280 Participants NeededMy employer runs this trial

Camoteskimab for Atopic Dermatitis

Recruiting at 84 trial locations
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment called camoteskimab for individuals with moderate-to-severe atopic dermatitis, also known as eczema. The goal is to evaluate the effectiveness and safety of camoteskimab compared to a placebo (a dummy treatment). Participants will receive one of three different doses of camoteskimab or a placebo. This trial suits those who have had eczema for at least a year and find that topical treatments (creams or ointments) haven't been effective enough. As a Phase 2 trial, the research focuses on assessing the treatment's effectiveness in an initial, smaller group of people.

Will I have to stop taking my current medications?

Yes, you may need to stop taking certain medications before joining the trial. Some medications, like specific topical treatments, systemic therapies, and certain antihistamines, need to be stopped for a period before the trial starts. It's best to discuss your current medications with the trial team to see if any changes are needed.

Is there any evidence suggesting that Camoteskimab is likely to be safe for humans?

Research has shown that camoteskimab was safe for patients in earlier studies. No serious side effects related to the treatment were reported, and no participants discontinued due to side effects. This indicates that participants generally did not experience severe or dangerous reactions to the medication. Patients also experienced significant improvements in their eczema symptoms, suggesting the treatment was both effective and safe.12345

Why do researchers think this study treatment might be promising for atopic dermatitis?

Researchers are excited about camoteskimab for atopic dermatitis because it offers a fresh approach compared to current treatments like topical steroids and immunosuppressants. Unlike these standard treatments, camoteskimab works by targeting specific pathways involved in the inflammatory process of atopic dermatitis, potentially reducing symptoms more effectively and with fewer side effects. Additionally, camoteskimab is designed to be more precise in its action, which could mean better management of the condition and improved quality of life for patients.

What evidence suggests that Camoteskimab might be an effective treatment for atopic dermatitis?

Research has shown that camoteskimab holds promise for treating atopic dermatitis, a condition causing itchy and inflamed skin. In earlier studies, camoteskimab significantly reduced eczema symptoms, with improvements observed as early as four weeks. By week 16, some patients experienced up to an 80% reduction in their Eczema Area and Severity Index (EASI) scores, which measure the severity of their condition. Approximately 60-65% of participants responded well to the treatment, underscoring its potential effectiveness. This trial will evaluate different doses of camoteskimab, and these findings suggest it could be a helpful option for those with moderate-to-severe atopic dermatitis.12346

Are You a Good Fit for This Trial?

This trial is for adults aged 18-65 with moderate-to-severe atopic dermatitis (eczema) affecting at least 10% of their skin, who have had the condition for over a year and haven't improved enough with creams or ointments. Participants must be able to use contraception and give consent.

Inclusion Criteria

Have you tried at least one prescription for your eczema that did not work?
Have you had eczema for more than a year?

Exclusion Criteria

Do you have psoriasis or lupus?
Do you have HIV or hepatitis?

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants are randomized to receive either camoteskimab or placebo for 24 weeks

24 weeks
Regular visits throughout the 24-week period

Extension

All participants receive camoteskimab in the extension period

Duration not specified

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Camoteskimab

Trial Overview

The study compares camoteskimab, an experimental drug, to a placebo in people with moderate-to-severe eczema. It is randomized and double-blind, meaning neither patients nor doctors know who gets which treatment.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Placebo Group

Group I: Dose 3Experimental Treatment1 Intervention
Group II: Dose 2Experimental Treatment1 Intervention
Group III: Dose 1Experimental Treatment1 Intervention
Group IV: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Apollo Therapeutics Ltd

Lead Sponsor

Trials
5
Recruited
330+

Citations

NCT06436183 | A Study of the Effects of Camoteskimab in ...

To further assess the efficacy of camoteskimab in participants with AD via the Eczema Area and Severity Index (EASI) which measures the severity of clinical ...

Apollo Therapeutics' Anti-IL-18 Antibody Camoteskimab ...

In the open-label phase, camoteskimab responses continued to deepen, with ~80% reduction in mean EASI score, and ~65% and ~60% responder rates ...

Camoteskimab Meets Primary Endpoint in Phase 2a ...

Camoteskimab significantly reduced atopic dermatitis symptoms by Week 16, with improvements seen as early as Week 4. The phase 2a study showed ...

A Phase 2b Study of the Effects of Camoteskimab in Adults ...

To further assess the efficacy of camoteskimab in participants with moderate-to-severe AD via the Eczema Area and Severity Index (EASI) which ...

A Study of the Effects of Camoteskimab in Adults With ...

This is a Phase 2a, multicenter, randomized, double-blind, placebo-controlled study with an open-label extension to evaluate the efficacy and safety of ...

camoteskimab (AVTX-007) / Avalo Therap, AstraZeneca, ...

... Camoteskimab was extremely well tolerated with no treatment-related serious adverse events or discontinuations." P2a data • Atopic Dermatitis. Print; Email ...