see later• International standardisation see later
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EudraVigilanceg• Contains 1.5 million case reports* of suspected serious adverse reactions for
medicinal products authorised in the EU- Average new case reports per month: 39.700*
S t th EU h i il d i k t ti iti• Supports the EU pharmacovigilance and risk management activities– All Member States can analyse world-wide data – repeated training
offered and ‘Eudravigilance support program’ for rapporteurs
• Facilitates the EU decision making process related to the benefit risk l ti f di i l d t evaluation of medicinal products
• Key tool to protect public health of EU citizens:– Allows new or changing risks to be detected early– Allows rare adverse effects to be detected
All t f i k f t d th ibiliti f i i i i – Allows assessment for risk factors and thus possibilities for minimising risk
– Allows comparisons between products
• MSs and EMA share safety ‘signals’ based on EV data
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• RMS and rapporteurs analyze the EV data to support their monitoring role
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EudraVigilanceg
• Eudravigilance validation study– Direct evidence that more than 54% of serious safety issues can
be detected earlier if Eudravigilance is used in addition to other pharmacovigilance resources
Why Analysis of pooled data:– Why – Analysis of pooled data:• Detection of rare ADRs• ADRs detected earlier as absolute numbers are greater
Reference:Drug Safety, 33(6), pp. 475-487
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EPITT (European Pharmacovigilance Issues Tracking Tool)
• Database facilitating the sharing of safety information of the medicinal products for human use between the National Competent Authorities (NCAs) and the Agency
• 4 “main modules”: Safety Issues, Safety Signals, PSURs, RMPs
• Objectives:– Tracking of the Safety Issues and Signals “life cycles” (independently of the g y g y ( p y
authorisation type)– Tracking of the PhVWP recommendations and SPC wordings within the EU– Tracking and monitoring of the PSURs cycles and Risk Management Plans together
with the implementation of the regulatory actions they require– Support to the European Incident Management Plan Procedure– Easy retrieval of the documents related to the safety of a medicinal product
• EPITT is:
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– 280 Users within the EU (Agency and NCAs)
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EU-RMP Annex 1 Updatep
• The EU-RMP Annex 1 is:
– The structured electronic representation of the EU Risk Management Plan (EU-RMP)
– The interface between EU-RMPs and EudraVigilance
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EU-RMP Annex 1 in the EudraVigilance webpagep g
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What is ENCePP? www.encepp.europa.eu
European Network of Centres for Pharmacoepidemiology (PhEpi) & Pharmacovigilance (PhV) is an Agency-led project to bring together the available expertise and research experience in the fields of PhEpi and PhV scattered across Europe in a Network of Excellence, [research centres, healthcare databases, electronic registries and existing networks] networks].
The aim is to further strengthen the post-authorisation monitoring of medicinal products in Europe by facilitating the g p p y gconduct of high quality, multi-centre, independent post-authorisation studies focusing on safety and on benefit: risk.
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ENCePP Resource Database
ENCePP aims to increase the capacity to conduct quality Post-
Authorisation studies in Europe.Authorisation studies in Europe.
→ Database describing resources in ENCePP and facilitating
searches.
• 60 research centres
• 8 specialised networks (e.g. cutaneous ADRS, psoriasis, paediatric population…)population…)
• Data sources (Eurocat, GPRD, Memo, etc)
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http://www.encepp.eu/encepp/resourcesDatabase.jsp
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2
An agency of the European Union
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ENCePP–Structure and main componentsp
Research Standards & Guidance
WGResearch Centres
WG
Steering GroupG
WGData Sources & Multi-
source Studies
WGTransparency
& Independence
Governance
ENCePPSecretariatSecretariat
EU R h
ENCePP Resources Database
EU Data Sources
EU Research Institutions
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ENCePP Code of Conduct for Studies
Govern the responsibilities of and interaction between stakeholders
(funder investigator) in the conduct of studies to ensure transparency(funder-investigator) in the conduct of studies to ensure transparency
and promote scientific independence.
Essentially a charter of rights and obligations covering the development
of the study protocol, study conduct, data ownership, access to data,
bli ti f lt i ti tpublication of results, communication, etc.
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ENCePP Register of Post-authorisation studies
Purpose: i) Reduce publication bias, ii) increase transparency, iii)
promote information exchange and iv) facilitate collaborations within the promote information exchange and iv) facilitate collaborations within the
scientific community.
