Printer Friendly
The Free Library
19,607,059 articles and books
Member login
User name  
Password 
 
Join us Forgot password?

Cubist Pharmaceuticals Receives Two Sbir Grants for Lipopeptide Research; Company Could Receive Almost $500,000.


Business Editors/High-Tech Writers

BIOWIRE2K

LEXINGTON, Mass.--(BUSINESS WIRE)--July 29, 2003

Cubist Pharmaceuticals, Inc. (Nasdaq: CBST CBST Center for Biophotonics Science and Technology
CBST Congregation Beth Simcha Torah (NYC)
CBST Complete Binary Search Tree
) today announced that it has recently been awarded two Phase I Small Business Innovation Research (SBIR SBIR Small Business Innovation Research (program/grant)
SBIR Space Based Infra-Red
SBIR Speaker-Boundary Interference
SBIR Site Backsurface-referenced Ideal Plane/Range (silicon wafers) 
) grants that could total almost $500,000 should all funding be received from the National Institutes of Health (NIH "Not invented here." See digispeak.

NIH - The United States National Institutes of Health.
). To date, Cubist has been awarded over $4.25 million in SBIR grants.

Both grants focus on Cubist's research on lipopeptides, a new class of compounds that may prove to be a source of additional antiinfective medicines. Cubist's lead investigational antibiotic Cidecin(R) (daptomycin for injection) is a member of this new class and a natural product of the fermentation of the bacterium Streptomyces Streptomyces (strĕp'təmī`sēz), bacterial genus of the order Actinomycetales, members of which resemble fungi in their branching filamentous structure. Various species produce such antibiotics as streptomycin and various tetracyclines.  roseosporus. The New Drug Application for CIDECIN is currently being reviewed by the U.S. Food & Drug Administration under priority review status with an action date of September 20, 2003.

The first SBIR grant, entitled "Modification of Daptomycin by Combinatorial Biosynthesis Biosynthesis

The synthesis of more complex molecules from simpler ones in cells by a series of reactions mediated by enzymes. The overall economy and survival of the cell is governed by the interplay between the energy gained from the breakdown of compounds
," will help support an ongoing project to rapidly manipulate the gene cluster responsible for the synthesis of daptomycin. The company is performing biosynthetic bi·o·syn·the·sis  
n.
Formation of a chemical compound by a living organism. Also called biogenesis.



bi
 modification of the daptomycin molecule to determine if analogues can be identified with broad spectra of bactericidal bactericidal /bac·te·ri·ci·dal/ (bak-ter?i-si´d'l) destructive to bacteria.
Bactericidal
An agent that destroys bacteria (e.g.
 (bacteria killing) activity and more potent activity against specific resistant species.

The second SBIR grant, entitled "Structure Activity Relationships Around Lipopeptides," will facilitate the exploration of the structure activity relationships around cyclic lipopeptide antibiotics. Cubist scientists will couple the use of more traditional methods of chemical synthesis of lipopeptides with biosynthetic techniques of swapping entire subunits responsible for the production of other lipopeptides in an attempt to create novel hybrid molecules with antibacterial activity.

Richard H. Baltz, Ph.D., Executive Director of Research at Cubist, commented on the grants: "Since the beginning of this year, our research efforts have focused on refining and advancing our natural product drug discovery technologies. We believe these government grants recognize the value of continuing these innovative programs, and we hope to continue to build our antiinfective franchise through the exploration of new molecular entities."

About Cubist

Cubist Pharmaceuticals, Inc. is a biopharmaceutical company focused on the research, development and commercialization of antiinfective drugs. Cubist has submitted a 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 ) to the U.S. Food & Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) for Cidecin(R) (daptomycin for injection) for the treatment of complicated skin and skin structure infections. The NDA for CIDECIN is currently being reviewed by the FDA under priority review status. Cubist's pipeline includes CAB-175, a next-generation parenteral parenteral /pa·ren·ter·al/ (pah-ren´ter-al) not through the alimentary canal, but rather by injection through some other route, as subcutaneous, intramuscular, etc.

par·en·ter·al
adj.
1.
 cephalosporin cephalosporin (sĕf'əlōspôr`ĭn), any of a group of more than 20 antibiotics derived from species of fungi of the genus Cephalosporium and closely related chemically to penicillin. Cephalosporins, e.g.  antibiotic in Phase 1 trials, and an oral version of ceftriaxone ceftriaxone /cef·tri·ax·one/ (cef?tri-ak´son) a semisynthetic, ß–resistant, third-generation cephalosporin effective against a wide range of gram-positive and gram-negative bacteria, used as the sodium salt.  (OCTX), a broad-spectrum cephalosporin antibiotic in pre-clinical development. Cubist is headquartered in Lexington, MA.

Cubist Safeharbor Statement

Statements contained herein that are not historical fact may be forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934, that are subject to a variety of risks and uncertainties. There are a number of important factors that could cause actual results to differ materially from those projected or suggested in any forward-looking statements made by the Company. These factors include, but are not limited to: (i) the Company's ability to successfully complete product research and development, including pre-clinical and clinical studies and commercialization; (ii) the Company's ability to obtain required governmental approvals; (iii) the Company's ability to attract and/or maintain manufacturing, sales, distribution and marketing partners; (iv) the Company's ability to develop and commercialize its products before its competitors; and (v) the Company's ability to finance its operations. Additional factors that would cause actual results to differ materially from those projected or suggested in any forward-looking statements are contained in the Company's filings with the Securities and Exchange Commission, including those factors discussed under the caption "Risk Factors" in the Company's recent SEC filings.

Cidecin is a registered trademark of Cubist Pharmaceuticals, Inc.

Additional information can be found at the Company's web site at www.cubist.com
COPYRIGHT 2003 Business Wire
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2003, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

 Reader Opinion

Title:

Comment:



 

Article Details
Printer friendly Cite/link Email Feedback
Publication:Business Wire
Geographic Code:1USA
Date:Jul 29, 2003
Words:652
Previous Article:New York Film Works Acquires Bladon Studios Limited.
Next Article:Software Armada and Fischer International Team to Provide the Higher Education Community with Affordable, Commercial Quality Identity Management and...
Topics:



Related Articles
Albany Molecular Research, Inc. Initiates Research Collaboration with Cubist Pharmaceuticals.
Thermal Wave Imaging, Inc., Ferndale, Mich., is being awarded a not-to-exceed $25,000,000 indefinite-delivery and indefinite-quantity contract.
FDA Accepts CIDECIN NDA and Grants Priority Review Status.
Genomatica awarded $765,000 Phase II SBIR grant from NIH.
Cubist Pharmaceuticals Names Michael Wood, M.D., and Martin Rosenberg, Ph.D., to Its Board of Directors.
Cubist Pharmaceuticals Selects ACS Dobfar as Single Source API Supplier.
Cubist Pharmaceuticals Reports Results from HepeX-B(TM) Phase 2 Study.
Cubist Pharmaceuticals to Present at Upcoming Investor Conferences; Presentations at the Merrill Lynch Global Pharmaceutical, Biotechnology & Medical...
Cubist Pharmaceuticals to Present at December Investor Conferences.
Cubist Pharmaceuticals Licenses Rights for Development and Commercialization of CUBICIN in Japan to Merck & Co., Inc.

Terms of use | Copyright © 2012 Farlex, Inc. | Feedback | For webmasters | Submit articles