US2013095065A1PendingUtilityA1
Methods for Treating Vascular Leak Syndrome and Cancer
Est. expiryOct 13, 2031(~5.2 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 7/00A61P 35/04A61P 9/14A61P 9/00A61P 31/04A61P 31/00A61P 35/00A61P 31/12A61P 33/02A61P 29/00A61P 31/10A61P 25/00A61P 17/02A61P 11/00A61P 17/00A61P 13/12A61P 27/02C07K 16/28C07K 16/40A61K 38/2013C07K 14/55A61K 2039/505
57
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Disclosed are methods for treating Vascular Leak Syndrome and preventing cancer metastasis. Further disclosed are methods for treating vascular leakage due to inflammatory diseases, sepsis, cancer or the presence of pathogens.
Claims
exact text as granted — not AI-modified1 . A method for treating or preventing vascular leak syndrome in a patient comprising administering to the patient a composition comprising an effective amount of an HPTPO-ECD binding agent or a pharmaceutically acceptable salt thereof.
2 . The method according to claim 1 , wherein the HPTPβ-ECD binding agent, or a pharmaceutically acceptable salt thereof, is administered in combination with an additional therapeutic agent, wherein the HPTPβ-ECD binding agent or pharmaceutically acceptable salt are administered together or in any order.
3 . The method according to claim 1 , wherein the patient is suffering from an inflammatory disease or condition, cancer, trauma, shock, sepsis, adult respiratory distress syndrome, acute lung injury, or infection with a pathogen.
4 . The method according to claim 3 , wherein the HPTPβ-ECD binding agent, or a pharmaceutically acceptable salt thereof, is administered in combination with an additional therapeutic agent, wherein the HPTPβ-ECD binding agent or pharmaceutically acceptable salt are administered together or in any order.
5 . The method according to claim 4 , wherein the additional therapeutic agent is IL-2.
6 . The method according to claim 4 , wherein patient is suffering from cancer and the additional therapeutic agent is a chemotherapeutic agent.
7 . The method according to claim 4 , wherein the patient suffering from an infection with a pathogen and the additional therapeutic agent is an anti-pathogenic agent.
8 . The method according to claim 7 , wherein the pathogen is a bacterium, a virus, or a fungus.
9 . The method according to claim 8 , wherein the anti-pathogenic agent is an antibacterial agent, an antiviral agent, an anti-fungal agent, or any combination thereof.
10 . The method according to claim 1 , wherein the dose of the HPTPβ-ECD binding agent, or pharmaceutically acceptable salt thereof, is from about 0.01 mg/kg to about 10 mg/kg by weight of the patient.
11 . The method according to claim 1 , wherein the dose is administered once daily, three-times weekly, twice weekly, once weekly, three times monthly, twice monthly, once monthly, and once every other month.
12 . The method according to claim 1 , wherein the HPTPβ-ECD binding agent is conjugated to a vehicle.
13 . The method according to claim 1 , wherein the HPTPβ-ECD binding agent is administered by intravenous injection or subcutaneous injection
14 . A method for determining the course of treatment for a patient suffering from vascular leak syndrome, comprising:
a) administering to a patient a composition comprising an effective amount of an HPTPβ-ECD binding agent; b) monitoring the level of angiopoietin-2 present in the patient during the course of treatment; and c) discontinuing treatment when the angiopoietin-2 level returns to within a normal range.
15 . A method for treating or preventing metastasis in a patient with cancer, by administering to a patient having cancer, a composition comprising an effective amount of an HPTPβ-ECD binding agent or a pharmaceutically acceptable salt thereof.
16 . The method according to claim 15 , wherein the HPTPβ-ECD binding agent or a pharmaceutically acceptable salt thereof, is administered in combination with an additional therapeutic agent wherein the HPTPβ-ECD binding agent or pharmaceutically acceptable salt are administered together or in any order.
17 . The method according to claim 16 , wherein the additional therapeutic agent is a chemotherapeutic agent.
18 . The method according to claim 17 , wherein the HPTPβ-ECD binding agent is administered before the chemotherapeutic agent.
19 . The method according to claim 15 , wherein the dose of the HPTPβ-ECD binding agent, or pharmaceutically acceptable salt thereof, is from about 0.01 mg/kg to about 10 mg/kg by weight of the patient.
20 . The method according to claim 15 , wherein the dose is administered once daily, three-times weekly, twice weekly, once weekly, three times monthly, twice monthly, once monthly, and once every other month.
21 . The method according to any one of claims 15 , wherein the HPTPβ-ECD binding agent is conjugated to a vehicle.
22 . The method according to claim 15 , wherein the HPTPβ-ECD binding agent is administered by intravenous injection or subcutaneous injection.
23 . A method for stabilizing the vasculature of a patient in need thereof, comprising administering to the patient a composition comprising an effective amount of an HPTPβ-ECD binding agent or a pharmaceutically acceptable salt thereof.
24 . The method of claim 23 , wherein the HPTPβ-ECD binding agent is administered prior to the patient undergoing a surgical treatment.
25 . The method of claim 23 , wherein the HPTPβ-ECD binding agent is administered prior to the patient undergoing chemotherapeutic treatment.Join the waitlist — get patent alerts
Track US2013095065A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.