IP Library Granted Patent US 11,524,056
Granted Patent B2
US 11,524,056 · App. 16/593,226 · Granted Dec 13, 2022

Thymosin alpha 1 for use in treatment of cystic fibrosis

Inventors: Luigina Romani (Perugia, IT); Enrico Garaci (Rome, IT)
Assignee: SciClone Pharmaceuticals International Ltd.
A61K38/2292
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,524,056
App. No.
16/593,226
Granted
Dec 13, 2022
Kind
B2
Abstract

The present invention concerns Thymosin alpha 1 (Tα1) for use in treatment of cystic fibrosis as a CFTR corrector, CFTR potentiator and anti-inflammatory agent.

Claims (10)

1. A method of treating inflammation attributed to infection associated with cystic fibrosis in a patient, comprising administering to the patient in need thereof a pharmaceutical composition comprising Thymosin alpha 1 .

2. The method of claim 1 , further comprising administering to the patient at least one agent selected from the group consisting of antibiotic, antifungal, cystic fibrosis transmembrane conductance regulator (CFTR) corrector, CFTR potentiator, and anti- inflammatory agent.

3. The method of claim 2 , wherein the antibiotic agent is selected from the group consisting of tobramycin, ciprofloxacin, and colistin.

4. The method of claim 2 , wherein the antifungal agent is selected from the group consisting of itraconazole and amphotericin B.

5. The method of claim 2 , wherein the CFTR corrector or potentiator agent is selected from the group consisting of ivacaftor and lumacaftor.

6. The method of claim 2 , wherein the anti-inflammatory agent is ibuprofen.

7. The method of claim 2 , wherein Thymosin alpha 1 and the at least one agent are administered to the patient together, separately, or sequentially.

8. The method of claim 1 , wherein the pharmaceutical composition comprises one or more excipients and/or coadjuvants.

9. The method of claim 1 , wherein the inflammation is chronic inflammation.

10. The method of claim 1 , wherein the patient has a CFTR mutation ΔF508.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2024
From: SCICLONE PHARMACEUTICALS INTERNATIONAL LTD.
To: SCICLONE PHARMACEUTICALS INTERNATIONAL (SG) PTE. LTD.
Reel/Frame 066730/0332 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2020
From: ROMANI, LUIGINA; GARACI, ENRICO
To: SCICLONE PHARMACEUTICALS INTERNATIONAL LTD.
Reel/Frame 053250/0554 →
Priority Claims (2)
IT RM2015A00056 · Feb 9, 2015 · national
IT 102015000053089 · Sep 18, 2015 · national
Continuity (2)
Continuation 15549073
Related Publication 20200023039A1 · Jan 23, 2020