Scope: mandatory only for “ENCePP studies” (largely non-Scope: mandatory only for ENCePP studies (largely non
interventional); voluntary for all others.
other registers of Post-authorisation studies exist (Spain, Italy, USA)…
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“ENCePP study” - CoRe Principlesy pAny PhV/PhEpi study whose main investigator works at a centre included in the ENCePP database of resources and for which the following (CoRe) criteria are met:
• ENCePP Code of Conduct: signed declaration and checklist
• Methodological standards for protocols: signed checklistThe completed and signed declaration and checklists and study protocol must be sent to the ENCePP Secretariat before the start of the study. The declaration and the checklists will be made public.
• e-Register of post-authorisation studies: Registration in the R i t b f t d t t Register before study start
Basically, the main investigator agrees to conduct the study according to ENCePP rules and methodological research standards.
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g
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Benefits of ENCePPENCePP will contribute to:• Identify, characterise and
promote access to PhV/promote access to PhV/PhEpi resources in the EU.
• Improve research standards
• Increase independency and transparency in research
• Stimulate collaboration/ exchange of information and experience
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Collaboration European Commission [FP-7]p [ ]List of priorities in drug safety research (off-patent or class effects)
Multinational research projects, including academic centres, hospitals, p j , g , p ,
SMEs, patient groups, industry, etc
Duration is ~ 5 years; Public funding ~ € 3 million
• 2nd Call (2007) – CV and GI Safety of NSAIDs
http://www.sos-nsaids-project.org/
3 d C ll (2008) A th i t ti l f l l f • 3rd Call (2008) – Arrythmogenic potential of several classes of medicines.http://www.aritmo-project.org/
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Collaboration European Commission [FP-7]p [ ]• 4th Call (2009)
EMA prepared summary of each priority and published on webLong term effects of methylphenidate in children treated for – Long-term effects of methylphenidate in children treated for ADHD *
– Long-term adverse effects of immunomodulators *– Long-term adverse skeletal effects of biphosphonates – Medicine use in pregnancy (design of effective pregnancy
prevention programmes, recommendation for safe use in pregnancy, etc) *
– Suicidal behaviour in relation to certain drug use (antidepressants, antipsychotics varenicline montelukast) *antipsychotics, varenicline, montelukast) *
– Safety aspects of antipsychotics in demented patient
• 5th Call (July 2010 ?)
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( y )
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PROTECT: Pharmacoepidemiological Research on Outcomes of Therapeutics by an European Outcomes of Therapeutics by an European
ConsorTium
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PROTECT is receiving funding from the European C it ' S th F k P Community's Seventh Framework Programme (FP7/2007-2013) for the Innovative Medicine
Initiative (www.imi.europa.eu).
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PROTECT Goal
To strengthen the monitoring of benefit-risk of medicines in Europe by developing innovative medicines in Europe by developing innovative methods
to enhance early detection and assessment of adverse drug reactions from different data sources (clinical
to enable the integration and presentation of data on
trials, spontaneous reporting and observational studies)
pbenefits and risks
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These methods will be tested in real-life situations.
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Rationale: what are the needs ?
• Data collection– efficient and simple methods for early data collection directly from patients– non-prescribed medicines– linkage to health event databases
• Signal detection– spontaneous reports: in-depth analysis of methods and good practice
recommendations– better use of electronic health records and clinical trials
• Signal evaluation– understanding of variability in results of studies of same safety issue in
same or different data sources– detailed guidance and standards regarding design of
pharmacoepidemiological studiesp p g• Benefit-risk assessment
– widely accepted method for integrating data on benefits and risks from clinical trials, observational studies and drug reaction reports
– display of benefit-risk assessment for use by patients, prescribers, regulators...
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regulators...
