due to its complexity it cannot be fully characterized by analytical … uimp 2014.pdf · 2014. 9....
TRANSCRIPT
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COMMISSION DIRECTIVE 2003/63/EC of 25 June 2003
due to its complexity it cannot be fully characterized by analytical testing alone
quality determined by a combination of physico-chemical and biological testing, together with the production process and its control
bioactivity and immunogenicity are dependent upon all its structural features
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well defined molecular structure, easy to characterize
impurity profile related to synthesis and degradation routes
Chemical med product
safety and efficacy are independent of the origin of the product
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IBUPROFENO (mol. mass 206.29 g/mol)
VANCOMICINA (mol. mass 1449.3 g/mol)
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INSULINA (5808 Da)
MoAb (150 000 Da)
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INSULINA (5808 Da)
MoAb (150 000 Da)
Trp (204.23
g/mol)
206.29 g/mol
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IBUPROFENO VANCOMICINA
INSULINA MoAb
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BIOTECNOLÓGICOS
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i) Idénticas a la molécula natural
ii) Moléculas modificadas/nuevas
Hormona de crecimiento
Insulina*
Proteínas de fusión (TNFR:Fc)
Anticuerpos monoclonales “humanizados”
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Yeast Saccharomyces
Mammalian cell lines CHO (Chinese hamster ovary)
NS0 (murine myeloma)
Bacteria E. coli
12
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Recombinant baculovirus expression system and the insect cell line Hi-5 Rix4446 derived from Trichoplusia ni
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FDA approval May 2012
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Year of approval
Commercial name
Active ingredient
Indication
1996 CEAScan Arcitumomab Diagnostic agent for carcinoma of the colon or rectum
1997 LeucoScan Sulesomab Diagnostic agent (location and extent of infection/inflammation of bones)
1998
Mabthera Rituximab Rheumatoid arthritis (RA)
Simulect Basiliximab Prophylaxis of acute organ rejection in de novo allogeneic renal transplantation in adult and paediatric patients (1-17 years)
1999
Remicade Infliximab RA
Zenapax Daclizumab Prophylaxis of acute organ rejection in de novo allogeneic renal transplantation
Synagis Pavilizumab Prevention of serious lower respiratory tract disease by RSV
2000 Herceptin Trastuzumab Treatment of patients with metastatic breast cancer whose tumours overexpress HER2.
2001 MabCampath Alentuzumab Treatment of patients with B-cell chronic lymphocytic leukaemia
2003 Trudexa Adalimumab RA
Humira Adalimumab RA, psoriasis
2004
Raptiva Efalizumab Chronic plaque psoriasis
Erbitux Cetuximab Treatment of patients with EGFR-expressing, KRAS wt metastatic colorectal cancer
Zevalin Ibritumomab
tiuxetan
Consolidation therapy after remission induction in previously untreated patients with follicular lymphoma
2005
Xolair Omalizumab Add-on therapy to improve asthma control in adult and adolescent patients (12 years of age and above) with severe persistent allergic asthma
Avastin Bevacizumab Treatment of patients with metastatic carcinoma of the colon or rectum, metastatic breast cancer, renal cell cancer, non small cell lung cancer
2006 Tysabri Natalizumab Single disease modifying therapy in highly active relapsing remitting multiple sclerosis
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2007
Soliris Eculizumab Treatment of patients with paroxysmal nocturnal haemoglobinuria (PNH)
Vectibix Panitumumab Treatment of patients with EGFR expressing metastatic colorectal carcinoma with non-mutated (wild-type) KRAS
Lucentis Ranibizumab Treatment of neovascular (wet) age-related macular degeneration (AMD)
2009
Removab Catumaxomab Intraperitoneal treatment of malignant ascites in patients with EpCAM positive carcinomas
RoActemra Tocilizumab Rheumatoid arthritis in combination with MTX
Stelara Ustekinumab Treatment of moderate to severe plaque psoriasis
Cimzia Certolizumab
pegol Rheumatoid arthritis in combination with MTX
Simponi Golimumab Treatment of rheumatoid arthritis , psoriatic arthritis and ankylosing spondylitis
Ilaris Canakinumab
Treatment of adults, adolescents and children aged 4 years and older with Cryopyrin-Associated Periodic Syndromes (CAPS), including Muckle-Wells Syndrome (MWS), Neonatal-Onset Multisystem Inflammatory Disease (NOMID) / Chronic Infantile Neurological, Cutaneous, Articular Syndrome (CINCA), and severe forms of Familial Cold Autoinflammatory Syndrome (FCAS).
