SBIR/STTR Research Award

Translating a Novel Therapeutic Approach to the Treatment for Idiopathic Pulmonary Fibrosis

Award identifier 65780571c378ae043ddfeea3391d49b4657683382e2479a2baac1505ed750e3bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$356,250

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
VASARYA THERAPEUTICS, INC.
Proposal award date
2024-09-15
Contract end date
2025-02-28
UEI
PFB5FMPM2666
Solicitation number
PA23-230
Topic code
NHLBI

Research abstract

Project Abstract The goal of this Fast-Track SBIR application is to develop a novel drug candidate to treat Idiopathic pulmonary fibrosis (IPF). IPF is a fatal disease that remains uncurable and carries a median survival of 2-3 years post diagnosis. The two current FDA-approved drugs Nintedanib and Pirfenidone marginally extend quality-adjusted life years while presenting severe life-altering side effects, resulting in extremely poor compliance. Current pipeline therapeutics are focused on more effective targets to improve functional outcomes but many, if not all, present significant safety concerns by targeting critical, systemically active receptors and intracellular signaling proteins. Our tool compound, VSR-H5, has demonstrated an ability to 1) specifically target only regions of ongoing fibrosis within diagnosed IPF patient lung tissues while not binding healthy tissues/regions; 2) selectively inhibit activation of patient-derived fibroblasts’ on pro-fibrotic mimetic extracellular matrix (ECM) in vitro; and 3) mitigate fibrosis progression in multiple in vivo mouse models of lung fibrosis and a clean tox profile. Our approach specifically avoids systemic disruption of critical, normal receptor engagement by targeting a unique, cryptic epitope that is only exposed in tissues undergoing active fibrosis. In this proposal we will first (Phase I) perform affinity maturation and liability assessment and removal to create a pool of candidate antibody drugs. Then in Phase II we will perform successive selection assays to establish our primary drug candidate from the pool generated in Phase I and then further establish its translatability through a series of PK/PD, toxicity/safety, and efficacy analyses in established animal models, while exploring potential formulations for future process development and manufacturing. At the successful conclusion of this project, we will be poised to design and initiate IND-enabling studies.

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

3 SBIR/STTR records share this UEI (2024–2025). Reported award amounts total $1,759,671. 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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