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12th European Biosimilars Congress, will be organized around the theme “”
European Biosimilars Congress 2019 is comprised of 22 tracks and 112 sessions designed to offer comprehensive sessions that address current issues in European Biosimilars Congress 2019.
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The development of biologics calls for overcoming lot many challenges. With initial steps of concepts of biologics, their considerations, essentials for early clinical developments it is very much needed that proper scientific and strategic approaches are taken for the successful development of follow-on-biologics. Moreover, the need for overcoming the challenges continues in the late clinical steps, drug safety factors and labelling requirements. Also it is much required now to develop a drug product in accordance to quality by design (QbD).This Euro biosimilars conference will look at the multiple facets of current challenges in Biosimilars development. This biosimilars conference will focus on multiple aspects of biosimilars product development to successfully deliver safe, potential and efficacious biologic products to the market.
- Track 1-1Biopharmaceuticals development
- Track 1-2Biologics in genetic disorders
- Track 1-3Early clinical development essentials
- Track 1-4Late clinical development essentials
- Track 1-5Drug safety essentials
- Track 1-6Comparability for biologics
- Track 1-7Unique considerations for biologics
- Track 1-8Advertising, promotion and labelling essentials
- Track 1-9Implimentation of the BPCI Act
- Track 1-10Quality by Design for Biologics and Biosimilars
- Track 1-11Biopharmaceuticals development
Management of cGMP facility calls for a strict monitoring all factors including analytical strategies, formulation procedures, packaging etc. For biologic products establishing comparability and interchangeability is a big hurdle. For this purpose employment of suitable analytical approach, bioassay, protein analysis, potency testing, safety assurances are highly important. LC/MS analysis for biologic products, characterization of biologics, peptide mapping, Isoelectric Focusing and Capillary Isoelectric Focusing, SDS-PAGE, Thermal Analysis, Particulate Matter Analysis, Thermogravimetric Analysis are some methods commonly used for analysis of biologics and Biosimilars products. On average, facilities outsource 32% of their analytical testing/bioassays (up from 28%) meaning that close to one-third of analytical testing is estimated to be outsourced by the industry.
While small changes in these parameters can impact the various chemical permutations for a given biotherapeutic, innovators can, under certain circumstances, change the host cell, fermentation process, purification process, and even manufacturing site, but the product can be validated without undertaking a complete new product development review
- Track 2-1Biosimilars multimodal techniques
- Track 2-2Biosimilars bioanalytical methods
- Track 2-3Bioassay for comparability and potency testing
- Track 2-4Biosimilars LC/MS analysis for discovery, preclinical and clinical programs
- Track 2-5Biosimilars GMP protein analysis
- Track 2-6Biosimilars electrophoresis
- Track 2-7Biochemical and Biosimilar Characterization
The safeguarding of product trade secret, its formulations and other process parameters by law is usually covered by IPR. It includes those as patents, copyrights, industrial design rights, trademarks etc. IPR is of prime importance in the field of biologics and biosimilars. Most scientist and industries tend to retain their monopoly business by exercising the IPR. The very name Biosimilars calls for the occurrence of Intellectual Property rights laws and by-laws. Hence this session is of utmost interest to the attorneys and law personnel. Currently, the US provides 12 years of exclusivity for new biological products under the Biologics Price Competition and Innovation Act (BPCIA).The provision providing 12 years exclusivity was buried inside the 20,000-page healthcare law. Eight years of exclusivity would keep biologic medicines out of the hands of many who need them. Prices frequently exceed $100,000.
- Track 3-1Pharma patent scenario
- Track 3-2Criteria for patentability and patent claims
- Track 3-3Critical research issues
- Track 3-4Patentable subject matter
- Track 3-5Recent patent disputes and litigations
- Track 3-6Evaluation of highly variable drugs and drug products
Biological Medicine works with the biology of the body and its natural healing capabilities as well as the spiritual, emotional and physical aspects of disease. Disease means that the body’s regulation is not working properly and needs to be brought back into its natural dynamic state where the immune system is in full regulation. It therefore looks for root causes for the presenting symptoms of disease the underlying factors causing a person to present with a certain illness. These root causes may consist of several factors which have built up over time and can include; diet, food allergies, intestinal disturbances, family history, stress, environmental factors, heavy metals, dental problems, hyperacidity, trauma, exposure to bacteria or viruses or electromagnetic disturbances.
