Jazz Pharmaceuticals Data to Showcase Ongoing Sleep Medicine Research at SLEEP 2019
DUBLIN, May 9, 2019 /PRNewswire/ -- Jazz Pharmaceuticals plc (Nasdaq: JAZZ) announced today that 14 abstracts sponsored by Jazz Pharmaceuticals and one abstract from an investigator-sponsored trial will be presented at the 33(rd) Annual Meeting of the Associated Professional Sleep Societies, known as "SLEEP," in San Antonio from June 8-12, 2019.
"Jazz is committed to making meaningful strides in researching medicines that can improve the lives of people living with sleep disorders," said Jed Black, M.D., senior vice president, Sleep and CNS Medicine at Jazz Pharmaceuticals and adjunct professor, Stanford University Medical Center, Stanford Center for Sleep Sciences and Medicine. "There continue to be large unmet needs in these patient populations, and we are looking forward to presenting new data from our sleep portfolio, including our newest sleep medicine to be approved by FDA, solriamfetol."
On March 20, 2019, Jazz announced that the U.S. Food and Drug Administration (FDA) approved Sunosi(TM) (solriamfetol) to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA). Sunosi is expected to be commercially available in the U.S. following the final scheduling decision by the U.S. Drug Enforcement Administration (DEA), which is typically within 90 days of FDA approval.
Highlights at SLEEP will include the following poster presentations:
-- Results from pooled analyses from 12-week randomized studies of
solriamfetol for the treatment of excessive daytime sleepiness in
patients with obstructive sleep apnea (OSA) or narcolepsy.
-- Long-term effects of solriamfetol on quality of life in patients with
excessive daytime sleepiness associated with narcolepsy or OSA.
-- Treatment patterns among patients with narcolepsy treated with sodium
oxybate.
-- Physician prescribing patterns for patients with narcolepsy treated with
sodium oxybate.
-- Evaluation of cataplexy-free days in children/adolescents with
narcolepsy with cataplexy treated with sodium oxybate.
A full list of Jazz-supported oral and poster presentations follows below:
Solriamfetol Poster Presentations
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Sodium Oxybate Presentations
Presentation Title Author Date / Time / Session/
Presentation Number/ Location
---
Treatment Patterns among Patients
with Narcolepsy Treated with
Sodium Oxybate
Bae et al.
Poster presentation:
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0604
Bridge Hall
Oral presentation:
Tuesday, June 11
10:30 a.m. - 12:30 p.m.
0604 / Bridge Hall
---
Physician Prescribing Patterns for
Patients with Narcolepsy Treated
with Sodium Oxybate
Roy et al.
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0608
Bridge Hall
---
Dosing, Titration, and Treatment
Compliance to Sodium Oxybate
Therapy in Pediatric Patients With
Narcolepsy Plazzi et al.
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0765
Bridge Hall
---
Evaluation of Cataplexy-Free Days
in Children/Adolescents with
Narcolepsy with Cataplexy Treated
with Sodium Oxybate Mignot et al.
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0766
Bridge Hall
---
Long-Term Safety of Sodium Oxybate
in Pediatric Narcolepsy with
Cataplexy: Open-Label
Continuation Post 1-Year of
Treatment Strunc et al.
Poster presentation:
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0767
Bridge Hall
Oral presentation:
Tuesday, June 11
10:30 a.m. - 12:30 p.m.
0767
Bridge Hall
---
Sodium Oxybate Dosing Utilization
Patterns in the Nexus Narcolepsy
Registry Ohayon et al.
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0605
Bridge Hall
---
Patient Survey Poster Presentation
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Narcolepsy Prevalence Poster Presentation
Presentation Title Author Date / Time / Session/
Presentation Number/ Location
---
Prevalence of
Diagnosed
Pediatric
Narcolepsy in the
United States Morse et al.
Sunday, June 9
5:15 p.m. - 7:15 p.m.
0761
Bridge Hall
---
Additionally, data from the following investigator-sponsored trial focusing on sodium oxybate will be presented.
