Supernus Pharma Stock Price, News & Analysis

Supernus Pharmaceuticals continues its collaboration with actress Busy Philipps to raise awareness about ADHD in women and promote Qelbree®, a non-stimulant ADHD treatment. Philipps shares her personal experience with ADHD and how Qelbree has helped manage her symptoms. The campaign aims to empower women to advocate for their ADHD care, especially as ADHD Awareness Month approaches.

Qelbree is a once-daily non-stimulant medication approved for patients 6 years and older with ADHD. It's the first non-stimulant approved for adults with ADHD in 20 years. The drug has no evidence of abuse or misuse and can be refilled without needing a new prescription each month.

The press release includes important safety information, noting that Qelbree may increase suicidal thoughts and actions in some patients. It also mentions potential side effects and drug interactions.

Supernus Pharmaceuticals (Nasdaq: SUPN), a biopharmaceutical company specializing in central nervous system (CNS) diseases, has announced its participation in the TD Cowen 4th Annual Novel Mechanisms in Neuropsychiatry Summit. The company's President and CEO, Jack Khattar, will engage in a virtual fireside chat on Thursday, September 26, 2024, at 8:40 a.m. ET.

Interested parties can access a live webcast of the presentation through a provided link or by visiting the Events & Presentations section in the Investor Relations area of the company's website at www.supernus.com. An archived replay of the webcast will remain available on the company's website for 60 days following the conference.

Supernus Pharmaceuticals (Nasdaq: SUPN), a biopharmaceutical company specializing in central nervous system (CNS) diseases, has announced its participation in the 2024 Wells Fargo Healthcare Conference. Jack Khattar, President and CEO, will engage in a fireside chat on September 4, 2024, at 4:30 p.m. ET at the Encore Boston Harbor Hotel in Everett, Massachusetts.

Investors can arrange meetings with company management through the Wells Fargo conference coordinator. A live audio webcast of the presentation will be available on the company's website, with an archived replay accessible for 60 days post-conference. This event provides an opportunity for Supernus to showcase its developments in CNS treatments to potential investors and industry professionals.

Supernus Pharmaceuticals (Nasdaq: SUPN) has announced that the FDA has accepted the resubmission of the new drug application (NDA) for SPN-830, its apomorphine infusion device. This device is designed for the continuous treatment of motor fluctuations (OFF episodes) in Parkinson's disease. The FDA has set a PDUFA target action date of February 1, 2025 for the review of the application. This development marks a significant step forward in Supernus's efforts to bring a new treatment option to market for Parkinson's disease patients experiencing motor fluctuations.

Supernus Pharmaceuticals (Nasdaq: SUPN) reported strong financial results for Q2 2024. Total revenues increased 24% to $168.3 million, driven by significant growth in Qelbree and GOCOVRI sales. Qelbree net sales surged 92% to $59.4 million, while GOCOVRI net sales grew 10% to $31.7 million. The company achieved operating income of $22.6 million and adjusted operating earnings of $45.5 million. Supernus raised its full-year 2024 guidance for total revenues and operating earnings. The company also made progress in its product pipeline, including SPN-820 for depression and SPN-817 for epilepsy.

Supernus Pharmaceuticals (Nasdaq: SUPN) has resubmitted its New Drug Application (NDA) for SPN-830, an apomorphine infusion device designed for the continuous treatment of motor fluctuations (OFF episodes) in Parkinson's disease. This resubmission addresses the FDA's questions from a Complete Response Letter (CRL) issued in April 2024. The CRL indicated that two areas required additional review or information, but no clinical safety or efficacy issues were identified as approval requirements. Supernus believes it has addressed the FDA's concerns and will continue to work closely with the agency during the review process. The company's CEO, Jack Khattar, expressed commitment to bringing SPN-830 to market, viewing it as a potentially important treatment option for Parkinson's disease patients and their families.

Supernus Pharmaceuticals (Nasdaq: SUPN), a biopharmaceutical company focused on central nervous system (CNS) diseases, has announced its plans to report second quarter 2024 financial and business results on August 6, 2024, after market close. The company will host a conference call at 4:30 p.m. ET on the same day, featuring Jack Khattar, President and CEO, and Tim Dec, Senior VP and CFO.

A live webcast will be available on the company's Investor Relations website. Participants can pre-register for the call and will receive a personalized dial-in number. The webcast replay will be accessible on the website for 60 days following the live call.

Supernus Pharmaceuticals (Nasdaq: SUPN), a biopharmaceutical company specializing in CNS disease treatments, announced its participation in the Jefferies Global Healthcare Conference. The event will feature a fireside chat with President and CEO Jack Khattar on June 6, 2024, at 1:30 p.m. ET, at the Marriott Marquis Hotel in New York City.

Investors can contact the Jefferies conference coordinator to arrange meetings with management. A live audio webcast of the presentation will be available on the company's website, with an archived replay accessible for 60 days post-conference.

Supernus announced interim results from its Phase 2a study of SPN-817 for treatment-resistant epilepsy. The study included 41 subjects, with 19 completing the maintenance period. Promising findings revealed a 75% median reduction in focal seizures at 3-4 mg doses twice daily. During the open-label extension period, this reduction increased to 86%. For subjects on three or more anti-seizure medications, a 70% median seizure reduction was observed initially, dropping to 60% in the extension period. Safety data showed SPN-817 to be well-tolerated with a 22% discontinuation rate due to adverse events in the titration period. Common side effects included nausea, diarrhea, and headache. Full results are expected in the second half of 2024, and a Phase 2b study is planned for later this year.