Claims for Patent: 10,233,242
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Summary for Patent: 10,233,242
Title: | CTLA4 fusion proteins for the treatment of diabetes |
Abstract: | A method of treating, preventing, or delaying the progression of Type 1 diabetes mellitus autoimmunity by administering an effective amount of a cytotoxic T-lymphocyte-associated antigen 4 (CTLA4) molecule is provided herewith. The CTLA4 molecule may be a fusion protein of a CTLA4 extracellular region and an immunoglobulin, such as abatacept. |
Inventor(s): | Orban; Tihamer (Brookline, MA) |
Assignee: | DMNOMORE (London, GB) |
Application Number: | 14/576,990 |
Patent Claims: | 1. A method of treating type 1 diabetes mellitus in a subject comprising administering an effective amount of a fusion protein composition which comprises a fusion
protein and an oil-based carrier, wherein the fusion protein comprises the extracellular domain of CTLA4 and a portion of an immunoglobulin molecule, and wherein the oil-based carrier is a water-in-oil emulsion.
2. The method of claim 1 wherein the composition comprises Abatacept. 3. The method of claim 1 wherein the composition is administered as a pharmaceutically acceptable salt. 4. The method of claim 1, wherein the composition is administered by intravenous infusion. 5. The method of claim 4, wherein the composition is administered by intravenous infusion in about 50 to 200 ml of physiological saline. 6. The method of claim 4, wherein the composition is administered at a dose ranging from about 5 mg/kg to about 50 mg/kg. 7. The method of claim 4, wherein the intravenous infusion of the composition is repeated over time. 8. The method of claim 4, wherein the intravenous infusion of the composition is repeated at least once following a time interval ranging from about one week to about two months. 9. The method of claim 4, wherein the composition is administered at a dose ranging from about 250 to 2000 mg. 10. The method of claim 9, wherein the composition is administered at a dose of 500 mg. 11. The method of claim 9, wherein the composition is administered at a dose of 750 mg. 12. The method of claim 9, wherein the composition is administered at a dose of 1000 mg. 13. The method of claim 1, wherein the subject is white. |
Details for Patent 10,233,242
Applicant | Tradename | Biologic Ingredient | Dosage Form | BLA | Approval Date | Patent No. | Expiredate |
---|---|---|---|---|---|---|---|
Bristol-myers Squibb Company | ORENCIA | abatacept | For Injection | 125118 | December 23, 2005 | ⤷ Try for Free | 2039-04-18 |
Bristol-myers Squibb Company | ORENCIA | abatacept | Injection | 125118 | July 29, 2011 | ⤷ Try for Free | 2039-04-18 |
Bristol-myers Squibb Company | ORENCIA | abatacept | Injection | 125118 | June 07, 2016 | ⤷ Try for Free | 2039-04-18 |
Bristol-myers Squibb Company | ORENCIA | abatacept | Injection | 125118 | March 30, 2017 | ⤷ Try for Free | 2039-04-18 |
>Applicant | >Tradename | >Biologic Ingredient | >Dosage Form | >BLA | >Approval Date | >Patent No. | >Expiredate |