Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
  • A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
  • A61K31/216—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acids having aromatic rings, e.g. benactizyne, clofibrate
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
  • A61P11/16—Central respiratory analeptics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

• the present invention provides pharmaceutical compositions comprising reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA) and methods of treating sleep apnea comprising administering reboxetine or a pharmaceutically acceptable salt thereof and an MRA.
• MRA muscarinic receptor antagonist
• OSA Obstructive Sleep Apnea
• One aspect of the present invention provides a method of treating a subject having a condition associated with pharyngeal airway collapse, the method comprising administering to a subject in need thereof an effective amount of (i) reboxetine or a pharmaceutically acceptable salt thereof and (ii) a muscarinic receptor antagonist (MRA).
• MRA muscarinic receptor antagonist
• Embodiments of this aspect of the invention may include one or more of the following optional features.
• the reboxetine or pharmaceutically acceptable salt thereof is administered at a dosage of from about 1 mg to about 8 mg.
• the reboxetine or pharmaceutically acceptable salt thereof is administered at a dosage of from about 2 mg to about 6 mg.
• the MRA and reboxetine are each administered daily.
• the MRA and reboxetine are administered in a single composition.
• single composition is an oral administration form.
• the oral administration form is a syrup, pill, tablet, troche, capsule, or patch.
• the MRA is selected from the group consisting of atropine, propantheline, bethanechol, solifenacin, darifenacin, tolterodine, fesoterodine, trospium, and oxybutynin, or or a pharmaceutically acceptable salt thereof.
• the MRA is selected from the group consisting of anisotropine, benztropine, biperiden, clidinium, cycrimine, dicyclomine, diphemanil, diphenidol, ethopropazine, glycopyrrolate, hexocyclium, isopropamide, mepenzolate, methixene, methscopolamine, oxyphencyclimine, oxyphenonium, procyclidine, scopolamine, tridihexethyl, and trihexyphenidyl, or a pharmaceutically acceptable salt thereof.
• the MRA is oxybutynin or a pharmaceutically acceptable salt thereof.
• the oxybutynin or pharmaceutically acceptable salt thereof is administered at a dosage of from about 1 mg to about 25 mg. In some embodiments, the oxybutynin or pharmaceutically acceptable salt thereof is administered at a dosage of from about 2 mg to about 15 mg.
• the MRA is (R)-oxybutynin or a pharmaceutically acceptable salt thereof. In some embodiments, the (R)-oxybutynin or pharmaceutically acceptable salt thereof is administered at a dosage of from about 1 mg to about 25 mg. In some embodiments, the (R)-oxybutynin or pharmaceutically acceptable salt thereof is administered at a dosage of from about 2 mg to about 15 mg. In some embodiments, the MRA is fesoterodine.
• the reboxetine or pharmaceutically acceptable salt thereof is (S,S)-reboxetine or a pharmaceutically acceptable salt thereof.
• the MRA is administered daily.
• the condition associated with pharyngeal airway collapse is sleep apnea, e.g., obstructive sleep apnea (OSA).
• the condition associated with pharyngeal airway collapse is snoring, e.g., simple snoring.
• the subject is in a non-fully conscious state. In some embodiments, the non-fully conscious state is sleep.
• Another aspect of the invention provides a pharmaceutical composition
• a pharmaceutical composition comprising (i) reboxetine or a pharmaceutically acceptable salt thereof and (ii) a muscarinic receptor antagonist (MRA), and (iii) a pharmaceutically acceptable carrier.
• MRA muscarinic receptor antagonist
• Embodiments of this aspect of the invention may include one or more of the following optional features.
• the reboxetine or pharmaceutically acceptable salt thereof is present in an amount of from about 1 mg to about 8 mg. In some embodiments, the reboxetine or pharmaceutically acceptable salt thereof is present in an amount of from about 2 mg to about 6 mg.
• the MRA is selected from the group consisting of atropine, propantheline, bethanechol, solifenacin, darifenacin, tolterodine, fesoterodine, trospium, and oxybutynin, or or a pharmaceutically acceptable salt thereof.
• the MRA is selected from the group consisting of anisotropine, benztropine, biperiden, clidinium, cycrimine, dicyclomine, diphemanil, diphenidol, ethopropazine, glycopyrrolate, hexocyclium, isopropamide, mepenzolate, methixene, methscopolamine, oxyphencyclimine, oxyphenonium, procyclidine, scopolamine, tridihexethyl, and trihexyphenidyl, or a pharmaceutically acceptable salt thereof.
• the MRA is oxybutynin or a pharmaceutically acceptable salt thereof.
