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Sachs Associates 5th Annual North American Forum: Investing & Partnering in Biotech Presenter Profiles
BOSTON --(Business Wire)-- March 9, 2006 -- Sachs Associates 5th Annual North American Forum: Investing & Partnering in Biotech takes place Mar. 13 - 14, 2006, at The Fairmont Copley Plaza in Boston.
For in-depth information about the event, visit http://www.sachsforum.com/boston06.html
Business Wire is the official news wire service for 5th Annual North American Forum: Investing & Partnering in Biotech. Below are profiles from presenting companies. News releases and advisories are available at http://www.tradeshownews.com, Business Wire's trade show, conference, and event news resource.
Company: Advaxis Inc.
Ticker Symbol & Exchange: ADXS. OB Bulletin Board
Investor Relations Contact: Erik Lux; 212-825-3210
Web: www.Advaxis.com
Date of Presentation: March 13, 2006
Time of Presentation: 4:30 p.m.
Advaxis is developing proprietary Listeria cancer vaccines based
on technology developed by Dr. Yvonne Paterson, professor of
microbiology at the University of Pennsylvania and chairperson of
Advaxis' Scientific Advisory Board. Advaxis is developing therapeutic
cancer vaccines that enhance the immune system's cancer-fighting
abilities through its proprietary Listeria monocytogenes based system,
which utilizes two immunological mechanisms (Innate and Classical
Immunity) to develop safer and more effective Listeria-based cancer
vaccines. Advaxis is the exclusive licensee of a patented broadly
enabling Listeria platform technology that can elicit effective
anti-tumor responses. Advaxis has entered a Phase I/II clinical trial
for its lead Listeria vaccine candidate, Lovaxin C, which targets
cervical and head and neck cancers. Further Listeria vaccines in
development target breast, ovarian and lung cancers. The Listeria
platform will also have applications in the fields of infectious
disease and autoimmune disorders.
Company: Aethlon Medical, Inc.
Ticker Symbol & Exchange: "AEMD" OTCBB
Investor Relations Contact: Jeff Richardson; 858-459-7800, x302
Web: www.aethlonmedical.com
Date of Presentation: March 13, 2006
Time of Presentation: 4:20 p.m. EST
Aethlon Medical is developing the first medical device to treat
infectious disease. The device, known as the Hemopurifier(TM), is a
broad-spectrum treatment countermeasure against drug and vaccine
resistant bioweapons, naturally evolving pandemic threats such as H5N1
Avian Flu, and chronic infectious disease targets including
Hepatitis-C (HCV) and the Human Immunodeficiency Virus (HIV). More
information on Aethlon Medical and the Hemopurifier(TM) technology can
be found at www.aethlonmedical.com.
Company: Allergy Therapeutics Plc
Ticker Symbol & Exchange: AGY (London Stock Exchange, AIM)
Investor Relations Contact: Mr Keith Carter; Mr. Ian Postlethwaite;
+44 1903 844720
Web: www.allergytherapeutics.com
Date of Presentation: 13 March
Time of Presentation: 17:25 - 17:40
Allergy Therapeutics(R) plc (AGY) is a Europe-based specialty
pharmaceutical company focused upon the treatment and prevention of
allergy. AGY has an existing sales base of approximately GBP 23m/$40m
per annum, an MHRA-approved manufacturing capability and an
established sales and marketing infrastructure. The Company has the
opportunity to transform the treatment of allergic disorders with its
specific immunotherapy products based upon the TLR4 agonist vaccine
adjuvant, MPL. It is developing ultra-shot course (4-shot) Allergy
vaccines, known as Pollinex(R)Quattro. The Pollinex(R)Quattro range
should improve the effectiveness of allergy immunotherapy, achieve it
more safely and increase patient take-up of this method through its
convenience and better compliance. Phase III studies for worldwide
registration for Pollinex Quattro are scheduled to initiate in 2006.
The company is also investigating MPL as an adjuvant to sub-lingual
vaccines, currently in Phase IIa.
