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Daily Dose Newsroom is a Daily Dose of Wall Street research and news in the Healthcare, Biotech, and Biomedical sectors.

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Entries in Conferences (28)

Tuesday
Jun192012

Keryx Biopharmaceuticals Announces Live Webcast of Upcoming Analyst Day (KERX)

Keryx Biopharmaceuticals (NASDAQ: KERX) is focused on the acquisition, development and commercialization of medically important pharmaceutical products for the treatment of renal disease. Keryx is developing Zerenex (ferric citrate), an oral, ferric iron-based compound that has the capacity to bind to phosphate and form non-absorbable complexes. The Phase 3 clinical program of Zerenex for the treatment of hyperphosphatemia (elevated phosphate levels) in patients with end-stage renal disease is being conducted pursuant to a Special Protocol Assessment (SPA) agreement with the FDA. Keryx is headquartered in New York City.

The Company has announced that its upcoming Analyst Day will be webcast live on Thursday, June 21, 2012 at 4:30 pm ET. Scheduled speakers include the following:

  • Julia Lewis, M.D. will provide her perspective on the Zerenex (ferric citrate) Phase 3 clinical program and the potential Zerenex product profile.-- Professor of Medicine, Division of Nephrology, Vanderbilt University School of Medicine
  • Geoffrey Block, M.D. will discuss the potential for Zerenex in pre-dialysis.-- Director of Research, Denver Nephrology and Associate Clinical Professor in Medicine, University of Colorado Health Sciences Center
  • David Goldfarb, M.D. will discuss the potential importance of citrate.-- Chief, Nephrology Division, NY Campus of NY Harbor Health Care Veterans Affairs System and Professor of Medicine & Physiology, NYU School of Medicine.

To access the live audio webcast, please visit the Company's Investor Relations section of their website ( http://investors.keryx.com ). An archived version of the webcast will become available following the conclusion of the live presentation.

Tuesday
Jun192012

Tonix Pharmaceuticals to Present at Marcum MicroCap Conference (TNXP)

Tonix Pharmaceuticals (OTCBB: TNXP) develops new treatments for challenging disorders of the central nervous system (CNS). The Company’s lead programs are potential new treatments for fibromyalgia and post-traumatic stress disorder, which are chronic CNS syndromes. In each of these programs, TONIX seeks to use new doses and formulations of cyclobenzaprine in new treatment regimens. Cyclobenzaprine is the active ingredient of two prescription muscle relaxants that have been approved by the U.S. Food and Drug Administration (FDA) and are marketed by other companies.

The company has announced that Chief Executive Officer Seth Lederman, M.D. will be presenting at the inaugural Marcum MicroCap Conference on June 20th at the Roosevelt Hotel in New York City. Dr. Lederman's presentation is scheduled to begin at 3:30 p.m. Eastern time.

A live audio webcast of this presentation will be available through the conference website: http://execvid.com/marcum-microcap-conference-2012


The Marcum MicroCap Conference is dedicated to introducing investors to the very best, undiscovered companies under $500 million in market capitalization and will feature presentations by CEOs and CFOs of approximately 60 promising high-growth companies, as well as panel discussions. This invitation-only event is expected to attract top fund managers who focus on small cap equities and qualified high-net-worth investors.

For full event details and registration information, please visit http://www.marcumllp.com/microcap.

 

Friday
Jun152012

CytoSorbents to Present at the Marcum MicroCap Conference - $CTSO

CytoSorbents Corporation (CTSO), a critical care-focused company using blood purification to modulate the immune system to prevent or treat organ failure caused by life-threatening illnesses, announced that Dr. Phillip Chan, Chief Executive Officer, will present at the Marcum MicroCap Conference on June 20th in New York City at the Roosevelt Hotel. The event is held by Marcum LLP and co-presented by CCG Investor Relations.

Presentation Details

  • Date: Wednesday, June 20, 2012
  • Time: 4:00PM
  • Location: The Roosevelt Hotel, 45 East 45th Street, New York, NY

A live audio webcast of this presentation will be available through the conference website: http://execvid.com/marcum-microcap-conference-2012

The Marcum MicroCap conference is designed for investors interested in the micro-cap arena, and is expected to gather over 500 participants, including institutional investors, mutual funds, hedge funds, wealth managers, and family offices. The conference will also feature panels on subjects highly relevant to small-cap corporate finance. The event is free to attend for qualified investors and the company will make a formal presentation and be available for one-on-ones.

