SBIR/STTR Research Award

Targeted RNA degradation assay for new antiviral drug discovery

Award identifier eb2bf5456c7a82ac0aa6ef8d59efac248af4034a80913f7d3f2abd843583cde4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$300,000

Program and phase

SBIR · Phase I

Award year

2024

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
LUCERNA INC
Proposal award date
2024-08-01
Contract end date
2025-07-31
UEI
J3MWGA6WFCG3
Solicitation number
PA23-230
Topic code
NIAID

Research abstract

PROJECT SUMMARY There are currently no effective vaccines or antiviral drugs for most of the viral diseases afflicting human. Development of new therapy is challenging and expensive, and often complicated by drug resistance. It is now known that viral transcripts contain many highly structured RNA elements in both the coding and noncoding regions, and they play key roles in the viral life cycle. Many of these elements are highly conserved and, thus, they are attractive new targets that potentially have lower likelihoods of viral resistance development. Targeted RNA degradation (TRD) is an emerging strategy in recent efforts to further discover new antiviral small molecules with privileged scaffolds and better resistance profiles. However, early-stage TRD drug discovery has been hindered by current high-throughput screening (HTS) assay technologies designed for protein targets. Virtually all cell-based drug screens used minigene reporters that rely on luciferase or fluorescent protein signals for assay read-out. Minigene reporter design is straightforward but minigene reporter requires mRNA export to the cytosol and protein translation. This significantly increases the rate of false hits per screen since compounds that inhibit global protein translation machinery or RNA export will also impact reporter read-out. Assays that monitor endogenous RNA levels are low-throughput or time-consuming, involve multiple steps, and not readily adaptable for high-throughput SM screening. Thus, there is an unmet need for a new cell-based HTS assay platform that monitors target RNA turnover directly, reflects real-time RNA dynamics, and compatible for different types of RNA and different TRD approaches. For proof-of-concept, this project aims to develop HTS-compatible reporters that can measure drug- induced changes of RNA levels of dengue and influenza viruses, two global pathogens with different genomic structures and life cycles. The ultimate product of this SBIR project will be a cell-based HTS assay platform that can accelerate the early-stage discovery of TRD drugs toward previously intractable viral diseases.

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

22 SBIR/STTR records share this UEI (2011–2025). Reported award amounts total $10,266,039. Reported amounts are not federal obligations.

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

Agencies: Department of Health and Human Services, National Science Foundation

Agency intelligence

Department of Health and Human Services

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