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About Sunosi(TM) (solriamfetol)
Sunosi is a dual-acting dopamine and norepinephrine reuptake inhibitor (DNRI) indicated to improve wakefulness in adults living with excessive daytime sleepiness due to narcolepsy or obstructive sleep apnea (OSA). In 2014, Jazz Pharmaceuticals acquired a license to develop and commercialize Sunosi from Aerial Biopharma. Jazz Pharmaceuticals has worldwide development, manufacturing, and commercialization rights to Sunosi, excluding certain jurisdictions in Asia. SK Biopharmaceuticals, the discoverer of the compound, maintains rights in 12 Asian markets, including Korea, China and Japan. Sunosi has orphan drug designation for narcolepsy in the United States.
Important Safety Information
SUNOSI is not for use to treat the underlying cause of airway obstruction in people with OSA. SUNOSI does not take the place of using your continuous positive airway pressure (CPAP) machine or other devices that your healthcare provider has prescribed for the treatment of OSA. It is important that you continue to use these treatments as prescribed by your healthcare provider.
SUNOSI can be a target for people who abuse prescription medicines or street drugs. Keep SUNOSI in a safe place to protect it from theft. Never give your SUNOSI to anyone else, because it may cause death or harm them. Selling or giving away SUNOSI may harm others and is against the law. Tell your doctor if you have ever abused or been dependent on alcohol, prescription medicines or street drugs.
Before taking SUNOSI, tell your doctor about all of your medical conditions, including if you:
-- have heart problems, high blood pressure, kidney problems, diabetes, or
high cholesterol
-- have had a heart attack or a stroke
-- have kidney problems or diabetes
-- have a history of mental health problems (including psychosis and
bipolar disorders), or of drug or alcohol abuse or addiction
-- are pregnant or planning to become pregnant. It is not known if SUNOSI
will harm your unborn baby.
-- are breastfeeding or plan to breastfeed. It is not known if SUNOSI
passes into your breast milk. Talk to your doctor about the best way to
feed your baby if you take SUNOSI.
What are the possible side effects of SUNOSI?
SUNOSI may cause serious side effects, including:
-- Increased blood pressure and heart rate. SUNOSI can cause blood pressure
and heart rate increases that can increase the risk of heart attack,
stroke, heart failure, and death. Your doctor should check your blood
pressure before and during treatment with SUNOSI. Your doctor may
decrease your dose or tell you to stop taking SUNOSI if you develop high
blood pressure that does not go away during treatment with SUNOSI.
-- Mental (psychiatric) symptoms including anxiety, problems sleeping
(insomnia), irritability, and agitation. Tell your doctor if you develop
any of these symptoms. Your doctor may change your dose or tell you to
stop taking SUNOSI if you develop side effects during treatment with
SUNOSI.
The most common side effects of SUNOSI include:
-- headache
-- decreased appetite
-- problems sleeping
-- nausea
-- anxiety
These are not all the possible side effects of SUNOSI. Call your doctor for advice about side effects.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
Please find full prescribing information here: http://pp.jazzpharma.com/pi/sunosi.en.USPI.pdf
About Xyrem
Xyrem(®) (sodium oxybate) oral solution, CIII, is the only product approved by the U.S. Food and Drug Administration (FDA) for both cataplexy and excessive daytime sleepiness in narcolepsy in adult and pediatric patients ages 7 and older. Xyrem may only be dispensed to patients enrolled in the Xyrem REMS Program. Xyrem was first approved in the U.S. in 2002, based on clinical trial data in adults.
Important Safety Information
WARNING: Taking XYREM with other CNS depressants such as medicines used to make you or your child fall asleep, including opioid analgesics, benzodiazepines, sedating antidepressants, antipsychotics, sedating anti-epileptic medicines, general anesthetics, muscle relaxants, alcohol, or street drugs, may cause serious medical problems, including trouble breathing (respiratory depression), low blood pressure (hypotension), changes in alertness (drowsiness), dizziness (syncope), and death.
XYREM is a form of gamma hydroxybutyrate (GHB). Abuse or misuse of illegal GHB alone or with other drugs that cause changes in alertness (or consciousness) has caused serious side effects. These effects include seizures, trouble breathing (respiratory depression), changes in alertness (drowsiness), coma, and death.
Because of these risks, you have to go through the XYREM REMS Program to have your or your child's prescription for XYREM filled.
Do not take XYREM if you take or your child takes other sleep medicines or sedatives (medicines that cause sleepiness), drink alcohol, or have a rare problem called succinic semialdehyde dehydrogenase deficiency.
