Claims for Patent: 8,282,966

Summary for Patent: 8,282,966

Title:	Methods of reducing the risk of occurrence of pulmonary edema in children in need of treatment with inhaled nitric oxide
Abstract:	The invention relates methods of reducing the risk or preventing the occurrence of an adverse event (AE) or a serious adverse event (SAE) associated with a medical treatment comprising inhalation of nitric oxide.
Inventor(s):	Baldassarre; James S. (Doylestown, PA), Rosskamp; Ralf (Chester, NJ)
Assignee:	INO Therapeutics LLC (Hampton, NJ)
Application Number:	12/821,020
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 8,282,966
Patent Claims:	1. A method of reducing the risk of occurrence of pulmonary edema associated with a medical treatment comprising inhalation of 20 ppm nitric oxide gas, said method comprising: (a) performing echocardiography to identify a child in need of 20 ppm inhaled nitric oxide treatment for pulmonary hypertension, wherein the child is not dependent on right-to-left shunting of blood; (b) determining that the child identified in (a) has a pulmonary capillary wedge pressure greater than or equal to 20 mm Hg and thus has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide; and (c) excluding the child from inhaled nitric oxide treatment based on the determination that the child has left ventricular dysfunction and so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide. 2. The method of claim 1, wherein the child is a neonate. 3. The method of claim 1, wherein step (b) comprises measuring the child's pulmonary capillary wedge pressure. 4. The method of claim 1, wherein the child's left ventricular dysfunction is attributable to congenital heart disease. 5. The method of claim 1, wherein the child is determined to be at particular risk not only of pulmonary edema, but also of other Serious Adverse Events, upon treatment with inhaled nitric oxide, and the child is excluded from inhaled nitric oxide treatment based on the determination that the child has left ventricular dysfunction and so is at particular risk not only of pulmonary edema, but also of other Serious Adverse Events, upon treatment with inhaled nitric oxide. 6. A method of reducing the risk of occurrence of pulmonary edema associated with a medical treatment comprising inhalation of 20 ppm nitric oxide gas, said method comprising: (a) carrying out a diagnostic process comprising measuring blood oxygen level, to identify a child as being in need of 20 ppm inhaled nitric oxide treatment for hypoxic respiratory failure, wherein the child is not dependent on right-to-left shunting of blood; (b) determine determining that the child has a pulmonary capillary wedge pressure greater than or equal to 20 mm Hg and thus has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide; and (c) excluding the child from treatment with inhaled nitric oxide based on the determination that the child has left ventricular dysfunction and so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide. 7. The method of claim 6, wherein the diagnostic process of step (a) further comprises performing echocardiography. 8. The method of claim 6, wherein the child is a neonate. 9. The method of claim 6, wherein step (b) comprises measuring the child's pulmonary capillary wedge pressure. 10. The method of claim 6, wherein the left ventricular dysfunction is attributable to congenital heart disease. 11. The method of claim 6, wherein the child is determined to be at particular risk not only of pulmonary edema, but also of other Serious Adverse Events, upon treatment with inhaled nitric oxide, and the child is excluded from inhaled nitric oxide treatment based on the determination that the child has left ventricular dysfunction and so is at particular risk not only of pulmonary edema, but also other Serious Adverse Events, upon treatment with inhaled nitric oxide. 12. The method of claim 11, wherein the left ventricular dysfunction is attributable to congenital heart disease. 13. A method of treatment comprising: (a) performing echocardiography to identify a plurality of children who are in need of 20 ppm inhaled nitric oxide treatment for pulmonary hypertension, wherein the children are not dependent on right-to-left shunting of blood; (b) determining that a first child of the plurality has a pulmonary capillary wedge pressure greater than or equal to 20 mm Hg and thus has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide; (c) determining that a second child of the plurality does not have left ventricular dysfunction; (d) administering the 20 ppm inhaled nitric oxide treatment to the second child; and (e) excluding the first child from treatment with inhaled nitric oxide, based on the determination that the first child has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide. 14. The method of claim 13, wherein step (a) further comprises measuring blood oxygen levels in the first and second children and thereby determining that the first and second children are hypoxic. 15. The method of claim 13, wherein the second child has congenital heart disease. 16. The method of claim 13, wherein step (b) comprises measuring the first child's pulmonary capillary wedge pressure. 17. The method of claim 13, wherein determining that the second child of the plurality does not have pre-existing left ventricular dysfunction comprises performing echocardiography. 18. The method of claim 13, wherein the left ventricular dysfunction is attributable to congenital heart disease. 19. The method of claim 13, wherein the left ventricular dysfunction of the first child is attributable to congenital heart disease. 20. The method of claim 13, wherein the first child is determined to be at particular risk not only of pulmonary edema, but also of other Serious Adverse Events, upon treatment with inhaled nitric oxide, and the first child is excluded from inhaled nitric oxide treatment based on the determination that the first child has left ventricular dysfunction and so is at particular risk not only of pulmonary edema, but also other Serious Adverse Events, upon treatment with inhaled nitric oxide. 21. The method of claim 20, wherein the pre-existing left ventricular dysfunction of the first child is attributable to congenital heart disease. 22. A method of treatment comprising: (a) identifying a plurality of children who are in need of 20 ppm inhaled nitric oxide treatment, wherein the children are not dependent on right-to-left shunting of blood; (b) in the first child of the plurality, measuring pulmonary capillary wedge pressure to determine that the first child of the plurality has a pulmonary capillary wedge pressure greater than or equal to 20 mm Hg and thus has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide; (c) in the second child of the plurality, performing echocardiography and/or measurement of pulmonary capillary wedge pressure to determine that the second child of the plurality does not have left ventricular dysfunction; (d) administering the 20 ppm inhaled nitric oxide treatment to the second child; and (e) excluding the first child from treatment with inhaled nitric oxide, based on the determination that the first child has left ventricular dysfunction, so is at particular risk of pulmonary edema upon treatment with inhaled nitric oxide. 23. The method of claim 22, wherein step (a) comprises performing echocardiography to determine that the first and second children have pulmonary hypertension. 24. The method of claim 22, wherein step (a) comprises measuring blood oxygen levels in the first and second children and thereby determining that the first and second children are hypoxic. 25. The method of claim 22, wherein the second child has congenital heart disease. 26. The method of claim 22, wherein the left ventricular dysfunction is attributable to congenital heart disease. 27. The method of claim 22, wherein the pre-existing left ventricular dysfunction of the first child is attributable to congenital heart disease. 28. The method of claim 22, wherein the first child is determined to be at particular risk not only of pulmonary edema, but also of other Serious Adverse Events, upon treatment with inhaled nitric oxide, and the first child is excluded from inhaled nitric oxide treatment based on the determination that the first child has pre-existing left ventricular dysfunction and so is at particular risk not only of pulmonary edema, but also other Serious Adverse Events, upon treatment with inhaled nitric oxide. 29. The method of claim 28, wherein the pre-existing left ventricular dysfunction of the first child is attributable to congenital heart disease.