US2017065589A1PendingUtilityA1

Methods of treating or preventing preterm labor

Individually held — no corporate assignee on recordPriority: May 6, 2014Filed: May 6, 2015Published: Mar 9, 2017
Est. expiryMay 6, 2034(~7.8 yrs left)· nominal 20-yr term from priority
Inventors:Anthony Visco
A61P 15/06A61K 31/137A61K 31/36A61K 31/4025A61K 31/445A61K 31/4525A61K 31/145A61K 31/222A61K 31/4725A61K 31/216A61K 31/196A61K 31/439A61K 31/4439A61K 31/4465A61K 31/215A61K 31/517A61K 31/135A61K 31/357A61K 31/46A61K 31/426A61N 7/00A61N 5/0619A61N 2/00
50
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Claims

Abstract

Described herein are methods for treating preterm labor, stopping labor prior to Cesarean delivery, preventing preterm labor, or controlling the timing of parturition by administering a chemical compound, such as a muscarinic receptor antagonist preferably a M, receptor antagonist, or a β-3 adrenergic agonist. Also described are methods for treating preterm labor, stopping labor preparatory to Cesarean delivers', preventing preterm labor, or controlling the timing of parturition by administering an effective amount of transdermal stimulation, posterior tibial nerve stimulation or another form of non-invasive or invasive neuromodulatton, unstimulated or stimulated acupuncture, magnetic field therapy, or vibratory stimulation. These methods may be practiced individually, in combination with each other, or in combination with known tocolytic methods or medications.

Claims

exact text as granted — not AI-modified
1 . A method for treating preterm labor, stopping labor preparatory to Cesarean delivery, preventing preterm labor, or controlling the timing of parturition comprising the step of:
 administering to a patient in need thereof an effective amount of a muscarinic antagonist.   
     
     
         2 . The method of  claim 1 , wherein the muscarinic antagonist has high selectivity for the M 3  receptor compared with the M 2  receptor. 
     
     
         3 . The method of  claim 1 , wherein the muscarinic antagonist has high affinity for the M 3  receptor. 
     
     
         4 . The method of  claim 1 , wherein the muscarinic antagonist is selected from the group consisting of (3R,2′R)-1-azabicyclo[2.2.2]octan-8-yl 2-cyclopentyl-2-hydroxy-2-phenylethanoate, ((3R)-1-[2-(1-,3-benzodioxol-5-yl)ethyl]-3-(diphenylmethoxy)piperidine, (aR)-a-cyclopentyl-a-hydroxy-N-[1-(4-methyl-3-pentenyl)-4-piperidinyl]benzeneacetamide, darifenacin, dicycloverine, a 1,1-dimethyl-4-diphenylacetoxypiperidinium salt, fesoterodine, 5-hydroxymethyltolterodine, hyoscyamine, ipratropium, 8-methyl-8-azabicyclo-3-enclo[1.2.3]oct-3-yl-1,4-dihydro-2-oxo-3(2H)-quinazolinecarboxylic acid ester, oxybutynin, propiverine, solifenacin, temiverine, a tiotropium salt, and trospium. 
     
     
         5 . A method for treating preterm labor, stopping labor preparatory to Cesarean delivery, preventing preterm labor, or controlling the timing of parturition comprising the step of:
 administering to a patient in need thereof an effective amount of a β-3 adrenergic agonist.   
     
     
         6 . The method of  claim 5 , wherein the β-3 adrenergic agonist has high selectivity for the β-3 adrenergic receptor compared with the β-2 adrenergic receptor. 
     
     
         7 . The method of  claim 5 , wherein the β-3 adrenergic agonist has high affinity for the β-3 adrenergic receptor. 
     
     
         8 . The method of  claim 5 , wherein the β-3 adrenergic agonist is selected from the group consisting of:
 amibegron, CL-316,243, L-742,791, L-796,568, LY-368,842, mirabegron, Ro40-2148, and solabegron. 
 
     
     
         9 . A method for treating preterm labor, stopping labor preparatory to Cesarean delivery, preventing preterm labor, or controlling the timing of parturition comprising the step of:
 administering to a patient in need thereof an effective amount of transdermal stimulation, posterior tibial nerve stimulation or another form of non-invasive or invasive neuromodulation, unstimulated or stimulated acupuncture, magnetic field therapy, or vibratory stimulation.   
     
     
         10 . The method of  claim 1 , wherein labor, delivery, or parturition is delayed or prevented for at least about 2 days. 
     
