by analytical testing alone - cdn.ymaws.com · ZALMOXIS T cells -HSV TK 05/2017 SPHEROX Spheroids...
Transcript of by analytical testing alone - cdn.ymaws.com · ZALMOXIS T cells -HSV TK 05/2017 SPHEROX Spheroids...
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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
biological activity and immunogenicity are dependent upon all its structural features
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Yeast Saccharomyces
Mammalian cell lines CHO (Chinese hamster ovary)
NS0 (murine myeloma)
Bacteria E. coli
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Nature Reviews Drug Discovery March 2003
Pegasys (PEG-IFNα 2a)
PegIntron (PEG-IFNα 2b)
Mircera (PEG-EPO)
Plegridy (PEG-IFN beta-1a)
Adynovi (PEG-FVIII)
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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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ATMP in the EU
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Specific rules regarding the authorization supervision pharmacovigilance of advanced therapy medicinal products (ATMPs)
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HIV
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Tissue engineered product means a product that:
— contains or consists of engineered cells or tissues,
and
— is administered to human beings with a view to regenerating, repairing or replacing a human tissue
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limbal stem cells
chondrocytes
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From EMA
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SHOULD COMPLY WITH THE LEGISLATION FOR MED PROD
• their use needs to be authorized: marketing authorization, clinical study, compassionate use…
• quality, safety and efficacy
• GMP (production & control), GLP (non-clinical) and GCP (clinical studies) apply
clinical studies, compassionate use hospital exemption
MA in the EU (centralized procedure)
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Advanced therapy medicinal products which are intended to be placed on the market in Member States and either prepared industrially or manufactured by a method involving an industrial process (Title II of Directive 2001/83).
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Advanced Therapy Medicinal Products
Regulation (EC) 1394/2007
Marketing authorisation required
Demonstration of Q, S & E
Post-authorisation vigilance of S & E
Centralised procedure mandatory
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Price and reimbursement decided by each member
state
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from EMA
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from EMA
ERA
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QUALITY
DRAFT OPINION
RMP
OVERALL FINAL OPINION
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• 1 member per MS (+1 alt) - 28
• 1 member from NO and ICE (+1 alt) (observers)
• 5 co-opted members (elected by the CHMP)
FINAL opinion on ALL medicines for HUMAN use
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45
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07/2009 CHONDROCELECT Autologous chondrocytes
07/2012 GLYBERA AAV-LPL
04/2013 MACI Matrix-induced autologous chondrocyte implantation
06/2013 PROVENGE Autologous PBMC activated with PAP-GM-CSF
12/2014 HOLOCLAR Autologous human corneal epithelial cells
10/2015 IMLYGIC Oncolytic HSV-1 - GM-CSF
04/2016 STRIMVELIS Autologous CD34+ - RV hu ADA
06/2016 ZALMOXIS T cells - HSV-TK
05/2017 SPHEROX Spheroids of human autologous matrix-associated
chondrocytes
12 / 2017 ALOFISEL Allogeneic expanded adipose stem cells
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07/2007 CEREPRO AdV-HSVtk
12/2008 ADVEXIN AdV-p53
01/2013 HYALOGRAFT C
AUTOGRAFT Autologous chondrocytes
03/2013 ORANERA Autologous oral mucosal epithelial
cells
10/2015 HEPARESC Human heterologous liver cells
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• NIBSC
• EDQM
Veronika Jekerle (Sci. secretariat)
Klara Tiitso (back-up)
Nadja Kriste (secretariat)
Angelo Pacifico (secretariat)
S. Ruiz (chair)
N. Kruse (vice-chair)
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HISTORY
1986 Working Party on Biotechnology and Pharmacy to advise the
CPMP on quality aspects of emerging medicinal products
produced by biotechnological processes. Develop specific
recommendations on quality and safety
1995 Biotechnology Working Party was established as a permanent
working party of the CPMP (now CHMP)
Now: 11 meetings / year (2-2,5 days/month)
57 V. Jekerle (EMA)
