university joins industry: clinical trials & drug safety
TRANSCRIPT
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University joins
Industry:
Clinical Trials & Drug Safety
Aula Magna-Facultad de Farmacia 11 Marzo 2015
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• Background, key points and basic knowledge
• Department tasks and responsibilities • Importance of the department within the
Pharmaceutical Industry • Career development • Personal skills
Contents
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Clinical Trials
Human research
CLINICAL TRIALS
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Ethics and Clinical Trials
• Nuremberg Code (1947) • Declaration of Helsinki (1964) • Belmont report (1978)
• Core principles: • Respect for persons • Beneficence • Justice
• Areas of application • Informed consent • Assessments of risks and benefits • Selection of subjects
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Regulation and Clinical Trials • Good Clinical Practise (GCP) • International Conference Harmonisation (ICH)
• Real Decreto 223/2004
• Directive 2001/20/EC • Regulation EU No 536/2014
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Definition of Clinical Trials
Clinical trials are studies that are intended to discover or verify the effects of one or more investigational medicines. The regulation of clinical trials aims to ensure that the rights, safety and well-being of trial subjects are protected and the results of clinical trials are credible.
Arguments in favour of performing clinical trials are those pointing out that the
alternative: uncertainty medical practice is always worst
Evidence Based Medicine
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Main objective of Clinical Trials
• DESCRIPTIVE : broaden knowledge
• ANALITYCAL : evaluate intervention
(hypothesis testing)
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CONFIDENCIAL © ESTEVE, 2015 8
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CONFIDENCIAL © ESTEVE, 2015 23.05.2006 Dr. Enrique Jiménez 9
Phase I : healthy subjects (ocasionally patients) to evaluate pharmacokinetic, pharmacodynamics giving preliminary information about safety and efficacy of the drug. Non therapeutic benefit.
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CONFIDENCIAL © ESTEVE, 2015 23.05.2006 Dr. Enrique Jiménez 10
Fases de los E.C.
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Fases de los E.C.
Phase II : patients to get the most effective dose of the drug for a specific disease. Preliminary information on efficacy and safety and first hints on therapeutic effect.
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Fases de los E.C.
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CONFIDENCIAL © ESTEVE, 2015 23.05.2006 Dr. Enrique Jiménez 13
Fases de los E.C.
Phase III : CT designed to know drug safety and efficacy compared to a drug of known efficacy in a sample of patients representative of the general population.
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Fases de los E.C.
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Fases de los E.C.
Phase IV : CT with a marketed drug to evaluate the effectivenes and long term use of a drug (both efficacy and safety).
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Stakeholders in Clinical Trials
• Sponsor • Monitor (Clinical Research Associate) • Investigator • Health Authorities: AEMPS, EMA, FDA……. • Ethics Committees • PATIENTS/SUBJECTS !!!
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Some figures in Clinical Trials
• In the EEA, approximately 4,000 clinical trials are authorised each year. This equals approximately 8,000 clinical-trial applications, with each trial involving two Member States on average.
• Approximately 61% of clinical trials are sponsored by the pharmaceutical industry and 39% by non-commercial sponsors, mainly academia.
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Some figures in Clinical Trials
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Some figures in Clinical Trials
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Spain competitivity in Clinical Research
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Department tasks and responsibilities
SPONSOR • PROTOCOL/INFORMED CONSENT/CASE REPORT FORM/INVESTIGATOR BROCHURE (IB)
• INVESTIGATOR/MONITOR selection
• ETHICS COMMITTEE AND HEALTH AUTHORITIES approval
• PROVIDE DRUG STUDY medication
• SUBMIT ANY SERIOUS ADVERSE EVENT occurred during study
• PROVIDE INSURANCE to patients participants
• COLLECTION and ANALYSIS of patient data
• ELABORATTE FINAL REPORT
• PUBLISH RESULTS following transparency policy
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Clinical Trials within Pharmaceutical Industry
Preclinical Phase I Phase II Phase III Submission LCM
Commercialization
Global Product Team
Commercial Team
Manufacturing Team
Regulatory Team
Clinical Team
Emerging BU Task Force
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Internal Interfaces
Data Management
Medical Monitor
Statistics
Clinical QA
Drug Safety
Trial supply group
Medical Writing
Regulatory Affairs
Finance Legal
Vendors Management
Clinical Pharmacology
TRIAL MANAGEMENT
TEAM
Clinical Trial Director
Clinical trial Manager
Clinical trial monitor
CLINICAL TRIAL TEAM
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External Interfaces
Manufacturing providers
Health Authorities
Steering Committees
Partner Due
dilligence
CROs
Ethics Committees
Media Press
World Couriers
Laboratory Data
Patients
Investigators
TRIAL MANAGEMENT
TEAM
Clinical Trial Director
Clinical trial Manager
Clinical trial monitor
CLINICAL TRIAL TEAM
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Career development
• EARLY CLINICAL DEVELOPMENT:
• Design of phase I/II studies for small and biotech companies (medical writing, monitoring, analysis and data entry, statistics and publication)
• LATEST CLINICAL DEVELOPMENT
• Operational aspects of clinical trials: monitor/CRA
• Regulatory: regulatory and GCP compliance
• Medical writing and publication
• Data management and statistics
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Personal Skills “Clinical Research Associate” Core Competencies: • Leadership skills • Team work • Negotiation skills • Conflict management
• Familiar with basic computer and database applications • Good leadership, analytical, problem solving and time
management skills
• Comunication skills
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Drug Safety/Pharmacovigilance Public health activity with the main objective of identification, quantification, evaluation and decission taking in front of the presence of durg risks once are marketed.
