Turkiyede klinik arastirma 2015 ing
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Transcript of Turkiyede klinik arastirma 2015 ing
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CLINICAL TRIALS IN TURKEY
Dr. Hamdi Akan [email protected] University Faculty of MedicineDept. of HematologyClinical Trials Unit
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What is a Clinical Trial?
A prospective trial, done with the purpose of comparing the effect and value of an intervention with the control group in a clinical situation, is called a
Friedman LM, Furberg CD, DeMets DL: Fundamentals of Clinical Trials (2nd edition). St. Louis, Mosby 1985.
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DRUG
SURGERY
MEDICAL DEVICE
DIET
PHYSICAL THERAPY
DIAGNOSTIC INTERVENTION
EDUCATION
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Drug Development Process
GLP
GMP
GCP
Pre-clinic1- 3 Year
Clinical trial3- 8 Years
Post-approval
Synthesis and Formulation
Idea
Animal/in vitrotest
Phase III
Phase IV
NDAIND
Phase II
Phase I
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Daily medical practice aims to gain a benefit to a patient by treating.
Clinical research aims to find a scientific answer that may help future patients.
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Although scientific rules regulate the daily medical practice, they can be modified when necessary.
Clinical research has to be performed according to previously defined rules and regulations. To deviate from them can be acceptable for the benefit of the patient but may be wrong on behalf of the clinical research.
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SCORBUT
A big problem for the English army in 1700’s.
James Lind separated 12 sailors in 6 groups. They all received the same diet plus; Vinegar
Diluted sulfuric acid
Apple vinegar
Garlic, radish
2 Orange and 1 lemon
No addition
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SEMMELWEIS
The mortality rates in the clinic dropped form 18.3% to 1.3% after hand washing of the medical students.
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No one believed him
Fired after 1 year
Went back to Budapest and conducted a new study
Mortality decreased to 1% from 15%
Vienna Medical Journal refused the paper summarizing his results
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Our rights are the result of our mistakes
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Massengil Co.
Harold Watkins
1937
SULFONILAMIDE DISASTER
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NOTHING RIGHT!
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TUSKEGEE STUDY
Started in 1932. Aimed to observe the natural course ofuntreated syphilis.
Volunteers were poor African Americans. Free medicalcare was offered and they entered an observationalstudy without information and consent.
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The study was terminated in 1972; 20 years after the discovery of teheffectiveness of Penicillin in syphilis. New York Times reported this as teh‘’longest study in medical history, performed on humans without anytreatment’’.
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Kefauver–Harris Drug Amendment ‘’Efficacy and
Safety’’
1962Frances Oldham Kelsey
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HELSINKI DECLARATION
Adopted by the 18th WMA General Assembly, Helsinki, Finland, June 1964, and amended by the:
29th WMA General Assembly, Tokyo, Japan, October 197535th WMA General Assembly, Venice, Italy, October 1983
41st WMA General Assembly, Hong Kong, September 198948th WMA General Assembly, Somerset West, Republic of South Africa,
October 199652nd WMA General Assembly, Edinburgh, Scotland, October 2000
53rd WMA General Assembly, Washington 2002 (Note of Clarification on paragraph 29 added)
55th WMA General Assembly, Tokyo 2004 (Note of Clarification on Paragraph 30 added)
59th WMA General Assembly, Seoul, October 2008
1964
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ICH-GCP
1980 – Harmonization of regulations in Europe
1989 – Europe, Japan and USA joining forces
1990 April - ICH meeting in Brussels
Partners:
European Commission, European Medicines Agency (EMEA), European Federation of Pharmaceutical Industries and Associations
(EFPIA), JapanMinistry of Health, Labour and Welfare, Japan Pharmaceutical Manufacturers Association (JPMA), Food and Drug Administration (FDA), Pharmaceutical Research and Manufacturers of America (PhRMA).
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ICH Guidelines
QSEM
QualitySafety
Efficacy
MultidisciplinaryGCP
E6-R1
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TURKEY
First Regulations:
Code of Pharmaceutical Products and Preparations -1928
Bakanlıkça İlaç İmal ve Satış İzni verilebilmesi için Tahlil ve Tetkik neticesinde formülüne uygun ve bildirilen tedavi vasıflarına haiz olması gereklidir (Madde 7.E)
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TURKEY
Code of the Application of Medical Practice –1928
Article 70: All medical doctors have to get consent from the patients; and from the parents of a child for every intervention
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TURKEY
The Constitutional Code– 1987
‘the scientific research with licensed or not licensed medicines on human subject cannot be done if the Ministry of Health (MOH) approval and the relevant patient’s consent are not in place’
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TURKEY
Medical Deontology Bylaw – 1960
Article 10: The regulation for the Investigator to apply and to offer his/her new diagnostic and therapeutic approach.
