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Jupiter Neurosciences, Inc. Common Stock

Jupiter Neurosciences, Inc., a clinical stage research and development pharmaceutical company, engages in the development of therapeutics for central nervous system disorders and rare diseases in the United States and internationally. It operates in two segments, Pharmaceutical Operations and Premium Nutritional Supplements. The company researches and develops JNS115, which is in Phase IIa clinical trial for the treatment of Parkinson's disease; JNS108, which is in Phase II clinical trial for the treatment of mild cognitive impairment/early Alzheimer's disease; JNS102, which is in Phase II clinical trial for the treatment of mucopolysaccharidosis type 1; and JNS107, which is in Phase II clinical trial for the treatment of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome. It is also involved in the commercialization and sale of GLO for skin beauty, MND for mental clarity, and PWR for energy, endurance, and muscle recovery under the Nugevia brand name. The company was formerly known as Jupiter Orphan Therapeutics, Inc. and changed its name to Jupiter Neurosciences, Inc. in August 2021. Jupiter Neurosciences, Inc. was incorporated in 2016 and is headquartered in Jupiter, Florida.

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JUNS

Jupiter Neurosciences prices $2M registered direct offering

Jupiter Neurosciences has entered into a securities purchase agreement for a registered direct offering of 307,692 shares of common stock. The gross proceeds are about $2 million, and the closing is expected on or about August 24. Shares of the company are up nearly 18% at $6.10.
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Biotech & Genomic Medicine

Jupiter Neurosciences Advances Parkinson's Trial

Jupiter Neurosciences is advancing its Phase 2a RESET trial of JOTROL in Parkinson's disease, with patient enrollment underway and topline data expected in the first quarter of 2027. The company's lead candidate is an oral, enhanced-bioavailability formulation of trans-resveratrol designed to address neuroinflammation, oxidative stress, and mitochondrial dysfunction. Jupiter reported approximately nine-fold higher plasma bioavailability than conventional resveratrol in a Phase 1 study of 24 patients, with measurable cerebrospinal-fluid exposure and no serious adverse events. The randomized, placebo-controlled Phase 2a trial is enrolling 30 patients and will evaluate safety, tolerability, pharmacokinetics, cerebrospinal fluid penetration, and inflammatory biomarkers alongside standard clinical assessments. Jupiter's market capitalization is approximately $5.0 million, compared with Parkinson's-focused peers ranging from roughly $76 million to more than $300 million.
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JUNS3

Jupiter Neurosciences Announces 1-for-75 Reverse Stock Split Effective August 6

Jupiter Neurosciences has approved a 1-for-75 reverse stock split of its common stock, effective after the market closes on August 6, 2026. The move, backed by shareholders at the July 22 annual meeting, aims to increase the per-share trading price and help the company regain compliance with Nasdaq's minimum bid price requirement. Trading on a split-adjusted basis will begin August 7 under the ticker JUNS and a new CUSIP number, reducing outstanding shares from approximately 57.76 million as of August 4 to about 770,081 shares. No fractional shares will be issued; instead, holders will receive cash payments based on the August 6 closing price. The stock is currently trading at $0.07, down 25%.
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Psychedelic Medicine

Jupiter Neurosciences Signs Up to $100 Million Deal for Exclusive U.S. Rights to Psychedelic MDMA Formulation

Jupiter Neurosciences has signed a definitive licensing agreement with PharmAla Biotech for perpetual exclusive U.S. rights to ALA-002, a patented formulation of MDMA, in a deal valued at up to $100 million including milestones. The transaction transforms Jupiter into a dual clinical-stage CNS company, adding ALA-002 to its existing Phase II Parkinson's disease program for JOTROL, a proprietary enhanced bioavailability resveratrol formulation. Chairman and CEO Christer Rosén and President Alison Silva discussed the acquisition during a fireside chat hosted by IPO Edge, noting the primary indication for ALA-002, its addressable market size, and potential revenue relative to the acquisition cost. They also addressed the status of the Phase II Parkinson's trial, the evolving U.S. regulatory landscape for psychedelics, and key milestones across the company's portfolio.
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