IP Library Granted Patent US 11,458,206
Granted Patent B2
US 11,458,206 · App. 16/793,094 · Granted Oct 4, 2022

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 (Andover, MA); Beata Sweryda-Krawiec (Marlborough, MA); Brian H. White (Malden, MA); Patrick Rosaire Bazinet (Somerville, MA); Richard Wooster (Natick, MA)
Assignee: TVA (ABC), LLC
A61K47/64A61K31/337A61K31/5383A61K47/55A61K47/65
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Quick Facts
Patent No.
US 11,458,206
App. No.
16/793,094
Granted
Oct 4, 2022
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 (15)

1. A method of treating lung cancer in a subject in need thereof comprising administering a therapeutically effective amount of a conjugate to the subject, wherein the conjugate comprises an active agent coupled to a somatostatin receptor (SSTR) targeting moiety by a linker, wherein the active agent is mertansine (DM1) and wherein the SSTR targeting moiety is a peptide, and wherein the conjugate has 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 method of claim 1 , wherein the molecular weight of the conjugate is less than about 50,000 Da, less than about 40,000 Da, less than about 30,000 Da, less than about 20,000 Da, less than about 15,000 Da, less than about 10,000 Da, less than about 8,000 Da, less than about 5,000 Da, or less than about 3,000 Da.

3. The method of claim 1 , wherein the linker is selected from the group consisting of an ester bond, disulfide, amide, acylhydrazone, ether, carbamate, carbonate, and urea.

4. The method of claim 1 , wherein the conjugate is selected from the group consisting of Compound 57, Compound 35, Compound 37, Compound 39, Compound 41, Compound 43, Compound 45, Compound 47, Compound 49, Compound 51, Compound 55, Compound 59, Compound 61, Compound 63, and Compound 65.

5. A method of inhibiting the rate of growth of a tumor, the size of a tumor or the volume of a tumor, the method comprising contacting the tumor with an effective amount of a conjugate comprising an active agent coupled to a somatostatin receptor (SSTR) targeting moiety by a linker, wherein the active agent is mertansine (DM1) and wherein the SSTR targeting moiety is a peptide, wherein the tumor is lung cancer, and wherein the conjugate has 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.

6. A method of delivering DM1 to a tumor in a subject, the method comprising administering a conjugate to the subject in need thereof, wherein the conjugate comprises an active agent coupled to a somatostatin receptor (SSTR) targeting moiety by a linker, wherein the active agent is mertansine (DM1) and wherein the SSTR targeting moiety is a peptide, wherein the tumor is lung cancer, and wherein the conjugate has 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.

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 Feb 21, 2020
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 051885/0130 →
CHANGE OF NAME Recorded Feb 21, 2020
From: BLEND THERAPEUTICS, INC.
To: TARVEDA THERAPEUTICS, INC.
Reel/Frame 051986/0771 →
Continuity (7)
Division 15652947 · Jul 18, 2017
Continuation 15382487 · Dec 16, 2016
Continuation PCTUS2015038569 · Jun 30, 2015
Provisional Application 62150413 · Apr 21, 2015
Provisional Application 62077487 · Nov 10, 2014
Provisional Application 62019001 · Jun 30, 2014
Related Publication 20200206356A1 · Jul 2, 2020