SBIR/STTR Research Award

Novel Plasmin-independent Thrombolytic Agent for Pulmonary Embolism

Award identifier 7b82ce48687187124fb7f22175fbc6b5da20b68433b116f17d32f4dbe300b21bAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$499,882

Program and phase

SBIR · Phase I

Award year

2025

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
SNJ PHARMA INC.
Proposal award date
2025-09-15
Contract end date
2026-08-31
UEI
KDZUVLP7VDH8
Solicitation number
PA24-245
Topic code
NHLBI

Research abstract

Project Summary Pulmonary embolism (PE) is the leading preventable cause of death among hospitalized patients, yet current thrombolytic therapies are hindered by significant limitations, including high bleeding risks and incomplete clot resolution. The high incidence and life-threatening nature of PE highlight the critical need for safer and more effective thrombolytic solutions. Despite decades of research, the available thrombolytics remain exclusively plasmin-based. These therapies activate plasminogen to plasmin, an enzyme that indiscriminately degrades essential hemostatic proteins, such as fibrinogen, necessary for clot stability and wound healing. This lack of specificity not only increases the risk of severe bleeding complications but also restricts the clinical applicability, leaving a substantial unmet need for innovative alternatives to address PE effectively and safely. SNJ Pharma, Inc. has developed a novel plasmin-independent thrombolytic enzyme, High-Temperature Requirement A1 (HtrA1), as a promising alternative to current plasmin-based therapies. The recombinant form of HtrA1 (rHtrA1) exhibits robust fibrinolytic activity, effectively dissolving intravascular clots while sparing essential hemostatic proteins, such as fibrinogen. This unique mechanism avoids plasmin generation, enabling rHtrA1 to selectively degrade pathological thrombi without increasing bleeding risk, a common limitation of traditional thrombolytics. In mouse models of PE, rHtrA1 demonstrated exceptional efficacy, completely dissolving clots and achieving a 100% survival rate. Building on this success, the proposed study will further evaluate the therapeutic potential of rHtrA1 in a murine PE model, focusing on establishing a dose-response relationship and determining the effective dose. Successful completion of this research will lay the groundwork for a groundbreaking therapeutic approach, addressing critical unmet needs in the thrombolytic treatment of PE while minimizing bleeding complications.

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

2 SBIR/STTR records share this UEI (2022–2025). Reported award amounts total $949,476. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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