SBIR/STTR Research Award

HLS- Cyclic CAR peptide: a targeted therapy for pulmonary hypertension

Award identifier e6efa495be8cb61d2aa0fc0fd98be4d80f6da19ef203f63de189764e277e7e07Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$2,001,569

Program and phase

STTR · Phase II

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
VASCULAR BIOSCIENCES, INC.
Proposal award date
2018-09-20
Contract end date
2020-08-31
UEI
ETJLM26WRKP5
Solicitation number
PA16-303
Topic code
NHLBI

Research abstract

PUBLIC ABSTRACT This projectin response to announcement HLSdescribes a development program for CARSKNKDCCARa synthetic cyclic peptide that selectively targets diseased pulmonary vascular endothelium and enhances the therapeutic effect of vasodilator therapiesfor the treatment of pulmonary hypertensionPHPH is a disorder of elevated pulmonary vascular resistance characterized by progressive thickening and obliteration of resistance determining vessels of the pulmonary circulationDespite current therapiessurvival following the diagnosis of PH remains slightly better thanatyearswith mortality a result of disease progression and right heart failureVasodilator therapies acting upon endothelinprostacyclinand nitric oxide pathways modestly improve functional statusbut are limited by systemic side effectstoxicityand tachyphylaxisNo current therapy selectively targets the diseased pulmonary circulationCARwhose peptide sequence has high sequence homology to protein heparinbinding domainswas identified by a phage screen for its enhanced binding to the vasculature of soft tissue woundsWe have demonstrated that CAR accumulates in the endothelium and adventitia of pulmonary vessels in animals with PHbut not systemic vesselsand not the pulmonary vessels of normal animalsWhen given with systemic vasodilator therapiesCAR potentiates selective vasodilatation of the pulmonary vascular bed without increasing systemic vasodilationCAR peptide appears to enhance the delivery of drugs to diseased vessels by a co administration effect without requiring conjugation to drugsBy virtue of its selective homing for damaged endotheliumwe propose that chronic administration CAR will synergize with prostacyclin and PDEinhibitor therapieswith greater impact on pulmonary vascular remodelingWe have devised a strategy that will optimize the dosingformulation and deliverypharmacokinetics and pharmacodynamics of this agent as an adjuvant therapy in combination with FDA approved vasodilator therapies for PHThis potentially groundbreaking approach would constitute the first example of a targeted therapy specifically designed to address pulmonary vascular diseaseand could address limitations of current PH therapy Project Narrative Pulmonary hypertension describes a diverse set of diseases characterized by elevated pressures and progressive obstruction of the lung vessels with a survival of approximatelyyears following diagnosis despite current treatmentsCurrent therapies are vasodilators that are not specific for lung vesselsand are limited in their use by their tendency to lower pressure in all blood vessels and cause side effects or toxicity in other organsThe current proposal examines a new type of drug molecule which targets only diseased lung blood vessels and which may improve the efficacy and reduce side effects of current treatments by concentrating their effects in diseased lung vessels

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

6 SBIR/STTR records share this UEI (2008–2021). Reported award amounts total $5,318,278. 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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