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APYX US Equity

Apyx Medical CorpHealth Care · Surgical & Medical Instruments & Apparatus · CIK 719135 · FY ends Dec 31
$3.11
+0.05 (+1.63%)
USD · as of 2026-08-18 · marketstack
10 registered studies · 0 active

Studies where APYX 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.

10 interventional · 10 with posted results

Held by 9 tracked-famous managers (RENAISSANCE TECHNOLOGIES LLC, MILLENNIUM MANAGEMENT LLC, MARSHALL WACE, LLP, SUSQUEHANNA INTERNATIONAL GROUP, LLP, CITADEL ADVISORS LLC, +4 more) · FINRA short interest 4.7 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionUpdated
Histological Evaluation of Human Skin Bx to Assess the Effects of APR Tx as an Adjunct Procedure in Facelift SurgeryNCT06243744results2026-03-24Analysis of Elasticity (Collagen & Elastin)Open-label · TreatmentStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR SystemSkin Laxity, Tissue Degeneration, Tissue Breakdown, Collagen Degeneration, Collagen Shrinkage72025-07-10actual2026-03-24
Measuring Renuvion Soft Tissue Contraction Using UltrasoundNCT05968495results2025-02-03Analysis of Contraction From Baseline to Day 365Open-label · TreatmentStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR HandpieceSkin Laxity52024-09-30actual2025-02-03
A Post-Market Study in Greece of a Minimally Invasive Breast Lift Procedure Utilizing the Renuvion APR SystemNCT05665335results2025-05-14Independent Photographic Review of Before and After Images Compared to Baseline Compared to D180.Open-label · TreatmentStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR SystemBreast Ptosis152024-04-26actual2025-05-14
Evaluation of the Use of the Renuvion APR System in the LabiaNCT05323630results2025-12-23Evaluation of Change Between Baseline and Follow-up Images as Determined by a Masked, Qualitative Assessment of Photographs at 90-days and 180-days Post-treatment Compared to Baseline.Open-label · TreatmentStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR SystemLabia Enlarged, Labium; Hypertrophy102024-04-23actual2025-12-23
Post-Market Lower Eyelid Treatment With Renuvion in GreeceNCT05605691results2025-03-26Day 180 Number of Participants With Improvement in Lower Eyelid Area as Determined by a Masked, Qualitative Assessment.Open-label · TreatmentStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR SystemSkin Laxity162024-03-05actual2025-03-26
Renuvion APR System When Used as an Adjunct Procedure In Gynecomastia SurgeryNCT05093049results2024-02-08Analysis of Bilateral Occurrence of Adverse EventsRandomized · Double-masked · TreatmentStudy ProtocolNot applicableCompletedDevice: Renuvion APR System · Procedure: Gynecomastia Correction SurgeryGynecomastia102022-08-17actual2024-02-08
Renuvion APR Device to Improve the Appearance of Lax Tissue in the Neck and Submental RegionNCT04146467results2022-07-08Day 180 Number of Participants With Improvement Measured By Independent Photographic ReviewNon-randomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanNot applicableCompletedDevice: Renuvion APR DeviceLax Skin822022-02-28actual2022-07-20
Renuvion Dermal System for Dermal ResurfacingNCT04185909results2022-06-03Independent Photo Reviewer Fitzpatrick Wrinkle and Elastosis Scale (FWS)Open-label · TreatmentStudy Protocol · Statistical Analysis PlanNot applicableCompletedDevice: Renuvion Dermal SystemWrinkle, Rhytides552021-03-23actual2022-06-22
The Use of J-Plasma® for Dermal ResurfacingNCT03286283results2019-08-07Improvement in Fitzpatrick Wrinkle and Elastosis Scale (FWS) ScoreOpen-label · TreatmentStudy Protocol · Statistical Analysis PlanNot applicableCompletedDevice: J-PlasmaFacial Wrinkles, Rhytides552018-08-20actual2022-07-27
Cold Plasma for the Reduction of Lymphoceles Following PLNDNCT02658851results2020-12-02Number of Participants With Incidence of Lymphocele FormationOpen-label · PreventionStudy Protocol and Statistical Analysis PlanNot applicableCompletedDevice: J-PlasmaLymphoceles Following Pelvic Lymph Node Dissection1002017-06-27actual2020-12-02

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