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BioWorld Today
the daily biopharmaceutical news source

FDA Adds Ampligen Experts to Roster for CFS Workshop

Volume 24, No. 49
published Thursday,
March 14,2013


A Double-Blind, Placebo-Controlled, Randomized, Clinical Trial of the TLR-3 Agonist Rintatolimod in Severe Cases of Chronic Fatigue Syndrome

published on March 14, 2012 at www.PLosONE.org


 

 

 

Our Mission

"Develop innovative therapies to improve the quality of life of patients suffering from severe chronic diseases.”
 
 

Company Profile

Hemispherx Biopharma, based in Philadelphia, is a biopharmaceutical company engaged in the manufacture and clinical development of new drug entities for treatment of viral and immune-based disorders.  Hemispherx’s flagship products include Alferon N Injection® and the experimental immunotherapeutics/antivirals Ampligen®. 

Alferon N Injection® is the company's registered trademark for its injectable formulation of Natural Alpha Interferon, and is approved by the FDA for a category of STD infection.  Alferon N Injection® (interferon alfa-n3 human leukocyte derived) is a highly purified, natural source, glycosylated, multispecies alpha interferon product, composed of eight forms of high-purified alpha interferon.

Alferon LDO® (Low Dose Oral) is a new experimental drug delivery platform for the Company’s highly purified, natural source alpha interferon.

Ampligen® (poly I:poly C12U) is a synthetic specifically configured double-stranded RNA containing regularly occurring regions of mismatching.  Ampligen® and Oragens® experimental nucleic acids are being developed for the potential treatment of globally important viral diseases and disorders of the immune system including HPV, HIV, Chronic Fatigue Syndrome (CFS), Hepatitis and influenza. 

Hemispherx’s platform technology includes large and small agent components for potential treatment of various severely debilitating and life threatening diseases.  Hemispherx has an extensive number of patents comprising its core intellectual property estate and a fully commercialized product (Alferon N Injection®).  The Company wholly owns and exclusively operates a GMP certified manufacturing facility in New Brunswick, New Jersey.  

Mail: Hemispherx Biopharma, Inc.
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One Penn Center
1617 JFK Blvd., 6th Floor
Philadelphia, PA 19103
Phone: (215) 988-0080
Fax: (215) 988-1739
E-mail: info@hemispherx.net

NOTE: We will do our best to respond to all inquires. However, we cannot guarantee individual answers.

Information contained on the Hemispherx website other than historical information, should be considered forward-looking and is subject to various risk factors and uncertainties. For instance, the strategies and operations of Hemispherx involve risks of competition, changing market conditions, changes in laws and regulations affecting these industries and numerous other factors discussed on the Hemispherx website and in the Company's filings with the Securities and Exchange Commission. Accordingly, actual results may differ materially from those in any forward-looking statements. Additionally, all the referenced investigational drugs and associated technologies of the company are experimental in nature and as such are not designated safe and effective by a regulatory authority for general use and are legally available only through clinical trials with the referenced disorders. The forward-looking statements represent the Company's judgment as of the date of this website. The Company disclaims, however, any intent or obligation to update these forward-looking statements.