Dosing regimen for a selective s1p1 receptor agonist
US-2019151292-A1 · May 23, 2019 · US
US12336980B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12336980-B2 |
| Application number | US-202218046492-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 13, 2022 |
| Priority date | Dec 11, 2014 |
| Publication date | Jun 24, 2025 |
| Grant date | Jun 24, 2025 |
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The present invention relates to a dosing regimen for (R)-5-[3-chloro-4-(2,3-dihydroxy-propoxy)-benz[Z]ylidene]-2-([Z]-propylimmo)-3-o-tolyl-thiazolidin-4-one.
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The invention claimed is: 1. A method of treating a human subject, diagnosed with multiple sclerosis, who has been orally administered once-daily titrating doses, successively over a period of two weeks, of a compound that is (R)-5-[3-chloro-4-(2,3-dihydroxy-propoxy)-benz [Z]ylidene]-2-([Z]-propylimino)-3-o-tolyl-thiazolidin-4-one or a pharmaceutically acceptable salt thereof, which successive titrating doses are 2 mg on days 1 and 2; 3 mg of on days 3 and 4; 4 mg on days 5 and 6; 5 mg on day 7; 6 mg on day 8; 7 mg on day 9; 8 mg on day 10; and 9 mg on day 11, and 10 mg on days 12, 13, and 14, comprising: administering, starting on the day following the last titrating dose, 20 mg of said compound. 2. The method of claim 1 , wherein the multiple sclerosis is relapsing multiple sclerosis. 3. The method of claim 2 , wherein the multiple sclerosis is relapsing-remitting multiple sclerosis.
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