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EVMN US Equity

Evommune, Inc.Health Care · Pharmaceutical Preparations · CIK 2044725 · FY ends Dec 31
$15.01
+0.79 (+5.56%)
USD · as of 2026-08-19 · marketstack
6 registered studies · 2 active

Studies where EVMN 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 · 2 with posted results

Held by 10 tracked-famous managers (Point72 Asset Management, L.P., Balyasny Asset Management L.P., JANE STREET GROUP, LLC, Holocene Advisors, LP, Squarepoint Ops LLC, +5 more) · FINRA short interest 8.7 days to cover (settled 2026-07-31) · insider 90d: 0 buys / 9 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Study of EVO756 in Adults With MigraineNCT07616128Mean change from baseline in the number of monthly migraine days (MMD)Randomized · Quadruple-masked · PreventionPhase 2RecruitingDrug: EVO756, Dose 1, EVO756, Dose 2, PlaceboMigraine330Oct 2027≤ 437 d2026-08-10
Phase 2b Study of EVO756 in Adults With Atopic DermatitisNCT07150845Percentage change in Eczema Area and Severity Index (EASI) from BaselineRandomized · Quadruple-masked · TreatmentPhase 2Active, not recruitingDrug: EVO756, EVO756, EVO756, Placebo controlAtoptic Dermatitis120Jul 20262026-05-18
Phase 2b Study of EVO756 in Adults With Moderate to Severe Chronic Spontaneous Urticaria (CSU)NCT06873516Mean change from baseline in UAS7Randomized · Quadruple-masked · TreatmentPhase 2CompletedDrug: EVO756, EVO756, EVO756, Placebo controlChronic Spontaneous Urticaria1822026-05-29actual2026-07-01
Efficacy Study of EVO301 in Moderate to Severe Atopic DermatitisNCT06723405Eczema Area and Severity Index (EASI)Randomized · Triple-masked · TreatmentPhase 2CompletedBiological: EVO301, PlaceboAtopic Dermatitis (AD), Eczema, Eczema Atopic Dermatitis712025-11-17actual2025-12-04
A Study Evaluating the Safety, Tolerability, and Efficacy of EVO756 in Adults With Chronic Inducible UrticariaNCT06603220results2026-05-19Safety and TolerabilityOpen-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: Oral EVO756 300 mg QD, Oral EVO756 50 mg BIDChronic Inducible Urticaria302025-05-08actual2026-05-19
Safety and Efficacy Study of EVO101 Topical Cream in Atopic DermatitisNCT05579899results2025-03-05Percent Change in Eczema Area and Severity Index (EASI) From Baseline to Week 8Randomized · Triple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: EVO101Atopic Dermatitis Eczema1192023-07-27actual2025-03-05

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