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
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 |