Methods for treating or preventing acute vascular leak

US2016256457A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016256457-A1
Application numberUS-201514735250-A
CountryUS
Kind codeA1
Filing dateJun 10, 2015
Priority dateJun 10, 2014
Publication dateSep 8, 2016
Grant date

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  2. Abstract

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  5. First independent claim

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Abstract

Official abstract text for this publication.

The invention features methods, devices, pharmaceutical compositions, and kits for treating or preventing acute vascular leak. Such methods may involve contacting an effective amount of bosutinib for treating or preventing acute vascular leak with a subject in need thereof. Conditions associated with acute vascular leak include ischemic brain injury, stroke, septic shock, anthrax lethal toxin, anaphylaxis, trauma, severe episodic vasculitis, acute lung injury, ventilator-induced lung injury, transfusion-related acute lung injury, acute respiratory distress syndrome, severe burn injury, circulatory shock, capillary leak syndrome, and ischemia-reperfusion injury. The invention also features automatic injection devices, resuscitation fluids, or pharmaceutical compositions comprising an effective amount of bosutinib for treating or preventing acute vascular leak. The invention further features kits for use in the methods of the invention.

First claim

Opening claim text (preview).

What is claimed is: 1 . A method of treating or preventing acute vascular leak in a subject in need thereof, wherein said method comprises contacting an effective amount of bosutinib with said subject, and wherein said acute vascular leak is associated with a condition selected from the group consisting of: ischemic brain injury, septic shock, anthrax lethal toxin, anaphylaxis, trauma, severe episodic vasculitis, acute lung injury, acute respiratory distress syndrome, severe burn injury, circulatory shock, capillary leak syndrome, and ischemia-reperfusion injury. 2 . (canceled) 3 . The method of claim 1 , wherein said ischemic brain injury is stroke, said acute lung injury is ventilator-induced lung injury or transfusion-related acute lung injury, or said trauma is selected from the group consisting of: severe tissue trauma, head trauma, lung trauma, cardiac trauma, and vascular trauma. 4 - 5 . (canceled) 6 . The method of claim 1 , wherein said subject is at risk for acute vascular leak associated with a condition selected from the group consisting of: ischemic brain injury, septic shock, anthrax lethal toxin, anaphylaxis, trauma, severe episodic vasculitis, acute lung injury, acute respiratory distress syndrome, severe burn injury, circulatory shock, capillary leak syndrome, and ischemia-reperfusion injury. 7 . The method of claim 1 , wherein said bosutinib is administered by autoinjection, as a component of a resuscitation fluid, sublingually, or by inhalation. 8 - 10 . (canceled) 11 . The method of claim 1 , further comprising administering a second therapeutic agent. 12 . The method of claim 11 , wherein said second therapeutic agent is selected from the group consisting of: a Src inhibitor, a Rho kinase inhibitor, a soluble epoxide hydrolase inhibitor, a TREM1 inhibitor, a TNF-α inhibitor, an antibiotic, a corticosteroid, vasopressin, a mechanical ventilation device, surgical drainage of infected fluid collections, fluid replacement, support for organ dysfunction, activated protein C therapy, corticosteroid treatment, vasopressin, an MLC kinase inhibitor, a VEGF inhibitor, a PIGF inhibitor, an NFκB inhibitor, an IL-1 inhibitor, an IL-6 inhibitor, an Ang-2 antagonist, and a TGF-β inhibitor. 13 . The method of claim 12 , wherein said Src inhibitor is selected from the group consisting of: Nilotinib, Ponatinib, Bafetinib, imatinib, dasatinib, PP1, PP2, sunitinib, and SKS-927, said Rho kinase inhibitor is Y-27632 or fasudil, said soluble epoxide hydrolase inhibitor is 12-(3-adamantan-1-yl-ureido)-dodecanoic acid butyl ester (AUDA-BE), 1-adamantan-3-(5-(2-(2-ethyl-ethoxy)ethoxy)pentyl)urea (compound 950), or any combination thereof, said TREM1 inhibitor is recombinant TREM-like transcript 1 (TLT-1), LR17 peptide, Inotrem MOTREM peptide, or SignaBlock SCHOOL peptide, said TNF-α inhibitor is infliximab, adalimumab, etanercept, or ADZ9773, said support for organ dysfunction is selected from the group consisting of: hemodialysis, mechanical ventilation, transfusion of blood plasma, platelets, and coagulation factors, and drug and fluid therapy, said activated protein C therapy is drotrecogin alfa, said VEGF inhibitor is avastin, or said NFκB inhibitor is panepoxydone. 14 - 27 . (canceled) 28 . A method of treating vascular leak in a subject identified as likely to benefit from bosutinib treatment by monitoring one or more measures reflective of vascular leak, said method comprising administering an effective amount of bosutinib to said subject if said one or more measures indicate increased vascular leak, thus treating said vascular leak in said subject. 