Archive for September, 2007
Secure Pharma supply chain key to blocking entry of counterfeit medicines
Last Updated on Saturday, 15 September 2007 08:30 Written by admin Saturday, 15 September 2007 08:30
-Â Â Â Demand planning and supply chain network moves from cost outgoing towards revenue generation
-Â Â Â Developing a robust and resilient distribution strategy and ensuring patient safety essential for Pharma manufacturers
10th September 2007 London,
As the Demand Planning and Supply Chain networks of major Pharma Manufacturers becomes more and more of a revenue generator, it’s role as a direct link between customers and patients has never before been more severely tested in ensuring patient safety and being able to resist counterfeit medicines, as now.
For the Pharma supply chain, the challenges are vast in that there are a variety of needs across multiple functional areas, diverse geographical areas and differing timelines which means it can be daunting to begin to put a secure network in place.
As a result, Eye for Pharma , world renowned for providing business information and conferences for the Pharma Industry are hosting the forthcoming ‘Demand Planning and Supply Chain Management Excellence Summit ” in Prospero House, London, 4th-5th December 2007.
Over 20 Pharma experts in this field are attending to put forward their views and excellence such as
Philip Till, Demand and Supply Chain Manager  Novartis
Alejandro Portilla, Business Excellence Manager at Abbott and
Christian Borel, head of Supply Chain Integration at Merck-Serono
In areas covering the complete Demand Planning and supply chain domain in
Inventory management and safety stocks, supply chain security, strategic planning, demand planning, sales and operations planning, parallel trade and long term perspectives- where the market is heading.
Eye for Pharma is also offering a FREE 30 page report on the findings of the market called ‘Pharma Futurology, Joined Up Healthcare 2016 and beyond’ which focuses on where Supply chain management will be essential in the future.
For more information visit www.eyeforpharma.com/supplychain07/txt
About EyeforPharma
Eyeforpharma is a global pharmaceutical business strategy information provider with a highly reputable and worldwide presence in the Pharma industry. It is renowned for producing top level conferences that attract the highest level of speakers to deliver presentations on cutting edge pharmaceutical business strategies. We provide business intelligence and analysis online at www.eyeforpharma.com and through an email briefing twice a month. Eyeforpharma also has a very strong foothold in the European, US and Japanese markets.
Posted under Europe, Europe, Press Releases | No Comments
Length of Pharma Sales Rep visit falls to 90 seconds
Last Updated on Saturday, 13 October 2007 08:41 Written by admin Saturday, 15 September 2007 02:32
Forthcoming eyeforpharma’s Sales Force Effectiveness Summit to focus on challenges of getting increased Sales force ROI
- New stats reveal growth in Pharma sector being influenced by generics and biotech
- 90% of revenues coming from products already in market for over 5 years (Pricewaterhouse Cooper)
10th September 2007 London,
Whilst the Pharma industry is showing an 8% growth year on year, the sector is under more and more competitive pressure, particularly in sales, to maintain this rate. The challenges for Pharma sales forces have become more acute than ever in how to bring increased ROI. These challenges will be the main focus for the forthcoming eyeforpharma’s Sales Force Effectiveness USA, which will take place in Philadelphia, November 12th 2007.
Eye for Pharma are world renowned for providing business information and conferences for the Pharma Industry and are bringing together over 300 pharma experts from around the globe and a wealth of new research to make the Summit one of the most eagerly awaited events of the year.
New statistics reveal that most of the positive factors come from the effects of Medicare Part D , generics and the biotech sector. Over the last 10 years there has been there has been almost twice as much money ploughed into sales than for R&D and yet currently 90% of the revenues come from products that have been in the market for over 5 years and sales force visits on average last no longer than 90 seconds.
It is therefore essential for pharma sales forces to get new strategies in place to find solutions for these challenges and the Sales Force Excellence Summit has previously been the catalyst for choosing the most effective and efficient sales force deployment, including sizing, for the product portfolio – and also sales effectiveness- creating the right processes and coaching climate to maximize sales force productivity.
The summit is designed to provide a complete and thorough analysis for any pharma executive to increase sales force effectiveness through the following modules.
” Implementation and execution of SFE strategies that will achieve sustainable ROI
” Sales force sizing and deployment – territory alignment
” Interpreting and analyzing impact of longitudinal and patient level data on SFE – Improving usage OF Rx data
” Performance measurement: Incentive plans/compensation schemes
” Training and Development: Improving sales techniques, recruiting star performers, retaining key reps
” Analytics and sales reporting – how marketing analytics can help with true CRM
” Targeting and segmentation – effective tools to better profile key prescribers
” Sales Accountability and measurement
” Selling Effectively in US managed care system
For more information visit www.eyeforpharma.com/salesusa07/index.shtml
About eyeforpharma
eyeforpharma is a global pharmaceutical business strategy information provider with a highly reputable and worldwide presence in the Pharma industry. It is renowned for producing top level conferences that attract the highest level of speakers to deliver presentations on cutting edge pharmaceutical business strategies. We provide business intelligence and analysis online at www.eyeforpharma.com and through an email briefing twice a month. eyeforpharma also has a very strong foothold in the European, US and Japanese markets.