• the oxybutynin or pharmaceutically acceptable salt thereof is present in amount of from about 1 mg to about 25 mg. In some embodiments, the oxybutynin or pharmaceutically acceptable salt thereof is present in amount of from about 2 mg to about 15 mg.
• the MRA is (R)-oxybutynin or a pharmaceutically acceptable salt thereof. In some embodiments, the (R)-oxybutynin or pharmaceutically acceptable salt thereof is present in amount of from about 1 mg to about 25 mg. In some embodiments, the (R)-oxybutynin or pharmaceutically acceptable salt thereof is present in amount of from about 2 mg to about 15 mg. In some embodiments, the MRA is fesoterodine.
• the reboxetine or pharmaceutically acceptable salt thereof is (S,S)-reboxetine or a pharmaceutically acceptable salt thereof.
• the composition is an oral administration form.
• the oral administration form is a syrup, pill, tablet, troche, capsule, or patch.
• the composition is for use in treating a subject having a condition associated with pharyngeal airway collapse.
• the condition associated with pharyngeal airway collapse is sleep apnea, e.g., obstructive sleep apnea (OSA).
• OSA obstructive sleep apnea
• the condition associated with pharyngeal airway collapse is snoring, e.g., simple snoring.
• the subject is in a non-fully conscious state.
• the non-fully conscious state is sleep.
• Another aspect of the invention provides reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA) for use in treating a subject having a condition associated with pharyngeal airway collapse.
• MRA muscarinic receptor antagonist
• kits comprising reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA).
• MRA muscarinic receptor antagonist
• the kit is for use in treating a subject having a condition associated with pharyngeal airway collapse.
• Another aspect of the invention provides a therapeutic combination of reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA) for use in treating a subject having a condition associated with pharyngeal airway collapse.
• MRA muscarinic receptor antagonist
• FIG. l is a graphic illustration of an obstructive apnea.
• the top channel shows the electroencephalogram (EEG) pattern of sleep.
• the next channel represents airflow.
• the next three channels show ventilator effort by movements of the rib cage and abdomen and changes in esophageal pressure, all of which reflect a respiratory effort against an occluded upper airway.
• the last channel indicates oxyhemoglobin saturation.
• FIG. 2 is a plot showing the total apnea-hypopnea index (AHI) of the individual subjects after placebo and after reb-oxy treatment for the study of Example 1.
• AHI total apnea-hypopnea index
• FIG. 3 is a bar chart showing the AHI reduction from baseline for subjects in the placebo and treatment (reb4-oxy5) groups for the study of Example 1.
• FIG. 4 is a plot showing the hypoxic burden (HB) of the individual subjects after placebo and after reb-oxy treatment for the study of Example 1.
• FIG. 5 is a bar chart showing the HB reduction from baseline for subjects in the placebo and treatment (reb4-oxy5) groups for the study of Example 1.
• the pharyngeal airway region has no bone or cartilage support, and it is held open by muscles. When these muscles relax during sleep, the pharynx can collapse resulting in cessation of airflow. As shown in Fig. 1, ventilatory effort continues and increases in an attempt to overcome the obstruction, shown by an increase in esophageal pressure change. Rib cage and abdominal movements are in the opposite direction as a result of the diaphragm contracting against an occluded airway, forcing the abdominal wall to distend out and the chest wall to cave inward.
• Fig. l is a graphic illustration of an obstructive apnea.
• the top channel shows the electroencephalogram (EEG) pattern of sleep.
• the next channel represents airflow.
• the next three channels show ventilatory effort by movements of the rib cage and abdomen and changes in esophageal pressure, all of which reflect a respiratory effort against an occluded upper airway.
• the last channel indicates oxyhemoglobin saturation.
• OSA When a stringent definition of OSA is used (an AHI of >15 events per hour or AHI >5 events per hour with daytime sleepiness), the estimated prevalence is approximately 15 percent in males and 5 percent in females. An estimated 30 million individuals in the United States have OSA, of which approximately 6 million have been diagnosed. The prevalence of OSA in the United States appears to be increasing due to aging and increasing rates of obesity. OSA is associated with major comorbidities and economic costs, including: hypertension, diabetes, cardiovascular disease, motor vehicle accidents, workplace accidents, and fatigue/lost productivity. (Young et al., WMJ 2009; 108:246; Peppard et al., Am J Epidemiol 2013; 177:1006.)
• CPAP continuous positive airway pressure
• the methods described herein include methods for the treatment of disorders associated with pharyngeal airway muscle collapse during sleep.
• the disorder is obstructive sleep apnea (OSA) or simple snoring.
