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Targanta Announces Review of Oritavancin at FDA Anti-Infective Drugs Advisory Committee Meeting.

CAMBRIDGE, Mass. -- Targanta Therapeutics Corporation (Nasdaq: TARG TARG Tatra Area Research Group
TARG Telescoped Ammunition Revolver Gun
TARG Transportability Analysis Reports Generator
TARG Target Alternative Relevant Groups
) announced today that the U.S. Food and Drug Administration's (FDA FDA
Food and Drug Administration

FDA, See Food and Drug Administration.

FDA, the abbreviation for the Food and Drug Administration.
) Anti-Infective Drugs Advisory Committee will review the Company's New Drug Application (NDA (Non Disclosure Agreement) An agreement signed between two parties that have to disclose confidential information to each other in order to do business. In general, the NDA states why the information is being divulged and stipulates that it cannot be used for any ) for oritavancin on November 19, 2008.

Targanta submitted the NDA in February to obtain approval for oritavancin for the treatment of complicated skin and skin structure infection (cSSSI) caused by gram-positive organisms, including methicillin-resistant Staphylococcus aureus methicillin-resistant Staphylococcus aureus Methicillin-aminoglycoside resistant Staphylococcus aureus, MRSA An organism with multiple antibiotic resistances–eg, aminoglycosides, chloramphenicol, clindamycin, erythromycin, rifampin, tetracycline, , or MRSA MRSA Methicillin-resistant Staphylococcus aureus. See MARSA. . The submission includes data from 19 clinical trials, including two pivotal Phase 3 clinical trials that examined the safety and efficacy of intravenous oritavancin for the treatment of cSSSI, both of which met their primary endpoints. The NDA dossier also includes data from more than 2,100 individuals and in vitro in vitro /in vi·tro/ (in ve´tro) [L.] within a glass; observable in a test tube; in an artificial environment.

in vi·tro
In an artificial environment outside a living organism.
 activity data on oritavancin against more than 9,000 clinical bacterial isolates, including a broad range of gram-positive strains resistant to commonly used antibiotics such as oxacillin oxacillin /ox·a·cil·lin/ (ok?sah-sil´in) a semisynthetic penicillinase-resistant penicillin used as the sodium salt in infections due to penicillin-resistant, gram-positive organisms. , methicillin methicillin /meth·i·cil·lin/ (meth?i-sil´in) a semisynthetic penicillin highly resistant to inactivation by penicillinase; used as the sodium salt.

, vancomycin, daptomycin and linezolid. The FDA's action date for the oritavancin NDA is December 8, 2008.

The Anti-Infective Drugs Advisory Committee plans to meet on November 18, 2008 to discuss justification of the non-inferiority margin for cSSSI. Targanta, as well as other companies, has been asked to present before the panel on this topic.

About Oritavancin

Oritavancin is a novel, semi-synthetic lipoglycopeptide antibiotic candidate with potent bactericidal bactericidal /bac·te·ri·ci·dal/ (bak-ter?i-si´d'l) destructive to bacteria.
An agent that destroys bacteria (e.g.
 (killing) activity against a broad spectrum of gram-positive bacteria. These types of gram-positive antibiotic-resistant infections have created a market that IMS Health estimated to be more than $1 billion in the U.S. in 2007 and growing rapidly. MRSA infections have become an increasingly serious problem both in the hospital and in the community. According to the Centers for Disease Control and Prevention Centers for Disease Control and Prevention (CDC), agency of the U.S. Public Health Service since 1973, with headquarters in Atlanta; it was established in 1946 as the Communicable Disease Center. , there are over 126,000 hospitalized persons infected with MRSA annually. More than $2.5 billion in healthcare costs can be attributed to MRSA infections.1

About Targanta Therapeutics

Targanta Therapeutics Corporation is a biopharmaceutical company focused on developing and commercializing innovative antibiotics to treat serious infections in the hospital and other institutional settings. The Company's pipeline includes an intravenous version of oritavancin, a semi-synthetic lipoglycopeptide antibiotic currently awaiting U.S. and EU regulatory approval, and a program to develop an oral version of oritavancin. The Company has operations in Cambridge, MA; Indianapolis IN; and Montreal, Quebec, Canada. For more information about Targanta, visit

1 CreditSuisse, Hospital-Associated Infections, pg. 18, January 18, 2008.

Safe Harbor Safe Harbor

1. A legal provision to reduce or eliminate liability as long as good faith is demonstrated.

2. A form of shark repellent implemented by a target company acquiring a business that is so poorly regulated that the target itself is less attractive.

This press release contains "forward-looking statements" that are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act The Private Securities Litigation Reform Act of 1995 (PSLRA) implemented several significant substantive changes affecting certain cases brought under the federal securities laws, including changes related to pleading, discovery, liability, class representation and awards fees and  of 1995. These are statements that are predictive in nature, that depend upon or refer to future events or conditions or that include words such as "potential," "may," "will," "expects," "projects," "anticipates," "estimates," "believes," "intends," "plans," "should," "seeks," "hope" and similar expressions. Such statements include the approval of oritavancin for the treatment of cSSSI caused by gram-positive organisms. Forward-looking statements involve known and unknown risks and uncertainties that may cause actual future results to differ materially from those projected or contemplated in the forward-looking statements. Forward-looking statements may be significantly impacted by certain risks and uncertainties described in Targanta's filings with the Securities and Exchange Commission. The risks and uncertainties referred to above include, but are not limited to, delays in obtaining or a failure to obtain regulatory approval for Targanta's product candidates; unfavorable clinical trial results; Targanta's potential inability to initiate and complete pre-clinical studies and clinical trials for its product candidates; the possibility that results of pre-clinical studies are not necessarily predictive of clinical trial results; and those other risk factors that are described more fully in the Company's filings with the Securities and Exchange Commission. Targanta does not undertake any obligation to update any of these forward-looking statements to reflect a change in its views or events or circumstances that occur after the date of this release.
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Publication:Business Wire
Date:Oct 14, 2008
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