Posted under Europe, Press Releases, USA and Canada | No Comments
Eyeforpharma announces new speakers and podcast series for their Pharma Marketing Congress
Last Updated on Friday, 14 September 2007 08:27 Written by admin Friday, 14 September 2007 08:27
Eyeforpharma announces new speakers and podcast series for their Pharma Marketing Congress
London, UK.–(Targetwire)-30 August 2007 – eyeforpharma, the global source of information and education for the pharmaceutical industry, announced today that they have recruited new speakers for the 7th annual Pharma Marketing ROI Congress in Barcelona on25th and 26th October.
Since launching the conference, 3 excellent and insightful pharma executives have agreed to speak at Marketing ROI. They are:
-Â Â Â Marta Wieldonk, Global Brand Manager, Novartis
-Â Â Â Paul Hooper, Marketing Director, Lundbeck
-Â Â Â Dave Clarke, Global eMarketing Manager, Established Brands, Astra Zeneca
In addition, eyeforpharma warmly welcomes the participation of IMS as Global Sponsors.
The latest updated brochure is available to download now at www.eyeforpharma.com/marketing07/43
Eyeforpharma are also working with their Gold Sponsors DigiRedo to produce a series of insightful podcasts with leading thinkers in the pharma industry. The first, with Fonny Schenck, is set to be ready before the end of August, with more to come in September. Updates will be sent to anyone asking to be kept updated: http://www.eyeforpharma.com/marketing07/info.shtml
Eyeforpharma’s Early Bird discount is also set to expire soon, on September 28TH with the €200 discount.
The secure registration page is: https://secure.firstconf.com/pharma/marketing07/register.htm
Further updates, full information on presentations and speakers, and details on ticket options can all be found by downloading the brochure a www.eyeforpharma.com/marketing07/brochure.shtml
About eyeforpharma
eyeforpharma is a leading global source of information for the pharmaceutical industry. Our reputation has been built on quality, in-depth conferences that have distinguished themselves from competitors by the depth and breadth of research we put into each conference to ensure it is covering the hottest and most pertinent issues of the industry. Months are spent talking directly to senior executives in the industry, as well as relevant consultants and journalists and well respected solutions providers.
eyeforpharma also provides a fortnightly newsletter to over 11 thousand leading executives from every major pharmaceutical company in the industry, and of course consultants, sponsors and academics as well.
The eyeforpharma wiki, launched last month, highlights our dedication to improving the communication between people in the industry and furthering learning and development within it.
Please visit www.eyeforpharma.com to find out more about us.
Posted under Europe, Europe, Press Releases | No Comments
EYE FOR PHARMA LOOKS TO INCREASE PHARMA SALES FORCE ROI THROUGH ONLINE MEANS AT FORTHCOMING SUMMIT
Last Updated on Thursday, 13 September 2007 03:11 Written by admin Thursday, 13 September 2007 03:11
2ND Ecommunications and Online Marketing 2007 for Pharma
Summit to be held in Philadelphia Convention Centre, November 12-13th.
-Â Â Â Emarketing Web 2.0 links web technology to the bottom line through the latest advanced strategies and methods .
-Â Â Â Leading speakers such as Simon Goldberg, Director, Electronic Communications, Abbott; Preeti Pinto, Sr. Director, Head of Promotional Regulatory Affairs,talk of the benefits of eDetailing and Online Promotion
14th August 2007 London,
In the rush to gain Share of Voice by increasing the frequency and reach of sales calls, pharmaceutical companies may have lost sight of the value that the “detail person” has given to physicians in past years.
The declining sales force return on investment may signal that a significant adjustment will take place in how pharma companies market and sell their products to physicians. Many experts believe that areas such as eDetailing and ePromotion fits the bill for a solution to declining physician marketing ROI.
EyeforPharma, world renowned leader in providing business strategy information and conferences for the Pharmaceutical Industry has announced dates for the 2nd Ecommunications and Online marketing 2007 Summit which will address such issues and provide a greater insight into how to take advantage of the new tools available through an impressive list of expert speakers.
The event promises to give key understand to the importance of ‘e’ strategies as part of a broader cross channel integrated marketing strategy
Eye for pharma brings together all the latest online developments and strategies to improve ROI such as,
Physician Relationship Marketing: Attendees will hear a strategic approach to eDetailing as a complimentary component of an integrated physician relationship marketing campaign
Create eDialog with your customers: How to create genuine two-way interactions with physicians to meet their needs and exceed their expectations
Examine the most effective metrics to evaluate, monitor and interpret an online marketing campaign
Web 2.0: Monitor and interpret user-generated content from social networks, blogs and forums to enhance your marketing strategy
Pharma eMarketing 2.0: Participants will understand how to harness and interpret the power of social media to ensure you brand leads the way.