Spain: - Real Decreto 1344/2007 - Reglamento 1235/2010 - Directiva 2010/84 - Buenas Prácticas de Farmacovigilancia ( 21 de Diciembre 2011)
EU: - Regulation 1235/2010 - Commission Implementing regulation (EU) No 520/2012 - Directive 2010(84 - Good Pharmacovigilance Practices (GVP)
Legal framework
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Background history 1937 • Renal failure by dietilenglicol/sulfamide elixir
1938 • FDA demands toxicological and preclinical
controls for drug investigation 1950 • Cloranfenicol, causal agent of aplastic
anemia 1960 • FDA initiates the collection of Adeverse Drug
Reactions in the Johns Hopkins H & Boston Collaborative Drug Surveillance Program: intrahospitalary monitorization
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Background history
• 1960-62 “The Thalidomide DISASTER” Cases of focomelia (congenital malformation). The first case was published in Lancet (WG McBridel) suggesting a relationship with the thalidomide ingestion. Thalidomide was withdrawn in 1962 after more than 4.000 cases were registered worldwide. • 1962 WHO initiates an international
program to collect and monitor adverse drug reactions.
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Drug safety tasks and responsibilities
Pharmacovigilance System Master File (PSMF) of the company Individual Case Safety Reports management § Data entry in database § Medical evaluation & reportability assessment to regulators and/or licensors; Interaction to obtain follow up. § Weekly Scientific/Medical Literature Search
Periodic Safety Update Reports (PSUR)s creation § Preparation and scientific assessment of data in Periodic Safety Update Reports (PSUR), Annual Safety Report
(ASR), etc. § Responses to R-PSURs assessment reports
Labeling § Review of safety data of all SmPCs/PILs to be created/harmonised according to guideline on SmPCs (October
2005) and legibility test. § Preparation and scientific assessment of data in Periodic Safety Update Reports (PSUR), Annual Safety Report
(ASR), etc.
Risk Management Plan (RMP) elaboration Benefit/risk evaluation SOP creation and update Safety Data Exchange Agreements (SDEA) § Maintenance and update
Training of sales network and Company employees Audits
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External Interfaces
Drug safety & Pharmacovigilance Department
Toxicology Services
Medical Literature
International Congresses
Cooperative Groups
Licensors Safety Data Exchange Agreements
Health Professionals
Consumers/ Patients
EMA FDA Other ROW
Hospitals Autonomous Community
AEMPS Local Health Authorities
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Internal Interfaces
Databases
Sales Network
Regulatory Affairs
Clinical Research
Legal Department
Medical Affairs
Licensors
Marketing Technical Director
CEO
Quality Control
Quality Assurance
Drug safety & Pharmacovigilance Department
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Career development • Every single company needs to have a Drug Safety Responsible:
• EU QPPV (Qualified Person for Pharmacovigilance) and back-up
• Local Safety Officer (multinational company)
• Regulatory and Good Pharmacovigilance Practises (GVP) compliance:
• Drug Safety Officer (DSO): pharmacist, biologist, chemistry
• Medical Drug Safety Officer (MDSO): benefit/risk assessment of the drugs
• Compilating of pharmacovigilance documents: PSURs, RMPs, PASS
• DSO
• MDSO
• EU QPPV
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Personal Skills “Drug Safety Officer”
Core Competencies: • Comprehensive knowledge of international drug safety and
pharmacovigilance principles and regulations • Extensive knowledge of drug safety and drug development
process and procedures • In-depth knowledge of coding principles, submission criteria,
regulatory timeline requirements, technical requirements and guidelines
• Possess sound communication skills, both in verbal and written • Familiar with basic computer and database applications • Good leadership, analytical, problem solving and time
management skills
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Highly appreciated Values
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