Claims for Patent: 6,743,590

Summary for Patent: 6,743,590

Title:	Methods for differentiating and monitoring parathyroid and bone status related diseases
Abstract:	The present invention relates to novel methods and devices for differentiating in a patient parathyroid diseases, such as hyperparathyroidism and related bone diseases, from normal or non-disease states. One detects whole or non-fragmented (1 to 84) parathyroid hormone in a biological sample and also a large non-whole parathyroid hormone peptide fragment that can function as a parathyroid hormone antagonist. By either comparing values or using independently the value of either the large non-whole parathyroid hormone peptide fragment, the whole parathyroid hormone, or the combination of these values one is able to differentiate parathyroid and bone related disease states, as well as differentiate such states from normal states.
Inventor(s):	Cantor; Thomas L. (El Cajon, CA), Gao; Ping (San Diego, CA)
Assignee:	Scantibodies Laboratory, Inc. (Santee, CA)
Application Number:	09/344,639
Patent Claims:	1. A method for differentiating between a person having substantially normal parathyroid function and having hyperparathyroidism comprising: a) obtaining a sample from a person to be tested; b) determining whole parathyroid hormone level in said sample using an antibody or an antibody fragment that distinguishes whole parathyroid hormone from a parathyroid hormone inhibitory peptide fragment, said antibody or antibody fragment being specific for the parathyroid hormone peptide SER-VAL-SER-GLU-ILE-GLN-LEU-MET (SEQ ID No:4), wherein at least four amino acids in said peptide sequence are part of a reactive portion with said antibody, determining total parathyroid hormone level in said sample and determining parathyroid hormone inhibitory peptide fragment level by subtracting said whole parathyroid hormone level from said total parathyroid hormone level; and c) comparing at least two parameters selected from the group consisting of said whole parathyroid hormone level, parathyroid hormone inhibitory peptide fragment level, and total parathyroid hormone level, thereby determining whetber said person has substantially normal parathyroid function or has hyperparathyroidism. 2. The method of claim 1, wherein the sample is selected from the group consisting of a serum, a plasma and a blood sample. 3. The method of claim 1, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level. 4. The method of claim 1, wherein the whole parathyroid hormone level is compared with the total parathyroid hormone level. 5. The method of claim 1, wherein the parathyroid hormone inhibitory peptide fragment level is compared with the total parathyroid hormone level. 6. The method of claim 1, wherein the comparison is in the form of a ratio or proportion. 7. The method of claim 1, wherein the antibody is a goat anti-(1-6) parathyroid hormone antibody. 8. The method of claim 7, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level. 9. The method of claim 1, wherein the parathyroid hormone inhibitory peptide fragment is a peptide having an amino acid sequence from between PTH.sub.3-84 (SEQ ID NO:2) and PTH.sub.34-84 (SEQ ID NO:3) and functions in vivo as a parathyroid hormone antagonist or inhibitor (PIN). 10. The method of claim 1, wherein the parathyroid hormone inhibitory peptide fragment is a peptide having an amino acid sequence of human PTH.sub.7-84 (SEQ ID No:6). 11. The method of claim 1, wherein the hyperparathyroidism is primary hyperparathyroidism. 12. The method of claim 1, wherein the hyperparathyroidism is secondary hyperparathyroidism. 13. The method of claim 1, wherein the hyperparathyroidism is caused by chronic renal failure. 14. A method for monitoring parathyroid related bone disease and treatment comprising: a) obtaining a sample from a person to be monitored; b) determining whole parathyroid hormone level using an antibody or an antibody fragment that distinguishes whole parathyroid hormone from a parathyroid hormone inhibitory peptide fragment, said antibody or antibody fragment being specific for the parathyroid hormone peptide SER VAL-SER-GLU-ILE-GLN-LEU-MET (SEQ ID NO:4), wherein at least four amino acids in said peptide sequence are part of a reactive portion with said antibody, determining total parathyroid hormone level in said sample and determining parathyroid hormone inhibitory peptide fragment level by subtracting said whole parathyroid hormone level from said total parathyroid hormone level; and c) comparing at least two parameter selected from the group consisting of said whole parathyroid hormone level, parathyroid hormone inhibitory peptide fragment level, and total parathyroid hormone level, thereby monitoring parathyroid related bone disease and treatment in said person. 15. The method of claim 14, wherein the comparison is in the form of a ratio or proportion. 16. The method of claim 14, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level. 17. The method of claim 14, wherein the parathyroid related bone disease is renal osteodystrophy. 18. The method of claim 17, wherein the renal osteodystrophy is selected from the group consisting of osteitis fibrosa, cystica, osteomalacia, extraskeletal calcification/ossification and an adynamic low bone turnover disease. 19. The method of claim 17, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level to monitor renal osteodystrophy and its event. 20. A method for monitoring effects of therapeutic treatment for hyperparathroidiem comprising: a) obtaining a sample from a person to be monitored; b) determining whole parathyroid hormone level using an antibody or an antibody fragment that distinguishes whole parathyroid hormone from a parathyroid hormone inhibitory peptide fragment, said antibody or antibody fragment being specific for the parathyroid hormone peptide SER-VAL-SER-GLU-ILE-GLN-LEU-MET (SEQ ID NO:4), wherein at least four amino acids in said peptide sequence are part of a reactive portion with said antibody, determine total parathyroid hormone level in said sample and determining parathyroid hormone inhibitory peptide fragment level by subtracting said whole parathyroid hormone level from said total parathyroid hormone level; and c) comparing at least two parathyroid selected from the group consisting of said whole parathyroid hormone level, parathyroid hormone inhibitory peptide fragment level, and total parathyroid hormone level, thereby monitoring effects of the therapeutic treatament for hyperparathyroidism in said person. 21. The method of claim 20, wherein the comparison is in the form of a ratio or proportion. 22. The method of claim 20, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level. 23. The method of claim 20, wherein the therapeutic treatment for hyperparathyroidism is vitamin D or vitamin D analogues treatment, calcium treatment, or parathyroidectomy. 24. The method of claim 23, wherein the whole parathyroid hormone level is compared with the parathyroid hormone inhibitory peptide fragment level to monitor the effects of vitamin D or vitamin D analogues treatment, calcium treatment, or parathyroidectemy. 25. The method of claim 23, wherein the hyperparathyroidism is selected from the group consisting of primary hyperparathyroidism, secondary hyperparathyroidism, renal bone disease, renal osteodystrophy, osteitis fibrosa, cystica, osteomalacia, extraskeletal calcification/ossification and an adynamic low bone turnover disease. 26. The method of claim 14, wherein the parathyroid hormone inhibitory peptide fragment is a peptide having an amino acid sequence of human PTH.sub.7-84 (SEQ. ID. No. 6). 27. The method of claim 20, wherein the parathyroid hormone inhibitory peptidc fragment is a peptide having an amino acid sequence of human PTH.sub.7-84 (SEQ. ID. No. 6).

Details for Patent 6,743,590

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Nps Pharmaceuticals, Inc.	NATPARA	parathyroid hormone	For Injection	125511	01/23/2015		2019-01-14