Key speakers include Simon Goldberg, Director, Electronic Communications, Abbott; Preeti Pinto, Sr. Director, Head of Promotional Regulatory Affairs, AstraZeneca; Christoph Ferse, Global eMarketing Director, Bayer Healthcare
For further information visit http://www.eyeforpharma.com/ecomm2007/
About EyeforPharma
Eyeforpharma is a global pharmaceutical business strategy information provider with a highly reputable and worldwide presence in the Pharma industry. It is renowned for producing top level conferences that attract the highest level of speakers to deliver presentations on cutting edge pharmaceutical business strategies. We provide business intelligence and analysis online at www.eyeforpharma.com and through an email briefing twice a month. Eyeforpharma also has a very strong foothold in the European, US and Japanese markets.
Posted under Europe, Europe, Press Releases | No Comments
Solving patient compliance: Pharma’s multidimensional challenge
Last Updated on Saturday, 13 October 2007 08:45 Written by admin Wednesday, 12 September 2007 01:34
LONDON (August 29, 2007) – Patient non-compliance with doctor prescribed medication regimens is a significant challenge for healthcare providers and pharmaceutical makers. Experts estimate that patient non-adherence costs the pharmaceutical industry in excess of $30 billion a year – not to mention, the chance at a fuller, healthier life for countless patients.
But the opportunity is even greater. Clinical researchers report that for most prescription drugs, patient compliance rates are 50-60%. With some disease states, however, compliance drops as low as 10-20%. So, even modest improvements in adherence and persistence can have significant, positive impacts on not only revenues for drug makers, but expenses for third party payers and outcomes for patients.
Improving compliance is a win-win for everyone in the patient care equation.
Solving the patient compliance challenge isn’t easy, however, according to Ganesh Vedarajan, a principal at ZS Associates.
“It’s a very multidimensional problem and there is usually a complex combination of reasons why patients are non-compliant with their medication regimens,” Vedarajan says. “Some of these reasons are easily addressable, but others are much more systemic and difficult to comprehend.”
Identifying and reaching the right patients is difficult, he says. But some emerging research and technologies offer new promise.
“There is a lot of research being done in patient psychographics that will allow us to better understand patient lifestyles and tailor programs and messages to have a greater impact,” Vedarajan says. “And new anonymous patient level data sources in the US and other places are making it easier to target programs to patients and their individual needs.”
But truly solving the patient compliance conundrum is a societal problem, he says, that will require a multi-stakeholder, collaborative effort among a broad range of important players, including doctors, payers, pharmacists, patients, pharmaceutical makers and others.
“Pharmas simply can’t say, ‘I have money and I can solve this problem on my own,’” Vedarajan says. “It’s a problem for society as a whole and one that will take a collaborative effort to solve.”
But he is quick to point out that pharma can lead the charge by bringing the right stakeholders to the patient compliance table.
Join Vedarajan and a first-rate panel of other industry experts at eyeforpharma’s 4th annual Patient Adherence & Persistence USA Summit November 12-13, 2007 at the Pennsylvania Convention Center in Philadelphia to see first-hand how leading pharmaceutical companies are strengthening communication with patients and sharpening their competitive advantage with new technologies to boost revenues.
As always, the emphasis will be on equipping you with the practical information and tools you need to tackle new patient adherence and persistence initiatives in your own company or make your existing approaches even more effective.
To learn more or to register to attend, please visit www.eyeforpharma.com/pcusa07
Posted under Europe, Press Releases, USA and Canada | No Comments
More than 90% of Pharma Companies in the US and 80% in Europe Are Thinking about or Already Implementing Physician-Centric Service Models.
Last Updated on Wednesday, 12 September 2007 09:48 Written by admin Wednesday, 12 September 2007 09:48
Eye for Pharma launches New live webinar aimed at Re engineering Physician Relationship Models
-   Features NEW Research on Physicians’ Experience Preferences and Sales Force Ratings. .
-Â Â Â Takes place 26th September 2007 12.00 EST / 18.00 CET
31st August 2007 London,
Physicians today want a new set of experiences from pharma, an integrated mix that includes patient support, educational programs and practice management services, as well as effective representative interactions.
The vast majority of companies recognize the need to transition to a service model that meets physicians’ new expectations. But most still struggle with how to move from traditional sales approaches to a physician-centric orientation.
EyeforPharma, world renowned leader in providing business strategy information and conferences for the Pharmaceutical Industry has announced an ALL NEW webinar called
‘Re-Engineering Physician Relationships:
Putting the New Service Model into Action
The webinar will feature new research conducted with Physicians to understand exactly what doctors want, what changes are they seeing in the Pharma market and who is not delivering. Expert help will also be given on how to transition to a successful Physician -centric model.