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PartnersPublic Private
Regulators:EMA (Co-ordinator)DKMA (DK)
GSK (Deputy Co-ordinator)
AEMPS (ES)MHRA (UK)
Academic Institutions:University of Munich
Sanofi- Aventis
Roche
Novartis
Pfizery
FICF (Barcelona)INSERM (Paris)Mario Negri Institute (Milan)
Amgen
Genzyme
Merck Serono
Bayer Schering
A t Z
Others:
WHO UMCUniversity of GroningenUniversity of UtrechtImperial College (London)University of Newcastle Upon Tyne
Astra Zeneca
Lundbeck
NovoNordisk
WHO UMC
GPRD
IAPO
CEIFE
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Upon Tyne SMEs:Outcome EuropePGRx
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Work PackagesgWP2: Framework for Pharmacoepidemiological StudiesTo develop, test and disseminate methodological standards for the design, conduct and analysis of pharmacoepidemiological studies, applicable to different safety issues using different data
WP3: Methods for Signal DetectionTo develop new methods and assess existing ones for signal detection To develop new methods, and assess existing ones, for signal detection from spontaneous reports, electronic health records and clinical trials
WP4: New tools for data collection from consumersTo develop modern methods of data collection directly from consumers To develop modern methods of data collection directly from consumers in their natural language in several EU countries, including using web-based data collection, and computerised telephone interviews.
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Work Packagesg
WP5: Benefit-Risk Integration and RepresentationTo develop methods for use in benefit-risk assessment including both the underpinning modelling and the presentation of the results with a the underpinning modelling and the presentation of the results, with a particular emphasis on graphical methods.
WP6: Validation studies involving an Extended AudienceT lid t th d d l d i WP2 t 5 i i d t To validate methods developed in WP2 to 5 in various data sources owned or managed by Consortium Partners or members of the Extended Audience.
WP7: Training and CommunicationTo identify training opportunities and support training programmes in the fields addressed by PROTECT.
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The PROTECT community
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International work
European Economic Area European Economic Area –– 30 30 member statesmember statesEMA/Commission bilaterals:EMA/Commission bilaterals:•• FDAFDA•• JapanJapan
H lth C dH lth C d•• Health CanadaHealth CanadaMultilateral / globalMultilateral / global•• CIOMSCIOMS•• ICHICH•• ICHICH•• ISOPISOP•• ISPEISPE•• WHOWHO
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•• ISO / CEN / HL7 / CDISCISO / CEN / HL7 / CDISC
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Advantages of International collaborationg
•• Pooling / sharing of expertisePooling / sharing of expertise•• Peer review of each others workPeer review of each others work•• BenchmarkingBenchmarking•• Sharing standardsSharing standards•• Bigger population from which to collect dataBigger population from which to collect datagg p pgg p p•• Bigger databases Bigger databases –– greater power to detect (e.g. EudraVigilance)greater power to detect (e.g. EudraVigilance)•• Different healthcare systems Different healthcare systems –– allows comparisons of use and impact allows comparisons of use and impact
of risk minimisation measuresof risk minimisation measureso s sat o easu eso s sat o easu es
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Standardisation
• Identification of Medicinal Products (IDMP)
• Individual Case Safety Report (ICSR)• Individual Case Safety Report (ICSR)
• Electronic Health Records
• Clinical Trial Registration and Reportingg p g
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From local to global: standardisationFrom local to global: standardisation - Joint Initiative
ICH
ISOTC215
CENTC251
CDISCLiaisingOrganisation
HL7
CDISCOrganisation
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Identification of Medicinal Products
Package
ProductRegulator
Manufacturer
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Substance
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IDMP: Conceptual Overviewp
MPIDPhPID
Medicinal Product - Regulatory Information
Pharmaceutical Product
Pharmaceutical Dose Form
Quantitative Composition
Substance(s)
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Vocabularies
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ICSR Standard
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Standardisation
ICSR – 2011 (mid)
(l )IDMP – 2011 (late)
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From risk to benefit riskFrom risk to benefit risk
• EU Paediatric Regulation: planning pharmacovigilance and effectiveness
• EU Advanced Therapies Regulation: planning pharmacovigilance and effectiveness
• Revised EU Risk management guideline 2010
• Pandemic monitoring
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The European Strategy for Influenza A/H1N1 Vaccine Benefit-Risk MonitoringVaccine Benefit Risk Monitoring
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The European Strategy for Influenza A/H1N1 Vaccine Benefit-Risk Monitoring
• April 2009 novel H1N1 influenza outbreak starts in Mexico
• June 2009 WHO declares pandemic• June 2009 WHO declares pandemic
• September 2009 Commission authorizes pandemic vaccines
• September 2009 Post-authorisation benefit-risk monitoring strategy • September 2009 Post authorisation benefit risk monitoring strategy in place
• How did they do that?
Pharmacovigilance. Building capacity and improving methods39
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Preparation and collaboration! Preparation and collaboration!