Company: Apoxis SA
Ticker Symbol & Exchange:
Investor Relations Contact: George Bates, CFO; +41 21 620 60 93
Web: www.apoxis.com
Date of Presentation: 14 March 2006
Time of Presentation: 13:55-14:10
Apoxis, a private Swiss company, exploits its world-class
understanding of the mechanisms underlying apoptosis, or cell death,
to develop first-in-class therapeutics for the treatment of cancer and
immunological diseases. Apoxis lead product, APO866, is a novel small
molecule therapeutic for the treatment of a range of cancers. APO866
is expected to enter Phase II trials in 2006. The product is also
being evaluated in a range of cancers in combination with commonly
used chemo- and radiotherapies in preclinical studies. The Apoxis
oncology portfolio also includes APO010, a protein therapeutic that
was developed using the company's proprietary multimerization
technology. It is expected to enter the clinic in 2006. Also based on
Apoxis multimerization technology, APO200 is currently being developed
as a treatment for a rare genetic disease.
Company: Biophan Technologies, Inc.
Ticker Symbol & Exchange: BIPH, OTC: BB
Investor Relations Contact: Carolyn Hotchkiss; 585-214-2441
Web: www.biophan.com
Date of Presentation: March 13, 2006
Time of Presentation: 11:25 a.m.
Biophan develops and markets cutting-edge technologies designed to
make biomedical devices safe and image compatible with the magnetic
resonance imaging (MRI) environment. The Company develops technologies
that enable implanted medical systems such as pacemakers,
interventional surgical devices such as catheters and guide wires, and
implants such as stents to be safely and effectively imaged under MRI.
The Company also recently announced a relationship with MYOTECH, LLC
to help develop and commercialize the MYO-VAD(TM) -- a novel, MRI
compatible ventricular assist device, which has significant potential
for improving the treatment of heart disease. Other applications in
development include novel MRI contrast agents, drug delivery
technologies and power systems, which derive energy from body heat.
Committed to growth through innovation and developmental leadership,
Biophan and its licensors now hold a total of 156 U.S. patents,
licenses, or applications. This total includes 50 issued U.S. patents
and 106 allowed or pending applications at various stages of
examination at the U.S. Patent and Trademark Office, plus
international applications. The patents cover areas including
nanotechnology (nanomagnetic particle coatings), medical device
designs, radio frequency filters, thermoelectric materials for
batteries, which generate power from body heat, and optical catheter
technologies. Biophan has joint development and licensing agreements
with Boston Scientific Corporation and NASA's Ames Center for
Nanotechnology. Biophan's goals are to make all biomedical devices
capable of safely and successfully working with MRI and to deliver
technologies that will improve healthcare delivery.
Company: BioSante Pharmaceuticals, Inc.
Ticker Symbol & Exchange: BPA Amex
Investor Relations Contact: Ritu Baral; 212-477-9007, ext. 25
Web: www.biosantepharma.com
Date of Presentation: March 13, 2006
Time of Presentation: 11:55 a.m.
BioSante Pharmaceuticals, Inc. is a U.S.-based pharmaceutical
company developing a pipeline of hormone therapy products for men and
women. Symptoms in women include menopausal symptoms such as hot
flashes and vaginal atrophy. Symptoms of low testosterone in women
include female sexual dysfunction. The hormone therapy products are
gel formulations for transdermal delivery including bio-identical
testosterone for men, bio-identical estradiol for women, and
bio-identical testosterone for women. BioSante also is developing its
calcium phosphate nanotechnology (CAP) for novel vaccines, including
biodefense vaccines for toxins such as anthrax and ricin, and drug
delivery systems. Key products in development include: Bio-E-Gela -- a
transdermal estradiol gel in development for treatment of menopausal
symptoms. An NDA was submitted to the FDA for Bio-E-Gel in Q1 2006;
and LibiGela -- a transdermal testosterone gel in clinical development
for treatment of female sexual dysfunction.
