IP Library Patent Application 14271749
Patent Application
App. No. 14/271,749

PHARMACEUTICAL COMPOSITION CONTAINING NEUREGULIN ISOFORMS

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Patent No.
US None
App. No.
14/271,749
Abstract

A pharmaceutical composition containing a soluble Neuregulin-1 isoform representing Posttranslational Neuregulin-1 modifications.

Claims (25)

1 . A pharmaceutical composition comprising a polypeptide which is a recombinant soluble Type I Neuregulin-1 β isoform which is an about 15 to about 35 kD N-terminal fragment of Type I Neuregulin-1 β and a pharmaceutically acceptable excipient, wherein said recombinant soluble Type I Neuregulin-1 β isoform is characterized in that it is capable of crossing the blood-brain barrier and is non-mutagenic in a mouse lymphoma thymidine kinase locus assay.

2 . The pharmaceutical composition of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 150 to 250 amino acids of Type I Neuregulin-1 β.

3 . The pharmaceutical composition of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform is the first 245 to 250 amino acids of Type I Neuregulin-1 β.

4 . The pharmaceutical composition of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform comprises the extracellular domain of Type I Neuregulin-1 β and has a molecular mass of between 25 and 32 kD.

5 . The pharmaceutical composition of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform comprises the extracellular domain of Type I Neuregulin-1 β and has a molecular mass of about 26 kD.

6 . The pharmaceutical composition of claim 1 , wherein said recombinant soluble Type I Neuregulin-1 β isoform has an isoelectric point (pl) of about 4 to about 10.

7 . The pharmaceutical composition of claim 1 , wherein said composition is formulated to be injectable.

8 . The pharmaceutical composition of claim 7 , wherein said composition is formulated to be injectable by intravenous (i.v.) injection.

9 . The pharmaceutical composition of claim 7 , wherein said composition is formulated to be injectable by subcutaneous (s.c.) injection.

10 . The pharmaceutical composition of claim 7 , wherein said composition is formulated to be injectable by intraperitoneal (i.p.) injection.

11 . The pharmaceutical composition of claim 1 , wherein said composition is formulated to be an inhalation product.

12 . The pharmaceutical composition of claim 1 , wherein said composition is formulated to be administered systemically.

13 . The pharmaceutical composition of claim 1 , further comprising a medicament for the treatment of neurological conditions.

14 . The pharmaceutical composition of claim 13 , wherein the further medicament is selected from the group consisting of acetylcholine esterase inhibitors, MAO-B-inhibitors, COMT-inhibitors, Memantine-type channel blockers, dopamine receptor agonists, serotonine receptor agonists or antogonists, catecholamine reuptake inhibitors, serotonine reuptake inhibitors.

15 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of psychotic disorders.

16 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of Parkinson's disease.

17 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of Alzheimer's disease.

18 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of Multiple Sclerosis (MS).

19 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of Amyotrophic Lateral Sclerosis (ALS).

20 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of epilepsy.

21 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of stroke.

22 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of traumatic brain injury.

23 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of spinal cord injury.

24 . The pharmaceutical composition of claim 13 , wherein the further medicament is selected from clozapine, olanzapine, or gabapentin.

25 . The pharmaceutical composition of claim 13 , wherein the further medicament is a medicament for the treatment of schizophrenia, bipolar disorders or depression.

Assignments (4)
CHANGE OF NAME Recorded Jul 8, 2016
From: MIND-NRG SA
To: MIND-NRG SARL
Reel/Frame 039289/0137 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE NAME PREVIOUSLY RECORDED AT REEL: 038506 FRAME: 0881. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 11, 2016
From: PROTEOSYS AG
To: MIND-NRG SA
Reel/Frame 038684/0686 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2016
From: PROTEOSYS AG
To: MING-NRG SA
Reel/Frame 038506/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2016
From: SCHRATTENHOLZ, ANDRE
To: PROTEOSYS AG
Reel/Frame 038241/0359 →