IP Library Granted Patent US 8,993,717
Granted Patent B2
US 8,993,717 · App. 13/502,781 · Granted Mar 31, 2015

Gadd45beta targeting agents

Inventors: Guido Franzoso (London, GB); Albert Andrzej Jaxa-Chamiec (London, GB); Caroline Minli Rachel Low (London, GB); Simona Maria Monti (Napoli, IT); Menotti Ruvo (Napoli, IT); Laura Tornatore (London, GB); Catherine Jane Tralau-Stewart (London, GB)
Assignee: Imperial Innovations Limited
C07K5/1016C07K5/06078C07K5/06104C07K5/06113C07K5/0812
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 8,993,717
App. No.
13/502,781
Granted
Mar 31, 2015
Kind
B2
Abstract

Compounds based around tetrapeptide, tripeptide and dipeptide moeties and corresponding peptiod moeties. Related methods and pharmaceutical compositions for use in treatment of cancer, inflammatory diseases, and other disorders.

Claims (34)

1. A method of treating hematological cancer comprising administering to a subject in need thereof a therapeutically effective amount of a compound of Formula I:

X 1 -A-X 2

wherein,

A is an oligopeptide moiety or an oligopeptoid moiety comprising the residues Y 1 -Y 2 -Y 3 -Y 4

Y1 is D-tryptophan

or D-tyrosine

Y4 is D-phenylalanine

D-tryptophan

or D-tyrosine

Y2 is an amino acid residue in the D-configuration or a residue of an amino acid derivative in the D-configuration or is absent;

Y3 is an amino acid residue in the D-configuration or a residue of an amino acid derivative in the D-configuration or is absent;

X 1 is absent, or is a moiety added to the -amino terminal of A in order to block the free amino group;

X 2 is absent or is an amino moiety added to the carbonyl acid terminal of the oligopeptide sequence so as to form an amide bond;

or derivatives thereof, said derivatives being selected from the group consisting of:

a) oligomers or multimers of molecules of the compound of formula I, said oligomers and multimers comprising two or more molecules of the compound of formula I each linked to a common scaffold moeity via an amide bond formed between an amino or carboxylic acid group present in molecules of the compound of formula I and an opposite amino or carboxylic acid group on a scaffold moiety said scaffold moiety participating in at least 2 amide bonds,

b) derivatives comprising a molecule of the compound of formula I or an oligomer or multimer thereof as defined above in part (a) conjugated via an amide bond, an ester bond, an ether bond or a thioether bond to:

PEG,

PEG-based compounds,

cell-penetrating peptides,

fluorescent dyes,

biotin or other tag moiety,

fatty acids,

nanoparticles of discrete size

or chelating ligands complexed with metallic or

radioactive ions, and

c) derivatives comprising a molecule of the compound of formula I or an oligomer or multimer thereof as defined in part (a) which has been modified by amidation, glycosylation, carbamylation, acylation, sulfation, phosphylation, cyclization, lipidation, pegylation or linkage to a peptide or peptiod fusion partner to make a fusion peptide or fusion peptiod,

and

d) salts and solvates of a molecule of the compound of formula I or of a derivative thereof as defined in part (a) or (b) above.

2. The method according to claim 1 wherein said hematological cancer depends on (a) NF-κB or Gadd45β or (b) NF-κB and Gadd45β for its survival, growth or survival and growth in human.

3. The method according to claim 1 comprising measuring (i) expression or activity level of Gadd45β or (ii) expression and activity level of Gadd45β in suspected hematological cancer cells of the subject prior to said administration of the compound.

4. The method of claim 1 , wherein said hematological cancer is multiple myeloma, Burkitt's lymphoma; promonocytic leukemia, or diffuse large B-cell lymphoma.

5. The method of treating hematological cancer comprising administering to a subject in need thereof a therapeutically effective amount of a pharmaceutical composition comprising a compound of Formula I in accordance with claim 1 .

6. The method according to claim 5 wherein said hematological cancer depends on (a) NF-κB or Gadd45β or (b) NF-κB and Gadd45β for its survival and/or growth in humans.

7. The method of claim 5 , wherein said hematological cancer is multiple myeloma, Burkitt's lymphoma; promonocytic leukemia, or diffuse large B-cell lymphoma.

Assignments (4)
CONFIRMATORY LICENSE Recorded Jan 22, 2024
From: IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 066360/0205 →
CHANGE OF NAME Recorded Dec 8, 2020
From: IMPERIAL INNOVATIONS LIMITED
To: IP2IPO INNOVATIONS LIMITED
Reel/Frame 054577/0166 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 8, 2020
From: IP2IPO INNOVATIONS LIMITED
To: IMPERIAL COLLEGE INNOVATIONS LIMITED
Reel/Frame 054577/0449 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2015
From: FRANZOSO, GUIDO; JAXA-CHAMIEC, ALBERT ANDRZEJ; LOW, CAROLINE MINLI RACHEL; MONTI, SIMONA MARIA; RUVO, MENOTTI; TORNATORE, LAURA; TRALAU-STEWART, CATHERINE JANE
To: IMPERIAL INNOVATIONS LIMITED
Reel/Frame 034961/0180 →
Priority Claims (1)
GB 0918579.4 · Oct 22, 2009 · national
Continuity (1)
Related Publication 20120277164A1 · Nov 1, 2012