Company: Chemokine Therapeutics
Ticker Symbol & Exchange: TSX: CTI & OTCBB: CHKT
Investor Relations Contact: Frederica Bell; 604-827-3131
Web: www.chemokine.net
Date of Presentation: Monday, March 13th
Time of Presentation: 11:40-11:55 a.m.
Chemokine Therapeutics is a product-focused biotechnology company
developing drugs that harness the therapeutic potential of stem cells
through chemokine pathways. Chemokines are a class of proteins which
signal biological responses from stem cells that play a critical role
in the growth, differentiation and maturation of cells necessary for
fighting infection, as well as tissue repair and regeneration. Stem
cells are the master primitive cells that give rise to all of the
cells and organs in the body. Chemokines are one of the major
mediators of stem cell activity including stem cell growth,
differentiation and maturation. Chemokine Therapeutics is a leader in
research in this field. The Company has five products with two lead
product candidates in clinical trials: CTCE-0214, for enhancing the
immune system, and CTCE-9908, to prevent the spread of cancer and its
continued growth. For more information, please visit our website at
www.chemokine.net.
Company: ConjuGon, Inc.
Ticker Symbol & Exchange: Private
Investor Relations Contact: Sal Braico, Chief Operating Officer;
1-608-441-2890
Web: www.conjugon.com
Date of Presentation: March 13, 2006
Time of Presentation: 5:40 p.m.
ConjuGon is developing fundamentally new therapeutics to combat
antibiotic resistant bacterial infections. ConjuGon's novel
technology, based on research done at the University of
Wisconsin-Madison, uses harmless bacteria to transfer genes into
targeted, pathogenic bacteria. The genes encode for potent
antibacterial proteins and compounds that quickly kill the pathogenic
bacteria. Through a collaboration with the Loyola University Medical
Center outside of Chicago, ConjuGon's technology effectively cured
infections caused by antibiotic-resistant bacteria, including bacteria
resistant to all antibiotics, in a murine wound infection model.
ConjuGon is currently raising a Series A round of financing from
venture capitalists.
Company: DeveloGenAG
Ticker Symbol & Exchange:
Investor Relations Contact: Mrs. Kathrin Shem-Tov; +49 551 50558525
Web: www.develogen.com
Date of Presentation: 14. March 2006
Time of Presentation: 13.40-13.55
DeveloGen is a biopharmaceutical company engaged in the discovery
and development of novel therapeutic drugs for the treatment of
metabolic disorders, such as type 1 and type 2 diabetes, as well as
diabetic complications. The objective of DeveloGen is to address unmet
medical needs by leveraging its expertise and in-depth understanding
of the disease-related biology and medical implications of autoimmune
and diabetic complications. The Company has a broad and innovative
pipeline from lead discovery to phase III clinical development.
DeveloGen is headquartered in Goettingen, Germany, with additional
sites in Rehovot, Israel, and Erkrath, Germany.
Company: Diamyd Medical AB (publ)
Ticker Symbol & Exchange: DIAM B OMXS (Stockholm Stock Exchanfe)
Investor Relations Contact: Anders Essen-Moller; +46 70 551 06 79
Web: www.diamyd.com
Date of Presentation: March 13
Time of Presentation: 11:40 - 11:55
Founded in 1996, Diamyd Medical (OMXS: DIAM B) is an emerging and
global biotechnology company based in Stockholm, Sweden, and
Pittsburgh, Pa., USA. The Company is focused on developing
therapeutics for diabetes, pain and cancer as well as on protein
delivery using a proprietary gene delivery technology platform. Diamyd
Medical conducts therapeutic development based on its GAD (Glutamic
Acid Decarboxylase) molecule. GAD is an enzyme that converts the
excitatory neurotransmitter glutamate to the inhibitory transmitter
GABA. In this context GAD may have an important role in CNS-related
disease. GAD is also a target pancreatic beta cell autoantigen in
autoimmune diabetes, such autoimmunity leading to development of
insulin-dependence. Diamyd Medical's furthest developed project is
Diamyd, which is currently employed in two ongoing clinical Phase II
trials of both Type 2 and Type 1 diabetes. Other mainstream
developments include using a proprietary Nerve-Target Delivery System
to deliver GAD to treat diabetes pain and neuropathy.
