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Camoteskimab

Phase 2

Atopic Dermatitis | Small molecule | Dermatology |cbdMD, Inc.|Last Updated: Aug 28, 2026

Target and mechanism

Molecular targetIL18
Target classCross-linking Agent
ModalitySmall molecule

Success Probability

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Market & Valuation

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Trial Design

RandomizedDouble-BlindPLACEBO_CONTROLLEDDMCBiomarker
Total Trials1
Total Enrollment280

FDA Designations

No designations recorded

Clinical trial landscape

Camoteskimab · 1 trial · 8 indications

Phase 2 1
NCT07599813A Phase 2b Study of the Effects of Camoteskimab in Adults With Moderate-to-Severe Atopic DermatitisAtopic Dermatitis
RECRUITING280 Analytics
PHASE2RECRUITING
A Phase 2b Study of the Effects of Camoteskimab in Adults With Moderate-to-Severe Atopic Dermatitis
Atopic DermatitisUnlock trial analytics

Study Endpoints

Primary Endpoints

Percentage change from baseline in Eczema Area and Severity Index (EASI) between camoteskimab and placebo at Week 24
From Baseline visit until Week 24 visit

An EASI score is a tool used to measure the extent (area) and severity of atopic eczema. The EASI utilizes area assessments that rate the four involved regions on a 0% to 100% scale for each region. The scores are added up for each of the four body regions (head, arms, trunk, and legs). For each of these components, the individual scores are added together to calculate the EASI score, which ranges from 0 to 72. The higher the EASI score, the more severe the AD.

Secondary Endpoints

Proportion of participants achieving at least 75% improvement from baseline in EASI (EASI-75)
24 weeks
Proportion of participants with vIGA-AD 0/1 and a decrease in vIGA-AD of ≥ 2 points from baseline
24 weeks
Proportion of participants with an improvement of ≥ 4 or more points from baseline in peak pruritus NRS (PP-NRS) weekly average of the daily scores
24 weeks
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Study Design & Arms

AllocationRANDOMIZED
MaskingQUADRUPLE
ModelPARALLEL
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Camoteskimab Dose Level 1EXPERIMENTALCamoteskimab administered subcutaneously
Camoteskimab Dose Level 2EXPERIMENTALCamoteskimab administered subcutaneously
Camoteskimab Dose Level 3EXPERIMENTALCamoteskimab administered subcutaneously
PlaceboPLACEBO_COMPARATORDummy version of the study drug administered subcutaneously

Interventions

NameTypeDescription
CamoteskimabDRUGDrug Product
PlaceboDRUGInactive substance
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Eligibility Criteria

Age Range18 Years to 65 Years
SexALL
Healthy VolunteersNo
Study Sites85

Inclusion Criteria: 1. Age 18-65 inclusive, at the time of signing the informed consent. 2. Chronic AD for at least 1 year based on clinically confirmed diagnosis of active AD, according to Hanfin and Rajka criteria. 3. Participants with moderate-to-severe AD defined by: 1. Investigator global ...

Countries:United StatesBulgariaCanadaCzechiaGermanyHungaryPolandSpain
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