Claims for Patent: 10,545,135

Summary for Patent: 10,545,135

Title:	Compositions comprising human embryonic stem cells and their derivatives, methods of use, and methods of preparation
Abstract:	The present invention relates to a pharmaceutical composition comprising of preparations of human embryonic stem (hES) cells and their derivatives and methods for their transplantation into the human body, wherein transplantation results in the clinical reversal of symptoms, cure, stabilization or arrest of degeneration of a wide variety of presently incurable and terminal medical conditions, diseases and disorders. The invention further relates to novel processes of preparing novel stem cell lines which are free of animal products, feeder cells, growth factors, leukaemia inhibitory factor, supplementary mineral combinations, amino acid supplements, vitamin supplements, fibroblast growth factor, membrane associated steel factor, soluble steel factor and conditioned media. This invention further relates to the isolation, culture, maintenance, expansion, differentiation, storage, and preservation of such stem cells.
Inventor(s):	Shroff; Geeta (New Delhi, IN)
Assignee:
Application Number:	12/224,839
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 10,545,135
Patent Claims:	1. A pharmaceutical composition for the treatment of diseases, disorders, or conditions comprising a therapeutic effective amount of human embryonic stem (hES) cells, derivatives of hES cells, or combinations thereof, wherein said hES cells, derivatives of hES cells, or combinations thereof are free from feeder cells, animal products, growth factors, leukemia inhibiting factor, fibroblast growth factor, vitamin supplements, membrane associated steel factor, soluble steel factor, and conditioned media, wherein the hES cells, derivatives of hES cells, or combinations thereof do not give rise to teratomas upon administration, wherein said hES cells, derivatives of hES cells, or combinations thereof are suspended in a pharmaceutically acceptable biocompatible solution, wherein said derivatives of hES cells are selected from the group consisting of hematopoietic stem cell progenitors, neuronal stem cell progenitors, a combination of hematopoietic stem cell progenitors and neuronal stem cell progenitors, mesenchymal stem cell progenitors, insulin producing stem cell progenitors, hepatocytic stem cell progenitors, cardiac stem cell progenitors, and epithelial stem cell progenitors, and wherein the composition contains trace amounts of a progestin and a .beta.-human chorionic gonadotrophin (.beta.hCG) agonist. 2. The pharmaceutical composition of claim 1 wherein said composition is in a ready-to-use form. 3. The pharmaceutical composition of claim 2, wherein said ready-to-use form is a prefilled syringe. 4. The pharmaceutical composition of claim 2 wherein the stem cells have sufficient viability to be therapeutically effective. 5. The pharmaceutical composition of claim 4 wherein the viability of the stem cells is greater than 40%. 6. The pharmaceutical composition of claim 1 wherein said biocompatible solution is saline. 7. The pharmaceutical composition of claim 1 wherein said biocompatible solution further comprises an antimicrobial agent, antibacterial agent or other pharmaceutical agent. 8. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of hematopoietic stem cell progenitors and neuronal stem cell progenitors. 9. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of mesenchymal stem cell progenitors. 10. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of insulin producing stem cell progenitors. 11. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of hepatocytic stem cell progenitors. 12. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of cardiac stem cell progenitors. 13. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of epithelial stem cell progenitors. 14. The pharmaceutical composition of claim 1 wherein the therapeutically effective amount of hES cells, derivatives or hES cells, or combinations thereof is about 750,000 to about 160 million cells in about 0.25 ml to about 100 ml of the biocompatible solution. 15. The pharmaceutical composition of claim 1 wherein the therapeutically effective amount of hES cells, derivatives or hES cells, or combinations thereof is 750,000 to about 80 million cells in about 0.25 ml to about 10 ml of the biocompatible solution. 16. The pharmaceutical composition of claim 1 wherein the diseases, disorders or conditions are selected from the group consisting of cancer, stroke, genetic disorders, liver disorders, developmental disorders, degenerative disorders, familial disorders or traumatic disorders of the nervous system, vascular disorders, skin diseases and disorders, auto immune disorders, eye disorders, kidney disorders, cardiac disorders, musculoskeletal disorders, reproductive and fertility disorders, arthritis, and blood disorders. 