Keep XYREM in a safe place to prevent abuse and misuse. Selling or giving away XYREM may harm others, and is against the law. Tell your doctor if you have ever abused or been dependent on alcohol, prescription medicines, or street drugs.
Anyone who takes XYREM should not do anything that requires them to be fully awake or is dangerous, including driving a car, using heavy machinery, or flying an airplane, for at least 6 hours after taking XYREM. Those activities should not be done until you know how XYREM affects you or your child.
XYREM can cause serious side effects, including the following:
-- Breathing problems, including slower breathing, trouble breathing,
and/or short periods of not breathing while sleeping (sleep apnea).
People who already have breathing or lung problems have a higher chance
of having breathing problems when they use XYREM.
-- Mental health problems, including confusion, seeing or hearing things
that are not real (hallucinations), unusual or disturbing thoughts
(abnormal thinking), feeling anxious or upset, depression, or thoughts
of killing yourself or trying to kill yourself. Tell your doctor if you
or your child have or had depression or have tried to harm yourself.
Call your doctor right away if you have or your child has symptoms of
mental health problems.
-- Sleepwalking. Sleepwalking can cause injuries. Call your doctor if you
or your child starts sleepwalking. Your doctor should check you or your
child.
Tell your doctor if you are or your child is on a salt-restricted diet or if you have or your child has high blood pressure, heart failure, or kidney problems. XYREM contains a lot of sodium (salt) and may not be right for you or your child.
The most common side effects of XYREM include nausea, sleepiness, dizziness, vomiting, bedwetting, and tremor (in adults). In pediatric patients, headache, decreased appetite, and weight decrease were also common. Your side effects may increase when you take higher doses of XYREM. XYREM can cause physical dependence and craving for the medicine when it is not taken as directed. These are not all the possible side effects of XYREM.
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.
Please find full prescribing information here: http://pp.jazzpharma.com/pi/xyrem.en.USPI.pdf
About Jazz Pharmaceuticals plc
Jazz Pharmaceuticals plc (Nasdaq: JAZZ), a global biopharmaceutical company, is dedicated to developing life-changing medicines for people with limited or no options. As a leader in sleep medicine and with a growing hematology/oncology portfolio, Jazz has a diverse portfolio of products and product candidates in development, and is focused on transforming biopharmaceutical discoveries into novel medicines. Jazz Pharmaceuticals markets Xyrem(®) (sodium oxybate) oral solution, Erwinaze(®) (asparaginase Erwinia chrysanthemi), Defitelio(® )(defibrotide sodium) and Vyxeos(®) (daunorubicin and cytarabine) liposome for injection in the U.S. and markets Erwinase(®), Defitelio(®) (defibrotide) and Vyxeos(®) 44 mg/100 mg powder for concentrate for solution for infusion in countries outside the U.S. For country-specific product information, please visit https://www.jazzpharma.com/medicines. For more information, please visit www.jazzpharmaceuticals.com and follow us on Twitter at @JazzPharma.
"Safe Harbor" Statement under the Private Securities Litigation Reform Act of 1995
This press release contains forward-looking statements, including, but not limited to, statements related to the expected timing of the commercial availability of Sunosi and other statements that are not historical facts. These forward-looking statements are based on the company's current plans, objectives, estimates, expectations and intentions and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, risks and uncertainties associated with: delays or problems in the supply or manufacture of Sunosi; complying with applicable U.S. regulatory requirements; any delays in, or the outcome of, DEA scheduling for Sunosi; and other risks and uncertainties affecting the company, including those described from time to time under the caption "Risk Factors" and elsewhere in Jazz Pharmaceuticals plc's Securities and Exchange Commission filings and reports (Commission File No. 001-33500), including the company's Quarterly Report on Form 10-Q for the quarter ended March 31, 2019 and future filings and reports by the company. Other risks and uncertainties of which the company is not currently aware may also affect the company's forward-looking statements and may cause actual results and the timing of events to differ materially from those anticipated. The forward-looking statements herein are made only as of the date hereof or as of the dates indicated in the forward-looking statements, even if they are subsequently made available by the company on its website or otherwise. The company undertakes no obligation to update or supplement any forward-looking statements to reflect actual results, new information, future events, changes in its expectations or other circumstances that exist after the date as of which the forward-looking statements were made.
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