Recent Updates
Recently added Catalysts

EVO301

Phase 2

Atopic Dermatitis (AD) | Monoclonal antibody | Immunology |Evommune, Inc.|Last Updated: Dec 4, 2025

Success Probability
Approval Probability 71%
TA Base Rate26%
Adjusted LOA41%
ML RiskLOW_RISK
Premium
Market & Valuation
rNPV $3.2B
Market Size $9.4B
Revenue Basis $1.6B
Competitors 6
Premium
Trial Design
RandomizedDouble-BlindPLACEBO_CONTROLLED
Total Trials1
Total Enrollment71
FDA Designations
No designations recorded
Clinical Trials (1)
NCT IDTitlePhaseStatusEnrollmentVelocityDesignStartCompletionLast UpdatedSitesCountries
NCT06723405Efficacy Study of EVO301 in Moderate to Severe Atopic DermatitisPHASE2 COMPLETED 71Feb 13, 2025Nov 17, 2025Dec 4, 202512 Australia, New Zealand
Unlock Drug Trial Details
Study Endpoints
Primary Endpoints
Eczema Area and Severity Index (EASI)
12 weeks

EASI assesses the extent and severity of atopic dermatitis. EASI is a composite index with scores ranging from 0 to 72. Higher values indicate more severe or extensive disease.

Secondary Endpoints
Investigator Global Assessment (IGA)
12 weeks
Body Surface Area (BSA)
12 weeks
Pruritus-NRS
12 weeks
Unlock Study Endpoints
Study Design & Arms
AllocationRANDOMIZED
MaskingTRIPLE
ModelPARALLEL
PurposeTREATMENT
Treatment Arms
ArmTypeDescription
Intravenous EVO301EXPERIMENTAL -
PlaceboPLACEBO_COMPARATOR -
Interventions
NameTypeDescription
EVO301BIOLOGICALIntravenous EVO301
PlaceboBIOLOGICALPlacebo
Unlock Study Design Details
Eligibility Criteria
Age Range18 Years — N/A
SexALL
Healthy VolunteersNo
Study Sites12

Inclusion Criteria: 1. Males or non-pregnant, non-lactating females, age 18 years or older 2. Chronic atopic dermatitis for at least 6 months 3. BSA of AD involvement of at least 10% 4. EASI score of at least 16. Exclusion Criteria: 1. Significant AD flare with 4 weeks 2. Use of biologic therapy ...

Countries:AustraliaNew Zealand
Unlock Eligibility Criteria