Key speakers include
Andrew Brana, Senior Global Consultant, Sales Performance Optimization, TNS Healthcare
Simon Roberts, Strategic Partnerships/Market Access, Roche
Tobias Weizel, Sales & Marketing Effectiveness, Amgen
Gregg Ciarelli, Executive Director – Sales Administration, Boehringer Ingelheim
Brad Fackler, Executive Vice President of Commercial Operations, Sucampo Pharmaceuticals
The webinar will be of particular interest where companies are already thinking about or already implementing Physician-Centric Service Model. Attendees will discover what changes doctors are reporting in their rep interactions, learn which sales forces doctors say deliver the best experiences and understand how to create a successful physician-centric model .
The webinar will take place 26th September 2007 -
12.00 EST / 18.00 CET
For more information visit www.eyeforpharma.com/virtual/salesmodel/
About EyeforPharma
Eyeforpharma is a global pharmaceutical business strategy information provider with a highly reputable and worldwide presence in the Pharma industry. It is renowned for producing top level conferences that attract the highest level of speakers to deliver presentations on cutting edge pharmaceutical business strategies. We provide business intelligence and analysis online at www.eyeforpharma.com and through an email briefing twice a month. Eyeforpharma also has a very strong foothold in the European, US and Japanese markets.
Posted under Asia, Europe, Europe, Press Releases, USA and Canada | No Comments
Cisbio has entered into a partnership agreement with Lumiphore to gain access to new fluorescence reporter molecules for use in its high throughput (HT) screening assays.
Last Updated on Tuesday, 11 September 2007 03:40 Written by Fred Tuesday, 11 September 2007 03:40
The agreement grants Cisbio exclusive access to the Lumi4 compounds for fluorescence applications in drug discovery, with Lumiphore free to develop partnerships to develop the technology in other areas.
Cisbio has played an important part in the development of HT drug screening technologies and has enabled researchers to conduct binding assays based on its homogenous time-resolved fluorescence (HTRF) system that combines Time-Resolved Fluorescence (TRF) and Fluorescence Resonance Energy Transfer (FRET).
“This agreement reinforces our position as real leaders the TR-FRET field, and is a very important step for us,” said François Degorce, head HTRF marketing and business development at Cisbio.
“We have plans to apply the technology in some of our current products as well as many of our mid-to-long term projects.”
Lumiphore’s lanthanide-based florescent reporter molecules will enable Cisbio to generate assays that provide more accurate results due to their long-emission lifetimes and strong luminescent properties that provide higher signal-to-noise (S/N) ratio.
“According the last figures I have, TR-FRET accounted for between 13 and 15 per cent of the HT screening market and the use of this technology is increasing rapidly compared with other competing technologies due to its increased sensitivity and robustness,” said Degorce.
During the TR-FRET process, fluorescent reporting molecules emit long-lived fluorescence signals when a fluorescence donor molecule binds to an acceptor / emitter molecule.
This is in contrast to many biological assay systems that use radioactive reagents, which pose health risks not just to the researchers themselves, but also to any live cell lines they may be conducting assays in.
The donor / acceptor molecules and proteins can be supplied from the company’s catalogue, or can be developed in-house or by Cisbio to enable researchers to study the binding of potential drug candidates.
This powerful new technology brings researchers increased assay sensitivity, higher throughput and greater reliability and flexibility than some other systems with Cisbio already providing a wide range of assays based on its original Europium cryptate technology.
These include assays for GPCRs (G Protein couple receptors), inflammation, metabolic diseases, central nervous system, biomarkers, kinase assays and other oncology related assays.
“The new technology will complement our existing catalogue offerings and quite a few of our existing assays will be upgraded to make use of it,” said Degorce.
In addition, the company also offer kits for monitoring bioprocesses such as protein or antibody engineering as well as enabling rapid quantification of antibodies during the production process.
“The Lumiphore technology is very bright and very stable, and will enable an upgraded version of the HTRF assays to be conducted on a expanded range of detection platforms,” said Degorce.
He continued by saying that because the Lumiphore technology uses a Terbium ion rather than the Europium ion that Cisbio currently uses a whole range of new possibilities could be accessed.
This could include the development of multicolour assays that use different donor-acceptor pairs that have very narrow excitation and emission bands.
The compounds resistance to bleaching allows samples to be archived allowing improved quality control comparisons between old and new data – a problem for more easily bleached organic dyes.
“When you run a screen with 100,000 samples and the detector system is not working properly, instead of throwing the plate away and having to start again because the lifetime of the dyes are too short lived to conduct the experiments the next day, you can store the plates in the fridge or freezer and study the plates the next week when the detector is back up and running,” said Degorce.
“Many luminescence screens actually destroy the reporter molecules such that any repeat read-outs are less sensitive than the first, with both our old Europium cryptate dye and this new Lumiphore technology you can just keep on reading the plates.”