     
         11 . The method of  claim 1 , wherein the patient in need thereof is
 a woman pregnant with a fetus at less than 40 weeks gestational ager   a woman pregnant with a fetus weighing less than about 2500 g;   a pregnant woman whose cervix is dilated less than about 4 cm;   a woman pregnant with a fetus who is not suffering from fetal distress;   a pregnant woman who smokes cigarettes, or smoked cigarettes prior to conception;   a pregnant woman who was overweight or obese prior to conception, or was underweight prior to conception;   a pregnant woman with limited access to prenatal care;   a pregnant woman who drinks alcohol during her pregnancy, or uses illegal drugs during her pregnancy;   a pregnant woman also suffering from high blood pressure, preeclampsia, diabetes, a blood clotting disorder, placenta previa, placental abruption, cervical insufficiency, or an infection;   a pregnant woman who has undergone surgical fetal intervention;   a pregnant woman who will undergo surgical fetal intervention;   a pregnant woman who is under 17 years of age;   a pregnant woman who is over 35 years of age;   a pregnant woman who is African American;   a pregnant woman who suffered from vaginal bleeding during the first or second trimester of her pregnancy;   a pregnant woman who suffered from anemia during the first or second trimester of her pregnancy;   a pregnant woman who suffers from stress;   a pregnant woman who suffers from polyhydramnios;   a pregnant woman who conceived via in vitro fertilization;   a pregnant woman who is pregnant with twins or other multiples;   a pregnant woman who has a family history or a personal history of premature labor;   a pregnant woman who conceived less than 14 months after giving birth to a previous child; or   a pregnant woman who is not also suffering from urinary incontinence.   
     
     
         12 - 34 . (canceled) 
     
     
         35 . The method of  claim 5 , wherein labor, delivery, or parturition is delayed or prevented for at least about 2 days. 
     
     
         36 . The method of  claim 5 , wherein the patient in need thereof is
 a woman pregnant with a fetus at less than 40 weeks gestational age;   a woman pregnant with a fetus weighing less than about 2500 g;   a pregnant woman whose cervix is dilated less than about 4 cm;   a woman pregnant with a fetus who is not suffering from fetal distress;   a pregnant woman who smokes cigarettes, or smoked cigarettes prior to conception;   a pregnant woman who was overweight or obese prior to conception, or was underweight prior to conception;   a pregnant woman with limited access to prenatal care;   a pregnant woman who drinks alcohol during her pregnancy, or uses illegal drugs during her pregnancy;   a pregnant woman also suffering from high blood pressure, preeclampsia, diabetes, a blood clotting disorder, placenta previa, placental abruption, cervical insufficiency, or an infection;   a pregnant woman who has undergone surgical fetal intervention;   a pregnant woman who will undergo surgical fetal intervention;   a pregnant woman who is under 17 years of age;   a pregnant woman who is over 35 years of age;   a pregnant woman who is African American;   a pregnant woman who suffered from vaginal bleeding during the first or second trimester of her pregnancy;   a pregnant woman who suffered from anemia during the first or second trimester of her pregnancy;   a pregnant woman who suffers from stress;   a pregnant woman who suffers from polyhydramnios;   a pregnant woman who conceived via in vitro fertilization;   a pregnant woman who is pregnant with twins or other multiples;   a pregnant woman who has a family history or a personal history of premature labor;   a pregnant woman who conceived less than 14 months after giving birth to a previous child; or   a pregnant woman who is not also suffering from urinary incontinence.   
     
     
         37 . The method of  claim 9 , wherein labor, delivery, or parturition is delayed or prevented for at least about 2 days. 
     
     
         38 . The method of  claim 9 , wherein the patient in need thereof is
 a woman pregnant with a fetus at less than 40 weeks gestational age;   a woman pregnant with a fetus weighing less than about 2500 g;   a pregnant woman whose cervix is dilated less than about 4 cm;   a woman pregnant with a fetus who is not suffering from fetal distress;   a pregnant woman who smokes cigarettes, or smoked cigarettes prior to conception;   a pregnant woman who was overweight or obese prior to conception, or was underweight prior to conception;   a pregnant woman with limited access to prenatal care;   a pregnant woman who drinks alcohol during her pregnancy, or uses illegal drugs during her pregnancy;   a pregnant woman also suffering from high blood pressure, preeclampsia, diabetes, a blood clotting disorder, placenta previa, placental abruption, cervical insufficiency, or an infection;   a pregnant woman who has undergone surgical fetal intervention;   a pregnant woman who will undergo surgical fetal intervention;   a pregnant woman who is under 17 years of age;   a pregnant woman who is over 35 years of age;   a pregnant woman who is African American;   a pregnant woman who suffered from vaginal bleeding during the first or second trimester of her pregnancy;   a pregnant woman who suffered from anemia during the first or second trimester of her pregnancy;   a pregnant woman who suffers from stress;   a pregnant woman who suffers from polyhydramnios;   a pregnant woman who conceived via in vitro fertilization;   a pregnant woman who is pregnant with twins or other multiples;   a pregnant woman who has a family history or a personal history of premature labor;   a pregnant woman who conceived less than 14 months after giving birth to a previous child; or   a pregnant woman who is not also suffering from urinary incontinence.

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