Company: Ensemble Discovery
Ticker Symbol & Exchange:
Investor Relations Contact: Richard Begley, Ph.D., President and CEO;
617-492-6977, x233
Web: www.ensemblediscovery.com
Date of Presentation: Monday March 13
Time of Presentation: 17.10-17.25
Ensemble Discovery Corporation is developing a novel approach to
chemical discovery based on a highly integrated set of processes that
combine chemistry, biology and nanotechnology. Central to our approach
is DNA Programmed Chemistry (DPC), an innovative method for chemical
synthesis based on the groundbreaking work of Professor David Liu of
Harvard University. DPC employs short complementary DNA strands with
chemical moieties attached at each end to drive chemical reactions,
creating new bonds and novel compounds. Libraries containing complex,
diverse, pure and soluble drug-like small molecules can be generated
in a single pot. A nanoscale affinity-based selection system is then
used to identify binders with a wide dynamic range and to efficiently
generate comprehensive, data-driven SAR. Ensemble is applying the
technology to identify unprecedented chemical bond formations as well
as to discover human therapeutics and detection products, including
research tools, clinical diagnostics, and other specialty chemicals.
The company has a broad intellectual property portfolio and has raised
capital from a premier group of investors. Located in Cambridge,
Mass., Ensemble has assembled a world-class team of scientists and
entrepreneurs and aims to generate new products that address
significant unmet needs.
Company: Evolutec Group plc
Ticker Symbol & Exchange: EVC Exchange - London AIM
Investor Relations Contact: Nicholas Badman; +44 118 922 4488
Web: www.evolutec.co.uk
Date of Presentation: Monday, 13th March
Time of Presentation: 11.55-12.10
Evolutec is a biopharmaceutical company focused on drug
development for allergy, inflammation and auto-immune diseases.
Evolutec is based in Reading, UK. Evolutec's lead drug candidate,
rEV131 appears to work in both acute and chronic respiratory
indications including asthma and COPD (bronchitis). Early stage
results also indicate potential efficacy in ophthalmic indications
including conjunctivitis and post-cataract surgery. This unusual
breadth of activity may result from rEV131's novel mechanism of
action. Evolutec recently announced a positive result for rEV131 in a
112 patient Phase IIa study in allergic rhinitis (severe hay fever).
rEV131 met the primary efficacy endpoint (p less than 0.05). In
addition, rEV131 showed efficacy against mucus and congestion, the
most difficult to treat symptoms of rhinitis, and a rapid onset of
action (less than 45 minutes). Evolutec intends to carryout a Phase
IIb 300-400 patient rhinitis trial using a multi-dose device. In
addition, rEV131 will undergo proof of concept trials in post-cataract
surgery and dry eye, such that by the end of 2006 Evolutec will have
Phase II data in three disease areas. Evolutec has two other
preclinical molecules, rEV576 and rEV598, which are currently being
evaluated. rEV576 is a complement inhibitor and is being assessed for
its potential in myasthenia gravis and certain acute coronary
conditions including acute myocardial infarction ("AMI"). Evolutec
recently announced positive preclinical results for rEV576 in
myasthenia gravis a severe autoimmune disease, and AMI. rEV598 binds
serotonin and is being examined for CINV (chemotherapy induced nausea
and vomiting). Evolutec's management intend to create a range of
commercial options across its family of proteins including licensing
out the sales rights in primary care markets and retaining the rights
in specialist markets. For example, Evolutec will seek a partner for
rEV131 in respiratory indications, including allergic rhinitis and
asthma, but will retain the rights to rEV131 in ophthalmic indications
including dry eye and post-cataract surgery.
Company: IBEX Technologies Inc.
