SBIR/STTR Research Award
A NOVEL TARGET FOR THE DEVELOPMENT OF ANTIFUNGAL AGENTS
Award amount
$100,000Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- CYTOKINETICS, 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 (Verbatim from Applicant's Abstract): The increase in opportunistic
fungal infections such as candidiasis, zygomycosis, cryptococcosis,
histoplasmosis, and Aspergillus and Fusarium infections in immunocompromised
individuals, including AIDS patients, the elderly, surgical patients, and burn
victims, has demonstrated that these infections are frequently fatal if
untreated. In addition, the two accepted therapies, amphotericin B and the
azoles, have limited effectiveness and toxic side-effects. There is a clear
need for more effective antifungal agents.
To address this need, we plan to exploit the opportunity to discover antifungal
compounds with a novel mechanism of action by targeting drug discovery efforts
on a microtubule motor essential for mitotic progression in Aspergillus. Using
a high-throughput screen developed by Cytokinetics, we will isolate inhibitors
of this molecule's activity from chemical libraries totaling 230,000 compounds.
We will test hits for antifungal activity against a panel of fungi and
determine mammalian toxicity using cell-based assays. We have isolated homologs
of the Aspergillus target from several pathogens, which we will use in in vitro
assays to support our efforts to develop broad-spectrum antifungal compounds.
In addition to their anticipated use in treating a number of opportunistic
fungal diseases in humans, we expect inhibitors of these targets to have
agricultural and animal health applications.
PROPOSED COMMERCIAL APPLICATION:
There has been a dramatic increase in opportunistic fungal infections in immunocompromised
individuals, including AIDS patients, the elderly, transplant patients, and burn victims. The
two accepted therapies, amphotericin B and the azoles, have limited effectiveness and
toxic side effects. We seek to identify new antifungal agents with a novel mechanism of
action. Current antifungals have potential market sales of $6.5 billion annually. Clearly, a
novel, broad-spectrum antifungal will have significant commercial value, and will increase
the quality of life for infected individuals.
Technology keywords
Not reported