Methods of administering anti-fibrotic therapy
US-11207304-B2 · Dec 28, 2021 · US
US11925624B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11925624-B2 |
| Application number | US-202117528537-A |
| Country | US |
| Kind code | B2 |
| Filing date | Nov 17, 2021 |
| Priority date | Nov 30, 2016 |
| Publication date | Mar 12, 2024 |
| Grant date | Mar 12, 2024 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure relates to methods of administering Compound I for treating fibrotic disorders, inflammatory disorders or autoimmune disorders.
Opening claim text (preview).
What is claimed is: 1. A method of providing Compound I therapy to a subject in need thereof: comprising: evaluating the renal function of the subject; and then administering a therapeutically effective amount of Compound I to the subject. 2. The method of claim 1 , wherein evaluating the renal function of the subject comprises determining the subject's creatinine clearance rate. 3. The method of claim 2 , wherein the subject has a creatinine clearance of ≥90 mL/min. 4. The method of claim 2 , wherein the subject has a creatinine clearance of 60-89 mL/min. 5. The method of claim 2 , wherein the subject has a creatinine clearance of 30-59 mL/min and <50 mL/min. 6. The method of claim 2 , wherein the subject has a creatinine clearance of 15-29 mL/min. 7. The method of claim 1 , wherein the subject does not have end stage renal disease requiring dialysis. 8. The method of claim 1 , further comprising monitoring changes in the subject's serum creatinine (Scr) level after said administering of Compound I. 9. The method of claim 8 , further comprising adjusting the amount of Compound I or discontinuing Compound I therapy after monitoring changes in the subject's Scr level. 10. The method of claim 8 , further comprising advising the subject to discontinue Compound I therapy when the subject's Scr level is 1.5 times baseline or higher, or shows a ≥0.3 mg/dL (≥26.5 μmol/L) increase. 11. The method of claim 1 , wherein the subject is suffering from a fibrotic disorder. 12. The method of claim 11 , wherein the subject is suffering from idiopathic pulmonary fibrosis (IPF).
the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline · CPC title
containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole (nicotine A61K31/465) · CPC title
the heterocyclic ring system containing a five-membered ring having oxygen as a ring hetero atom · CPC title
Drugs for disorders of the respiratory system · CPC title
Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.