Posted under Collaborations, Europe, HT Screening, North America, Press Releases | No Comments
Tikvah Therapeutics, Inc. And Chakra Biotech Pte. Ltd. Establish Collaboration To Accelerate The Development Of Novel Antipsychotic Compounds
Last Updated on Tuesday, 11 September 2007 03:29 Written by Fred Tuesday, 11 September 2007 03:29
SINGAPORE, Norway, Sept 6, 2007 – (Hugin via ACN Newswire) – ATLANTA and SINGAPORE, Sept. 6, 2007 (PRIME NEWSWIRE) — Tikvah Therapeutics, Inc., a biopharmaceutical company focused on new treatment options to better manage central nervous system diseases, and Chakra Biotech Pte. Ltd., a drug discovery and development company focusing on central nervous system disorders, yesterday announced a collaboration and option agreement designed to advance and accelerate the development of four compounds targeted at a broad range of psychiatric conditions, including schizophrenia and bipolar disorder from Chakra Biotech Pte. Ltd.’s developmental pipeline. These compounds have shown robustly positive results in the chakragati (ckr) mouse model, a patented transgenic mouse model for dopamine dysfunction that has been validated as a model for screening antipsychotic compounds.
“These novel compounds are potentially important new agents because they have been identified through a unique physiologically based transgenic mouse model of dopamine function. This greatly increases the likelihood of success in the clinic and reduces the time needed for successful development,” said Daniel E. Casey, M.D., professor of psychiatry and neurology at Oregon Health and Science University, in Portland. “Combining the Central Nervous System drug development experience of Tikvah Therapeutics’ personnel with the novel drug discovery capability of Chakra Biotech forges a strong partnership for advancing new treatments for a number of serious psychiatric and neurological illnesses.”
The social and financial consequences of schizophrenia and bipolar disorder are substantial. Currently, there is a lack of adequate treatment options to alleviate positive, negative, and mood symptoms for many patients utilizing available antipsychotic medications; furthermore, significant side effects are frequently associated with the available medications.
“There is a considerable need for new broad-spectrum treatments with low side effect burdens for many psychiatric illnesses, including schizophrenia and bipolar disorder,” said Dr. Harold H. Shlevin, President and Chief Executive Officer of Tikvah Therapeutics, Inc. “We are very excited by the opportunity to work closely with Chakra Biotech Pte. Ltd. to further the development of these potentially significant compounds with the goal of bringing hope to patients with these debilitating illnesses.”
The four Chakra Biotech Pte. Ltd.’s compounds are fully synthetic and easily manufactured as single optical isomers. The lead compound CB030006 has been evaluated by in vitro and in silico analysis to be a dopamine D2 receptor antagonist with affinity levels unlikely to cause extrapyramidal side effects. The compound also has high affinity at the 5-HT2 receptors, particularly the 5-HT2A receptor. CB030006 also has 5-HT2C and 5-HT6 receptor antagonism similar to the current medications, olanzapine and clozapine. Additionally, CB030006 exhibits inhibition of noradrenaline reuptake, which may be associated with antidepressant and precognitive effects. CB030006 is predicted not to interact with the hERG channel decreasing the risk for drug-induced cardiac arrhythmia and sudden death. Results from in silico binding studies predict no interaction with histamine receptors associated with sedation, weight gain and associated drug-induced diabetes.
“We believe Tikvah Therapeutics is an ideal partner. The Tikvah team has extensive experience in the development of new pharmaceuticals for Central Nervous System disorders, including schizophrenia and bipolar disorder,” said Anthony Bishop, Director at Chakra Biotech Pte. Ltd. “The collaboration with Tikvah Therapeutics will propel our development program forward toward human clinical trials.”
About Schizophrenia and Bipolar Diseases
The social and financial consequences of schizophrenia and bipolar disorder are substantial. Schizophrenia is characterized by symptoms of hallucinations, delusional beliefs, disorganized thinking or speech, social withdrawal and apathy. Bipolar disorder also known as manic depressive disorder is characterized by extreme shifts in mood, energy, and functioning. Examples of adverse side effects of commonly used medications for treatment of schizophrenia and bipolar include sedation; extrapyramidal effects such as tremors, acute muscle contractions, inner restlessness, stiffness and shuffling gait; cardiovascular effects including QTc prolongation; and metabolic effects including weight gain and diabetes.
About Tikvah Therapeutics, Inc.
Tikvah Therapeutics, Inc., Atlanta, Ga., focuses on exploring new uses for late-stage pharmaceutical compounds in selected therapeutic indications of Central Nervous System diseases – neurology and psychiatry. Its focus is on new therapeutic uses which have been confirmed in multiple, clinical proof-of-concept studies. This strategy shortens product development timelines and substantially decreases the risk associated with the research and development efforts. A second prong of its strategy is to focus on specialized products with multiple stepping-stone indications and strong patent protections, thus helping to ensure long product life cycles and manageable commercial risk. For further information, please see www.tikvahtherapeutics.com.
