IP Library › Granted Patent US 12,662,523
Granted Patent B2
US 12,662,523 · App. 17/608,546 · Granted Jun 23, 2026

Pharmaceutical formulations containing CD80 extracellular domain-Fc fusion proteins

Inventor: Yong Quan (Dublin, CA)
Assignee: FIVE PRIME THERAPEUTICS, INC.
C07K14/70532A01K67/0271A61K9/0019A61K47/26A61P35/00A01K2227/105A01K2267/0331A61K38/00
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Quick Facts
Patent No.
US 12,662,523
App. No.
17/608,546
Filed
Nov 3, 2021
Granted
Jun 23, 2026
Kind
B2
Examiner
KIM, YUNSOO
Art Unit
1641
USPC
424/130.1
Abstract

The present disclosure provides pharmaceutical compositions comprising CD80 extracellular domain (ECD)-fragment crystallizable (Fc) fusion molecules. The present disclosure also provides methods for treating solid tumors by administering such pharmaceutical compositions.

Claims (16)

1 . A pharmaceutical composition consisting of (i) sialylated CD80 ECD-Fc fusion molecules, (ii) about 20 mM L-histidine, (iii) about 270 mM sucrose, and (iv) about 0.05% weight/volume polysorbate 20, wherein the pH of the composition is about 6.7.

2 . A pharmaceutical composition consisting of (i) sialylated CD80 ECD-Fc fusion molecules, (ii) about 20 mM L-histidine, (iii) about 270 mM sorbitol, and (iv) about 0.05% weight/volume polysorbate 20, wherein the pH of the composition is about 6.7.

3 . A syringe or vial comprising the pharmaceutical composition of claim 1 .

4 . The pharmaceutical composition of claim 1 , wherein the concentration of CD80 ECD-Fc fusion molecules is about 5 mg/ml to about 15 mg/ml.

5 . The pharmaceutical composition of claim 4 , wherein the concentration of the CD80 ECD-Fc fusion molecules is about 10 mg/ml.

6 . The pharmaceutical composition of claim 1 , wherein the composition is a liquid.

7 . The pharmaceutical composition of claim 1 , wherein the composition is for intravenous administration.

8 . The pharmaceutical composition of claim 1 , wherein the CD80 ECD-Fc fusion molecules comprise a human CD80 ECD and a human IgG1 Fc domain.

9 . The pharmaceutical composition of claim 1 , wherein the CD80 ECD-Fc fusion molecules comprise 15-60 moles sialic acid (SA) per mole of fusion protein.

10 . The pharmaceutical composition of claim 2 , wherein the concentration of CD80 ECD-Fc fusion molecules is about 5 mg/ml to about 15 mg/ml.

11 . The pharmaceutical composition of claim 10 , wherein the concentration of the CD80 ECD-Fc fusion molecules is about 10 mg/ml.

12 . The pharmaceutical composition of claim 2 , wherein the composition is a liquid.

13 . The pharmaceutical composition of claim 2 , wherein the composition is for intravenous administration.

14 . The pharmaceutical composition of claim 2 , wherein the CD80 ECD-Fc fusion molecules comprise a human CD80 ECD and a human IgG1 Fc domain.

15 . The pharmaceutical composition of claim 2 , wherein the CD80 ECD-Fc fusion molecules comprise 15-60 moles sialic acid (SA) per mole of fusion protein.

16 . A syringe or vial comprising the pharmaceutical composition of claim 2 .

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA NAME FROM FIVE PRIME THERAPEUTICS TO FIVE PRIME THERAPEUTICS, INC. PREVIOUSLY RECORDED ON REEL 58633 FRAME 239. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded May 22, 2026
From: QUAN, YONG
To: FIVE PRIME THERAPEUTICS, INC.
Reel/Frame 075622/0309 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2022
From: QUAN, YONG
To: FIVE PRIME THERAPEUTICS
Reel/Frame 058633/0239 →
Continuity (2)
Provisional Application 62842722 · May 3, 2019
Related Publication 20220227834A1 · Jul 21, 2022
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