• Recommendations developed by a Working group composed of members of the Pharmacovigilance Working Party, the EMA and vaccine manufacturersPharmacovigilance Working Party, the EMA and vaccine manufacturers
• This document describes additional pharmacovigilance activities and additional risk minimisation activities that should be presented, if applicable, by vaccine manufacturers in the Risk Management Plan to be submitted at the same time as an authorisation application.Recommendations made legally mandatory in the European Commission Decision
Pharmacovigilance. Building capacity and improving methods40
• Recommendations made legally mandatory in the European Commission Decision.
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The European Strategy for Influenza A/H1N1 Vaccine Benefit-Risk Monitoring: Rationale
• CHMP Recommendations for the RMP provide obligations to VM
• Other research needs may not be covered• Other research needs may not be covered
• ‘Research groups’ may generate useful data for the B/R of the vaccines or data with high media interest
• These data need to be rapidly evaluated by regulators in order to take quick decisions or respond quickly to public concerns
• Principles of exchange of information to be defined in advance• Principles of exchange of information to be defined in advance
• Proposals for roles and responsibilities
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The European Strategy for Influenza /H1N1 Vaccine Benefit-Risk Monitoring:
• Operational formally since October 09
• Publicly announced November 09
• First EMA pandemic pharmacovigilance report: published 3 December 2009December 2009
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A few results A few results
Spontaneous reports: main data source for vaccine safety monitoringSpontaneous reports: main data source for vaccine safety monitoring
Estimated exposure to pandemic A/H1N1 influenza vaccines (EEA, up to 25 Apr 2010)
40,000,000
20,000,000
25,000,000
30,000,000
35,000,000
ted
ex
po
su
re
Pandemic A/H1N1 influenza vaccines: Reports of ADRs (EEA; up to 25 Apr 2010)
14 35916,000
ed
0
5,000,000
10,000,000
15,000,000
3- 9- 16- 23- 6- 13- 20- 27- 3- 10- 17- 24- 10- 24- 08- 21- 05-
Esti
ma
t
14,456
14,359
14,243
14,015
11,64912,057
12,377 12,705
12,915
13,13013,354
8,745
11,126
13,725
8,000
10,000
12,000
14,000e
re
po
rts r
ece
ive
3-Dec-09
9-Dec-09
16-Dec-09
23-Dec-09
6-Jan-10
13-Jan-10
20-Jan-10
27-Jan-10
3-Feb-10
10-Feb-10
17-Feb-10
24-Feb-10
10-Mar-10
24-Mar-10
08-Apr-10
21-Apr-10
05-May-10
Date of update publication3,882
1,469800
2,644
523 408 320 328 210 215 224 371 228 116 97
2,381
290
5,301 6,101
0
2,000
4,000
6,000
3- 9- 16- 23- 6- 13- 20- 27- 3- 10- 17- 24- 10- 24- 08- 21- 05-
Nu
mb
er
of
ca
se
Exposure ADR reports P d i 30 6 illi 10 912
Pharmacovigilance. Building capacity and improving methods43
3Dec-09
9Dec-09
16Dec-09
23Dec-09
6Jan-10
13Jan-10
20Jan-10
27Jan-10
3Feb-10
10Feb-10
17Feb-10
24Feb-10
10Mar-10
24Mar-10
08Apr-10
21Apr-10
05May-10
Date of update publication
New cases since last report Total received over time
Pandemrix: 30.6 million 10,912Focetria: 6.5 million 3,018Celvapan: 0.6 million 551
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Be informed• Be informed about key strategic developments:
– EMA working to ensure stakeholders have the information needed for excellence pharmacovigilance and risk management:for excellence pharmacovigilance and risk management:• The European Network for Pharmacoepidemiology and
Pharmacovigilance (ENCePP) is now operational. Opportunity to engage: ENCePP Info-Day 26 Nov 2010
• EudraVigilance is the EU system for managing safety reports and detecting safety signals. EudraVigilance Info-Days: 22 June and 19 October 2010I t t k i t ti l t d di ti • Important work on international standardisation on pharmacovigilance. New individual case safety report Info-Day 25 June 2010
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EMA is the hub of the European NetworkEMA is the hub of the European Networkpp
k h h bWorking with the Member States,
industry, sponsors, health
professionals and patients to build
capacity and improve methods.
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