About Chakra Biotech Pte. Ltd
Chakra Biotech Pte. Ltd. is a Singapore-based drug discovery and development company aiming to improve the lives of people with Central Nervous System disorders. We have a portfolio of antipsychotic compounds and an exclusive license to a transgenic mouse model for dopamine dysfunction. The model exhibits a number of behavioral, anatomical and pharmacological characteristics of schizophrenia that parallel those found in humans and has been validated as a screen for antipsychotic compounds. The company is combining its unique screening model with an exclusively licensed library of novel compounds. This provides a solid foundation for discovering novel leads and advancing its pipeline towards human clinical trials. For more information please see www.chakrabiotech.com.
FORWARD-LOOKING STATEMENTS
This press release contains certain forward-looking information that is intended to be covered by the safe harbor for “forward-looking statements” provided by the Private Securities Litigation Reform Act of 1995. Forward- looking statements are statements that are not historical facts. Words such as “expect(s),” “feel(s),” “believe(s),” “will,” “may,” “anticipate(s)” and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, financial projections and estimates and their underlying assumptions; statements regarding plans, objectives and expectations with respect to future operations, products and services; and statements regarding future performance. Such statements are subject to certain risks and uncertainties, many of which are difficult to predict and generally beyond the control of Tikvah Therapeutics Inc., that could cause actual results to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include: those generally associated with developmental stage biopharmaceutical companies; the progress or likelihood of success of our product research and development programs; potential benefits from our collaboration with Chakra Biotech Pte. Ltd.; the status of our preclinical and clinical development of potential drugs; the likelihood of success of our drug products in clinical trials and the regulatory approval process; our drug products’ efficacy, abuse and tamper resistance, onset and duration of drug action, ability to provide protection from overdose, ability to reduce the development of tolerance, ability to improve symptomatology or otherwise improve patients’ symptoms; the incidence of adverse events; the ability to develop, manufacture, launch and market our drug products; our projections for future revenues, profitability and ability to achieve certain sales targets; our estimates regarding our capital requirements and our needs for additional financing; the likelihood of obtaining favorable scheduling and labeling of our drug products; the likelihood of regulatory approval under the Federal Food, Drug, and Cosmetic Act; our ability to develop safer and improved versions of widely-prescribed drugs using our technology; and our ability to obtain favorable patent claims. Readers are cautioned not to place undue reliance on these forward- looking statements that speak only as of the date hereof. Tikvah Therapeutics Inc. does not undertake any obligation to republish revised forward-looking statements to reflect events or circumstances after the date hereof or to reflect the occurrence of unanticipated events.
“TIKVAH THERAPEUTICS, INC.”, “Bringing Hope to Life”, and the above logo design are trademarks of Tikvah Therapeutics, Inc., Atlanta, Georgia USA
CONTACT: Tikvah Therapeutics, Inc. Jack Callicutt +1 404-920-3182 jcallicutt@tikvahtherapeutics.com
Chakra Biotech Anthony Bishop +65 9767 0227 anthony@chakrabiotech.com
Copyright © Hugin ASA 2007. All rights reserved.
Chakra Biotech Pte Ltd.
Posted under Asia, Collaborations, Drug-Like Compounds, Europe, Press Releases | No Comments
PepCon-2008, China Apr.22-23, 2008 Shenzhen, China
Last Updated on Tuesday, 11 September 2007 03:49 Written by admin Tuesday, 11 September 2007 03:05
Advances in peptide and protein researches are occurring at an ever increasing pace, in a wide range of fields and scientific disciplines. At this exciting time, it is especially important to promote scientific and technological exchange and cooperation at the international level.
To establish of a new educational and networking platform for protein and peptide sciences for international academic and industrial institutions and professionals in the area, PepCon Committee has assembled an exciting scientific program, PepCon-2008, of local and international invited speakers, covering the areas of cutting edge peptide and protein researches. More than 500 participants are expected, including 300 scientists from academic, industrial and government research institutions, 100 best local and international academic and medical research institutions as well as 80 world-famous bio-pharmaceutical and instrumentation industries. The conference will take the form of lectures, workshops, round table conferences and posters around the theme of Peptide & Protein Technology: From Concept to Market .
The sessions will be tailored around:
Part â… : Emerging Enabled Technologies
1 Proteomics
2 Structure and Activity Relationship
3 Folding Misfolding and Structure with Disease
4 Peptide Materials
Part â…¡ : Peptide / Protein Drug Discovery
1 Protein and Peptide in Immunity Studies
2 Protein Receptor and Drug Target
3 Peptide / Protein Drug Delivery Technology
4 Protein / Peptide as Diagnostic Tools
5 Protein/Peptide Vaccine
Part â…¢ : Peptide / Protein Based Therapeutics
1 Peptide / Protein in Anti-Tumour
2 Peptide / Protein in Anti-Infection
3 Protein/Peptide Drug in CNS
4 Protein in Cardiovascular & Cerebrovascular Disease
Part â…£ : BioProcess for Peptide / Protein
1 Protein and Peptide Design & Expression
2 New Technologies in Protein Peptide Synthesis and Analysis
Part â…¤ : Business Development
1 Outsourcing Service for Protein/Peptide
2 Market Research of Protein/Peptide Drug and Health Care Products
The conference will be held in Shenzhen during April 19-21, a world-renowned coastal city in southern China , Hong Kong being shortly near in the south. During the April 22-23, we arrange a two-day tour, “Charming Sanya, Romantic Heaven†, in Sanya of Hainan Island. The region is famous for beautiful local scenery, beaches, temples and rich ethnic folklore and at this time of the year you will be able to enjoy the weather and surroundings of this beautiful region of China , at their finest.