• OSA obstructive sleep apnea
• the methods include administering a therapeutically effective amount of reboxetine or a pharmaceutically acceptable salt thereof and a muscarinic receptor antagonist (MRA) as known in the art and/or described herein, to a subject who is in need of, or who has been determined to be in need of, such treatment.
• MRA muscarinic receptor antagonist
• to “treat” means to ameliorate at least one symptom of the disorder associated with pharyngeal airway collapse.
• pharyngeal airway collapse during sleep results in snoring and/or an interruption in breathing (apnea or hypopnea), arousal from sleep, and reduced oxygenation (hypoxemia); thus, a treatment can result in a reduction in snoring, apneas/hypopneas, sleep fragmentation, and hypoxemia.
• Administration of a therapeutically effective amount of a compound described herein for the treatment of a subject with OSA may result in decreased AHI.
• Measurement of OS A disease and symptoms may be, for example, by polysomnography (PSG).
• an “effective amount” of a compound refers to an amount sufficient to elicit the desired biological response, e.g., to treat a condition associated with pharyngeal airway collapse, e.g., to treat sleep apnea or snoring.
• the effective amount of a compound of the invention may vary depending on such factors as the desired biological endpoint, the pharmacokinetics of the compound, the disease being treated, the mode of administration, and the age, weight, health, and condition of the subject.
• An effective amount encompasses therapeutic and prophylactic treatment.
• An effective amount can be administered in one or more administrations, applications or dosages.
• the compositions can be administered from one or more times per day to one or more times per week; including once every other day.
• the compositions are administered daily.
• the compositions are administered daily before sleep time, e.g., immediately before sleep time or 15-60 minutes before sleep time.
• sleep time e.g., immediately before sleep time or 15-60 minutes before sleep time.
• treatment of a subject with a therapeutically effective amount of the therapeutic compounds described herein can include a single treatment or a series of treatments.
• a “therapeutically effective amount” of a compound is an amount sufficient to provide a therapeutic benefit in the treatment of a disease, disorder or condition, or to delay or minimize one or more symptoms associated with the disease, disorder or condition.
• a therapeutically effective amount of a compound means an amount of therapeutic agent, alone or in combination with other therapies, which provides a therapeutic benefit in the treatment of the disease, disorder or condition.
• the term “therapeutically effective amount” can encompass an amount that improves overall therapy, reduces or avoids symptoms or causes of disease or condition, or enhances the therapeutic efficacy of another therapeutic agent.
• the terms “subject” and “patient” are used interchangeably.
• the terms “subject” and “patient” refer to an animal (e.g., a bird such as a chicken, quail or turkey, or a mammal), specifically a "mammal” including a non-primate (e.g., a cow, pig, horse, sheep, rabbit, guinea pig, rat, cat, dog, and mouse) and a primate (e.g., a monkey, chimpanzee and a human), and more specifically a human.
• a non-primate e.g., a cow, pig, horse, sheep, rabbit, guinea pig, rat, cat, dog, and mouse
• a primate e.g., a monkey, chimpanzee and a human
• the subject is a non-human animal such as a farm animal (e.g., a horse, cow, pig or sheep), or a pet (e.g., a dog, cat, guinea pig or rabbit). In a preferred embodiment, the subject is a human.
• a farm animal e.g., a horse, cow, pig or sheep
• a pet e.g., a dog, cat, guinea pig or rabbit.
• the subject is a human.
• “pharmaceutically acceptable” means approved or approvable by a regulatory agency of the Federal or a state government or the corresponding agency in countries other than the United States, or that is listed in the U.S. Pharmacopoeia or other generally recognized pharmacopoeia for use in animals, and more particularly, in humans.
• the term “unit dosage form” is defined to refer to the form in which the compound is administered to a subject. Specifically, the unit dosage form can be, for example, a pill, capsule, or tablet. In some embodiments, the unit dosage form is a capsule.
• “solid dosage form” means a pharmaceutical dose(s) in solid form, e.g. tablets, capsules, granules, powders, sachets, reconstitutable powders, dry powder inhalers and chewables.
• Reboxetine is the generic name of the pharmaceutical substance with the chemical name of 2-((2-ethoxyphenoxy)(phenyl)methyl)morpholine or 2-[a-(2- ethoxyphenoxy)benzyl]-morpholine, and its pharmaceutically acceptable salts.
• reboxetine may be a racemic mixture of R,R- and S,S-enantiomers, or an isolated enantiomer, e.g., the S,S-enantiomer.
• reboxetine may be reboxetine hydrochloride.