For full event details and registration information, please visit http://www.marcumllp.com/microcap

About Marcum LLP
Marcum LLP is one of the largest independent public accounting and advisory services firms in the nation. Ranked among the top firms in the nation, Marcum offers the resources of more than 1,100 professionals, including more than 150 partners, in 23 offices throughout New York, New Jersey, Massachusetts, Connecticut, Pennsylvania, California, Florida, Grand Cayman, China and Hong Kong. The Firm's presence runs deep with full service offices strategically located in major business markets. Marcum is a member of the Marcum Group , the gateway to a group of organizations that provide a variety of professional services including accounting and advisory, technology solutions, recruiting, and wealth management. These organizations include Marcum LLP ; Marcum Technology LLC ; MarcumBuchanan Associates LLC ; Marcum Search LLC ; Marcum Financial Services LLC ; Marcum Cronus Partners LLC ; Marcum Bernstein and Pinchuk LLP ; and Marcum Healthcare LLC .

About CCG Investor Relations
CCG is a leading global investor relations and strategic communications consulting firm. In business for more than 30 years, the agency provides a complete range of investor communications, counseling, and IT and data solutions through our global network to over 100 clients across multiple capital markets. CCG has been awarded a number of industry honors for its handling of complex investor relations and crisis communications matters. The agency's corporate headquarters is in Los Angeles with additional offices in New York, Beijing, Shanghai, Hong Kong, London and Tel Aviv. For further information, contact CCG directly, or visit the Company's web sites at http://www.ccgir.com/ and http://www.ccgirasia.com.

About CytoSorbents, CytoSorb®, and HemoDefend
CytoSorbents Corporation is a critical care focused therapeutic device company using blood purification to modulate the immune system and fight multi-organ failure in life-threatening illnesses. Its purification technology is based on biocompatible, highly porous polymer beads that can actively remove toxic substances from blood and other bodily fluids by pore capture and adsorption. In March 2011, CytoSorb®, the Company's flagship product, achieved European regulatory approval as an extracorporeal cytokine filter, and can now be sold throughout the European Union (E.U.) under the CE Mark to be used in clinical situations where cytokines are elevated. The goal of CytoSorb® is to modulate the immune system by removing excessive cytokines, often called "cytokine storm," in critically-ill patients that can lead to deadly inflammation, multiple organ failure, immune dysfunction, and often death in common illnesses such as sepsis, trauma, burn injury, acute respiratory distress syndrome, and pancreatitis. CytoSorb® has demonstrated statistically significant reductions in mortality in septic patients at high risk of death and is now available for sale in Germany for the treatment of critical care illnesses under a controlled market release, with a planned broad product launch in Germany starting in the first half of 2012 and availability in other E.U. countries, assuming adequate and timely funding, and continued positive results from our clinical studies. HemoDefend is a development-stage blood purification technology platform for the blood transfusion industry intended to reduce transfusion reactions and safeguard the quality and safety of blood products. The HemoDefend technology utilizes the Company's polymer bead technology to remove many substances, such as antibodies, free hemoglobin and inflammatory mediators that can cause potentially serious and sometimes fatal transfusion reactions. CytoSorb® and HemoDefend are just two of a number of different polymers the Company has designed for various medical applications, including improved dialysis, reduction of post-surgical complications, the potential treatment of inflammatory and autoimmune disorders, rhabdomyolysis in trauma, drug detoxification, and others. Additional information is available for download on the Company's website: www.cytosorbents.com

Forward-Looking Statements
This press release includes forward-looking statements intended to qualify for the safe harbor from liability established by the Private Securities Litigation Reform Act of 1995. Forward-looking statements in this press release are not promises or guarantees and are subject to risks and uncertainties that could cause our actual results to differ materially from those anticipated. These statements are based on management's current expectations and assumptions and are naturally subject to uncertainty and changes in circumstances. We caution you not to place undue reliance upon any such forward-looking statements. Actual results may differ materially from those expressed or implied by the statements herein. CytoSorbents Corporation and CytoSorbents, Inc believe that its primary risk factors include, but are not limited to: obtaining government approvals including required FDA and additional CE Mark approvals; ability to successfully develop commercial operations; dependence on key personnel; acceptance of the Company's medical devices in the marketplace; the outcome of pending and potential litigation; compliance with governmental regulations; reliance on research and testing facilities of various universities and institutions; the ability to obtain adequate and timely financing in the future when needed; product liability risks; limited manufacturing experience; limited marketing, sales and distribution experience; market acceptance of the Company's products; competition; unexpected changes in technologies and technological advances; and other factors detailed in the Company's Form 10-K filed with the SEC on March 30, 2012, which is available at http://www.sec.gov.

