IP Library Granted Patent US 11,046,746
Granted Patent B2
US 11,046,746 · App. 15/560,944 · Granted Jun 29, 2021

Method of treatment of cerebral amyloid angiopathy with P75ECD peptide and/or P75ECD-FC fusion protein

Inventors: Xinfu Zhou (Adelaide, AU); Yanjiang Wang (Chongqing, CN)
C07K14/70578A61K38/179A61K47/6811A61P9/10A61P25/28C07K14/71C07K16/2878C12N15/86G01N33/6896A61K38/00A61K2039/505C07K2319/30C12N2750/14143G01N2333/71
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Quick Facts
Patent No.
US 11,046,746
App. No.
15/560,944
Granted
Jun 29, 2021
Kind
B2
Abstract

A method of treating and/or preventing neurological conditions, comprising administering to a subject in need thereof a therapeutically effective amount of a p75 extracellular domain (p75ECD) or a functional fragment, variant, analogue or derivative thereof. Also provided is a method of diagnosing and/or prognosing Alzheimer's disease (AD) in a test subject comprising comparing the concentration of p75ECD and/or p75FL and/or the ratio of p75ECD:p75FL in a biological sample of the test subject to non-demented control subject(s).

Claims (4)

1. A method of treating cerebral amyloid angiopathy (CAA) in a human, comprising administering to a human in need thereof, a therapeutically-effective amount of a pharmaceutical formulation comprising: (a) an isolated p75 extracellular domain (p75ECD) peptide that consists of the sequence of SEQ ID NO:4; (b) an isolated p75ECD-Fc fusion protein that consists of the amino acid sequence of SEQ ID NO:6; or (c) a combination thereof, in an amount and for a time effective to treat the CAA in the human.

2. The method of claim 1 , wherein the isolated p75ECD peptide or the isolated p75ECD-Fc fusion protein is a recombinant peptide.

3. The method of claim 2 , wherein the isolated p75ECD peptide or the isolated p75ECD-Fc fusion protein is administered via one or more of intraperitoneal, intraventricular, intravenous, intrathecal, and intramuscular injections.

4. The method of claim 3 , wherein the isolated p75ECD peptide or the isolated p75ECD-Fc fusion protein is administered at a dosage of between about 0.1 mg/kg and about 250 mg/kg of body weight.

Assignments (4)
CHANGE OF NAME Recorded Jan 9, 2025
From: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD
To: SHANGHAI AUZONE BIOLOGICAL TECHNOLOGY CO., LTD
Reel/Frame 069801/0053 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2019
From: FUZHOU TIANTAI MEDICAL TECHNOLOGY CO. LTD
To: SUZHOU AUZONE BIOLOGICAL TECHNOLOGY CO., LTD
Reel/Frame 048868/0701 →
CHANGE OF NAME Recorded Apr 12, 2019
From: FUJIAN TIANTAI MEDICAL TECHNOLOGY CO. LTD
To: FUZHOU TIANTAI MEDICAL TECHNOLOGY CO. LTD
Reel/Frame 048878/0265 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 25, 2017
From: ZHOU, XINFU; WANG, YANJIANG
To: FUJIAN TIANTAI MEDICAL TECHNOLOGY CO. LTD
Reel/Frame 043999/0376 →
Priority Claims (1)
AU 2015901100 · Mar 26, 2015 · national
Continuity (1)
Related Publication 20180170996A1 · Jun 21, 2018