- Track 4-1Advances in biological products
- Track 4-2Biological drugs
- Track 4-3Generic biological drugs
- Track 4-4Biotechnology medicinal products for different drugs
- Track 4-5Future of next generation biosimilars
- Track 4-6Biopharmaceuticals development
Biosimilars Market is experiencing a growth at an exponential rate. Presently around 700 biologics are making progress in the research pipelines of nearly 250 biopharma companies. Biosimilar insulins have already started revolutionizing the future drug development in the realm of diabetology. Biosimilars of Adalimumab, Etanercept, Rituximab, Peg-Filgrastim, Trastuzumab are expected to hit the market soon. Biosimilar of Humatrope, biosimilar of Eprex, biosimilar of Neupogen, biosimilar of Remicade have already been enjoying a greater market share in Europe than the reference product itself. The proportion of different biosimilars that reached market are Low Molecular Weight Heparins 44%, Epoetins 19%, HGH 11%, G-CSFs 7%, Interferons 6%, Insulins 5%, Others 8%.
- Track 5-1Biologics in cancer
- Track 5-2Biologics for psoriasis
- Track 5-3Biosimilar monoclonal antibodies
- Track 5-4Recombinant therapeutic proteins
- Track 5-5Insulin biosimilars
- Track 5-6Biologics in autoimmune disease
Clinical trials for biosimilars must exhibit practically identical security what's more, viability to the reference item, including consecutive PK/ PD and viability/security trials. Controllers expect PK/PD similarity information from a Phase I trial will bolster encourage viability/ wellbeing evaluations in crucial Phase III trials. Remain solitary Phase III investigations or joined Phase I/III outlines without supporting PK information are probably not going to be acknowledged. Clinical similarity prerequisites may fluctuate on a case-by-case premise subject to a risk based approach. Three-arm Phase I trials are progressively being used to show equivalence between the biosimilars and two authorized adaptations of a similar reference item that may exist in various markets, allowing developers to proceed with pivotal trials using a single version of the reference product
- Track 6-1Biosimilars clinical trials
- Track 6-2Clinical PK/PD studies
- Track 6-3Toxicological studies
- Track 6-4Risk management and quality affairs
- Track 6-5Risk management and quality affairs
- Track 6-6Targeted cell line development
- Track 6-7Case studies and clinical models
- Track 6-8Biologics product life cycle and sustainable market returns
Competitions and/or success in the present pharma industry are determined by the winning patent strategy which mostly pertains to the generic market entry. Generic and branded drug manufacturers both the patent strategy proximally belongs to the Hatch-Waxman Act statutory scheme and ANDA litigations. The Hatch-Waxman Act enacted in 1984 with amendment in 2003 facilitated the entry of generics at an early stage-thereby finishing the battle of branded generic ANDA of blockbuster drugs. All the same the Biologics Price Competition and Innovation (BPCI) Act has maximized the branded-generic patent duel in the biologics realm by imposing a litigated framework on follow-on-biologics.
An FDA analysis of drug prices from 1999 to 2004 found that the discount from generic competition was just 6% with one generic competitor, but jumps to 48% with two generic competitors, 56% with three, 61% with four and 67% with five generic producers in a market. Within 2 years of the expiration of the patent of the popular drug Zantac in 1997, generics of Zantac accounted 90% of the treatment’s total sales, and the price for patients was about 10% of its pre-generic price. European patents on biologic treatments began to expire in 2000, and in April 2006, Sandoz and Biopartners successfully received EMEA approval for the first European biogenerics, two products containing human growth hormone.