29 . The method of claim 28 , wherein said one or more measures reflective of vascular leak comprises measuring blood pressure, edema, severity of organ dysfunction, red blood cell (RBC) velocity, RBC supply rate, percent oxygen saturation, capillary diameter, or any combination thereof. 30 . The method of claim 29 , wherein said edema is measured by conducting physical examination of ankle thickness or tissue swelling, or said severity of organ dysfunction is measured by conducting one or more Sequential Organ Failure Assessments (SOFA). 31 . (canceled) 32 . The method of claim 28 , wherein said indication of increased vascular leak comprises a decrease in blood pressure, an increase in edema, an increase in severity of organ dysfunction, a decrease in RBC velocity, a decrease in RBC supply rate, decrease in oxygen saturation, or any combination thereof. 33 . The method of claim 32 , wherein said increase in edema comprises increased ankle thickness or increased tissue swelling. 34 . The method of claim 28 , further comprising monitoring said one or more measures reflective of vascular leak after said administration, wherein a reduction of said indication of increased vascular leak indicates treatment of said vascular leak. 35 . The method of claim 28 , wherein said bosutinib has not been previously administered to said subject to treat said vascular leak, or wherein said bosutinib has been previously administered to said subject to treat said vascular leak. 36 . (canceled) 37 . The method of claim 28 , wherein said vascular leak is an acute vascular leak. 38 . The method of claim 37 , wherein said acute vascular leak is associated with a condition selected from the group consisting of: ischemic brain injury, stroke, septic shock, anthrax lethal toxin, anaphylaxis, trauma, severe episodic vasculitis, acute lung injury, ventilator-induced lung injury, transfusion-related acute lung injury, acute respiratory distress syndrome, severe burn injury, circulatory shock, capillary leak syndrome, and ischemia-reperfusion injury. 39 . The method of claim 28 , wherein said bosutinib is administered by autoinjection, as a component of a resuscitation fluid, sublingually, or by inhalation. 40 - 42 . (canceled) 43 . A pharmaceutical composition in unit dosage form comprising an effective amount of bosutinib for treating or preventing acute vascular leak, wherein said unit dosage form comprises: an automatic injection device comprising a pre-loaded charge of medicament for automatically self-administering said medicament upon actuation thereof, wherein said medicament comprises said bosutinib; a resuscitation fluid comprising said bosutinib; a tablet to be administered sublingually, said tablet comprising said bosutinib; a liquid to be administered sublingually, said liquid comprising said bosutinib; a powder to be administered sublingually, said liquid comprising said bosutinib; or an aerosol comprising said bosutinib. 44 - 48 . (canceled) 49 . The pharmaceutical composition of claim 43 , wherein said acute vascular leak is associated with a condition selected from the group consisting of: ischemic brain injury, stroke, septic shock, anthrax lethal toxin, anaphylaxis, trauma, severe episodic vasculitis, acute lung injury, ventilator-induced lung injury, transfusion-related acute lung injury, acute respiratory distress syndrome, severe burn injury, circulatory shock, capillary leak syndrome, and ischemia-reperfusion injury. 50 . A kit for treating or preventing acute vascular leak in a subject in need thereof, comprising an effective amount of bosutinib and instructions for administering said bosutinib to said subject according to the method of claim 1 .

Assignees

Inventors

Classifications

  • A61K31/496Primary

    Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin · CPC title

  • Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca · CPC title

  • Oral mucosa, e.g. mucoadhesive forms, sublingual droplets; Buccal patches or films; Buccal sprays · CPC title

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What does patent US2016256457A1 cover?
The invention features methods, devices, pharmaceutical compositions, and kits for treating or preventing acute vascular leak. Such methods may involve contacting an effective amount of bosutinib for treating or preventing acute vascular leak with a subject in need thereof. Conditions associated with acute vascular leak include ischemic brain injury, stroke, septic shock, anthrax lethal toxin, …
Who is the assignee on this patent?
Beth Israel Deaconess Medical Ct Inc, Brigham & Womens Hospital Inc
What technology area does this patent fall under?
Primary CPC classification A61K31/496. Mapped technology areas include Human Necessities.
When was this patent published?
Publication date Thu Sep 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).