Composition and method for treating peripheral t-cell lymphoma and cutaneous t-cell lymphoma
US-2020289520-A1 · Sep 17, 2020 · US
US11466006B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11466006-B2 |
| Application number | US-202016865034-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 1, 2020 |
| Priority date | Jun 7, 2013 |
| Publication date | Oct 11, 2022 |
| Grant date | Oct 11, 2022 |
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The present invention relates to dual delta (δ) and gamma (γ) PI3K protein kinase modulators, methods of preparing them, pharmaceutical compositions containing them and methods of treatment, prevention and/or amelioration of Pi3K kinase mediated diseases or disorders with them.
Opening claim text (preview).
What is claimed is: 1. A method of treating T-cell lymphoma in a patient in need thereof, the method comprising administering to the patient an effective amount of (S)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof. 2. A method of treating T-cell lymphoma in a patient in need thereof, the method comprising administering to the patient an effective amount of a compound that is (S)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof, wherein the compound contains less than about 5% by weight of (R)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof. 3. The method of claim 2 , wherein the compound contains less than about 2.5% by weight of (R)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof. 4. The method of claim 2 , wherein the compound contains less than about 1% by weight of (R)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof. 5. The method of claim 2 , wherein the compound contains less than about 0.1% by weight of (R)-2-(1-(9H-purin-6-ylamino)propyl)-3-(3-fluorophenyl)-4H-chromen-4-one or a pharmaceutically acceptable salt thereof. 6. The method of claim 1 , wherein the patient is a human patient. 7. The method of claim 2 , wherein the patient is a human patient. 8. The method of claim 3 , wherein the patient is a human patient. 9. The method of claim 4 , wherein the patient is a human patient. 10. The method of claim 5 , wherein the patient is a human patient.
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