• the methods include administering a dose of from about 0.2 mg to about 12 mg of reboxetine or a pharmaceutically acceptable salt thereof.
• the dose of reboxetine or a pharmaceutically acceptable salt thereof is from about 1 mg to about 8 mg.
• the dose of reboxetine or pharmaceutically acceptable salt thereof is from about 0.5 mg to about 6 mg.
• the dose of reboxetine or pharmaceutically acceptable salt thereof is from about 2 mg to about 6 mg.
• the dose of reboxetine or pharmaceutically acceptable salt thereof is about 4 mg. In some embodiments, the dose of reboxetine or pharmaceutically acceptable salt thereof is about 6 mg. In some embodiments, the dose of reboxetine or pharmaceutically acceptable salt thereof is about 2 mg. In some embodiments, the dose of reboxetine or pharmaceutically acceptable salt thereof is about 3 mg. In some embodiments, the reboxetine or pharmaceutically acceptable salt thereof is (S,S)-reboxetine or a pharmaceutically acceptable salt thereof.
• the dose of oxybutynin or (R)-oxybutynin or a pharmaceutically acceptable salt thereof may be from about 1 mg to about 25 mg (or a dose equivalent thereof of another MRA), or in some embodiments, from about 2 mg to about 15 mg.
• the dose of oxybutynin or pharmaceutically acceptable salt thereof is from about 2.5 mg to about 10 mg, e.g., 5 mg.
• the dose of (R)-oxybutynin or pharmaceutically acceptable salt thereof is from about 1 mg to about 10 mg, e.g., 2.5 mg.
• the dose of oxybutynin or (R)-oxybutynin or pharmaceutically acceptable salt thereof is from about 1 mg to about 5 mg.
• the methods include administering 4 mg reboxetine hydrochloride and 5 mg oxybutynin chloride. In some embodiments, the methods include administering 4 mg reboxetine hydrochloride and 5 mg (R)-oxybutynin chloride. In some embodiments, the methods include administering 4 mg reboxetine hydrochloride and 2.5 mg (R)-oxybutynin chloride. In some embodiments, the methods include administering 6 mg reboxetine hydrochloride and 5 mg oxybutynin chloride.
• the methods include administering 6 mg reboxetine hydrochloride and 5 mg (R)-oxybutynin chloride. In some embodiments, the methods include administering 6 mg reboxetine hydrochloride and 2.5 mg (R)-oxybutynin chloride.
• compositions comprising reboxetine or a pharmaceutically acceptable salt thereof and an MRA as active ingredients.
• the MRA and reboxetine can be in a single composition or in separate compositions.
• exemplary muscarinic receptor antagonists include atropine, propantheline, bethanechol, solifenacin, darifenacin, tolterodine, fesoterodine, trospium, and oxybutynin, or pharmaceutically acceptable salts thereof, which have activity on the M2 receptor.
• antimuscarinics include anisotropine, benztropine, biperiden, clidinium, cycrimine, dicyclomine, diphemanil, diphenidol, ethopropazine, glycopyrrolate, hexocyclium, isopropamide, mepenzolate, methixene, methscopolamine, oxyphencyclimine, oxyphenonium, procyclidine, scopolamine, tridihexethyl, and trihexyphenidyl, or pharmaceutically acceptable salts thereof.
• the muscarinic receptor antagonist is oxybutynin or (R)- oxybutynin, or a pharmaceutically acceptable salt thereof.
• (R)-oxybutynin refers to the (R)-oxybutynin stereoisomer substantially free of other stereoisomers of oxybutynin.
• the muscarinic receptor antagonist is fesoterodine.
• the reboxetine or pharmaceutically acceptable salt thereof is (S,S)-reboxetine or a pharmaceutically acceptable salt thereof.
• (S,S)- reboxetine refers to the (S,S)-reboxetine stereoisomer substantially free of other stereoisomers of reboxetine.
• compositions typically include a pharmaceutically acceptable carrier.
• pharmaceutically acceptable carrier includes saline, solvents, dispersion media, diluents, fillers, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like, compatible with pharmaceutical administration.
• oxybutynin is oxybutynin chloride.
• (R)-oxybutynin is (R)-oxybutynin chloride.
• reboxetine is reboxetine hydrochloride.
• Oxybutynin is the generic name for the pharmaceutical substance with the chemical name 4-diethylamino-2-butynylphenylcyclohexylglycolate or 4-(di ethyl amino)but-2-ynyl 2- cyclohexyl-2-hydroxy-2-phenylacetate, and its pharmaceutically acceptable salts.
• oxybutynin may be a racemic mixture of R- and S- enantiomers, or an isolated enantiomer, e.g., the R-enantiomer.
