SBIR/STTR Research Award

New Aminoglycosides to Treat Drug-Resistant Bacteria

Award identifier ebe0d8472ae43b4652a46fe99688d9fc2d17d2bb55f949945dba85596e5bde9fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$100,000

Program and phase

SBIR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
OPTIMER PHARMACEUTICALS, INC.
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
Not reported
Topic code
Not reported

Research abstract

DESCRIPTION (provided by applicant): Aminoglycosides (AMGs) are an important class of antibiotics, which are active against a broad rage of difficult to treat bacterial infections. AMGs are particularly useful for the treatment of serious Gram-negative infections resulting from Pseudomonas aeruginosa. AMG resistance in P. aeruginosa continues to grow at an alarming rate and there is an immediate need to develop new AMGs against drug-resistant strains. In the past, the difficulty of complex carbohydrate synthesis has limited the ability of medicinal chemists to develop AMGs with these improved properties. We plan to use our complex carbohydrate synthesis platform, OPopSTM, to tackle the medicinal chemistry of AMGs. The long-term objectives of this program are to identify and develop a novel broad-spectrum AMG, active against drug-resistant bacteria and to develop an AMG with an improved safety profile relative to the currently available alternatives using OPopSTM technology. Furthermore, we believe the OPopSTM platform will be a valuable toot to study carbohydratebased medicinal chemistry in a host of other disease areas. Broadly, the specific aims of our program are to: i) Design efficient syntheses for large numbers of AMG antibiotics, which incorporate Optimer's OPopSTM carbohydrate synthesis technology. ii) Synthesize large numbers of novel AMGs. iii) Screen the resulting AMGs against panels of bacteria including drug-resistant strains of P. aeruginosa, Enterococci sp., E.coli, and S. aureus. iv) Identify a few promising lead compounds for advancement into in vivo efficacy studies, safety studies and ultimately clinical development.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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