Ticker Symbol & Exchange: TO.IBT
Investor Relations Contact: Paul Baehr, President and Chief Executive
Officer
Investor Relations Contact Phone: Donna Lavoie or Bryan Murphy;
781-596-0200, x 103 or X 105
Web: www.ibex.ca
Date of Presentation: March 13
Time of Presentation: 12:10
IBEX Technologies Inc. (TSX: IBT) is a biopharmaceutical company
utilizing its expertise in disease related biomolecules to develop
therapeutics and diagnostics for the management of cancer and
arthritis. The Company's cancer program is based on a novel family of
genes known as kallikreins. IBEX is investigating the role of
kallikreins in metastatic disease, as well as developing
kallikrein-based diagnostics for the screening and monitoring of
cancer. The Company's arthritis program is based on a series of
biomarkers of cartilage degradation and synthesis. IBEX arthritis
assays are used by leading pharmaceutical companies for research
purposes. The Company also markets a number of products, including its
proprietary enzymes (heparinases and chondroitinases) and a series of
arthritis and kallikrein assays. IBEX(TM) Heparinase I is used in many
leading point-of-care hemostasis monitoring devices. IBEX's central
business strategy is to develop its core oncology products in-house
through demonstration of clinical efficacy, prior to establishing
commercial partnerships.
Company: immatics
Investor Relations Contact: Joerg Scheidle (Managing Director, CFO);
+49 (0)7071 565 125 14
Web: www.immatics.com
Date of Presentation: Monday, 13 March 2006
Time of Presentation: 5:10 p.m.
immatics is a biopharmaceutical company dedicated to the
development of innovative cancer vaccines. immatics' proprietary basis
of tumor-associated peptides (TUMAPs) provides a huge opportunity for
development of novel anti-cancer vaccines. With the discovery engine
XPRESIDENT(TM), immatics owns a unique technology allowing the
identification of thousands of TUMAPs directly from primary tumor
tissue. Having shown promising clinical results for first TUMAPs in
pilot trials, immatics has entered clinical Phase 1 trials in November
2005 for its first multi-TUMAP product candidate IMA901 treating renal
cell carcinoma (RCC) and recently completed enrollment well ahead of
plan. Final study results for this product candidate are expected for
3Q 2006. Several product candidates for even larger oncology
indications, including a product candidate for the treatment of
colorectal cancer, are currently in pre-clinical development and will
be ready for transition to phase 1 clinical testing in the next 12 to
18 months. immatics was founded in 2000 as a spin-off from the
Institute of Immunology at the University of Tuebingen (Hans-Georg
Rammensee).
Company: Ingenium Pharmaceuticals AG
Ticker Symbol & Exchange:
Investor Relations Contact: Michael Grau; 0049-89-8565-2300 (main)
Web: www.ingenium-ag.com
Date of Presentation: Monday, 13th March
Time of Presentation: 17.55 - 18.15
Ingenium Pharmaceuticals is leveraging its expertise in drug
target discovery and genetics-based therapeutic research toward the
development of novel treatments for pain and inflammatory disease. To
date, Ingenium has successfully used its unique forward and reverse
genetics approaches for its internal drug development programs and for
its partners. Ingenium's largest partnership is a multi-year drug
discovery and development collaboration with Elan in the area of
neuropathic pain. In addition, Ingenium has signed numerous agreements
across the biopharmaceutical industry and academia to provide genetic
expertise and animal models. As the lead program in its portfolio,
Ingenium has identified a novel mechanism for the treatment of
neuropathic and inflammatory pain. This mechanism is based on the
suppression of pro-inflammatory cytokines through a novel kinase-class
target. Using advanced lead compounds, Ingenium scientists have
established proof of concept in various animal models for both
neuropathic and inflammatory pain. To date, the compound series has
demonstrated good, pharmacokinetic properties, and Ingenium will
continue its drug discovery efforts toward defining a preclinical
developmental candidate by the end of 2006.
Company: Liponex Inc
Ticker Symbol & Exchange: LPX:TSX
Investor Relations Contact: Nick Hurst; 416-815-0700, ext. 226
Web: www.liponex.ca
Date of Presentation: Monday, March 13, 2006
Time of Presentation: 12:25 p.m. E.S.T.
