Claims for Patent: 7,998,477

Summary for Patent: 7,998,477

Title:	Spherical protein particles and methods for making and using them
Abstract:	This invention relates to SPPs, spherical nanocrystalline composite particles or crystalline SPPs of biologically active proteins or compositions, including formulations, comprising such SPPs, spherical nanocrystalline composite particles or crystalline SPPs. More particularly, methods are provided for the production of SPPs, spherical nanocrystalline composite particles or crystalline SPPs of high concentrations of biologically active proteins, and for the preparation of stabilized SPPs, spherical nanocrystalline composite particles or crystalline SPPs for use alone, or in dry or slurry compositions. This invention also relates to methods for stabilization, storage and delivery of biologically active proteins using SPPs, spherical nanocrystalline composite particles or crystalline SPPs. The present invention further relates to methods using SPPs, spherical nanocrystalline composite particles or crystalline SPPs, or compositions or formulations comprising such SPPs, spherical nanocrystalline composite particles or crystalline SPPs, for biomedical applications, including biological delivery to humans and animals.
Inventor(s):	Yakovlevsky; Kirill (Cambridge, MA), Shamashkin; Michael (Somerville, MA), Khalaf; Nazer (Worcester, MA), Govardhan; Chandrika P. (Lexington, MA), Jung; Chu W. (Arlington, MA)
Assignee:	Althea Technologies Inc. (San Diego, CA)
Application Number:	10/741,861
Patent Claims:	1. A crystalline spherical protein particle wherein said protein is an antibody or a single-chain Fv fragment of said antibody, wherein said protein has a conformation which is the same as that of the native, soluble counterpart of the protein, as indicated by an ELISA using a monoclonal antibody which specifically binds the native, soluble counterpart. 2. A crystalline spherical protein particle wherein said protein is an antibody or a single-chain Fv fragment of said antibody, wherein said protein has a .beta.-sheet structural content that is less than about 20% different from the .beta.-sheet structural content of the native, soluble counterpart of the protein, and has lost less than about 20% of the .alpha.-helical structural content of its native, soluble counterpart, as indicated by FTIR or Circular Dichroism (CD) spectroscopy. 3. The crystalline spherical protein particle according to claim 2, wherein said protein has a .beta.-sheet structural content that is less than about 20% different from the .beta.-sheet structural content of the native, soluble counterpart of the protein, as indicated by a correlation spectra as compared to its native, soluble counterpart, as indicated by FTIR. 4. The crystalline spherical protein particle according to claim 2, wherein said protein loses less than about 20% of its .beta.-helical structural content after storage from about 4 days to about 180 days at from about 4.degree. C. to about 50.degree. C., as compared to its native, soluble counterpart after storage under identical conditions. 5. The crystalline spherical protein particle according to claim 2, wherein said protein has a .beta.-sheet structural content that is less than about 20% different from the .beta.-sheet structural content of the native, soluble counterpart of the protein, and has lost less than about 20% of the .alpha.-helical structural content of the native, soluble counterpart of the protein, as indicated by Circular Dichroism (CD) spectroscopy. 6. A crystalline spherical protein particle wherein said protein is an antibody or a single-chain Fv fragment of said antibody, wherein said protein has about 100% of the biological activity of the native, soluble counterpart of the protein. 7. The crystalline spherical protein particle according to claim 6, wherein said protein has about 100% of the biological activity of the native, soluble counterpart of the protein. 8. The crystalline spherical protein particle according to claim 6, wherein said protein has about 90% of the biological activity of the native, soluble counterpart of the protein. 9. The crystalline spherical protein particle according to claim 6, wherein said protein has about 80% of the biological activity of the native, soluble counterpart of the protein. 10. The crystalline spherical protein particle according to claim 6, wherein said protein has about 70% of the biological activity of the native, soluble counterpart of the protein. 11. The crystalline spherical protein particle according to claim 6, wherein said protein has about 60% of the biological activity of the native, soluble counterpart of the protein. 12. The crystalline spherical protein particle according to claim 6, wherein said protein has about 50% of the biological activity of the native, soluble counterpart of the protein. 13. A crystalline spherical protein particle wherein said protein is an antibody or a single-chain Fv fragment of said antibody, wherein said protein has greater than about 50% to about 100% of the biological activity of the native, soluble counterpart of the protein as determined by a bioimmunoassay. 14. The crystalline spherical protein particle according to claim 13, wherein said bioimmunoassay is a direct cytotoxicity bioimmunoassay. 15. The crystalline spherical protein particle according to claim 13, wherein said bioimmunoassay is a complement dependent cytotoxicity (CDC) bioimmunoassay. 16. The crystalline spherical protein particle according to claim 13, wherein said bioimmunoassay is an antibody-dependent cell-mediated cytotoxicity (ADCC) bioimmunoassay. 17. A crystalline spherical protein particle wherein said protein is an antibody or a single-chain Fv fragment of said antibody, wherein said antibody is a therapeutic antibody. 18. The crystalline spherical protein particle according to claim 17, wherein said antibody has a greater half life in vivo than the soluble counterpart of said antibody. 19. The crystalline spherical protein particle according to claim 17, wherein said antibody is a polyclonal antibody or a monoclonal antibody. 20. The crystalline spherical protein particle according to claim 17, wherein said antibody is selected from the group consisting of: Rituximab, Infliximab, Trastuzumab and Etanercept. 21. The crystalline spherical protein particle according to claim 17, wherein said antibody is selected from the group consisting of: Abciximab, Palivizumab, Murumonab-CD3, Gemtuzumab, Basiliximab, Daclizumab, and Zevalin. 22. The crystalline spherical protein particle according to claim 17, wherein said antibody is selected from the group consisting of: an antibody for treating cardiovascular disease, an antibody for treating respiratory disease, an antibody for treating tissue transplant rejection, an antibody for treating organ transplant rejection, an antibody for treating cancer, an antibody for treating inflammatory disease and an antibody used in radioimmunotherapy. 23. The crystalline spherical protein particle according to claim 17, wherein said crystalline spherical protein particle is a dried crystalline spherical protein particle. 24. The crystalline spherical protein particle according to claim 17, wherein said crystalline spherical protein particle is a carrier-free pharmaceutical controlled release crystalline spherical protein particle. 25. The crystalline spherical protein particle according to claim 17, wherein said antibody is selected from the group consisting of: a chimeric antibody, a humanized antibody, a non-glycosylated antibody, a bispecific antibody, a human antibody and a mouse antibody.

Details for Patent 7,998,477

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Janssen Biotech, Inc.	REOPRO	abciximab	Injection	103575	12/22/1994		2021-06-21
Genentech, Inc.	RITUXAN	rituximab	Injection	103705	11/26/1997		2021-06-21
Idec Pharmaceuticals Corp.	RITUXAN	rituximab	Injection	103737	02/19/2002		2021-06-21
Hoffmann-la Roche Inc.	ZENAPAX	daclizumab	Injection	103749	12/10/1997		2021-06-21
Novartis Pharmaceuticals Corporation	SIMULECT	basiliximab	For Injection	103764	05/12/1998		2021-06-21
Novartis Pharmaceuticals Corporation	SIMULECT	basiliximab	For Injection	103764	01/02/2003		2021-06-21