Article 11: No medical experiment can be conducted on human, but if the available treatment options are not sufficient to benefit the patient, a conditioned permission can be granted
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Nerium oleander case
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REGULATIONS IN TURKEY
Regulation on Clinical Trials 29.01.1993
Regulation on the evaluation of Bioavailability and
Bioequivalance of pharmaceutical products
27.05.1995
Good Clinical Practice Guideline 29.12.1995
Bylaw on Patient Rights 01.08.1998
Criminal Code 2005
Bylaw on Animal Experiments 16.05.2004
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ETHICAL COMMITTEES
The Central Ethical Committee was formed in 23/01/1993 and the first meeting was in 1994.
107 Ethical Committees in Turkey
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There will be a penalty of imprisonment from one to three years for those conducting medical experiments on human
Criminal CodeArticle: 90
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Criminal CodeArticle: 90
To preclude a penalty the following are mandatory:
Approval from authorities
Preclinical and animal studies
A rationale for experimenting on human from the initial scientific information
No permenant risk and harm, no pain
Evaluation of Risk/Benefit ratio
Informed Consent
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Criminal CodeArticle: 90
The following are the requirements for medical experimentation on children not to raise criminal liability:
Same conditions for the adults
Obligatory to conduct on children
Child assent + Parent consent
A pediatrician in Ethical Committees
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Türk Ceza Kanunu Madde: 90
İnsan üzerinde gerekliliklere uyulmaksızın deney yapılması sonucu:
Mağdurun yaralanması veya ölmesi halinde kasten yaralama veya kasten adam öldürme suçuna ilişkin hükümler uygulanır.
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Drug
• Regulation on Clinical Trials of Medicinal and Biological Products (2014)
Medical Device
•Bylaw on Clinical Trials with medical Devices (2014)
Observational Drug Studies
•Guideline on Observational Drug Studies (2014)
Cosmetic Products
•Bylaw on Clinical trials with Cosmetic Products (2015)
Herbal Products
•Bylaw on Medical GelenekselBitkisel TıbbiÜrünlerYönetmeliği(2010)
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INFRASTRUCTURE OF CLINICAL TRIALS IN TURKEY
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2014
Number of Hospitals: 1528
Number of Beds: 206.836
Number of Medical Doctors: 135.616
Number of specialists: 75.251
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Clinical Trials Journey of Turkey-Long and Thin Road. Hilal Ilbars, Kaan Kavaklı, Hamdi Akan, Duygu Koyuncu Irmak. J Clin Trials 2015, 5:2
Number of Hospitals: 1528
Number of Beds: 206.836
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Clinical Trials Journey of Turkey-Long and Thin Road. Hilal Ilbars, Kaan Kavaklı, Hamdi Akan, Duygu Koyuncu Irmak. J Clin Trials 2015, 5:2
Number of Medical Doctors: 135.616
Number of specialists: 75.251
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Total 201.701
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Clinical Trials Journey of Turkey-Long and Thin Road. Hilal Ilbars, Kaan Kavaklı, Hamdi Akan, Duygu Koyuncu Irmak. J Clin Trials 2015, 5:2
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0
5
10
15
20
25
30
35
40
45
2009 2010 2011 2012 2013 2014
21 1
13
29
44
Approved Medical Device Clinical Trials
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Başvuru dosyalarınınhazırlanması
Sözleşme ve Bütçe
İthalat İzniDosyalarınınhazırlanması
SağlıkBakanlığına
Başvuru
Kontratlarıntamamlanması
İthal izni içinSağlık
Bakanlığınabaşvuru
Start
AraştırmaHastaneleri
ÜniversiteHastaneleri
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CLINICAL RESEARCH UNIT
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ÇA
Y
OC
AĞ
I
ÇALIŞMA 4 ÇALIŞMA 5İLAÇ
ODASI
ÇALIŞMA 3 ÇALIŞMA 2 ÇALIŞMA 1
ASANSÖR
SEKRETERLİK
DOKTOR
ODASI
ANA GİRİŞ-ÇIKIŞ KAPISI
KLİNİK ARAŞTIRMA 1.KAT
SU
NU
M O
DA
SI
GÖNÜLLÜ
BEKLEME.