17. The pharmaceutical composition of claim 1 wherein the diseases, disorders, or conditions are selected from the group consisting of Acute Myeloid Leukaemia, Adenocarcinoma, Arthritis, Astrocytoma, Auditory Nerve Atrophy, Autism, Auto Immune Disorders, Alzheimer's disease, Ankylosing Spondylitis, Becker's Muscular Dystrophy, Brain Damage, Burns, Cerebro Vascular Accident, Cerebral Palsy, Coma, Corneal Ulcers, Corneal Graft Rejection, Cortico-Basal Degeneration of the Nervous System, Coronary Artery Disease, Diabetes, Dementia, Downs Syndrome, Duchenne's Muscular Dystrophy, End-Stage Renal Disease, Erb's Palsy, Fascio Scapular Muscular Dystrophy, Fertility Disorders, Friedereich's Ataxia, Heart Failure, Hepato Cellular Carcinoma, Hereditary Spino Motor Neuron Disease, Huntington's Chorea, Krabbe's Disease, Limb Girdle Dystrophy, Liver Cirrhosis, Macular Degeneration, Mental Retardation, Multiple Sclerosis, Motor Neuron Disease, Myocardial Infarction, Nephrotic Syndrome, Niemann Pick Disease, Non-Healing Ulceration of the Skin, Olivo-Ponto Cerebellar Atrophy, Optic Nerve Atrophy, Parkinson's Disease, Post Electric Shock Encephalopathy, Post-Rabies Vaccine Encephalopathy, Pressure Sores, Progressive Supranuclear Palsy, Psoriasis, Pthysis Bulbi, Restrictive Cardiomyopathy, Retinitis Pigmentosa, Right Bundle Branch Block, Sarcoidosis, Sinus Bradycardia, Spinal Cord Tumour, Spinal Muscular Dystrophy, Spino Cerebellar Ataxia, Steven Johnson's Syndrome, Systemic Lupus Erythematosus, Thrombocytopenia, Thalassemia, Ulcerative Colitis, Vegetative State, Cystic Fibrosis, Interstitial Lung Disease, Azoospermia, Primary Ovarian Failure, Aphthous Ulcers, Hormone Imbalance, Osteo-Arthritis, Homer's Syndrome, Osteogenic Imperfecta, Channelopathy, and Hypogammaglobulinemia. 18. The pharmaceutical composition of claim 1, wherein the pharmaceutical composition comprises combinations of hES cells and derivatives of hES cells. 19. The pharmaceutical composition of claim 1, wherein the total population of (hES) cells, derivatives of hES cells, or combinations thereof contains no more than 40% undifferentiated stem cells. 20. The composition of claim 19, wherein the hES cells and derivatives of hES cells were obtained by expanding in a cell culture medium consisting of minimal essential medium, a progestin, and a .beta.hCG agonist. 21. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of hematopoietic stem cell progenitors. 22. The pharmaceutical composition of claim 21 wherein the therapeutically effective amount of hematopoietic stem cell progenitors in the composition is about 750,000 to about 160 million cells. 23. The pharmaceutical composition of claim 1 wherein the composition comprises a therapeutically effective amount of neuronal stem cell progenitors. 24. The pharmaceutical composition of claim 23 wherein the therapeutically effective amount of neuronal stem cells in the composition is about 750,000 to about 160 million cells. 25. A composition of matter comprising hES cells, derivatives of hES cells, or combinations thereof, wherein said hES cells, derivatives of hES cells, or combinations thereof are free from feeder cells, animal products, growth factors, leukemia inhibiting factor, fibroblast growth factor, vitamin supplements, membrane associated steel factor, soluble steel factor, and conditioned media, wherein the hES cells, derivatives of hES cells, or combinations thereof do not give rise to teratomas upon administration, wherein said hES cells, derivatives of hES cells, or combinations thereof are entrapped in a biocompatible structure or matrix, wherein the biocompatible structure or matrix is selectively permeable, wherein said hES cell derivatives are selected from the group consisting of hematopoietic stem cell progenitors, neuronal stem cell progenitors, a combination of hematopoietic stem cell progenitors and neuronal stem cell progenitors, mesenchymal stem cell progenitors, insulin producing stem cell progenitors, hepatocytic stem cell progenitors, cardiac stem cell progenitors, and epithelial stem cell progenitors, and wherein the composition contains trace amounts of a progestin and a .beta.-human chorionic gonadotrophin (.beta.hCG) agonist. 26. The composition of matter of claim 25 wherein the hES cells, derivatives of hES cells, or combinations thereof comprise hematopoietic stem cell progenitors. 27. The composition of matter of claim 25, wherein the hES cells, derivatives of hES cells, or combinations thereof comprise neuronal stem cell progenitors. 28. The composition of matter of claim 25, wherein the hES cells, derivatives of hES cells, or combinations thereof comprise a combination of hematopoietic stem cells and neuronal stem cell progenitors. 29. The composition of matter of claim 25, wherein the biocompatible, selectively permeable structure or matrix is selected from the group consisting of biopolymers, polypeptides, proteins, polysaccharides, fibronectin, collagen, laminin, keratin, fibrin, fibrinogen, hyaluronic acid, heparin sulfate, chondroitin sulfate, agarose, and gelatin. 30. The composition of matter of claim 25, wherein the hES cells, derivatives of hES cells, or combinations thereof are entrapped in a mixture of agarose and collagen or a mixture of agarose and gelatin. 31. The composition of claim 25, wherein the composition comprises combinations of hES cells and derivatives of hES cells. 32. The composition of claim 25, wherein the total population of (hES) cells, derivatives of hES cells, or combinations thereof contains no more than 40% undifferentiated stem cells. 33. The composition of claim 32, wherein the hES cells and derivatives of hES cells were obtained by expanding in a cell culture medium consisting of minimal essential medium, a progestin, and a .beta.hCG agonist.

Details for Patent 10,545,135

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Bavarian Nordic A/s	RABAVERT	rabies vaccine	For Injection	103334	10/20/1997		2026-03-07
Sanofi Pasteur Sa	IMOVAX RABIES	rabies vaccine	For Injection	103931	02/04/2000		2026-03-07