News & Press
2010 | 2009 | 2008 | 2007 | 2006 | 2005 | 2004 | 2002 | 2001 |

(12.17.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at the 27th Annual J.P. Morgan Healthcare Conference

(11.25.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at the 20th Annual Piper Jaffray Health Care Conference

(11.10.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Reports Positive Data from its North American Phase 3 CDI Study of OPT-80

(11.5.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Reports Third Quarter 2008 Financial Results

(10.29.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at Oppenheimer Annual Healthcare Conference

(10.20.2008) SAN DIEGO, CA
Data from Optimer Pharmaceuticals Prulifloxacin Phase 3 Trial in Travelers Diarrhea and Strain Typing Data from OPT-80 Study to be Presented at ICAAC/IDSA Annual Meeting

(9.10.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at Two Upcoming Investor Conferences

(9.2.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Completes Enrollment in Second Prulifloxacin Phase 3 Clinical Trial

(8.28.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at BioCentury NewsMakers Conference

(8.6.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Reports Second Quarter 2008 Financial Results

(7.30.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at August 2008 Investor Conferences

(7.28.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Completes $14.8 Million Registered Direct Offering

(7.23.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Completes Enrollment in OPT-80 Phase 3 Clinical Trial in Patients with Clostridium difficile Infection

(7.21.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Raise $12.2 Million in Registered Direct Offering

(7.17.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Announces Change to Board of Directors

(7.16.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Announces Positive Results in Prulifloxacin Phase 3 Study

(6.26.2008) SAN DIEGO, CA
Optimer Reports Additional Data on Investigational Compound OPT-80 at Anaerobe 2008 Congress

(6.17.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at Two Upcoming Investor Conferences

(6.11.2008) SAN DIEGO, CA
Optimer to Present Additional Data from OPT-80 Phase 2A Study for Clostridium difficile Infection at Anaerobe 2008 Congress

(6.3.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at Needham Biotechnology & Medical Technology Conference

(5.27.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Receives Polymorph Patent for Lead Product Candidate OPT-80

(5.7.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Reports First Quarter 2008 Financial Results

(5.6.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Present at Upcoming Investor Conferences

(4.21.2008) BARCELONA, SPAIN
Clostridium difficile Infection 'Epidemic' Leads to Calls for Emerging Next-Generation Therapies

(4.15.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Sponsors ECCMID Symposium on Clostridium difficile-Associated Disease: Current Treatment and Challenges

(4.8.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Receives Notice of Allowance for OPT-80 Patent Application

(4.2.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Announces Peer-Reviewed Publication of OPT-80 Phase 1 Clinical Results for the Treatment of Clostridium Difficile Infection

(3.26.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Reports Fourth Quarter and Full Year 2007 Financial Results

(3.19.2008) SAN DIEGO, CA
Optimer Pharmaceuticals to Host Conference Call and Webcast to Discuss Fourth Quarter and Full Year 2007 Financial Results

(3.11.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Completes Enrollment in Phase 3 Clinical Trial of Prulifloxacin in Patients with Travelers’ Diarrhea

(1.7.2008) SAN DIEGO, CA
Optimer Pharmaceuticals Awarded Grant from the National Institutes of Health for Development of OPT-80 to Treat Deadly Hospital Associated Infection

(4.15.2008) SAN DIEGO, CA

Optimer Pharmaceuticals Sponsors ECCMID Symposium on Clostridium difficile-Associated Disease: Current Treatment and Challenges



Leading Experts convene to define the challenges of CDAD and discuss strategies for combating this emerging ‘global epidemic’

 

SAN DIEGO, CA – Tuesday April 15, 2008 –Leading world experts in infectious disease will convene on Saturday April 19th to discuss the limitations of current and emerging therapies used to combat Clostridium difficile-associated disease (CDAD), also referred to as Clostridium difficile infection (CDI).  CDI is recognized as the most common cause of hospital-acquired diarrhea[1].

 

The educational symposium at the 18th European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) in Barcelona, Spain, will compare current treatment options for CDI and highlight future therapies.   The meeting titled, ‘Clostridium difficile-Associated Disease: Current Treatments and Challenges’ will also address the global and epidemic nature of this potentially fatal disease. 

