One of the largest gatherings of people with epilepsy, care partners, and healthcare practitioners to address unmet needs for increased education
SAN DIEGO, Nov. 18, 2024 /PRNewswire/ -- Neurelis, Inc., today announced it will participate in the 12th Annual Sofie's Journey Epilepsy Awareness Day & Education Expo at Disneyland (EADDL), one of the largest gatherings of people with epilepsy, care partners, and healthcare practitioners. The event was established to help address the unmet need for increased education for people with epilepsy and their families. Neurelis will participate in the free education expo November 18th and 19th, 9:00 AM to 5:00 PM at the Disneyland Hotel Convention Center. Epilepsy Awareness Day will take place on Nov. 20th at Disneyland Resort, where families will spend the day in the park together.
"Participating in the Epilepsy Awareness Day event is such a valuable opportunity for me and people in the epilepsy community to learn about progress in the field and exchange information with other families and medical professionals," commented Colleen, care partner and Neurelis Ambassador. "It is an honor to represent Neurelis at the Expo and share my experience with VALTOCO® (diazepam nasal spray), an immediate-use seizure medication which has been key to having my son, Paul, and I feel prepared to address his seizure clusters."
"Since I found VALTOCO, I feel I have more freedom to go out and do things and want to help others with seizure clusters realize there may be treatment options to help them experience that too. It means a lot to be able to share my story with kids and young adults with epilepsy, so they understand that they have support from a community of their peers," added Paul, person with epilepsy and Neurelis Ambassador.
Neurelis will sponsor a presentation on its FDA-approved product, VALTOCO, a treatment for episodes of frequent seizures in patients six years of age or older, on Monday Nov. 18th from 11:00 AM to 11:30 AM in the Expo Center, Room D. The presentation will feature Paul with his care partner and mother Colleen, who will speak about their journey with epilepsy and answer questions during a live Q&A.
Paul was diagnosed with epilepsy when he was 12 years old. Navigating his diagnosis and effectively managing his seizures and seizure clusters, as well as advocating for proper care of students with epilepsy have been a key focus for both Paul and Colleen following his diagnosis. Together they helped create legislation for seizure safe schools in the state of New Jersey, Paul's Law. Paul is now successfully attending college and enjoys golf. Colleen continues her advocacy efforts and is currently working on advancing the Seizure Awareness and Preparedness Act.
Joining Neurelis and the epilepsy community at the Expo will also be Neurelis Ambassador Danielle. Danielle was diagnosed with epilepsy almost 25 years ago, after she was unable to wake up for school one day. Epilepsy significantly impacted her life during her adolescence and college years. Now with proper management, a detailed seizure action plan, and a strong support system, Danielle has been able to increase her independence. She served as president of a regional epilepsy nonprofit focused on helping people with epilepsy to manage the logistics of accessing appropriate healthcare. She continues to be dedicated to increasing advocacy and awareness for people with epilepsy. Danielle spoke about her experiences living with and managing seizure clusters on Sunday Nov. 17 at a dinner co-sponsored by Epilepsy Alliance of America for families attending the meeting.
"VALTOCO has enabled me to have more freedom to travel and give back to the epilepsy community through my advocacy work," said Danielle. "It is exciting to participate in the Epilepsy Awareness Day Expo which is such a powerful event for learning and creating a community. Having the opportunity to engage with doctors, caregivers, and others who live daily with the challenges of epilepsy gives a sense of empowerment and support."
"Our focus at Neurelis has been on improving overall care and increasing awareness of the unmet needs of people with epilepsy," said Neurelis Founder and CEO Craig Chambliss. "We are proud to join the epilepsy community at this important event to promote education and to help advance the discussion on how to empower people with epilepsy and improve the quality of their lives."
Additionally, Neurelis has committed to sponsoring two new seizure detection and response puppies through Little Angels Service Dogs, an Assistance Dog International accredited organization that specializes in training service dogs for seizure alert and several other types of assistance. The puppies will be featured at the VALTOCO exhibit booth.
EADDL is part of November's National Epilepsy Awareness Month, which promotes the importance of epilepsy education and awareness, and improving the lives of those impacted by the condition. For more information about EADDL, visit https://epilepsyawarenessday.org/ and to register for the Expo, click here.
About EADDL and Sofie's Journey
EADDL is the combined effort of one family's thankfulness for their own daughter's recovery (10+ years seizure free) and a united community with a passion for winning the fight against epilepsy. It is operated by the Irvine, Calif.-based, non-profit foundation, Sofie's Journey, to drive epilepsy awareness by bringing together patients, families/caregivers, physicians, advocates, non-profits, services, and the biopharmaceutical industry. EADDL and Sofie's Journey were launched by Candy and Brad Levy, whose daughter Sofie, now 19 years old, underwent surgery in 2013 to remove a part of her brain that caused her seizures. Their mission is to drive epilepsy awareness, the key to overcoming challenges created by epilepsy.
