SBIR/STTR Research Award

A First-in-class Topical Immunoregulatory Therapeutic for Psoriasis

Award identifier d6e88c8ed678587ead5da13d0d1716b17c2da90295018cde677b4c5cf6ed1db3Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$295,294

Program and phase

SBIR · Phase I

Award year

2023

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Biotherapeutics, Inc.
Proposal award date
2023-09-20
Contract end date
2024-03-31
UEI
DKZNEQL174E3
Solicitation number
PA22-176
Topic code
NIAMS

Research abstract

A First-in-class Topical Immunoregulatory Therapeutic for Psoriasis BioTherapeutics Inc (BTI) is an emerging biotech company that synergistically combines the power of advanced computational modeling with translational experimentation to accelerate the development of novel product candidates for precision immunology. An unmet clinical need for safer, more effective drugs for plaque psoriasis remains as current therapies have limited efficacy and adverse side effects. The Technology and Product. Psoriasis (PsO) is a global health concern that affects 125 million people worldwide. PsO is presented as scaly and erythematous skin plaques in the scalp, elbows, knees, and lower back, associated with severe itchiness and persistent rashes that have a significant detrimental impact on quality of life. Despite advancements in treatments, an unmet clinical need remains for the development of novel therapeutics against plaque psoriasis. This SBIR application aims to advance the development of a novel first- in-class therapeutic that is being evaluated for the treatment of multiple autoimmune diseases as a well-tolerated, topical therapeutic for the treatment of plaque psoriasis. The Specific Aims for the SBIR Phase I application are to:1. Evaluate the permeability and long-term stability of the novel topical drug product formulation.We will further characterize the topical formulation developed by in vitro permeation testing and long-term stability in preparation for the initiation of the clinical studies.2. Compare the therapeutic efficacy of our product candidate to current approved PsO therapeuticsin a mouse model of psoriasis. We will use the imiquimod mouse model of psoriasis to evaluate diseaseactivity, histological lesions, plus local and systemic inflammation.3. Determine the translational potential in human primary cells. We will use blood samples frompsoriasis patients to investigate the new candidate’s functional ability to induce immunoregulatorychanges in patients. Expected successful outcomes: i) rt10% permeation by IVPT; ii) rt40% decrease in composite score on day 7 compared to other drugs; and iii) rt40% decrease in Th17 differentiation in human primary cells. Our long-term goal is to develop safer, more effective first-in-class immunoregulatory therapeutics for PsO with a novel mechanism of action that address an unmet clinical need for a market exceeding $12 billion and growing 5% annually.

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

28 SBIR/STTR records share this UEI (2013–2025). Reported award amounts total $12,395,941. 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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