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Nemolizumab

Alternative Names: nemolizumab, cim331, CD14152, CD-14152
Latest Update: 2024-12-18
Latest Update Note: Clinical Trial Update

Product Description

Nemolizumab is a subcutaneously administered humanized monoclonal antibody against interleukin-31 receptor A, which is involved in pruritus and inflammation in atopic dermatitis.Nemolizumab is a subcutaneously administered humanized monoclonal antibody against interleukin-31 receptor A, which is involved in pruritus and inflammation in atopic dermatitis.

Mechanisms of Action: IL31 Inhibitor

Novel Mechanism: No

Modality: Antibody

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Approved

Approved Countries: Japan

Approved Indications: None

Known Adverse Events: None

Company: Galderma
Company Location:
Company CEO:
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Nemolizumab

Countries in Clinic: Australia, Austria, Belgium, Bulgaria, Canada, Czech Republic, Denmark, Estonia, France, Georgia, Germany, Hungary, Italy, Japan, Korea, Latvia, Lithuania, Netherlands, New Zealand, Poland, Singapore, Spain, Sweden, Switzerland, United Kingdom, United States

Active Clinical Trial Count: 32

Highest Development Phases

Phase 3: Dermatitis, Atopic|Kidney Diseases|Kidney Failure, Chronic|Neurodermatitis|Prurigo|Pruritus

Phase 2: Scleroderma, Diffuse|Scleroderma, General|Scleroderma, Systemic

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

RD-06-SPR-202699

P3

Unknown Status

Prurigo

2027-08-15

jRCT2031230174

P3

Not yet recruiting

Dermatitis, Atopic|Pruritus

2027-04-30

RD.06.SPR.202699

P3

Active, not recruiting

Prurigo|Neurodermatitis

2026-10-26

RD.06.SPR.118163

P3

Unknown Status

Dermatitis, Atopic

2026-08-31

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