Liponex Inc. is a publicly traded biopharmaceutical research
company that is developing a proprietary technology to treat heart
disease, cancer, and infectious disease, the world's three biggest
health care markets. Liponex has a lead product for the treatment of
heart disease, called CRD5, which raises High Density Lipoprotein
(HDL), often called "good cholesterol." CRD5 has successfully
completed three Phase I human trials that demonstrated the product was
safe and well tolerated with no significant adverse events. These
studies confirmed preclinical animal data findings and demonstrated
that CRD5 can cause a significant increase in HDL levels (~20%) while
also lowering triglyceride levels (~40%). Liponex intends to conduct
its first Phase I/II clinical trial with CRD5 in 2006. Data from this
trial will be used to determine an optimal dose for a second Phase II
trial. The Company also intends to selectively advance preclinical
development of other compounds in its pipeline.
Company: Manhattan Pharmaceuticals, Inc.
Ticker Symbol & Exchange: AMEX: MHA
Investor Relations Contact: Michelle Carroll - Corporate
Communications; 212-582-3950; mcarroll@manhattanpharma.com
Web: www.manhattanpharma.com
Date of Presentation: 13-March-06
Time of Presentation: 12:55 - 1:10 p.m.
Manhattan Pharmaceuticals, Inc. (AMEX: MHA), a development stage
pharmaceutical company, acquires and develops proprietary prescription
drugs for large, underserved patient populations. In view of the
worldwide obesity epidemic, the company is developing OE, an orally
administered novel therapeutic for weight loss. To meet the needs of
other major, underserved medical markets while lowering development
risks, Manhattan Pharmaceuticals is also developing PTH (1-34), a
peptide believed to be a regulator of epidermal cell growth, for
psoriasis and Propofol Lingual Spray, a convenient, proprietary
lingual spray formulation of propofol, the world's best-selling
general anesthetic, as a sedative-hypnotic for use during diagnostic
and therapeutic procedures.
Company: Meditech Research Limited
Ticker Symbol & Exchange: MTR (ASX)
Investor Relations Contact: Mary Bennett; +61 3 9296 2043
Web: www.mrl.com.au
Date of Presentation: 13th March 2006
Time of Presentation: 16.40 - 16.55
Meditech is an Australian biotechnology company focused on
developing and commercialising drugs that improve the health and
quality of life of patients with cancer and other chronic diseases.
The company has internationally recognised expertise in
carbohydrate-based therapies, particularly products based upon the
glycosaminoglycan, hyaluronic acid. Building on this expertise,
Meditech has created its patented HyACT(TM) (Hyaluronic Acid
Chemotransport Technology) platform, which it is applying to the
development of improved formulations of cancer drugs. The lead product
from the HyACT(TM) platform is HyCAMP(TM), which is in phase II
clinical trials. In addition to HyCAMP(TM), Meditech has taken the
anti-cancer products HyDOX(TM) (doxorubicin and hyaluronic acid) and
HyFIVE(TM) (5-fluorouracil and hyaluronic acid) into clinical testing.
HyACT(TM) (Hyaluronic Acid Chemotransport Technology) is a proprietary
platform technology, which can potentially be applied to a wide range
of cytotoxic cancer drugs, both proprietary and generic. The
formulations of HA with cytotoxic drugs results in increased efficacy
and a reduction in treatment toxicities through novel delivery
mechanisms.
Company: MorphoSys AG
Ticker Symbol & Exchange: Frankfurt Stock Exchange (FSE): MOR
Investor Relations Contact: Dr. Claudia Gutjahr-Loser;
gutjahr@morphosys.com; +49 89 89927 122
Web: www.morphosys.com
Date of Presentation: March 13, 2006
Time of Presentation: 12:.10-12.25
MorphoSys is one of the world's leading biotechnology companies
focusing on fully human antibodies. With its proprietary technologies,
MorphoSys is developing not only the next generation of therapeutic
antibodies, but also antibodies for research and diagnostics purposes.
