BioVie Completes Last Patient Evaluation for SUNRISE-PD Phase 2 Trial
Written by Emily J. Thompson, Senior Investment Analyst
Updated: May 18 2026
0mins
BioVie announced that the last patient evaluation visit has been completed for the company's SUNRISE-PD Phase 2 trial evaluating its drug candidate bezisterim in early-stage Parkinson's disease. "With this last patient's treatment visit completed, our team will start the study closeout process, and the Company plans announce topline results in Q3," said Cuong Do, BioVie's president and CEO. "This trial was designed to assess bezisterim's magnitude of therapeutic impact on a series of motor and non-motor endpoints so that we can finalize the design for the Phase 3 registrational trials. We look forward to unblinding the data later this year to understand the molecule's true potential."
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About BIVI
BioVie Inc. is a clinical-stage company developing innovative drug therapies for the treatment of neurological and neurodegenerative disorders and advanced liver disease. In neurodegenerative disease, the Company's drug candidate bezisterim inhibits inflammatory activation of extracellular signal-regulated kinase and the transcription factor nuclear factor-kB, and the associated neuroinflammation and insulin resistance, but not ERK and NFkB homeostatic functions (such as insulin signaling and neuron growth and survival). Both neuroinflammation and insulin resistance are drivers of Alzheimer’s disease (AD) and Parkinson’s disease (PD). Persistent systematic inflammation and neuroinflammation are key features in patients with neurological symptoms of long COVID. In liver disease, the Company's orphan drug candidate BIV201, is being evaluated for Phase III clinical testing for the reduction of further decompensation in participants with liver cirrhosis and ascites.
About the author
Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- Trial Enrollment Completed: BioVie Inc. announced the completion of enrollment in its Phase 2 ADDRESS-LC trial for Bezisterim, targeting the neurological symptoms of Long COVID affecting approximately 15 million people in the U.S., indicating significant progress in addressing this unmet medical need.
- Drug Mechanism and Applications: Bezisterim (NE3107) is an investigational oral drug that crosses the blood-brain barrier to modulate key neuroinflammatory pathways, aimed at alleviating symptoms in patients with Long COVID, Alzheimer's, and Parkinson's disease, showcasing its broad clinical application potential.
- Trial Design and Funding: The trial is a randomized, placebo-controlled, multicenter study fully funded by the U.S. Department of War, primarily assessing the safety and efficacy of Bezisterim in improving neurocognitive and fatigue-related symptoms, reflecting governmental support for this research initiative.
- Market Performance and Outlook: Despite BioVie’s current trading price of $1.46, down 3.95%, the upcoming topline results from the Phase 2 SUNRISE-PD trial are expected to generate optimism in the market, particularly regarding potential breakthroughs in Parkinson's disease treatment.
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- Importance of Participation: Shareholder involvement can improve company policies and oversight mechanisms, thereby enhancing shareholder value and increasing the effectiveness of corporate management.
- Legal Fee Arrangement: Halper Sadeh LLC will handle the case on a contingency fee basis, meaning shareholders will not incur out-of-pocket legal fees, reducing the financial burden of participation.
See More
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- Trial Enrollment Completed: BioVie Inc. announced the completion of enrollment in its Phase 2 ADDRESS-LC trial for Bezisterim, targeting the neurological symptoms of Long COVID affecting approximately 15 million people in the U.S., indicating significant progress in addressing this unmet medical need.
- Drug Mechanism and Applications: Bezisterim (NE3107) is an investigational oral drug that crosses the blood-brain barrier to modulate key neuroinflammatory pathways, aimed at alleviating symptoms in patients with Long COVID, Alzheimer's, and Parkinson's disease, showcasing its broad clinical application potential.
- Trial Design and Funding: The trial is a randomized, placebo-controlled, multicenter study fully funded by the U.S. Department of War, primarily assessing the safety and efficacy of Bezisterim in improving neurocognitive and fatigue-related symptoms, reflecting governmental support for this research initiative.
- Market Performance and Outlook: Despite BioVie’s current trading price of $1.46, down 3.95%, the upcoming topline results from the Phase 2 SUNRISE-PD trial are expected to generate optimism in the market, particularly regarding potential breakthroughs in Parkinson's disease treatment.
See More
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- KOL Event Announcement: BioVie will host a virtual KOL event on May 7, 2026, featuring Dr. Suzanne de la Monte from Brown University, aimed at discussing the mechanism of action of bezisterim and its implications for understanding neurodegenerative diseases, particularly Parkinson's disease.
- Clinical Trial Progress: BioVie’s Phase 2 trial indicates that Parkinson's patients receiving bezisterim in conjunction with levodopa exhibited improved motor control and reported fewer morning symptoms, highlighting the drug's potential to enhance patient quality of life.
- Long COVID Research: The ADDRESS-LC trial is enrolling around 200 patients to evaluate bezisterim's effects on lingering neurological symptoms associated with Long COVID, with preliminary hypotheses suggesting these symptoms may be linked to persistent inflammation, with topline data expected in mid-2026.
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See More
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- Biotech Advancements: BioVie Inc. is advancing a clinical trial for Parkinson's disease with 60 patients enrolled, expecting topline data in May 2026, which could significantly bolster its market position in the biopharmaceutical sector if successful.
- Obstructive Sleep Apnea Solutions: Vivos Therapeutics Inc.'s FDA-cleared non-surgical oral appliance aims to provide a long-term solution for the estimated one billion people affected by OSA globally, with strategic growth initiatives targeting direct-to-patient markets.
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- Shareholder Rights Protection: Long-term shareholders of BioVie may seek corporate governance reforms, fund returns, or court-approved financial incentive awards, enhancing their rights and interests.
- Transparency Improvement: Shareholder involvement can improve the company's policies, practices, and oversight mechanisms, promoting more transparent and effective management, thereby increasing shareholder value.
- Legal Fee Arrangement: Halper Sadeh LLC will handle the case on a contingent fee basis, meaning shareholders will not be responsible for out-of-pocket legal fees or expenses, reducing the financial burden of participation.
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- Legal Relief Options: Long-term shareholders of BioVie may seek corporate governance reforms, fund recovery, or court-approved financial incentives, aimed at enhancing company transparency and accountability.
- Importance of Participation: Shareholder involvement can improve company policies and oversight mechanisms, thereby enhancing shareholder value and increasing the effectiveness of corporate management.
- Legal Fee Arrangement: Halper Sadeh LLC will handle the case on a contingency fee basis, meaning shareholders will not incur out-of-pocket legal fees, reducing the financial burden of participation.
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