Contact:
CytoSorbents Corporation
David Lamadrid
Chief Financial Officer
(732) 329-8885 ext. *816
DavidL@cytosorbents.com

Source: CytoSorbents Corporation

Monday
Jun042012

UPDATE: New Speaker at "The Age Of 'Big Data' In Bioscience Is Here, But Are We Prepared For It?" Panel Discussion in NYC on June 7, 2012

The panel discussion entitled "The Age of Big Data in Bioscience is Here, But are we prepared for it?" will be held June 7, 2012 at K&L Gates, LLP, located at 599 Lexington Ave. - 32d Floor - Seminar Room, New York, NY. It is hosted by the MIT Enterprise Forum Of NYC and LES NYC. See more information about the panel discussion here

UPDATE: Wanmei Ou Ph.D., Healthcare Product Strategist for Oracle Health Sciences will be speaking instead of Brett Davis, Senior Director of Oracle Health Sciences. See Wanmei's biography below:

"Wanmei Ou Ph.D. is a Healthcare Product Strategist in Oracle’s Health Sciences Global Business Unit responsible for the Translational Research Center solution. She works closely with leaders in healthcare and life sciences to understand their requirements and transform them into development activities shaping the product functions. In addition to this product strategy role, she is also an R&D liaison with multiple research laboratories in bioinformatics and natural language processing. 

Prior to joining Oracle, Wanmei obtained a Ph.D. degree in computer sciences from Massachusetts Institute of Technology with focus on biomedical imaging. While completing this work, she worked closely with scientists at both Massachusetts General Hospital and Brigham and Women’s Hospital. She also received the NSF Graduate Research and the Advanced Multimodal Neuroimaging fellowships during her graduate studies. Previous industry experience includes work at Siemens Corporate Research where she received a U.S. patent on her work on multimodal image registration. She also worked as a programmer analyst at the New York Blood Center focusing on population genetics." 
Monday
Jun042012

Islet Sciences Announces Participation at the 2012 American Transplant Congress (ISLT)

Islet Sciences, Inc., (OTCBB: ISLT) is a development-stage biotechnology company with patented technologies focused on transplantation therapy for people with insulin-dependent diabetes. The Company's transplantation technology includes methods for the culturing, isolation, maturation, and immunoprotection (microencapsulation) of islet cells. The Company's mission includes the introduction of commercial products with applications to cell-based replacement therapy in the healthcare marketplace.

The company has announced that it will be presenting at the upcoming 12th Joint Annual Meeting of the American Society of Transplant Surgeons and the American Transplantation (2012 American Transplant Congress).

The event will be held from June 2nd - June 6th at the John B. Hynes Convention Center in Boston, MA. Islet Sciences will present an update on work with their xenotransplantation model for islet transplantation on June 5, 2012 at 5:30 PM ET. Read more at PRNewswire.com
Overview of the American Transplant Congress (ATC), from 2012.atcmeeting.org
  • "To provide a forum for exchange of new scientific and clinical information relevant to solid organ and tissue transplantation.
  • To create an arena for the interchange of ideas regarding care and management of organ and tissue transplant recipients.
  • To facilitate discussions of the socioeconomic, ethical and regulatory issues related to solid organ and tissue transplantation.
A variety of formats are planned that will encourage the exchange of new scientific and clinical information and support an interchange of opinions regarding care and management issues, as well as socioeconomic, ethical, and regulatory issues relevant to organ and tissue transplantation.

Scientific material will be presented through symposia, oral abstracts, concurrent workshops, and poster presentations as well as small group sessions designed for in-depth exploration of both clinical and basic science topics." Read more at 2012.atcmeeting.org
Thursday
May312012

Biotech and related conferences in June 2012

June 2012 is a busy month for biotech and related conferences. Below are a few of the conferences taking place:

International Society for Cellular Therapy Annual Meeting 

Date: June 5-8, 2012
Venue: Sheraton Seattle, Seattle, WA

SeeThruEquity.com SmailCap Equity Conference - sponsored by ProActive Capital
Date: June 5, 2012
Venue: The Cornell Club
 
National Investment Banking Association Conference
 
Date: June 7-8, 2012
Venue: Le Parker Meridien Hotel, New York, NY

International Society for Stem Cell Research 10th Annual Meeting
 
Date: June 13-16, 2012
Venue: Pacifico Yokohama, Yokohama, Japan
 
The Biotechnology Industry Organization (BIO) International Conference
 
Date: June 18-21, 2012,
Venue: Boston Convention & Exhibition Center, Boston, MA
 
Alliance for Regenerative Medicine - Clinical Outlooks for Regenerative Medicine 2012
 
