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BIVI US Equity

Biovie Inc.Health Care · Pharmaceutical Preparations · CIK 1580149 · FY ends Jun 30
$1.34
+0.38 (+38.95%)
USD · as of 2026-08-19 · marketstack
6 registered studies · 1 active

Studies where BIVI is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

6 interventional · 1 with posted results

Held by 3 tracked-famous managers (RENAISSANCE TECHNOLOGIES LLC, CITADEL ADVISORS LLC, JANE STREET GROUP, LLC) · FINRA short interest 4.4 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
NE3107 in Adults With Neurological Symptoms of Long COVIDNCT06847191Change from Baseline in performance on the Cogstate Cognition battery*Randomized · Triple-masked · TreatmentPhase 2Active, not recruitingDrug: NE3107, PlaceboLong COVID203Aug 2026≤ 11 d2026-05-29
A Study of NE3107 in Early Parkinson'sNCT06757010Monocyte Lymphocyte Ratio (MLR)Randomized · Quadruple-masked · TreatmentPhase 2CompletedDrug: NE3107, PlaceboParkinsons Disease (PD)572026-05-01actual2026-08-11
A Phase 3 Study of NE3107 in Probable Alzheimer's DiseaseNCT04669028Change in Clinical Dementia Rating Scale Sum of Boxes (CDR-SB)Randomized · Quadruple-masked · TreatmentPhase 3CompletedDrug: NE3107, PlaceboAlzheimer Disease4392023-09-30actual2023-11-21
A Study for Evaluation of BIV201 to Reduce Ascites and Complications in Patients With Cirrhosis and Refractory AscitesNCT04112199Incidence of complications, at least grade 2 severityRandomized · Open-label · TreatmentPhase 2Terminatedsponsor's stated reason: For reasons unrelated to safety or efficacyDrug: BIV201 continuous infusionAscites, Decompensated Cirrhosis152023-05-08actual2024-05-08
NE3107 Activity and Safety in Patients With Parkinson's Disease Using LevodopaNCT05083260Change from baseline (day 1) in Motor disease society- Unified Parkinson's disease rating scale Part III total score for the patient in the "off-state" (without L-dopa for previous eight hours)Randomized · Quadruple-masked · TreatmentPhase 1/2CompletedDrug: NE3107, placeboParkinson Disease462022-11-21actual2023-02-08
Continuous Infusion Terlipressin for Patients With Cirrhosis and Refractory AscitesNCT03107091results2021-07-13Clinical Safety of Terlipressin Infusion in Cirrhotic Patients With Refractory AscitesOpen-label · TreatmentStudy Protocol and Statistical Analysis PlanPhase 2CompletedDrug: Terlipressin acetate continuous infusionCirrhosis, Ascites Hepatic62019-04-01actual2021-07-13

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19