 

Experts participating in the symposium and their topics include:

·         Carl Erik Nord, M.D., Ph.D., Co-Chair of the symposium and Professor of Clinical Microbiology from the Department of Laboratory Medicine at the Karolinska University Hospital of the Karolinska Institute in Stockholm, Sweden

- Introduction

·         Ed Kuijper, M.D., Ph.D., Vice President of the European Society of Clinical Microbiology and Infectious Diseases and Professor of Medical Microbiology at the Leiden University Medical Centre in Leiden, Netherlands

       - Clostridium Difficile – A Global Epidemic

·         Frédéric Barbut, Pharm.D., Ph.D., Infection Control Practitioner from the Infection Control Unit at Hôpital Saint-Antoine in Paris, France

- Infection Control and the prevention of CDAD

·         Ian R. Poxton, Ph.D., D.Sc., Professor of Microbial Infection and Immunity at the University of Edinburgh College of Medicine and Veterinary Medicine, Edinburgh, Scotland

      - Risk Factors and Disease Severity: Implications for Treatment

·         John G. Bartlett, M.D., Co-Chair of symposium and Professor of Medicine at the Johns Hopkins University School of Medicine in Baltimore, Maryland, United States

       - Current Treatments for CDAD: Successes and Failures

·         Mark A. Miller, M.D., FRCPC., M.Sc., Chair of Infection Prevention and Control, Chief of the Division of Clinical Microbiology and Head of the Division of Infectious Diseases at the Jewish General Hospital, Montreal, Canada

- Therapeutics in Development

 

CDI is a major concern within the international medical community due to the growing incidence and spread of hypervirulent strains of Clostridium difficile responsible for more severe disease symptoms[2].

 

CDI is known to affect approximately 500,000 people in the US[3] and is responsible for one in every 1,000 hospital admissions in Europe[4].  CDI is a serious infection of the lining of the colon by Clostridium difficile bacteria, which in severe cases can result in death.  Deaths from C. difficile (6,480)[5] surpassed MRSA (1,650)[6] in England and Wales in 2006.

 

“CDI remains a very serious health concern with increases in incidence and severity reported across the world. With the limitations of current therapies and limited clinical responses, there is a need for better therapeutic alternatives to treat CDI.  Optimer is delighted to be working with leading global experts in meeting the challenges of CDI, and to inform ECCMID delegates about the latest advances, “said Emmanuelle A. Hugentobler, M.D., Senior Director Medical Affairs, Optimer Pharmaceuticals.

 

For further information / an invitation to this event please contact:

Resolute Communications                                                   Optimer Pharmaceuticals, Inc.

Con Franklin                                                                          Christina Donaghy

+44 (0) 20 7015 1354                                                              +1 858 909-0736 ext. 154

+44 (0) 79 7443 4151 (cell)                                                     cdonaghy@optimerpharma.com

con.franklin@resolutecommunications.com

 

Miranda Sykes

+44 (0) 20 7397 7481

+44 (0) 7810 698 099 (cell)

Miranda.sykes@resolutecommunications.com

         

        

                                   

About Optimer

Optimer Pharmaceuticals, Inc. (NASDAQ:OPTR), is a biopharmaceutical company focused on discovering, developing and commercializing innovative anti-infective products for the treatment of serious infections. Optimer has two late-stage anti-infective product candidates.  OPT80, currently in two pivotal Phase 3 clinical trials, is being developed for the treatment of Clostridium difficile infection, the most common hospital-acquired diarrhea.  Prulifloxacin, also in two pivotal Phase 3 clinical trials, is an antibiotic being developed for the treatment of travelers’ diarrhea, a form of infectious diarrhea.  Additional information regarding Optimer can be found at http://www.optimerpharma.com

  

Forward-looking Statements

Statements included in this press release that are not a description of historical facts are forward-looking statements, including without limitation all statements related to incidence of CDI deaths associated with CDI, and anticipated symposia discussing CDI. Words such as "believes," "anticipates," "plans," "expects," "intend," "will," "goal" and similar expressions are intended to identify forward-looking statements. The inclusion of forward-looking statements should not be regarded as a representation by Optimer that any of its plans will be achieved. Actual results may differ materially from those set forth in this release due to the risks and uncertainties inherent in Optimer's business including, without limitation, risks relating to: the timing, progress and likelihood of success of its product research and development programs, the timing and status of its preclinical and clinical development of potential drugs and other risks detailed in Optimer's filings with the Securities and Exchange Commission.


[1] ESGCD, September 2004

[2] McDonald et al (2005)

[3] Centres for Disease Control

[4] ‘ECSMID Study Group Report: A European survey of diagnostic methods and testing protocols for Clostridium difficile’,     Clinical Microbiology and Infection, 2003; 9 (10): 989