SUPN: Supernus Pharmaceuticals, Inc. - Summary | Jitta

Supernus Pharmaceuticals, Inc.

NASDAQ:SUPN

Price
$44.07
Loss Chance
49.2%
4.03JITTA SCORE
63.68%Over Jitta Line
Jitta Ranking
166 / 714
1,760 / 4,216
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HISTORICAL JITTA SCORE
Jitta Factors
Growth Opportunity (37)
Recent Business Performance (32)
Financial Strength (91)
Return to Shareholders (6)
Competitive Advantage (39)
Jitta Signs
Debt LevelLow Long Term Debt
CapExVery Low
Revenue and EarningEarning decline from 2022-2025
Operating MarginDeclined
Recent Business PerformanceEarning decline 34.73% in the last year
SG&A to SalesIncreasing
Cash Conversion CycleMore than 1 year
Key Stats
Jitta Score
Jitta Line
4.03
63.68%
3.05
179.36%
3.06
156.55%
Pharmaceuticals
4.95
58.77%
5.05
81.75%
5.69
91.21%
COMPANY DESCRIPTION
Supernus Pharmaceuticals, Inc., a biopharmaceutical company, engages in the development and commercialization of products for the treatment of central nervous system (CNS) diseases in the United States. It offers Qelbree, a non-stimulant indicated for the treatment of attention-deficit hyperactivity disorder (ADHD); GOCOVRI for the treatment of dyskinesia and levodopa/carbidopa in patients with Parkinson's Disease (PD); Oxtellar XR, an extended-release oxcarbazepine product indicated for the monotherapy treatment of partial onset epilepsy seizures; and APOKYN for the acute and intermittent treatment of hypomobility or off episodes in patients with advanced PD. It also provides Trokendi XR, an extended release topiramate product indicated for the treatment of epilepsy, as well as for the prophylaxis of migraine headache; XADAGO for the treatment of levodopa/carbidopa in patients with PD experiencing off episodes; and MYOBLOC, a Type B toxin product indicated for the treatment of cervical dystonia and chronic sialorrhea. In addition, the company develops ONAPGO, which received FDA approval, for the treatment of motor fluctuations in adults with advanced PD; SPN-817, a first-in-class selective acetylcholinesterase inhibitor, which is in Phase 2 clinical trial, for the treatment of epilepsy, partial seizures, Dravet syndrome, and Lennox-Gaustaut syndrome; SPN-820, a small molecule in Phase 2 clinical trial for treating resistant depression; and SPN-443, a stimulant in Phase 1 trial for the treatment of ADHD/CNS. It markets and sells its products through pharmaceutical wholesalers, specialty pharmacies, and distributors. It has a development agreement with Navitor Inc. for the conduct of Phase 2 clinical program of SPN-820. Supernus Pharmaceuticals, Inc. was incorporated in 2005 and is based in Rockville, Maryland.