Cargando…
FDA approves Ruxolitinib (Opzelura) for Vitiligo Therapy: A breakthrough in the field of dermatology
The Food and Drug Administration (FDA) has authorized Ruxolitinib (Opzelura), as first at-home treatment for non-segmental vitiligo, an autoimmune condition that causes spots and patches of paler skin. Previously, it was used to treat atopic dermatitis, myelofibrosis, essential thrombocythemia, and...
Autores principales: | Sheikh, Ayesha, Rafique, Warisha, Owais, Rabia, Malik, Farheen, Ali, Eman |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486756/ https://www.ncbi.nlm.nih.gov/pubmed/36147080 http://dx.doi.org/10.1016/j.amsu.2022.104499 |
Ejemplares similares
-
Olumniant (Baricitinib) oral tablets: An insight into FDA-approved systemic treatment for Alopecia Areata
por: Ali, Eman, et al.
Publicado: (2022) -
Celebrating breakthrough in dental diagnostics: FDA approval of an AI model for diagnosis of periodontal diseases: A correspondence
por: Khan, Ayesha, et al.
Publicado: (2023) -
Recently FDA-approved drug: A new hope for vitiligo patients?
por: Siddiq, Mohammad Arham, et al.
Publicado: (2022) -
Pharmacists’ Knowledge and Perceptions of FDA Approval Standards and the Breakthrough Therapy Designation
por: Herink, Megan C., et al.
Publicado: (2022) -
SOBA (soluble oligomer binding assay): A breakthrough or the early diagnosis of Alzheimer's disease
por: Sheikh, Ayesha, et al.
Publicado: (2023)