IP Library Granted Patent US 8,691,771
Granted Patent B2
US 8,691,771 · App. 13/112,907 · Granted Apr 8, 2014

Bi-specific fusion proteins for tissue repair

Inventors: Ulrik Nielsen (Quincy, MA); Thomas Wickham (Groton, MA); Birgit Schoeberl (Cambridge, MA); Brian Harms (Roslindale, MA); Bryan Linggi (Richland, WA); Matthew Onsum (Jamaica Plain, MA); Byron DeLaBarre (Cambridge, MA)
Assignee: Merrimack Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 8,691,771
App. No.
13/112,907
Granted
Apr 8, 2014
Kind
B2
Abstract

Bi-specific fusion proteins with therapeutic uses are provided, as well as pharmaceutical compositions comprising such fusion proteins, and methods for using such fusion proteins to repair damaged tissue. The bi-specific fusion proteins generally comprise: (a) a targeting polypeptide domain that binds to an ischemia-associated molecule; and (b) an activator domain that that detectably modulates the activity of a cellular network.

Claims (24)

1. A bi-specific fusion protein comprising:

(a) a targeting domain consisting of an amino acid sequence of SEQ ID NO 31; and

(b) an activator domain consisting of an amino acid sequence of SEQ ID NO 3.

2. The bi-specific fusion protein of claim 1 further comprising a linker.

3. The bi-specific fusion protein of claim 2 wherein the linker is a non-immunogenic protein.

4. The bi-specific fusion protein of claim 2 , wherein the linker comprises SEQ ID NO 10.

5. The bi-specific protein of claim 1 or claim 2 further comprising a leader polypeptide.

6. The bi-specific protein of claim 5 wherein the leader polypeptide consists of an amino acid sequence of SEQ ID NO: 41 or SEQ ID NO 42.

7. The bi-specific fusion protein of claim 1 wherein the targeting domain is at the amino terminus of the activator domain or wherein the targeting domain is at the carboxy terminus of the activator domain.

8. The bi-specific fusion protein of claim 1 consisting of an amino acid sequence selected from the group consisting of:

(a) SEQ ID NOs 42, 3, 10 and 31, wherein the amino acid sequence of SEQ ID NO 3 is fused to the C terminus of the amino acid sequence of SEQ ID NO 42 and to the N-terminus of the amino acid sequence of SEQ ID NO 10 and wherein the amino acid sequence of SEQ ID NO 10 is fused to the N-terminus of the amino acid sequence of SEQ ID NO 31,

(b) SEQ ID NOs 42, 31, 10 and 3, wherein the amino acid sequence of SEQ ID NO 31 is fused to the C terminus of the amino acid sequence of SEQ ID NO 42 and to the N-terminus of the amino acid sequence of SEQ ID NO 10 and wherein the amino acid sequence of SEQ ID NO 10 is fused to the N-terminus of the amino acid sequence of SEQ ID NO 3,

(c) SEQ ID NOs 42, 3 and 31, wherein the amino acid sequence of SEQ ID NO 3 is fused to the C terminus of the amino acid sequence of SEQ ID NO 42 and to the N-terminus of the amino acid sequence of SEQ ID NO 31,

(d) SEQ ID NOs 3, 10 and 31, wherein the amino acid sequence of SEQ ID NO 10 is fused to the C terminus of the amino acid sequence of SEQ ID NO 3 and to the N-terminus of the amino acid sequence of SEQ ID NO 31,

(e) SEQ ID NOs 42, 31 and 3, wherein the amino acid sequence of SEQ ID NO 31 is fused to the C terminus of the amino acid sequence of SEQ ID NO 42 and to the N-terminus of the amino acid sequence of SEQ ID NO 3,

(f) SEQ ID NOs 31, 10 and 3, wherein the amino acid sequence of SEQ ID NO 10 is fused to the C terminus of the amino acid sequence of SEQ ID NO 31 and to the N-terminus of the amino acid sequence of SEQ ID NO 3,

(g) SEQ ID NOs 41, 3, 10, 31, wherein the amino acid sequence of SEQ ID NO 3 is fused to the C terminus of the amino acid sequence of SEQ ID NO 41 and to the N-terminus of the amino acid sequence of SEQ ID NO 10 and wherein the amino acid sequence of SEQ ID NO 10 is fused to the N-terminus of the amino acid sequence of SEQ ID NO 31,

(h) SEQ ID NOs 41, 31, 10 and 3, wherein the amino acid sequence of SEQ ID NO 31 is fused to the C terminus of the amino acid sequence of SEQ ID NO 41 and to the N-terminus of the amino acid sequence of SEQ ID NO 10 and wherein the amino acid sequence of SEQ ID NO 10 is fused to the N-terminus of the amino acid sequence of SEQ ID NO 3,

(i) SEQ ID NOs 41, 3, and 31, wherein the amino acid sequence of SEQ ID NO 3 is fused to the C terminus of the amino acid sequence of SEQ ID NO 41 and to the N-terminus of the amino acid sequence of SEQ ID NO 31, and

(j) SEQ ID NOs 41, 31 and 3, wherein the amino acid sequence of SEQ ID NO 31 is fused to the C terminus of the amino acid sequence of SEQ ID NO 41 and to the N-terminus of the amino acid sequence of SEQ ID NO 3.

9. A bi-specific fusion protein comprising:

(a) a targeting domain consisting of an amino acid sequence of SEQ ID NO 31,

(b) an activator domain consisting of an amino acid sequence of SEQ ID NO 3; and

(c) a polypeptide linker consisting of an amino acid sequence of SEQ ID NO 10.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2019
From: MERRIMACK PHARMACEUTICALS, INC.
To: SILVER CREEK PHARMACEUTICALS, INC.
Reel/Frame 049112/0597 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE PREVIOUSLY RECORDED ON REEL 026734 FRAME 0945. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Apr 1, 2014
From: NIELSEN, ULRIK; WICKHAM, THOMAS; SCHOEBERL, BIRGIT; HARMS, BRIAN; LINGGI, BRYAN; ONSUM, MATTHEW; DELABARRE, BYRON
To: MERRIMACK PHARMACEUTICALS, INC.
Reel/Frame 032588/0274 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2011
From: NIELSEN, ULRIK; WICKHAM, THOMAS; SCHOEBERL, BIRGIT; HARMS, BRIAN; LINGGI, BRYAN; ONSUM, MATTHEW; DELABARRE, BYRON
To: MERRIMACK PHARMACEUTICALS
Reel/Frame 026734/0945 →
Continuity (2)
Provisional Application 61347040 · May 21, 2010
Related Publication 20110286976A1 · Nov 24, 2011