- Track 7-1Licensing of biosimilars
- Track 7-2BLA filing for biosimilars
- Track 7-3Regulatory prospects of BRIC countries
- Track 7-4Biowaiver approval for biosimilars
A Biosimilars bio therapeutic item is comparative (but not identical) as far as quality, wellbeing, and viability to an effectively authorized reference item. Not at all like nonspecific little particles, it’s hard to institutionalize such naturally complex items in light of convoluted assembling forms. The worldwide biosimilars advertise is developing quickly as licenses on blockbuster biologic medications terminate and other medicinal services parts centre on lessening of expenses. Biologics are among the most elevated cost medicines on the worldwide market today, which suggests the requirement for minimal effort choices. In developing markets, biosimilars officially offer more moderate costs, which are alluring, as well as crucial to economies where costly medications are not monetarily achievable
- Track 8-1Biosimilars China and Asia Pacific
- Track 8-2Biosimilars India
- Track 8-3Biosimilars USA
- Track 8-4Biosimilars Europe
Biological medicines are much more structurally complex and extremely sensitive to manufacturing conditions and therefore more difficult to characterize and produce than small molecule drugs. Even minor changes in manufacturing may lead to significant variations of the cellular systems used for biological production, as well as to differences in the structure, stability, or other quality aspects of the end product, all of which have the potential to affect tolerability and/or efficacy and increase the risk of immune responses. Owing to these issues, specific regulatory guidance on biosimilars is continuously evolving, and there is some disagreement on which studies need to be implemented to approve a biosimilars. According to current literature, the following points on biosimilars deserve consideration: Biosimilars development is characterized by global harmonization, although several not fully answered questions remain regarding extrapolation of indications, switching or interchange ability, and tolerability; in patients with rheumatic diseases, the tolerability and efficacy of biosimilars in clinical practice remain to be established; several medical and patient associations have published position papers on biosimilars requesting that safety, efficacy, and traceability be carefully considered; long-term post marketing studies should be implemented to allow physicians to gain confidence in biosimilars.
- Track 9-1Biotechnologic drug
- Track 9-2Monoclonal antibody
- Track 9-3Fusion protein
- Track 9-4Biologic drug
- Track 9-5Anti–tumor necrosis factor
Biopharmaceutical informatics endeavors to use information technology, sequence-and structure-based bioinformatics analyses, molecular modelling and simulations, and statistical data analyse towards biologic drug development. Development of databases containing the experimental data on biophysical stability, safety along with molecular sequence
- Track 10-1Applications of computation in biologic drug development
- Track 10-2Physics-based molecular modelling
- Track 10-3Protein sequence-structural contexts and degradation reaction mechanisms
- Track 10-4De risk biopharmaceutical development
- Track 10-5Creation of databases and data mining
- Track 10-6Pre-clinical immunogenicity risk assessment of biotherapeutics
With Europe that paved way to the uptake of biosimilars over a decade ago, the consequences of Brexit would be potentially harder on UK. Presently UK is no more bound to follow the guidelines of EMA. Also research grants from Innovative Medicines Initiative and Horizon 2020 would no more be available to UK. All the same, EMA has its headquarters in London, UK. The thus arising complications would definitely have certain consequences on the Biosimilars scenario in UK and EU.
- Track 11-1Brexit- Pros and Cons to European pharma market
- Track 11-2Post Brexit changes in biosimilars regulation in UK
- Track 11-3Fate of biosimilars clinical trials in UK
- Track 11-4Research funding from European organizations to UK based research laboratories
The objective of this work was to suggest the biowaivers potential of biopharmaceutical classification system which are known to increase the solubility, dissolution, oral absorption of water insoluble drugs. Biopharmaceutics Classification System and invitro and invivo classification discusses about ADME pathways of different drugs. This also includes BCS biowaivers, In vitro diffusion cells for dissolution testing in formulation development, In vitro preclinical ADME/BCS testing. Until in vitro and in vivo correlation achieves the required degree, the biosimilars drug will not be able to meet the needs of the original drug candidate. Hence the proportion of BCS and IVIVC based biowaivers are fairly low ~0.5-1% of total pharmaceutical products.
