IP Library Granted Patent US 10,624,967
Granted Patent B2
US 10,624,967 · App. 15/652,947 · Granted Apr 21, 2020

Targeted conjugates and particles and formulations thereof

Inventors: Rossitza G. Alargova (Brighton, MA); Mark T. Bilodeau (Waltham, MA); Craig A. Dunbar (Needham, MA); Sudhakar Kadiyala (Newton, MA); Rajesh R. Shinde (Lexington, MA); Patrick Lim Soo (Ridgewood, NJ); Beata Sweryda-Krawiec (Marlborough, MA); Brian H. White (Malden, MA); Patrick Rosaire Bazinet (Somerville, MA); Richard Wooster (Natick, MA)
Assignee: TARVEDA THERAPEUTICS, INC.
A61K47/64A61K31/337A61K31/5383A61K47/55A61K47/65
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Quick Facts
Patent No.
US 10,624,967
App. No.
15/652,947
Granted
Apr 21, 2020
Kind
B2
Abstract

Nanoparticles and microparticles, and pharmaceutical formulations thereof, containing conjugates of an active agent such as a therapeutic, prophylactic, or diagnostic agent attached to a targeting moiety, such as a somatostatin receptor binding moiety, via a linker have been designed. Such nanoparticles and microparticles can provide improved temporospatial delivery of the active agent and/or improved biodistribution. Methods of making the conjugates, the particles, and the formulations thereof are provided. Methods of administering the formulations to a subject in need thereof are provided, for example, to treat or prevent cancer or infectious diseases.

Claims (16)

1. A conjugate or a pharmaceutically acceptable salt thereof, comprising an active agent coupled to a somatostatin receptor (SSTR) targeting moiety by a linker,

wherein the active agent is mertansine (DM1),

wherein the SSTR targeting moiety is a peptide,

wherein the linker binds to the C-terminus of the peptide with a covalent bond,

wherein the molecular weight of the conjugate is less than 5000 Da, and

wherein the conjugate comprises a formula of

wherein

R is selected from the group consisting of H, alkyl, aryl, and amide groups; and

Ar 1 and Ar 2 are independently selected from the group consisting of heterocyclyl, aryl, and heteroaryl groups.

2. The conjugate of claim 1 , wherein the bond between the linker and the SSTR targeting moiety is an amide bond.

3. The conjugate of claim 1 , wherein the linker is a cleavable linker.

4. The conjugate of claim 1 , wherein the linker comprises an ester bond, disulfide, amide, acylhydrazone, ether, carbamate, carbonate, or urea.

5. A pharmaceutical formulation comprising the conjugate in claim 1 and at least one pharmaceutically acceptable excipient.

6. A conjugate or a pharmaceutically acceptable salt thereof, wherein the conjugate is selected from the group consisting of Compound 35, Compound 37, Compound 39, Compound 41, Compound 43, Compound 45, Compound 47, Compound 49, Compound 51, Compound 55, Compound 57, Compound 59, Compound 61, Compound 63, and Compound 65.

7. The conjugate of claim 6 , wherein the conjugate is

8. A pharmaceutical formulation comprising the conjugate in claim 6 and at least one pharmaceutically acceptable excipient.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 25, 2022
From: TARVEDA THERAPEUTICS, INC.
To: TVA (ABC), LLC
Reel/Frame 059788/0518 →
SECURITY INTEREST Recorded Oct 4, 2021
From: TARVEDA THERAPEUTICS, INC.
To: OXFORD FINANCE LLC
Reel/Frame 057988/0232 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2017
From: ALARGOVA, ROSSITZA G.; BILODEAU, MARK T.; DUNBAR, CRAIG A.; KADIYALA, SUDHAKAR; SHINDE, RAJESH R.; LIM SOO, PATRICK; SWERYDA-KRAWIEC, BEATA; WHITE, BRIAN H.; BAZINET, PATRICK ROSAIRE; WOOSTER, RICHARD
To: BLEND THERAPEUTICS, INC.
Reel/Frame 043052/0879 →
CHANGE OF NAME Recorded Jul 20, 2017
From: BLEND THERAPEUTICS, INC.
To: TARVEDA THERAPEUTICS, INC.
Reel/Frame 043269/0617 →
Continuity (6)
Continuation 15382487 · Dec 16, 2016
Continuation PCTUS2015038569 · Jun 30, 2015
Provisional Application 62019001 · Jun 30, 2014
Provisional Application 62077487 · Nov 10, 2014
Provisional Application 62150413 · Apr 21, 2015
Related Publication 20180000959A1 · Jan 4, 2018