IP Library Granted Patent US 10,232,006
Granted Patent B2
US 10,232,006 · App. 15/592,911 · Granted Mar 19, 2019

Pharmaceutical composition comprising refined indigo naturalis extract and the use thereof

Inventors: Laurent Chantalat (Antibes, FR); Philippe Andres (Peymeinade, FR)
Assignee: Galderma S.A.
A61K36/70A61K8/492A61K8/4953A61K8/97A61K9/0014A61K9/0053A61K9/06A61K31/404A61K31/519A61K36/19A61K36/315A61K36/48A61Q19/08A61K2236/00A61K2800/92
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 10,232,006
App. No.
15/592,911
Granted
Mar 19, 2019
Kind
B2
Abstract

A refined Indigo Naturalis extract or Indigo-producing plant extract containing at least 65% (w/w) an indirubin derivative based on total weight of active ingredients is described. Also described are a pharmaceutical composition containing the refined extract, and the use of the pharmaceutical composition for treating or alleviating a disease or condition.

Claims (29)

1. A solid extract of Indigo Naturalis comprising, relative to the total weight of the extract:

65% to 90% (w/w) indirubin;

0.1-15% (w/w) indigo; and

0.01-5% (w/w) tryptanthrin.

2. The solid extract of claim 1 , comprising 0.1-5% (w/w) tryptanthrin relative to the total weight of the extract.

3. The solid extract of claim 2 , further comprising 0.1-5% (w/w) qingdainone relative to the total weight of the extract.

4. The solid extract of claim 3 , being micronized and comprising particles having a particle size of less than or equal to 30 μm in 99% of the particles.

5. A pharmaceutical composition comprising a solid extract of Indigo Naturalis and a pharmaceutically acceptable carrier, wherein the solid extract comprises, relative to the total weight of the extract:

65% to 90% (w/w) indirubin;

0.1-15% (w/w) indigo; and

0.01-5% (w/w) tryptanthrin.

6. The pharmaceutical composition of claim 5 , comprising 0.002% to 0.077% (w/w) of the solid extract relative to the total weight of the pharmaceutical composition, and a pharmaceutically acceptable carrier comprising at least one of an oil, an emulsifier, a thickening agent, and a preservative.

7. The pharmaceutical composition of claim 6 , wherein the solid extract comprises 0.1-5% (w/w) tryptanthrin relative to the total weight of the extract.

8. The pharmaceutical composition of claim 7 , wherein the solid extract further comprises 0.1-5% (w/w) qingdainone relative to the total weight of the extract.

9. The pharmaceutical composition of claim 8 , wherein the solid extract is micronized and comprises particles having a particle size of less than or equal to 30 μm in 99% of the particles.

10. The pharmaceutical composition of claim 5 , wherein the composition is in the form for topical administration or oral administration.

11. A topical pharmaceutical composition comprising a micronized solid extract of Indigo Naturalis and a pharmaceutically acceptable carrier, wherein the solid extract comprises, relative to the total weight of the extract:

65% to 90% (w/w) indirubin;

0.1-15% (w/w) indigo; and

0.01-5% (w/w) tryptanthrin.

12. The topical pharmaceutical composition of claim 11 , comprising 0.002% to 0.077% (w/w) of the solid extract relative to the total weight of the pharmaceutical composition, and a pharmaceutically acceptable carrier comprising at least one of an oil, an antioxidant, an emulsifier, a thickening agent, and a preservative.

13. The topical pharmaceutical composition of claim 12 , wherein the solid extract comprises 0.1-5% (w/w) tryptanthrin relative to the total weight of the extract.

14. The topical pharmaceutical composition of claim 13 , wherein the solid extract further comprises 0.1-5% (w/w) qingdainone relative to the total weight of the extract.

15. The topical pharmaceutical composition of claim 14 , wherein the solid extract comprises particles having a particle size of less than or equal to 30 μm in 99% of the particles.

16. A method of treating a disease or condition selected from the group consisting of psoriasis, an inflammatory skin condition, onychomycosis, skin cancer, abnormal keratinization induced diseases, skin aging, pustular dermatosis, comprising administering to a subject in need thereof a pharmaceutical composition of claim 5 .

17. A method of treating a disease or condition selected from the group consisting of psoriasis, an inflammatory skin condition, onychomycosis, skin cancer, abnormal keratinization induced diseases, skin aging, pustular dermatosis, comprising topically administering to a subject in need thereof a pharmaceutical composition of claim 11 .

18. The method of claim 17 , wherein the disease or condition is psoriasis, an inflammatory skin condition, onychomycosis, skin aging or pustular dermatosis.

19. The method of claim 18 , wherein the disease or condition is the inflammatory skin condition selected from the group consisting of atopic dermatitis (AD), eczema and superinfected skin.

20. The method of claim 17 , wherein the disease or condition is the abnormal keratinization induced disease selected from the group consisting of acne, ichtyosis and palmoplantar keratoderma.

Assignments (3)
MERGER AND CHANGE OF NAME Recorded Mar 10, 2022
From: NESTLÉ SKIN HEALTH SA; GALDERMA HOLDINGS SA
To: GALDERMA HOLDING SA
Reel/Frame 060044/0523 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 10, 2021
From: GALDERMA S.A.
To: NESTLÉ SKIN HEALTH SA
Reel/Frame 058962/0638 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 11, 2017
From: CHANTALAT, LAURENT; ANDRES, PHILIPPE
To: GALDERMA S.A.
Reel/Frame 042345/0333 →
Priority Claims (1)
EP 15163061 · Apr 9, 2015 · regional
Continuity (2)
Continuation PCTEP2016057763 · Apr 8, 2016
Related Publication 20170304381A1 · Oct 26, 2017