- Track 12-1BCS biowaivers
- Track 12-2Preclinical and clinical testing for oral drug delivery
- Track 12-3Waiver for In vivo bioavailability or bioequivalence
- Track 12-4Consideration of biowaiver extensions for BCS class III drugs
- Track 12-5In vitro diffusion cells for dissolution testing in formulation development
- Track 12-6Dissolution testing in drug formulation
- Track 12-7In vitro preclinical ADME/BCS testing
- Track 12-8In vitro drug product research
The global biosimilars market is growing at an exponential rate. The CAGR from 2015 to 2020 is projected at over 22%. The biosimilars market is expected to be around $6.2 billion by 2020 from only $2.3 billion in 2015. By the end of this decade the biosimilars would surely occupy 27% of the total pharmaceutical market. Moreover, with the global rise in concern for more accessible-improved- cost effective healthcare, biosimilar drugs would be a more apt choice to the payers, end users, manufacturers over the costly reference biologics. Originator biologics are as costly as about $100,000 per year per patient. Biosimilars on the contrary can be offered at a 30-40% lower price than that of the reference product. However, with all the success stories and opportunities there also lies a sobering 50% failure rate in developing and obtaining license towards marketing of biosimilars. The biosimilars market is categorized into mainly four zones – North America(USA and Canada); Europe(UK, Germany, Spain, Italy, France and Rest of Europe); Aisa-Pacific( China, India, Japan, South Korea) and rest of the world ( LATAM and MENA). Key players of the biosimilars market include Amgen, Hospira, Teva, Sandoz International GmbH, Dr. Reddy’s Laboratory, Biocon, Roche, Celltrion, Catalent, Mylan and Merck. There are also certain other companies which are gaining importance in biosimilar development like LeanBio Pro-Spain, PPD-USA, SGS Life Sciences-UK, Therapeutic Proteins International-USA. The biosimilars development is mainly concentrated in the therapeutic domains of oncology, blood disorders, autoimmune disorders, endocrine disorders and infectious diseases.
- Track 13-1Biosimilars pharmacoeconomic modelling
- Track 13-2Return on Investment(ROI) for biosimilars
- Track 13-3CAGR of biologics and biosimilars in Europe
- Track 13-4Penetration and uptake of biosimilars in different disease sectors
This session of the Biosimilars 2018 will look into the future and FDA initiatives that have already been announced to include enhanced tracking and follow-up of post marketing surveillance issues, planned improvements in AERS, and pilots of new post market drug-monitoring strategies and ADR related issues. Biosimilar guidelines for pharmacovigilance practice and pharmacoepidemiology are the points that shall be laid emphasis in this session. U.S. average annual spending growth from 2002 to 2007 was 16% for biologics, compared with 3.7% for drugs. In same proportion pharmacovigilance for biosimilars has been comparatively more than other pharmaceutical products.
- Track 14-1Current problems in biosimilars pharmacovigilance
- Track 14-2Adverse drug reactions with biologics and biosimilar products
- Track 14-3Detection and evaluation of drug safety signals
- Track 14-4Role of pharma industries in the improvement of pharmacovigilance system
- Track 14-5Good pharmacovigilance practice and pharmacoepidemiology
The legal issues pertaining to the follow-on-biologics and biosimilars are one of the most aspects that requires an open discussion. Before the actual advent of biosimilars to the market legal issues have risen in numbers in their developmental stages. Renowned organizations have filed cases against each other two claim their rights and for other legal allegations related to the products. This track is dedicated to discussion of all such cases which has been argued in the court of law.
By 2002, the FDA had approved 36 new biologics, followed by 37 more in 2003, another 40 in 2004 and 39 more in 2005. By 2006, the leading category of biologic treatment, the red blood cell enhancer recombinant erythropoietin (EPO), generated $14 billion in sales revenues, or 40 percent more than the best-selling traditional pharmaceutical, Lipitor. More than 300 therapeutic antibodies currently are in clinical development and trials, compared to just 13 that already are widely available due to legal issues.
