IP Library Granted Patent US 9,701,967
Granted Patent B2
US 9,701,967 · App. 15/189,159 · Granted Jul 11, 2017

Aptamers to PDGF and VEGF and their use in treating PDGF and VEGF mediated conditions

Inventors: Thale C. Jarvis (Boulder, CO); John C. Rohloff (Boulder, CO); Amy D. Gelinas (Lafayette, CO); Chi Zhang (Superior, CO); Daniel W. Drolet (Boulder, CO); Sheela M. Waugh (Erie, CO); Nebojsa Janjic (Boulder, CO)
Assignee: SomaLogic, Inc.
C12N15/115C12N2310/16C12N2310/315C12N2310/318C12N2310/321C12N2310/335C12N2320/30
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Quick Facts
Patent No.
US 9,701,967
App. No.
15/189,159
Granted
Jul 11, 2017
Kind
B2
Abstract

Aptamers that bind PDGF and aptamers that bind VEGF are provided. In addition, aptamer constructs comprising a PDGF aptamer and a VEGF aptamer are provided. Pharmaceutical compositions comprising the aptamers and aptamer constructs are provided, as well as methods of treating conditions using the aptamers and aptamer constructs.

Claims (17)

1. An aptamer comprising the sequence:

5′-GZZQAAEZECZZEZDRGAZZZAAAZGG-3′ (SEQ ID NO. 513)

wherein;

each Z is a modified pyrimidine;

Q is selected from any modified or unmodified nucleotide and a substituted or unsubstituted C 2 -C 50 linker, or is absent;

each E is independently selected from a G and a substituted or unsubstituted C 2 -C 50 linker;

D is selected from A and a substituted or unsubstituted C 2 -C 50 linker; and

R is selected from any modified or unmodified nucleotide and a substituted or unsubstituted C 2 -C 50 linker.

2. The aptamer of claim 1 , wherein each Z is independently selected from 5-(N-benzylcarboxyamide)-2′-deoxyuridine (BndU), 5-(N-benzylcarboxyamide)-2′-O-methyluridine, 5-(N-benzylcarboxyamide)-2′-fluorouridine, 5-(N-phenethylcarboxyamide)-2′-deoxyuridine (PedU), 5-(N-thiophenylmethylcarboxyamide)-2′-deoxyuridine (ThdU), 5-(N-isobutylcarboxyamide)-2′-deoxyuridine (iBudU), 5-(N-isobutylcarboxyamide)-2′-O-methyluridine, 5-(N-isobutylcarboxyamide)-2′-fluorouridine, 5-(N-tryptaminocarboxyamide)-2′-deoxyuridine (TrpdU), 5-(N-tryptaminocarboxyamide)-2′-O-methyluridine, 5-(N-tryptaminocarboxyamide)-2′-fluorouridine, 5-(N-[1-(3-trimethylamonium) propyl]carboxyamide)-2′-deoxyuridine chloride, 5-(N-naphthylmethylcarboxyamide)-2′-deoxyuridine (NapdU), 5-(N-naphthylmethylcarboxyamide)-2′-O-methyluridine, 5-(N-naphthylmethylcarboxyamide)-2′-fluorouridine, and 5-(N-[1-(2,3-dihydroxypropyl)]carboxyamide)-2′-deoxyuridine).

3. The aptamer of claim 1 , wherein each of E and R is independently, for each occurrence, selected from the group consisting of a substituted or unsubstituted C 2 -C 10 linker, a substituted or unsubstituted C 2 -C 8 linker, a substituted or unsubstituted C 2 -C 6 linker, a substituted or unsubstituted C 2 -C 5 linker, a substituted or unsubstituted C 2 -C 4 linker, a substituted or unsubstituted C 3 linker and a G.

4. The aptamer of claim 1 , wherein D is independently, for each occurrence, selected from the group consisting of a substituted or unsubstituted C 2 -C 10 linker, a substituted or unsubstituted C 2 -C 8 linker, a substituted or unsubstituted C 2 -C 6 linker, a substituted or unsubstituted C 2 -C 5 linker, a substituted or unsubstituted C 2 -C 4 linker, a substituted or unsubstituted C 3 linker and an A.

5. The aptamer of claim 1 , wherein Q is independently, for each occurrence, selected from the group consisting of a substituted or unsubstituted C 2 -C 10 linker, a substituted or unsubstituted C 2 -C 8 linker, a substituted or unsubstituted C 2 -C 6 linker, a substituted or unsubstituted C 2 -C 5 linker, a substituted or unsubstituted C 2 -C 4 linker, a substituted or unsubstituted C 3 linker and a C.

6. The aptamer of 1 further comprising at least one, at least two, at least three, at least four, or at least five nucleosides comprise a 2′-OMe.

7. The aptamer of 1 further comprising at least one, at least two, at least three, at least four, or at least five internucleoside linkages are phosphorothioate linkages.

8. The aptamer of 1 , wherein the aptamer binds VEGF-121 with an affinity of less than 10 nM, less than 5 nM, less than 2 nM, or less than 1 nM.

9. The aptamer of claim 1 , wherein the aptamer inhibits VEGF-121-mediated phosphorylation of a VEGF receptor.

10. A method comprising administering to a subject in need a therapeutically effective amount of an aptamer of claim 1 , wherein the method treats and/or prevents a conditions selected from the group consisting of macular degeneration, an ophthalmic condition, fibrosis, a cardiovascular disease and a cancer.

Assignments (3)
CHANGE OF NAME Recorded Feb 4, 2022
From: SOMALOGIC INC.
To: SOMALOGIC OPERATING CO. INC.
Reel/Frame 058885/0983 →
RELEASE OF SECURITY INTEREST Recorded Apr 20, 2021
From: MADRYN HEALTH PARTNERS, LP, FORMERLY VISIUM HEALTHCARE PARTNERS, LP
To: SOMALOGIC, INC.
Reel/Frame 055981/0884 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2016
From: JARVIS, THALE C.; ROHLOFF, JOHN C.; GELINAS, AMY D.; ZHANG, CHI; DROLET, DANIEL W.; WAUGH, SHEELA M.; JANJIC, NEBOJSA
To: SOMALOGIC, INC.
Reel/Frame 038984/0741 →
Continuity (6)
Division 14381679
Provisional Application 61616881 · Mar 28, 2012
Provisional Application 61648394 · May 17, 2012
Provisional Application 61719354 · Oct 26, 2012
Provisional Application 61722099 · Nov 2, 2012
Related Publication 20160298118A1 · Oct 13, 2016