HuCAL(R) (Human Combinatorial Antibody Library) is a very powerful
technology for the rapid and automated production of specific
antibodies. The most distinctive feature of the library is the
capability to optimize fully human antibodies to predefined
specifications, allowing MorphoSys to "Engineer the Medicines of
Tomorrow." MorphoSys' goal is to establish HuCAL(R) as the technology
of choice for antibody generation in all market sectors.
Company: Santhera Pharmaceuticals AG
Investor Relations Contact: Barbara Heller; +41 61 906 89 54
Web: www.santhera.com
Date of Presentation: 14 March 2006
Time of Presentation: 2:10 p.m.
Santhera Pharmaceuticals AG is a Swiss biopharmaceutical company
focused on the discovery, development and marketing of small molecule
pharmaceutical products for the treatment of neuromuscular diseases.
The company's lead product, SNT-MC17 (idebenone), is in a European
Phase III for the treatment of Friedreich's Ataxia, a rare but
devastating disease, which is ultimately fatal. Santhera has orphan
drug designations for this indication in both the U.S. and EU. The
Company intends to market the product in the U.S. and has exclusively
licensed the rights to market the product for FRDA in Europe to
Takeda. Santhera is also conducting a Phase II trial in Duchenne
Muscular Dystrophy with SNT-MC17 (idebenone). Santhera has developed a
pipeline of preclinical drug candidates, which it will progress in
neuromuscular diseases and outlicense in areas outside its core
therapeutic focus. Santhera's program on novel DPP IV inhibitors for
the treatment of metabolic diseases, including Type II diabetes, is
licensed to Biovitrum (Sweden). Santhera was formed in 2004 through
the merger of MyoContract AG and Graffinity Pharmaceuticals AG. The
Company has operations in Basel, Switzerland, and Heidelberg, Germany.
Santhera has attracted investment from leading global industry
investors including NGN Capital, Oxford Bioscience Partners, Merlin
Biosciences Limited, 3i Group plc, Carnegie Asset Management, Varuma
AG, The Novartis Venture Fund, GIMV, Heidelberg Innovation, Altana
Innovationsfonds, Clariden Bank, The Dow Chemical Company,
TechnoStart, tbg, the Swiss Foundation for Research on Muscle
Diseases, and private investors.
Company: Sapphire Therapeutics, Inc.
Ticker Symbol & Exchange: NA
Investor Relations Contact: Gary C. Cupit, PharmD, President and CEO;
908-203-6545
Web: www.sapphirethera.com
Date of Presentation: Monday, March 13, 2006
Time of Presentation: 5:25 p.m.
Sapphire Therapeutics is a private biopharmaceutical company
committed to developing and commercializing promising compounds ready
for clinical or preclinical testing. Sapphire's drug development team
collectively has brought over 80 approved drugs to market and includes
senior management from Merck, Novartis, Aventis, Akros and Alexion,
whose responsibilities ranged from research, to safety assessment, to
process research, to development and commercialization. The Company
utilizes its breadth of experience in drug development and contacts in
the pharmaceutical industry to select early stage compounds for
commercialization. Sapphire's first portfolio of novel compounds, a
collection of orally deliverable, small molecular ghrelin agonists,
have entered Phase II human clinical studies for cancer anorexia and
cachexia (CAC). This affects an estimated 70% of patients diagnosed
with neoplastic disease. Current treatments for CAC are utilized in a
relatively small percentage of patients and are limited in their
therapeutic effect. However, studies with ghrelin and ghrelin mimetics
have been shown to stimulate appetite and reverse nitrogen loss.
Management believes this will translate into a market opportunity
greater than $600 million. A second compound with an oncology
therapeutic indication is in Phase I.
Company: Swiss Medica
Ticker Symbol & Exchange: SWME. OB, NASD OTC
Investor Relations Contact: Dave Jones; djones@swissmedica.com;
705-495-5500
Web: www.swissmedica.com
Date of Presentation: March 13, 2006
Time of Presentation: 11:40-11:55 a.m.