- Track 15-1Implimentation of the BPCI Act
- Track 15-2Patent protection and infringement issues
- Track 15-3Patent negotiation and litigation phase
- Track 15-4Market exclusivities
For this rapidly growing industry sector, little consensus or authoritative information is available yet regarding how and where biosimilar products will be produced. The future of their manufacturing is still up in the air. Much discussion among experts has focused on a dramatic up-tick in Contract Manufacturing Organizations (CMOs) involvement with process development projects and clinical-scale manufacturing for biosimilars. None have really set up commercial-scale projects (yet), however. Many such companies are publicly discussing large-scale partnerships for production in India and elsewhere in Asia. On the other hand, some biosimilars sponsors are establishing relationships with smaller biotech CMOs that have demonstrated expertise in efficiency or lower-cost business models
- Track 16-1Multiproduct or dedicated single product plants
- Track 16-2Major markets or developing countries
- Track 16-3Single-use, stainless steel or hybrid
- Track 16-4Continuous bioprocessing
Biosimilars are a relatively new subset of biopharmaceuticals, with the biotechnology industry finally maturing such that off-patent generic-type products increasingly will be entering major markets. So far, more than 20 biosimilars for a limited number of reference products have been approved in major markets, primarily the European Union. Only two products have been formally approved as biosimilars in the United States. The parent field of biopharmaceuticals itself continues to exhibit a poor supporting infrastructure of information resources. Those biopharmaceutical and biosimilar information resources that do exist generally are limited in number, diversity, and sophistication.
- Track 17-1Drug safety of biosimilars products
- Track 17-2Regulatory aspects
- Track 17-3Regulatory affairs and IPR of biosimilars products
Biosimilars is a biologic medical product which is copy of an original product that is manufactured by a different company. Biosimilars are officially approved "innovative" versions of original products, and can be manufactured when the original product's patent expires. Reference to the innovator product is an integral component of the approval. This session also finds place for all the biosimilars exhibitors associated with the field of biosimilars and biologics. Biosimilars innovative products are on the rise. The number of new drugs seeking approvals is growing at a compounded rate of around 5% half early. Almost 1.5 times the number of biosimilars is expected to be in the market in 2016 compared to in the last 5 years.
- Track 18-1Biotechnology medicinal products for different drugs
- Track 18-2Future of next generation biosimilars
- Track 18-3Biopharmaceuticals development
- Track 18-4Biotechnology medicinal products for different drugs
- Track 18-5Future of next generation biosimilars
This track discuses about the generic drugs impact on global biosimilars market , Cost and risk management, Adopting innovative mechanisms such as risk-sharing arrangement, European market for biosimilars. The global market scenario with the launch of first biosimilars in the market forecasts some radical changes. This track will look upon such key concerns which are witnessed by the global pharma market and that are coming up with the subsequent launch of the other biosimilars and biologics. Despite these emerging facilities, biotherapeutic developers are most comfortable off-shoring to established markets—the US and Europe
- Track 19-1Global impact of biosimilars over generics
- Track 19-2Economic aspect towards biosimilars
- Track 19-3Biosimilars in global market
- Track 19-4Investment and returns on biosimilars
- Track 19-5Cost and risk management
- Track 19-6Adopting innovative mechanisms such as risk sharing arrangement
- Track 19-7Global P&R models for the biosimilars and generics market
Drug Delivery Companies and Market session is beginning to change for small, medium, and large scale pharmaceutical Co, biopharmaceutical Manufacturing and Industries, generic drugs companies, contract drug delivery companies which can manifest from development to manufacturing. Addressing these instabilities is a great challenge, because of the complexity of the Clinical bio therapeutics themselves
- Track 20-1New approaches to enhance drug performance
- Track 20-2Drug delivery technologies
- Track 20-3Drug delivery companies and markets
- Track 20-4Recent advances in drug delivery
- Track 20-5Biosimilars pharmacoeconomic modelling
The first mAb biosimilars to be approved in Europe and elsewhere was the infliximab biosimilars (Inflectra and Remsima), which originator is Remicade. In October 2013, after the European Medicines Agency (EMA) gave a positive opinion for infliximab biosimilars, the European Commission granted a marketing authorization (MA) for these two biosimilars in the various therapeutic indications that are authorized for Remicade (i.e. indications in gastroenterology, rheumatology, and dermatology). As for previously approved biosimilars, the two aforementioned European institutions did not make a stand on the issues of substitution, and with good reason, as answering these questions does not fall within their areas of expertise and is the sole responsibility of EU Member States
In the United States, the Food and Drug Administration (FDA) held that new legislation was required to enable them to approve Biosimilars to those biologics originally approved through the PHS Act pathway. Since 2004 the FDA has held a series of public meetings on Biosimilars. The FDA has previously approved biologic products using comparability, for example, Omnitrope in May 2006, but this like Enoxaparin was also to a reference product, Genotropin originally approved as a biologic drug under the FD&C Act.