IP Library Granted Patent US 10,987,361
Granted Patent B2
US 10,987,361 · App. 14/860,680 · Granted Apr 27, 2021

Treating auto-immune and auto-inflammatory diseases

Inventors: Tao Tom Du (North Potomac, MD); Chang Lee (Bethesda, MD)
Assignee: Shenzhen Evergreen Therapeutics Co., Ltd.
A61K31/573A61K9/0075A61K9/0078A61K31/56A61K31/57A61K31/58
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Quick Facts
Patent No.
US 10,987,361
App. No.
14/860,680
Granted
Apr 27, 2021
Kind
B2
Abstract

The present invention relates to the formulations, methods and kits for reducing cytokine interleukin-17 (IL-17 or IL-17A) levels in both broncheoalveolar lavage fluid (BALF) and blood/serum and/or for the inhibition of p38 mitogen activating protein kinase (MAPK) activity involving the use of 17α-hydroxyprogesterone caproate (17-OHPC) or derivatives thereof. The formulation may be in the form of an inhalant containing effective amounts of 17-OHPC, and the formulation may be used in a method to treat IL-17 cytokine and/or p38 MAPK mediated auto-immune and auto-inflammatory diseases. Such diseases may include glucocorticoid (GC) insensitive related diseases or conditions. In alternate embodiment, the formulation may include the combined use of budesonide (BUD) with 17-OPHC.

Claims (18)

1. A method for treating a disease selected from chronic obstructive pulmonary disease, oliterative bronchitis, or asthma with symptoms of reduced airflow to lungs due to smooth muscle hypercontractility and airway remodeling of a patient, said method comprising administering to said patient by inhalation a pharmaceutical composition comprising a first treatment agent comprising 17alpha-hydroxyprogesterone caproate (“17-OHPC”) in an amount of from 0.03 mg/L to 0.3 mg/L, a second treatment agent comprising budesonide (“BUD”) at 0.2 g/L, and a pharmaceutically acceptable carrier, wherein the disease is mediated by interleukin-17 (“IL-17”) and an IL-17 level is reduced in said patient after administration of the pharmaceutical composition compared to an IL-17 level in a patient having the disease and without administration of the pharmaceutical composition.

2. The method of claim 1 , wherein said disease comprises symptoms of glucocorticoid insensitivity.

3. The method of claim 1 , wherein the 17-OHPC is administered according to a dosing regimen selected from the group of an administration interval less than once per week, once weekly, or exceeding once per week.

4. The method of claim 1 , wherein said pharmaceutical composition is administered according to a dosing regimen selected from the group of an administration interval less than once per week, once weekly, or exceeding once per week.

5. A method for reducing IL-17 expression in a patient affected by a disease selected from chronic obstructive pulmonary disease, oliterative bronchitis, or asthma, comprising administering to said patient by inhalation a pharmaceutical composition comprising a first treatment agent comprising 17-OHPC in an amount of from 0.03 mg/L to 0.3 mg/L and a second treatment agent comprising BUD at 0.2 g/L.

6. The method of claim 5 , wherein the patient is affected by a condition comprising symptoms of glucocorticoid insensitivity that is associated with said disease.

7. The method of claim 5 , wherein the pharmaceutical composition further comprises 17alpha-hydroxyprogesterone acetate or 17-alpha hydroxyprogesterone valproate.

8. A method of treating a respiratory inflammatory disease selected from chronic obstructive pulmonary disease, oliterative bronchitis, or asthma that is mediated by IL-17 in a subject, wherein the respiratory inflammatory disease is characterized by a detectable clinical symptom or change in level of a biochemical marker with respect to the normal range of the marker, the method comprising:

administering to the subject by inhalation a pharmaceutical composition comprising a first treatment agent comprising 17-OHPC in an amount of from 0.03 mg/L to 0.3 mg/L and a second treatment agent comprising BUD at 0.2 g/L,

continuing said administration until there is a return of the marker level to a normal range or a desired change in the clinical symptom,

where the marker or the clinical symptom comprises:

a decrease in expression of IL-17 in combination with,

(a) p38 mitogen activated protein kinase activity,

(b) lung structure, or

(c) lung function;

wherein the decrease in expression of IL-17 is compared to an expression level of IL-17 from a subject without administration of the pharmaceutical composition.

9. The method of claim 8 , wherein the second treatment agent is administered before, coincident with, or after administration of the first treatment agent.

10. A method for treating a disease mediated by interleukin-17 (“IL-17”) selected from chronic obstructive pulmonary disease, oliterative bronchitis, or asthma in a patient in need thereof comprising administering to said patient by inhalation from 0.03 mg/L to 0.3 mg/L of 17alpha-hydroxyprogesterone caproate (“17-OHPC”) and 0.2 g/L budesonide (“BUD”), and wherein said treatment comprises a reduction in IL-17 level in said patient after the treatment.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 16174938 PREVIOUSLY RECORDED ON REEL 052384 FRAME 0051. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 14, 2020
From: PRAIRIE PHARMACEUTICALS LLC
To: SHENZHEN EVERGREEN THERAPEUTICS CO., LTD.
Reel/Frame 053500/0266 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2020
From: PRAIRIE PHARMACEUTICALS LLC
To: SHENZHEN EVERGREEN THERAPEUTICS CO., LTD.
Reel/Frame 052384/0051 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 22, 2015
From: DU, TAO TOM; LEE, CHANG
To: PRAIRIE PHARMACEUTICALS, LLC
Reel/Frame 036627/0532 →
Continuity (5)
Continuation In Part 13174939 · Jul 1, 2011
Continuation In Part 13021950 · Feb 7, 2011
Provisional Application 62195649 · Jul 22, 2015
Provisional Application 61302325 · Feb 8, 2010
Related Publication 20160045517A1 · Feb 18, 2016