Swiss Medica commercializes patented, clinically tested,
all-natural, OTC products that relieve chronic ailments:
-- O24 Pain Neutralizer is a topical analgesic and
anti-inflammatory, which has been praised for its safe and
fast-acting pain reduction benefits by physicians.
-- O24 Fibromyalgia is the first clinically tested OTC product
for Fibromyalgia available in North American pharmacies and
was awarded the first Seal of Approval by the National
Fibromyalgia Association.
-- PMS Escape is clinically proven to reduce the mood and
appetite symptoms that women experience during the
premenstrual period.
Swiss Medica's products are available in over 21,000 retailers
including Walgreens, CVS and Rite-Aid.
Company: TOPIGEN Pharmaceuticals Inc.
Investor Relations Contact: John Mohr; 973-809-5582
Web: www.topigen.com
Date of Presentation: March 14, 2006
Time of Presentation: 1:55 p.m.
TOPIGEN is a privately-held biopharmaceutical company focused on
respiratory care. The company is developing several new classes of
drugs and is actively progressing two drug candidates in Phase II
trials for COPD and asthma. These drugs are uniquely focused on
inhibiting multiple inflammation targets underlying the chronic
pulmonary diseases. TOPIGEN also has a number of discovery research
programs focused on the identification of novel compounds for the
treatment of COPD and allergic rhinitis. By applying its knowledge and
expertise in respiratory care, along with its proprietary mRNA-based
chemistry, TOPIGEN is seeking to make a positive difference for
patients. TOPIGEN is uniquely focused on developing products for the
treatment of pulmonary diseases using both traditional small molecule
chemistry and mRNA-based chemistry to target multiple inflammation
pathways and mediators. The drugs are delivered directly to the site
of action using topical inhalation technology. We are seeking
licensing and co-development arrangements on our lead drug candidates.
In addition, we are building our pipeline and actively seek
clinical-stage respiratory and pulmonary drug candidates that
complement our development expertise and meet our commercial criteria.
Ideal in-licensing candidates are programs with sufficient pulmonary
activity and toxicological data. For more information, visit
www.topigen.com.
Company: VioQuest Pharmaceuticals
Ticker Symbol & Exchange: OTCBB: VQPH
Investor Relations Contact: Daniel E. Greenleaf and Brian Lenz;
212-825-3210
Web: www.vioquestpharm.com
Date of Presentation: Monday, March 13, 2006
Time of Presentation: 12:25 - 12:40 p.m. ET
VioQuest's strategy is to acquire, develop, and commercialize
targeted late preclinical and early clinical stage therapies with
unique mechanisms of action for oncology, viral and autoimmune
disorders. The Company is developing two novel targeted anti-cancer
agents, VQD-001 and VQD-002, for the treatment of melanoma, myeloma,
lymphoma; and breast, leukemia, ovarian, pancreatic, colorectal
cancers, respectively. VioQuest's subsidiary Chiral Quest, a pioneer
in asymmetric chemocatalysis and custom synthesis, offers its
proprietary technology products to well-known pharmaceutical and fine
chemical companies worldwide to improve their production efficiencies
and, in some instances, to increase the overall safety and efficacy of
the underlying drug.
Company: VIRxSYS
Investor Relations Contact: Dr. Riku Rautsola; 301-987-0480, ext. 223
Web: www.virxsys.com
Date of Presentation: March 13, 2006
Time of Presentation: 16:20
The Company founded in Gaithersburg, Md., in 1998, is a private
biotechnology company whose mission is to develop gene-based therapies
using its proprietary lentiviral vector-based delivery system. The
first application of the Company's novel gene delivery technology has
been for treatment of HIV, the virus that causes AIDS. After a
successful first-in-class Phase I clinical trial that demonstrated the
safety profile of the Company's product VRX496, this new ex-vivo
anti-HIV treatment using a lentivector currently is being evaluated in
the first ever phase II clinical trial approved by the FDA involving a
lentiviral vector. The Company's lentiviral vector platform is an
ideal delivery system for the effective treatment of disease. The
Company's vector technology is also being investigated for
applications in anti-cancer therapies and the treatment of other
various life threatening diseases.
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