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Analysis of the expression construct in cell lines used for production of r-DNA derived proteins (1995)
Stability testing of biotechnological/biological products (1995)
Validation of analytical procedures(1996)
Viral safety evaluation of medicinal products derived from cell lines of human or animal origin (1997)
Early guidelines
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V. Jekerle (EMA)
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V. Jekerle (EMA)
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V. Jekerle (EMA)
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J-H Trouvin
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J-H Trouvin
Some examples…
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J-H Trouvin
Some examples…
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J-H Trouvin
Some examples…
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J-H Trouvin
Some examples…
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J-H Trouvin
Summary
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07/2009 CHONDROCELECT Autologous chondrocytes
07/2012 GLYBERA AAV-LPL
04/2013 MACI Matrix-induced autologous chondrocyte implantation
06/2013 PROVENGE Autologous PBMC activated with PAP-GM-CSF
12/2014 HOLOCLAR Autologous human corneal epithelial cells
10/2015 IMLYGIC Oncolytic HSV-1 - GM-CSF
04/2016 STRIMVELIS Autologous CD34+ - RV hu ADA
06/2016 ZALMOXIS T cells - HSV-TK
05/2017 SPHEROX Spheroids of human autologous matrix-associated
chondrocytes
12 / 2017 ALOFISEL Allogeneic expanded adipose stem cells
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Provenge
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76
Provenge® (sipuleucel-T) manufacturing
process overview
36-44 hrs
18 hr shelf life
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CHALLENGES VS OTHER BIOLOGICALS
New type of products
Gene therapy
Cell therapy
Tissue Engineered products
New challenges in terms of
Definition of the product
Characterisation and setting specifications
Validation and quality control parameters
Potency assay
Validation of a process
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• Manufacture, characterisation and control of the DS • Specifications • Comparability / biosimilarity • Plasma-derived medicinal products • Plasma master file (PMF) • Vaccines • Stability
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• Pharmaceutical Development
• Product Information
• Adventitious Agents / Viral Safety
• Transmissible Spongiform Encephalopathies (TSE)
• CJD related
• Investigational Medicinal Products
• GMO
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OUTPUT FOR 2017
86
• BWP report Pre-authorisation dossiers: 120 (9 to
CAT)
• BWP reports for Scientific Advices: 135 (32 to CAT)
• Plasma Master File – annual updates: 30
• Plasma Master File – variations: 13
V. Jekerle (EMA)
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PCV-1
Rotarix
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as a reagent for cell culture (vaccines, ATMP…) to activate virus particles as a protein processing reagent.
Trypsin purified from porcine pancreatic glands for use as a reagent in the manufacture of human medicinal products:
EMA/CHMP/BWP/814397/2011
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97
Quality, non-clinical and clinical aspects of medicinal products containing genetically
modified cells (CHMP/GTWP/671639/2008)
Leading group CAT
Target date Preparation of first draft of revised guideline for public
consultation by Q2 2018
Comments Contribution to preparation of first revised draft
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BWP WORKPLAN 2018
Workshops, stakeholder & expert meetings:
Stakeholder workshop on accelerated access and quality
Training on overview guidance for D80 Overview CHMP/CAT AR
Interested Parties meeting
Annual strain selection meeting (Seasonal Influenza)
98 V. Jekerle (EMA)
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EMA Annual Report 2014. Available at: http://www.ema.europa.eu/docs/en_GB/document_library/Annual_report/2015/04/WC500186306.pdf (accessed October 2016)
EMA. Available at: http://www.ema.europa.eu/ema/index.jsp?curl=pages/regulation/general/general_content_000660.jsp&mid=WC0b01ac058096f643 (accessed October 2016)
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Biologics – challenging field including new
concepts & approaches
Open mind required (adapt and reconsider
established criteria, if necessary)
Develop (and maintain) the spirit of experience-
and competence-sharing
Propose sound and scientifically-based advice
and recommendations
Adapted from J-H Trouvin
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