Methods for treating mucopolysaccharidosis
US-2024374534-A1 · Nov 14, 2024 · US
US12558365B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12558365-B2 |
| Application number | US-202017438712-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 12, 2020 |
| Priority date | Mar 13, 2019 |
| Publication date | Feb 24, 2026 |
| Grant date | Feb 24, 2026 |
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The invention provides methods for treating and preventing acute coronary syndromes (ACS). The methods involve initiation of the administration of glucose-insulin-potassium (GIK) soon (e.g., within 3 hours) after the onset of ACS symptoms.
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The invention claimed is: 1 . A method of treating, inhibiting, or preventing acute coronary syndromes (ACS) in a patient, the method comprising initiating the administration of a solution of glucose-insulin-potassium (GIK) to the patient within one hour or less of ACS symptom onset. 2 . The method of claim 1 , further comprising assessment by emergency medical service personnel. 3 . The method of claim 1 , wherein the administration of GIK is initiated upon assessment in (a) the emergency department (ED), (b) the hospital upon cardiac arrest, (c) a medical office setting, or (d) under the care of paramedics in the community. 4 . The method of claim 1 , wherein the patient has or is at risk of developing one or more ACS symptom selected from the group consisting of: chest pain, angina, radiating pain from the chest to the shoulders, arms, upper abdomen, back, neck, or jaw; nausea or vomiting; indigestion; shortness of breath; heavy sweating; lightheadedness; dizziness; fainting; unusual or unexplained fatigue; and feeling restless or apprehensive. 5 . The method of claim 1 , wherein the patient experiences an improvement in progression to myocardial infarction, 30-day survival, in-hospital mortality, or cardiac arrest due to the GIK treatment. 6 . The method of claim 1 , wherein the patient experiences a significant clinical improvement, or a group of patients experiences a statistically significant improvement, with respect to 30-day survival, 30-day heart failure, or in-hospital cardiac arrest. 7 . The method of claim 1 , wherein the patient is further treated with aspirin, P2Y 12 receptor antagonist, anticoagulant, beta blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blocker, fibrinolytic agent, statin, morphine, nitroglycerin, oxygen, interventional angioplasty, surgery or any combination thereof. 8 . The method of claim 1 , wherein the GIK comprises 25-35% glucose, 45-55 U/l regular insulin, and 70-90 mEq potassium chloride per liter. 9 . The method of claim 8 , wherein the GIK comprises 30% glucose, 50 U/l regular insulin, and 80 mEq of potassium chloride per liter. 10 . The method of claim 1 , wherein the GIK is administered at a speed of 1 to 2 ml/kg/hour for 10-14 hours. 11 . The method of claim 10 , wherein the GIK is administered at a speed of 1.5 ml/kg/hour for 12 hours. 12 . A method of treating, inhibiting, or preventing acute coronary syndromes (ACS) in a patient, the method comprising initiating the administration of a solution of glucose-insulin-potassium (GIK) to the patient within 3 to 6 hours of ACS symptom onset. 13 . The method of claim 12 , further comprising assessment by emergency medical service personnel. 14 . The method of claim 12 , wherein the administration of GIK is initiated upon assessment in (a) the emergency department (ED), (b) the hospital upon cardiac arrest, (c) a medical office setting, or (d) under the care of paramedics in the community. 15 . The method of claim 12 , wherein the patient has or is at risk of developing one or more ACS symptom selected from the group consisting of: chest pain, angina, radiating pain from the chest to the shoulders, arms, upper abdomen, back, neck, or jaw; nausea or vomiting; indigestion; shortness of breath; heavy sweating; lightheadedness; dizziness; fainting; unusual or unexplained fatigue; and feeling restless or apprehensive. 16 . The method of claim 12 , wherein the patient experiences an improvement in progression to myocardial infarction, 30-day survival, in-hospital mortality, or cardiac arrest due to the GIK treatment. 17 . The method of claim 12 , wherein the patient experiences a significant clinical improvement, or a group of patients experiences a statistically significant improvement, with respect to 30-day survival, 30-day heart failure, or in-hospital cardiac arrest. 18 . The method of claim 12 , wherein the patient is further treated with aspirin, P2Y 12 receptor antagonist, anticoagulant, beta blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blocker, fibrinolytic agent, statin, morphine, nitroglycerin, oxygen, interventional angioplasty, surgery or any combination thereof. 19 . The method of claim 12 , wherein the GIK comprises 25-35% glucose, 45-55 U/l regular insulin, and 70-90 mEq potassium chloride per liter. 20 . The method of claim 19 , wherein the GIK comprises 30% glucose, 50 U/l regular insulin, and 80 m Eq of potassium chloride per liter. 21 . The method of claim 12 , wherein the GIK is administered at a speed of 1 to 2 ml/kg/hour for 10-14 hours. 22 . The method of claim 21 , wherein the GIK is administered at a speed of 1.5 ml/kg/hour for 12 hours.
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