KLİNİK ARAŞTIRMA 2.KAT
GİRİŞİM
ODASI/
KAN ALMA
BİLİŞİM ODASIARŞİV
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ARŞİV
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GİRİSİM
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BEKLEME
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Ankara University Dept. of Hematology CR Software
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Database
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SOP’s
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PHASE I CENTERS
Ege University ARGEFAR Phase I and BA/BE Center
Ege University Medical Faculty Pediatric Hematology Phase I Center
Erciyes University Hakan Çetinsaya Phase I and BA/BE Center
Gaziantep Phase I and BA/BE Center
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INSPECTIONSYIL DENETİCİ KURUM
2004 FDA Ege University, Gastroenterology İzmir
2006 FDA Istanbul University, Romatology İstanbul
2006 FDA Ege University, Pulmonary Diseases İzmir
2007 FDA Ege University, General Surgery İzmir
2007 FDA Dokuz Eylül, General Surgery İzmir
2009 EMA Ege University General Surgery İzmir
2010 FDA İstanbul University, Medical Oncology İstanbul
2013 FDA Yüzüncü Yıl, Pediatrics Van
2013 EMA Ankara University, Hematology Ankara
Clinical Trials Journey of Turkey-Long and Thin Road. Hilal Ilbars, Kaan Kavaklı, Hamdi Akan, Duygu Koyuncu Irmak. J Clin Trials 2015, 5:2
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AUTHORITY (MoH)
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NGO’s/Academic organizations
Clinical Research Association (KAD)
Istanbul Clinical Research Initiative (IKAI)
Istanbul University Clinical Research Excellence Center
Association of Contract Research Organizations (SAKDER)
Turkey Clinical Research Infrastructure Network (TUCRIN)
Association of Research-Based Pharmaceutical Companies (AIFD)
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GOOD CLINICAL PRACTICE CERTIFICATION
Not legally obligatory for clinical investigator but needed to participate in a clinical trial,
Legally binding for Ethical Committee members
GCP educated health care personnel ≈ 10.000
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Clinical Research Distance Learning Program
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Clinical Research Distance Learning Program
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Book on Clinical Research
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Handbook on GCP
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GCP Journal
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Clinical Research
Dictionary
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Book on Good Presentation Skills
Book on Medical Publications
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MANUSCRIPTS on CLINICAL RESEARCH
1. Patients’ Motivation about Clinical Trials: A Local Perspective from Turkey. Hakan TABAN, Osman GörkemMURATOGLU, Bulut GÜÇ, Abdurahim HAJYOUSSEF, Atila KARAALP. Marmara Medical Journal 2011;24:181-6
2. Turkey’s Trial Status. Hilal İlbars, Gülbin Özçelikay. GCP Journal, 2005: 17-19
3. Clinical Scientific Research Potentials in Turkey. Emin Kansu et al. Monitor 2006: 51-54
4. New GCP Rules in Turkey. Hamdi Akan et al. Monitor 2007: 41-44
5. Turkey’s Position Regarding Clinical Drug Trials. Nüket Örnek Büken. Clinical Research and Regulatory Affairs 2003: 20(3); 349–355, 2003
6. Clinical Trials in Turkey. Hilal İlbars. Turkish Journal of Hematology 2013;30:111-114
7. Transparency in Clinical Research and Status in Turkey & Middle East. Nursah O. Cetinkaya. Applied Clinical Research, Clinical Trials & Regulatory Affairs, 2015 (2)
8. Orphan Drugs: R&D Challenges with Updates from Turkey and Middle East Countries. Hilal İlbars, Duygu K. Irmak, Hamdi Akan. Journal for Clinical Studies 2014: 6(2): 58-6
9. Clinical Trials Journey of Turkey-Long and Thin Road. Hilal Ilbars, Kaan Kavakli, Hamdi Akan, Duygu KoyuncuIrmak. J Clin Trials 2015, 5:2
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TRANSPERANCY IN CLINICAL TRIALS
Presenting information on clinical trials in a publicly accessible database
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Obligatory in Turkey
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www.klinikarastirmalar.org.tr/en