http://www.bitlifesciences.com/Pepcon2008/
Posted under Asia, Press Releases | No Comments
Global Pharma R&D Summit October 22 & 23, 2007 Boston Marriott Newton, Boston, MA
Last Updated on Tuesday, 11 September 2007 02:29 Written by admin Tuesday, 11 September 2007 02:29
Sharing Insight
The 4th Annual Global Pharma R&D Summit brings together leading pharmaceutical professionals to analyze and discuss key industry challenges and developments. Be a part of this influential meeting and engage in business, networking and innovative discussions regarding the future of Pharma R&D. Â
Key topics:
- Omics & RNA profiling – Developing more precision therapeutics and examining the current state of the industry
- Bottlenecks – Removing them in translational medicine
- Collaboration – Analyzing the impact the trend towards industry/FDA partnering has had on R&D productivity
- Safety – Resolving safety issues in small and large molecule drug development
- Predictive strategies – Evaluating emerging technologies
- Global information management – Are local needs being met?
- Biomarker insights – Assessing the ever-wider range of markers
- Adaptive trials -Â Designing for the real world
For more information, visit www.globalpharmasummit.com
Posted under Press Releases, USA and Canada | No Comments
The 5th International Bird Flu Summit
Last Updated on Wednesday, 5 September 2007 02:06 Written by admin Wednesday, 5 September 2007 02:06
US AI Experts, Public Health, Military and Homeland Security Officials, Vaccine Manufacturers and Other Stakeholders to Join Their Counterparts from 35 Nations this September in the 5th International Bird Flu Summit
More than 400 bird flu policy makers representing 35 countries are expected to gather at the 5th International Bird Flu Summit to examine the worlds preparedness and response plans against a bird flu pandemic.
Washington, DC (New-Fields) September 5, 2007 – More than 400 registered participants are expected to attend the 5th International Bird Flu Summit (IBFS) in Las Vegas on September 27 and 28, 2007.
The summit, which will have the participation of delegates from 35 countries, is expected to create a global perspective as well as offer practical approaches to the bird flu threat, to protect nations, communities, businesses, and way of life. With the number of delegates exceeding that of the last four summits, issues on health, economics, security and related concerns are expected to be tackled on a more global scale.
“The heightened interest and participation in the IBFS is a strong indication that the world needs to continue to reinforce its defenses against a possible pandemic bird flu,” explains Samir Farajallah, president and CEO of New-Fields, the summit organizer.
“Practical applications of breakthroughs in science, technology and infection control are some of the significant additions top the topics to be presented at the 5th Summit. These practical means to beat the avian influenza (AI) virus are seen as a boost in the global preparation against AI. This is very important as it is coming at the wake of bird flu related deaths in Indonesia,” Farajallah explains further.
As in the previous summits, distinguished scientists, public health officials, business leaders, law enforcers, first responders and other experts will discuss the latest in pandemic prevention, preparedness, response, and recovery.
The summit will also address the threat of a bird flu pandemic and a possible human-to-human transmission.
Participants, like in the past summits, will have a unique chance to come face-to-face with doctors who have treated fatal human cases of bird flu, such as Dr. Sardikin Giripatro of the Indonesian Investigation and Verification Team for Avian Influenza Outbreaks.
More participants are expected to join the 5th IBFS. Since its first staging in February 2006, the IBFS has established a strong global network of partners dedicated to the fight against the bird flu. The Summit continues to build on the success of the four previous summits held in Washington and Geneva, Switzerland.
This global event is open to all interested businesses and organizations from all countries. To obtain further information about the conference, please contact our Washington DC office at 202.536.5000 or visit us at www.new-fields.com.
About New-Fields
New-Fields Exhibitions, Inc. is a leading emerging markets and business information provider, producing trade shows that produce results for companies worldwide. Woth offices in the Asia Pacific Region and Washington DC, the company provides marketing services in the areas of construction, energy, oil & gas, telecommunications and health care.
Posted under Bird Flu Research, North America, Press Releases, USA and Canada | No Comments
Windhover Information’s 2nd Annual Therapeutic Area Partnerships
Last Updated on Saturday, 1 September 2007 02:47 Written by admin Saturday, 1 September 2007 02:47
Windhover Information’s 2nd Annual Therapeutic Area Partnerships is the industry’s most targeted and efficient partnering meeting for life science companies seeking partnerships in the top therapeutic areas: Oncology, Cardiovascular/Metabolic and Neuroscience. Decision-makers (business development and R & D) focusing on these therapeutic categories can meet to develop strategic alliances between their companies. Also, attendees enjoy the personal and interactive setting that combines company presentations, 1:1 meetings and networking functions.