Date: June 19, 2012
Venue: The Starr Center, Schepens Eye Research Institute, Boston, MA

Marcum's Inaugural MicroCap Conference

Date: June 20, 2012
Venue: The Roosevelt Hotel, New York, NY
Friday
May252012

Advaxis Awarded Best Therapeutic Vaccine at the 5th Annual Vaccine Industry Excellence Awards (ADXS)

Advaxis, Inc. (ADXS) is a clinical-stage biotechnology company developing the next generation of immunotherapies for cancer and infectious diseases. Advaxis immunotherapies are based on a novel platform technology using live, attenuated bacteria that are bio-engineered to secrete an antigen/adjuvant fusion protein that is designed to redirect the powerful immune response all human beings have to the bacterium to the cancer itself.

Advaxis was the recipient of the Novartis sponsored Best Therapeutic Vaccine Award at the 5th Annual Vaccine Industry Excellence Awards, which were "created to honor and generate recognition of the efforts, accomplishments, and positive contributions of companies and individuals in the vaccine industry."

Advaxis received the award due to "progress made to date through clinical trials and/or achieved milestones" and "advanced efficacy, safety, and risk management data where appropriate."

In February, Advaxis announced encouraging results from "the first of 3 dose cohorts in the single blind, placebo controlled Phase II dose escalation study assessing the safety and efficacy of ADXS-HPV in the treatment of cervical intraepithelial neoplasia (CIN) 2/3."

Below is a summary of the Cohort 1 results:
  • "In the ADXS-HPV arm, 52% of CIN 2/3 lesions regressed from CIN 2/3 to CIN 1 or normal.  This means surgery is longer be required.  The dose in cohort 1 is about 1/20th of the dose being used in trials of ADXS-HPV in cervical cancer.
  • This 52% regression rate of ADXS-HPV with the lowest dose tested is very encouraging. According to the American Academy of Clinical Research’s Task Force on the Treatment and Prevention of Intraepithelial Neoplasia, 50% objective regression rate with a new treatment agent is considered clinically meaningful.
  • Further, according to O’Shaughnessy, et al 2002, CCR, 8:314, “An improvement in CIN 2/3 to either pathologically normal cervix or of CIN 3 to CIN 1, with no new CIN 2/3 lesions appearing in at least 50% of the treated patients, is evidence of clinical benefit of the new agent.”
  • In the cohort 1 trial, 40% of CIN 2/3 lesions spontaneously regressed in the placebo arm. This is within the range reported in the scientific literature of 35%-43% (Wright, et. al. 2003. Am J Obstet Gynecol, Am. J. Obstet. Gynecol. 289:295).
  • ADXS-HPV is safe. Less than 1/3 (29%) of the patients treated reported any side effects associated with treatment. Those that occurred were mild and self-resolved or responded quickly to treatment.
  • No SAEs (serious adverse events) were reported." Read more about the trial at Advantage.Numoda.com

Chairman & CEO of Advaxis Thomas A. Moore commented,

"We are delighted to receive recognition for our Company's achievements in developing ADXS-HPV. Our team continues to bring our proprietary platform technology from the laboratory into the clinic and meet major milestones in development in HPV caused cancers and soon in prostate and breast cancer, as well."

Read more at FierceVaccines.com

Thursday
May242012

Bavarian Nordic's PROSTVAC® update & reception June 4, 2012 in Chicago


Bavarian Nordic's PROSTVAC® update & reception will be held in Chicago on Monday, June 4, 2012.


PROSTVAC® is a therapeutic vaccine currently enrolling in a pivotal Phase 3 trial (PROSPECT) of 1,200 patients with asymptomatic or minimally symptomatic castration-resistant prostate cancer that was initiated in November 2011 and is expected to form the basis for approval of the vaccine for this patient population. 

Pre-registration for the June 4 event is required and attendance is limited, so please click "Register Now!" to RSVP today.

Speakers at the event include:
  • Dr. James L. Gulley (NCI)
  • Dr. Philip W. Kantoff (Dana-Farber)
  • Anders Hedegaard (Bavarian Nordic)
  • Dr. Reiner Laus (Bavarian Nordic)
Contacts:
Mettes Buhls 
Bavarian Nordic 
or
Michael Becker 
MD Becker Partners