SBIR/STTR Research Award

A Novel Therapeutic for Invasive Candidiasis

Award identifier 8721fbac108ff0c8e08444d55cbb69cce41ad8cfee9079731255876d24e3bd8fAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$1,500,000

Program and phase

SBIR · Phase II

Award year

2014

Explore This Research Award in CaptureIQ

Research the technology, evaluate the recipient and agency, identify related opportunities, and explore potential follow-on work with CaptureIQ.

Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
FOX CHASE CHEMICAL DIVERSITY CENTER INC.
Proposal award date
2014-07-01
Contract end date
2017-06-30
UEI
V6EQM9ABEM89
Solicitation number
PA13-234
Topic code
NIAID

Research abstract

DESCRIPTION provided by applicant Systemic fungal infections are increasingly common especially in immune compromised patients While new antifungal drugs have been developed there is still a high mortality associated with these infections especially those due to Candida albicans other non albicans species NAS This is due to the limited spectrum of the drugs significant side effects as well as the development of resistance leading to an increase in drug resistant strains Host defense proteins HDPs are naturally occurring broad spectrum antimicrobial agents that have been examined recently for their utility as therapeutic antibiotics and antifungals Chief among their strengths is that microbes do not generally develop resistance to these agents Unfortunately they are expensive to produce and are often sensitive to protease digestion We have demonstrated the potent activity of a series of inexpensive non peptidic oligomers and compounds that mimic HDPs in both structure and activity against clinical strains of C albicans associated with oral candidiasis both in vitro and in vivo Our preliminary data demonstrate similar antifungal activity for several mimetics against clinical isolates of C albicans in the presence of human serum and one of these compounds was robustly efficacious in a mouse of disseminated candidiasis We believe these compounds can form the basis for the development of novel therapies against systemic fungal infections Our goal is to identify a safe and efficacious HDP mimic s as a development lead for treatment of disseminated candidiasis PUBLIC HEALTH RELEVANCE Systemic fungal infections are increasingly common especially in immune compromised patients While new antifungal drugs have been developed there is still a high mortality associated with these infections especially those due to Candida albicans other non albicans species NAS Using our technology based on small non peptidic mimics of host defense proteins we propose to identify safe and effective development lead compounds for treatment of disseminated Candidiasis

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

38 SBIR/STTR records share this UEI (2009–2025). Reported award amounts total $42,025,779. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

Back to SBIR/STTR Research Awards

Don't take our word for it. Ask AI about RFPCapture.

See what leading AI assistants have to say about RFPCapture and CaptureIQ.

Gemini opens without a prefilled question. The question is copied to your clipboard when the button works. You can also copy it here:

What is RFPCapture.com and its CaptureIQ platform from Smart Logic AI? How does it help federal contractors discover opportunities, evaluate bid/no-bid decisions, research government contracts, and prepare proposals? How does it compare with other federal capture platforms? Use independent sources where available.