Why attend TA Partnerships 2007? Use partnering software to pre-arrange and schedule partnership meetings that take place. PLUS:
- Capitalize on potential new business and collaboration opportunities with the hottest TA-focused companies
- Network with hundreds of potential pharmaceutical and biotech partners through 1:1 meetings, cocktail parties, luncheons and refreshment breaks
- Hear exciting new statistics, deal case studies and trends in therapeutic area partnering from an unbeatable line-up of senior level speakers
- Take back the most current conference and detailed information on delegates, their companies, projects and technologies
- Get pre-conference access to a database that includes detailed technical, non-confidential information on projects available for partnering (pre-clinical and clinical stage)
Benefit from Windhover’s carefully crafted Therapeutic-Specific sessions:
- Examining the Oncology/CV/Metabolic/Neuroscience marketplaces – where are the opportunities?
- Developing a commercial strategy
- Developing your value proposition in a highly competitive marketplace
- Drug reimbursement trends
- The most problematic and most exciting mechanisms under development
TA Partnerships 2007 is focused on the business of dealmaking, hosting partnering meetings all scheduled using our Industry-leading partnering software. Windhover hand-picks the presenting companies that grace our stage to ensure they represent the most exciting partnering candidates available, and a nice balance of opportunities across therapeutic categories, product types and geographies.
More Therapeutic Focus
Benefit from senior-level case studies from 4 therapeutic-specific tracks
- Track 1-Neuroscience
- Track 2-Cardiovascular
- Track 3-Metabolic
- Track 4-Oncology
More workshops (Included with your registration fees)
Take home practical insight on how to develop and commercialize your therapeutics through the following workshops :
Workshop 1
The Endless Challenge: Best Practices Demonstrating Safety and Proof of Concept In Clinical Development
Workshop 2
The New World of Commercialization and Reimbursement
Workshop 3
The Good, the Bad and the Ugly in Dealmaking
More content
1. Therapeutic Area Partnering – Predicting What Pharma Wants: Roger Longman on Therapeutic Alliances
- Which therapeutic areas attracts the most number of deals and alliance dollars
- Clinical development by indication – where are the clinical dollars going?
2. Large Pharma Panel with Merck, AstraZeneca and Bristol-Myers Squibb
- What is your interest level in the different TAs?
- Which TAs are attractive and why
- Are you open to going outside of stated TAs?
3. Top 10 Sessions – The Top 10 Most Licensable Projects in neuro, cardiovascular, metabolic and oncology, with each area analyst explaining the selection process and criteria and briefly describing the programs and companies chosen
Matchmaking in Drug Partnering: Identifying the Right Drugs and the Right Partners
Challenges in identifying good science
Market statistics and market potential
Competitive landscape
Where the most promising neuro drug programs are coming from
For a complete description of projects, click here.
4. Pharma’s New World Order: Mid-Size and Specialty Pharmaceuticals Take Center Stage
The panel will include three to four VP or C-level executives from midsize and large specialty pharma companie, and will cover:
Why Big Pharma isn’t always better pharma
Win-win alliances
How specialty differs from primary care deals
The impact of Big Pharma’s emerging interest in specialty products
Specialty and blockbuster are no longer contradictory terms; where to look for the next blockbuster specialty products
5. Poster sessions with the handpicked, Top 10 Most Licensable Projects in:
- Neuroscience
- Cardiovascular
- Metabolic
- Oncology
6. Challenges and Opportunities in Translating Advances into Prescribed Drugs with Some of the Industry’s Most Reputable R & D Leaders
- Challenges and opportunities in innovative discovery tools: what the industry needs
- How the industry is improving preclinical and toxicity predictors and human safety biomarkers
- Your view of the most problematic and most exciting mechanisms now under development
More Potential Partnering Opportunities
Schedule partnering meetings with global life science companies using Windhover’s proprietary partnering software
- Meet potential partners using software to pre-arrange and schedule several partnership meetings that take place at TA Partnerships
- Capitalize on potential new business and collaboration opportunities with the hottest global biotechs
- Take back the most current conference and detailed information on delegates, their companies, projects and technologies
Just a Sample of Past Attending Companies:
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More Networking Opportunities
Network with hundreds of potential pharmaceutical and biotech partners through 1:1 meetings, 2 cocktail parties, 2 luncheons and 4 refreshment breaks
Benefit from Windhover Editorial’s first hand-case studies, best practices and lessons learned to help you build your own drug pipeline. Spaces are limited so Register Now for THE therapeutic specific meeting that brings you the latest cutting-edge compounds and partnering opportunities under one roof.
We look forward to greeting you in Philadelphia!
Posted under Press Releases, USA and Canada | No Comments
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