About Neurelis
Neurelis, Inc., is a neuroscience company focused on the development and commercialization of therapeutics for the treatment of epilepsy and neurologic disorders characterized by high unmet medical need. The FDA has approved Neurelis' VALTOCO® (diazepam nasal spray) as an acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from an individual's usual seizure pattern in adult and pediatric patients 6 years of age and older. VALTOCO is a proprietary formulation of diazepam incorporating the science of INTRAVAIL®, a transmucosal absorption enhancement technology that enables the noninvasive delivery of a broad range of protein, peptide, and small-molecule drugs. For more information on VALTOCO, please visit www.valtoco.com. For the latest scientific information on VALTOCO, please visit http://www.neurelismedicalaffairs.com/. Neurelis is also developing NRL-1004, an investigational, Phase 1 stage intranasal olanzapine for treatment of acute agitation episodes associated with schizophrenia and bipolar disorder. In addition, Neurelis is also developing NRL-1049 (previously known as BA-1049), an investigational, Phase 1 new chemical entity Rho kinase (ROCK) inhibitor, for the treatment of cerebral cavernous malformations (CCMS), a rare disorder of the central nervous system (CNS). For more information on Neurelis, please visit www.neurelis.com.
Important Safety Information about VALTOCO:
Indication
VALTOCO® (diazepam nasal spray) is indicated for the acute treatment of intermittent, stereotypic episodes of frequent seizure activity (i.e., seizure clusters, acute repetitive seizures) that are distinct from a patient's usual seizure pattern in patients with epilepsy 6 years of age and older.
WARNING: RISKS FROM CONCOMITANT USE WITH OPIOIDS; ABUSE, MISUSE, AND ADDICTION; and DEPENDENCE AND WITHDRAWAL REACTIONS
Contraindications: VALTOCO is contraindicated in patients with:
Central Nervous System (CNS) Depression
Benzodiazepines, including VALTOCO, may produce CNS depression. Caution patients against engaging in hazardous activities requiring mental alertness, such as operating machinery, driving a motor vehicle, or riding a bicycle, until the effects of the drug, such as drowsiness, have subsided, and as their medical condition permits.
The potential for a synergistic CNS-depressant effect when VALTOCO is used with alcohol or other CNS depressants must be considered, and appropriate recommendations made to the patient and/or care partner.
Suicidal Behavior and Ideation
Antiepileptic drugs (AEDs), including VALTOCO, increase the risk of suicidal ideation and behavior. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or unusual changes in mood or behavior.
Glaucoma
Benzodiazepines, including VALTOCO, can increase intraocular pressure in patients with glaucoma. VALTOCO may only be used in patients with open-angle glaucoma only if they are receiving appropriate therapy. VALTOCO is contraindicated in patients with narrow-angle glaucoma.
Neonatal Sedation and Withdrawal Syndrome
Use of VALTOCO late in pregnancy can result in sedation (respiratory depression, lethargy, hypotonia) and/or withdrawal symptoms (hyperreflexia, irritability, restlessness, tremors, inconsolable crying, and feeding difficulties) in the neonate. Monitor neonates exposed to VALTOCO during pregnancy or labor for signs of sedation and monitor neonates exposed to VALTOCO during pregnancy for signs of withdrawal; manage these neonates accordingly.
Risk of Serious Adverse Reactions in Infants due to Benzyl Alcohol Preservative
VALTOCO is not approved for use in neonates or infants. Serious and fatal adverse reactions, including "gasping syndrome," can occur in neonates and low-birth-weight infants treated with benzyl alcohol–preserved drugs, including VALTOCO. The "gasping syndrome" is characterized by central nervous system depression, metabolic acidosis, and gasping respirations. The minimum amount of benzyl alcohol at which serious adverse reactions may occur is not known.
Adverse Reactions
The most common adverse reactions (at least 4%) were somnolence, headache, and nasal discomfort.
Diazepam, the active ingredient in VALTOCO, is a Schedule IV controlled substance.
To report SUSPECTED ADVERSE REACTIONS, contact Neurelis, Inc. at 1-866-696-3873 or FDA at 1-800-FDA-1088 (www.fda.gov/medwatch).
Please read full Prescribing Information, including Boxed Warning.
Contacts:
Brittany Bradrick, Chief Operating Officer and Chief Financial Officer, +1 858 251 2100
SOURCE Neurelis, Inc.