IP Library Granted Patent US 10,548,924
Granted Patent B2
US 10,548,924 · App. 14/017,152 · Granted Feb 4, 2020

Use of adipose tissue-derived stromal stem cells in treating fistula

Inventors: Maria Gema Fernandez Miguel (Madrid, ES); Manuel Angel Gonzalez De La Pena (Madrid, ES); Rosa Ana Garcia Castro (Madrid, ES); Mariano Garcia Arranz (Madrid, ES); Damian Garcia-Olmo (Madrid, ES)
Assignees: TIGENIX, S.A.U.; UNIVERSIDAD AUTONOMA DE MADRID
A61K35/35A61B17/1659A61B17/32A61K45/06A61L24/0015A61L24/106A61L27/3604A61L27/3834A61L27/3839A61L27/3869A61L27/3895C12N5/0667A61B2017/320008A61K35/12A61L2300/64C12N2509/00C12N2510/00C12N2533/56
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,548,924
App. No.
14/017,152
Granted
Feb 4, 2020
Kind
B2
Abstract

Provided herein are novel methods and compositions utilizing adipose tissue-derived stromal stem cells for treating fistulae.

Claims (14)

1. A method of preparing a pharmaceutical composition, comprising thawing a cryopreserved composition and formulating the thawed composition with human serum albumin (HSA) and Dulbecco's Modified Eagle's Medium (DMEM) to produce the pharmaceutical composition, wherein the cryopreserved composition comprises an isolated cell population comprising adipose tissue-derived stromal stem cells, wherein the isolated cell population was ex vivo generated by passaging adherent cells obtained from adipose tissue at least four times so that fewer than 10% of the adipose tissue derived stromal cells in the cryopreserved composition express the CD34 marker as measured by flow cytometry and at least 50% of the adipose-tissue derived stromal cells in the cryopreserved composition express the CD90 marker as measured by flow cytometry, wherein the concentration of the adipose tissue-derived stromal stem cells in the cryopreserved composition is at least about 5×10 6 cells/mL.

2. The method of claim 1 wherein at least 85% of the adipose tissue-derived stromal stem cells in the cryopreserved composition express the CD44 marker and more than 50% of the adipose tissue-derived stromal stem cells express the CD29 and CD105 markers as measured by flow cytometry.

3. The method of claim 1 wherein at least 95% of the adipose tissue-derived stromal stem cells in the cryopreserved composition express the CD44 marker as measured by flow cytometry.

4. The method of claim 1 wherein at least 99% of the adipose tissue-derived stromal stem cells in the cryopreserved composition express the CD44 marker as measured by flow cytometry.

5. The method of claim 1 wherein the adherent cells obtained from adipose tissue were passaged at least six times.

6. The method of claim 1 , wherein the cryopreserved composition further comprises HSA.

7. A method of preparing a pharmaceutical composition, comprising formulating an isolated cell population with HSA and DMEM to produce the pharmaceutical composition, wherein the isolated cell population comprises adipose tissue-derived stromal stem cells, wherein the isolated cell population was ex vivo generated by and passaging adherent cells from adipose tissue at least four times so that fewer than 10% of the adipose tissue-derived stromal stem cells in the pharmaceutical composition express the CD34 marker as measured by flow cytometry and at least 50% of the adipose tissue derived stromal stem cells in the pharmaceutical composition express the CD90 marker as measured by flow cytometry, wherein the concentration of the adipose tissue-derived stromal stem cells in the pharmaceutical composition is at least about 5×10 6 cells/mL.

8. The method of claim 7 , further comprising aliquoting the pharmaceutical composition into one or more doses of at least about 10×10 6 cells/dose.

9. The method of claim 7 , further comprising aliquoting the pharmaceutical composition into one or more doses of at least about 20×10 6 cells/dose.

10. The method of claim 1 , wherein the pharmaceutical composition further comprises an adhesive.

11. The method of claim 10 , wherein the adhesive comprises a fibrin glue or gel.

12. The method of claim 1 , wherein the pharmaceutical composition further comprises a therapeutic agent.

13. The method of claim 12 , wherein the therapeutic agent comprises an anti-inflammatory agent, an immunosuppressive agent, a biological agent, an antibiotic, an antidiarrheal agent or a combination thereof.

14. The method of claim 7 wherein the adherent cells obtained from adipose tissue were passaged at least six times.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 15, 2022
From: TIGENIX, S.A.U.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 060516/0532 →
CONVERSION Recorded Jun 6, 2018
From: CELLERIX, S.L.
To: CELLERIX, S.A.
Reel/Frame 047141/0720 →
CONVERSION Recorded Jun 6, 2018
From: CELLERIX, S.A.
To: CELLERIX, S.A.U.
Reel/Frame 046314/0287 →
CHANGE OF NAME Recorded Feb 22, 2018
From: CELLERIX, S.A.U.
To: TIGENIX, S.A.U.
Reel/Frame 045417/0609 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2018
From: FERNANDEZ MIGUEL, MARIA GEMA; GONZALEZ DE LA PEÑA, MANUEL A.; GARCIA CASTRO, ROSA ANA
To: CELLERIX, S.L.
Reel/Frame 044989/0856 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2018
From: GARCIA ARRANZ, MARIANO; GARCIA-OLMO, DAMIAN
To: UNIVERSIDAD AUTONOMA DE MADRID
Reel/Frame 045384/0210 →
Priority Claims (2)
ES 200402083 · Aug 25, 2004 · national
ES 200402355 · Oct 4, 2004 · national
Continuity (5)
Continuation 13457053 · Apr 26, 2012
Continuation 11167061 · Jun 24, 2005
Continuation In Part 11065461 · Feb 25, 2005
Continuation In Part 11056241 · Feb 14, 2005
Related Publication 20140072539A1 · Mar 13, 2014