SBIR/STTR Research Award

Novel antibacterial agents derived from natural products

Award identifier 3c0c378f8fd32186d527ca94863a1dfb28807c9bc81aae8f9b79f50a4881f1f3Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$295,729

Program and phase

STTR · Phase I

Award year

2016

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Promiliad Biopharma Incorporated
Proposal award date
2016-07-15
Contract end date
2018-07-14
UEI
NVGDWKLM5RR7
Solicitation number
PA14-072
Topic code
NIAID

Research abstract

DESCRIPTION provided by applicant Antibiotic resistance among common bacterial pathogens is a serious public health problem as it compromises our ability to treat infectious disease The resistance problem is compounded by the lack of discovery of new antibiotics especially those with novel mechanisms of action New antibiotics are critically needed as resistance to recently developed antibiotics is growing The goal of this project is to develop our triazolononactate antibiotics as exemplified by our lead compound PBI G as broad spectrum agents active against Gram positive pathogens Specifically we will improve the antibacterial activity and selectivity of our current lead compounds against S aureus including MRSA E faecalis including VRE and S pyogenes We will obtain data that will allow us to make a hypothesis concerning the MOA of the triazolononactate compound class and to identify the target so that we may employ structure based drug design to achieve our goals of potency and spectrum of activity In addition to using classic tracer studies we will use several resistant bacterial strains in hand to determine the genetic modifications leading to resistance Beyond the improvement of potency and identification of the cellular target we will initiate DMPK studies to determine if the triazolononactate compound class has any critical liabilities such as metabolic instability a poor resistance profile or off target pharmacology We will determine the maximal tolerated dose and basic pharmacodynamic properties Cmax AUC t oral bioavailability of the compound class We will then assess whether our best compounds show effectiveness in a murine S aureus infection model In summary this Phase I project seeks to obtain analogs of our lead compound that have improved potency and selectivity identify a mechanism of action and to evaluate DMPK properties We envisage a Phase II project wherein we fully address ADMET issues and greatly expand animal studies with an improved compound set to move our compound class to our eventual goal of an IND filing PUBLIC HEALTH RELEVANCE The ability to treat infections has become compromised by growing resistance to current antibiotics and has become a serious threat to public health The significance of the threat is greater as there have been fewer antibiotics being approved for use in recent years and the discovery of a new class of antibiotic is a rare event By employing natural product chemistry we have been able to identify a set of novel antibiotics These compounds are active against a range of pathogens including methicillin resistant Staphylococcus aureus MRSA This project seeks to demonstrate that these compounds can be developed into drugs

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

13 SBIR/STTR records share this UEI (2004–2020). Reported award amounts total $7,445,939. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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