• oxybutynin may be oxybutynin chloride or (R)-oxybutynin chloride.
• compositions are typically formulated to be compatible with its intended route of administration. Examples of routes of administration include systemic oral or transdermal administration.
• routes of administration include systemic oral or transdermal administration.
• Methods of formulating suitable pharmaceutical compositions are known in the art, see, e.g., Remington: The Science and Practice of Pharmacy, 21st ed., 2005; and the books in the series Drugs and the Pharmaceutical Sciences: a Series of Textbooks and Monographs (Dekker, NY).
• oral compositions generally include an inert diluent or an edible carrier.
• the active compound(s) can be incorporated with excipients and used in the form of pills, tablets, troches, or capsules, e.g., gelatin capsules.
• Oral compositions can also be prepared using a fluid carrier.
• a composition according to the present invention may be a unit dosage form.
• a composition according to the present invention may be a solid dosage form, e.g., a tablet or capsule.
• compositions can be included as part of the composition.
• the tablets, pills, capsules, troches and the like can contain any of the following ingredients, or compounds of a similar nature: a binder such as microcrystalline cellulose, gum tragacanth or gelatin; an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch; a lubricant such as magnesium stearate or Sterotes; a glidant such as colloidal silicon dioxide; a sweetening agent such as sucrose or saccharin; or a flavoring agent such as peppermint, methyl salicylate, or orange flavoring.
• a binder such as microcrystalline cellulose, gum tragacanth or gelatin
• an excipient such as starch or lactose, a disintegrating agent such as alginic acid, Primogel, or corn starch
• a lubricant such as magnesium stearate or Sterotes
• a glidant
• Systemic administration of the compounds as described herein can also be by transdermal means, e.g., using a patch, gel, or lotion, to be applied to the skin.
• transdermal administration penetrants appropriate to the permeation of the epidermal barrier can be used in the formulation. Such penetrants are generally known in the art.
• the active compounds can formulated into ointments, salves, gels, or creams as generally known in the art.
• the gel and/or lotion can be provided in individual sachets, or via a metered-dose pump that is applied daily; see, e.g., Cohn et ak, Ther Adv Urol. 2016 Apr; 8(2): 83-90.
• the therapeutic compounds are prepared with carriers that will protect the therapeutic compounds against rapid elimination from the body, such as a controlled release formulation, including implants and microencapsulated delivery systems.
• a controlled release formulation including implants and microencapsulated delivery systems.
• Biodegradable, biocompatible polymers can be used, such as ethylene vinyl acetate, polyanhydrides, polyglycolic acid, collagen, polyorthoesters, and polylactic acid.
• Such formulations can be prepared using standard techniques, or obtained commercially, e.g., from Alza Corporation and Nova Pharmaceuticals, Inc.
• Liposomal suspensions can also be used as pharmaceutically acceptable carriers. These can be prepared according to methods known to those skilled in the art, for example, as described in U.S. Patent No. 4,522,811.
• compositions can be included in a container, pack, or dispenser together with instructions for administration or use in a method described herein.
• Example 1 A Randomized, Placebo-controlled, Double-blind Crossover, 1- week Trial
• the study design was as follows: up to 28 days to conduct screening and baseline PSG, followed by 7 days randomized at-home study treatment, then an in-lab PSG night, followed by 7 days washout (up to 10 days if necessary, for scheduling), then 7 days cross over to the other treatment arm, and a final in-lab PSG night.
• Results 16 subjects with (median [interquartile range]) age 57 [51-61] years and body mass index 30 [26-36] kg/m 2 completed the study.
• AHI went from 49 [35-57] events/h at baseline to 18 [13-21] events/h (59% median reduction) on reb-oxy and to 39 [29-48] events/h (6% median reduction) on placebo (p ⁇ 0.001).
• Figure 2 shows the total AHI of the individual subjects after placebo and after reb- oxy treatment.
• Figure 3 shows the improvement in AHI reduction from baseline for reb-oxy compared to placebo.
• Hypoxic burden (HB) was also measured and calculated during the study. Hypoxic burden was measured and calculated as described in A. Azarbarzin et al.,
• the hypoxic burden of sleep apnoea predicts cardiovascular disease-related mortality: the Osteoporotic Fractures in Men Study and the Sleep Heart Health Study, Eur Heart J, 2019 Apr 7; 40(14): 1149-1157.
• Figure 4 shows the hypoxic burden of the individual subjects after placebo and after reb-oxy treatment.
• Figure 5 shows the improvement in HB reduction from baseline for reb-oxy compared to placebo.

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