SBIR/STTR Research Award

Preclinical Evaluation of a Novel Immunomodulatory Vaccine for Preventing and Treating HSV Infections

Award identifier 5b20c3e46ecc0bac0c5c1a3bc7bf781d654de0a539d2f81cad4e3b27df436cc1Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$986,717

Program and phase

SBIR · Phase II

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
RATIONAL VACCINES INC
Proposal award date
2025-01-24
Contract end date
2026-12-31
UEI
PKJWJVTMUS63
Solicitation number
PA21-259
Topic code
R

Research abstract

PROJECT SUMMARY: Herpes Simplex Virus (HSV) infections are common, infecting more than half of the world’s population. While most cases of genital herpes are caused by HSV type 2 (HSV-2), it is estimated that more than 150 million people aged 15-49 have genital HSV type 1 (HSV-1) infections. Although several vaccines have been evaluated for preventing/treating HSV infections, none have received FDA approval. Through an exclusive license with Louisiana State University, Rational Vaccines is developing a novel immunomodulatory vaccine engineered not to enter neuronal axons, rendering it incapable of establishing latency within the host. This vaccine was shown to be safe and effective at protecting female mice and guinea pigs from lethal intravaginal challenges with virulent HSV-1 and HSV-2. Further, this vaccine prevented HSV from establishing latency in vaccinated animals, and it induced prolonged immune responses in rhesus macaques. Moreover, the vaccine also exhibited therapeutic potential in guinea pigs latently infected with HSV-2. During the funding period of this Fast-Track proposal, Rational Vaccines will complete the studies required to submit an Investigational New Drug (IND) application to the FDA. In Phase I, process parameters will be developed, pilot batches of the RVx1001 will be manufactured, and product specifications will be drafted. This material will be used to validate the vaccine’s efficacy using the guinea pig model. Phase II will include IND-enabling GLP toxicology studies and scale-up production of the vaccine under current Good Manufacturing Practices (cGMP) to generate clinical trial material. The successful completion of the proposed work will extend to first-in-human clinical studies (beyond the scope of this proposal). Funding the development of this vaccine will play a key role in curbing the spread of HSV-associated conditions.

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.

Research funding history

4 SBIR/STTR records share this UEI (2022–2025). Reported award amounts total $1,835,901. 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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