Scintimun Besilesomab A radiopharmaceutical intended for use in scintigraphic imaging in adults with suspected osteomyelitis
Prolia Denosumab Treatment of osteoporosis in postmenopausal women
2010 Arzerra Ofatumumab Arzerra is used to treat chronic lymphocytic leukaemia (CLL)
2011
Benlysta Belimumab Add-on therapy in adult patients with active autoantibody-positive systemic lupus erythematosus with a high degree of disease activity
Yervoy Ipilimumab Treatment of advanced (unresectable or metastatic) melanoma in adults who have received prior therapy
Xgeva Denosumab Prevention of skeletal-related events in adults with bone metastases from solid tumours
June 2012
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• Una autorización única para toda la UE
• 210 días
• Mismas indicaciones y ficha técnica (prospecto)
El precio y la financiación las decide cada país
individualmente
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SCIENTIFIC COMMITTEES
CVMP COMP HMPC
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FINAL opinion on medicines for human
use
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• Chair & Vice-Chair • 1 scientific expert member nominated by each MS (+1 alternate) - 28
• 1 scientific expert member from NO and ICE (+1 alternate) (observers)
• 5 co-opted members (experts in specific areas of interest for the CHMP)
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Centralised Procedure
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RIESGO
BENEFICIO
– –
+
PLAN MANEJO DE RIESGOS
–
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EPAR European Public Assessment Report
= available in all EU languages
Summary Presentations
Package Leaflet
Summary of Product Characteristics
Scientific discussion
Steps taken before authorisation of the product
Steps taken after granting the Marketing Authorisation (if applicable)
= available in English
Labelling
all readers
patients
pharmacists/patients
health professionals
scientific community / health professionals
anyone interested
PRODUCT INFORMATION
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General information to the public
Name, INN, therapeutic area, MAH
SmPC, Labelling, Package leaflet, Presentations, Manufacturers (MAH, AS), Conditions to the MA
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Current sales of the drug are modest, at 70 million pounds ($106 million) in 2012, but GSK hopes it will become a major seller.
(http://www.reuters.com/article/2013/04/03/glaxosmithkline-benlysta-idUSL5N0CQ2NN20130403)
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March 2014
January 2014
EMA >> Committees >> CHMP>> Agendas, minutes and highlights
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May 2014
June 2014
July 2014
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2013
LEMTRADA Alentuzumab (anti-CD52) Relapsing remitting MS
REMSIMA
INFLECTRA Infliximab (anti-TNF) Same indications as Remicade
KADCYLA Trastuzumab emtansine HER2-positive breast cancer
2014
SYLVANT Siltuximab (anti-IL-6) Multicentric Castleman’s disease
ENTYVIO Vedolizumab (anti-integrin α4β7) Moderately to severely active Crohn’s disease
GAZYVARO Obinutuzumab (anti-CD20) Chronic lymphocytic leukaemia
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16 April 2010
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Marketing authorization through the centralized procedure (biotechnological products)
Same pharmaceutical form, dose and route of administration as the reference product
No extrapolation between different routes of administration
The reference product should be the same throughout the dossier and it should be available in the EU
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Preclinical Comparative studies in vitro and in vivo
– - PK – - PD – - Immunogenicity – - Toxicity
Efficacy and safety data showing comparability
Immunogenicity data
Pharmacovigilance system and risk management plan
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Guideline on Similar Biological Medicinal Products
Guideline on Similar Biological Medicinal Products Containing Biotechnology-Derived Proteins as Active
Substance: Quality Issues
Overarching
Quality
Annexes
Guideline on Similar Biological Medicinal Products Containing Biotechnology-Derived Proteins as Active
Substance: Nonclinical & Clinical Issues
Nonclinical & Clinical
Directives 2003/63 - 2004/27
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30/07/2014
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07/2007 CEREPRO AdV-HSVtk. Withdrawn by the applicant before the final negative opinion on the 2nd application
12/2008 ADVEXIN AdV-p53. Withdrawn by the applicant before the final negative opinion
07/2009 CHONDROCELECT Autologous chondrocytes. Marketing authorization granted
07/2012 GLYBERA AAV-LPL. Marketing authorization granted after 4rd evaluation
01/2013 HYALOGRAFT C
AUTOGRAFT
Autologous chondrocytes. Withdrawn by the applicant before the negative opinion
03/2013 ORANERA Autologous oral mucosal epithelial cells. Withdrawn by the applicant before the negative opinion
04/2013 MACI Matrix-induced autologous chondrocyte implantation. Marketing authorization granted
06/2013 PROVENGE Autologous peripheral blood mononuclear cells activated with PAP-GM-CSF (sipuleucel-T). Marketing authorization granted
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