IP Library Granted Patent US 10,370,413
Granted Patent B2
US 10,370,413 · App. 15/309,781 · Granted Aug 6, 2019

Kv1.3 potassium channel antagonists

Inventors: Andreas Klostermann (Martinsried, DE); Jörg Stockhaus (Martinsried, DE)
Assignee: cgtx-Peptide Development GmbH
C07K14/00C07K14/4703C07K14/705A61K38/00
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Quick Facts
Patent No.
US 10,370,413
App. No.
15/309,781
Granted
Aug 6, 2019
Kind
B2
Abstract

Compounds which selectively bind to and inhibit the activity of the potassium channel Kv1.3 are described. Pharmaceutical compositions comprising such compounds and the use of said compounds and said pharmaceutical compositions for the treatment or prevention of autoimmune diseases, obesity, parodontitis and/or tissue transplant rejection are also described.

Claims (50)

1. A composition comprising a peptide having the amino acid sequence X 1 -X 2 -X 3 -N-V-X 4 -C-X 5 -X 6 -X 7 -X 8 -X 9 C-X 10 -X 11 -X 12 -C-X 13 -X 14 -X 15 -T-G-C-P-X 16 -X 17 -K-C-M-N-R-K-C-X 18 -C-X 19 -X 20 -C as set forth in SEQ ID NO: 23:

wherein X 1 is selected from the group consisting of T, Q, S, Y and N;

wherein X 2 is selected from the group consisting of I, F, V, A, L and W;

wherein X 3 is selected from the group consisting of I, T, Y, S, V, A and L;

wherein X 4 is selected from the group consisting of K, S, T, Y and R;

wherein X 5 is selected from the group consisting of R, T, K, S and Y;

wherein X 6 is selected from the group consisting of T, G, S, N, I, K, Q, A, V, L and Y;

wherein X 7 is selected from the group consisting of P, S and T;

wherein X 8 is selected from the group consisting of R, K and P;

wherein X 9 is selected from the group consisting of D, Q, N and E;

wherein X 10 is selected from the group consisting of A, Y, I, L, W, S, T, V, L and F;

wherein X 11 is selected from the group consisting of D, R, P, K, E, S, T and Y;

wherein X 12 is selected from the group consisting of P, H, V, I, L and A;

wherein X 13 is selected from the group consisting of R, K, Q and N;

wherein X 14 is selected from the group consisting of K, D, A, R, E, V, L and I;

wherein X 15 is selected from the group consisting of E, Q, A, L, D, N, V and I;

wherein X 16 is selected from the group consisting of Y, N, S, T and Q;

wherein X 17 is selected from the group consisting of A, G, V, I and L;

wherein X 18 is selected from the group consisting of K and R;

wherein X 19 is selected from the group consisting of Y, N, Q, T and S; and

wherein X 20 is selected from the group consisting of G, R and K.

2. The composition of claim 1 :

wherein X 1 is Thr;

wherein X 2 is Ile;

wherein X 3 is Ile;

wherein X 4 is Lys;

wherein X 5 is Thr;

wherein X 6 is Ser;

wherein X 7 is Pro;

wherein X 5 is Lys;

wherein X 9 is Gln;

wherein X 10 is Leu;

wherein X 11 is Pro;

wherein X 12 is Pro;

wherein X 13 is Lys;

wherein X 14 is Ala;

wherein X 15 is Gln;

wherein X 16 is Tyr;

wherein X 17 is Gly;

wherein X 18 is Lys;

wherein X 19 is Asn; and

wherein X 20 is Arg.

3. A pharmaceutical composition comprising the composition of claim 1 and a pharmaceutically acceptable carrier.

4. A pharmaceutical composition comprising the composition of claim 2 and a pharmaceutically acceptable carrier.

5. The composition of claim 3 , wherein the composition is formulated for intravenous, subcutaneous, or intramuscular administration.

6. The composition of claim 4 , wherein the composition is formulated for intravenous, subcutaneous, or intramuscular administration.

7. A method of treating an autoimmune disease in a subject in need thereof, comprising administering the composition of claim 1 to a subject selected as having an autoimmune disease, wherein the autoimmune disease is rheumatoid arthritis, psoriasis, or atopic dermatitis.

8. The method of claim 7 , wherein the composition is the composition of claim 2 .

9. The method of claim 7 , wherein administering the composition comprises administering the composition to the subject intravenously, subcutaneously, or intramuscularly.

10. The method of claim 8 , wherein administering the composition comprises administering the composition to the subject intravenously, subcutaneously, or intramuscularly.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 17, 2019
From: CGTX-PEPTIDE DEVELOPMENT GMBH
To: SELECTION THERAPEUTICS GMBH
Reel/Frame 050751/0013 →
SECURITY INTEREST Recorded Feb 22, 2019
From: CONOGENETIX BIOSCIENCES GMBH
To: CGTX-PEPTIDE DEVELOPMENT GMBH
Reel/Frame 048414/0463 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2017
From: KLOSTERMANN, ANDREAS; STOCKHAUS, JÖRG
To: CONOGENETIX BIOSCIENCES GMBH
Reel/Frame 041299/0191 →
Priority Claims (1)
GB 1408135.0 · May 8, 2014 · national
Continuity (1)
Related Publication 20170137470A1 · May 18, 2017