AbbVie Seeks FDA Approval for Vitiligo Treatment

MT Newswires Live
Feb 03

AbbVie (ABBV) said Tuesday it filed regulatory applications with the US Food and Drug Administration and the European Medicines Agency for upadacitinib to treat adults and adolescents with vitiligo, an autoimmune skin condition.

In a phase 3 trial, participants achieved a 50% improvement in total body pigment, and about 75% showed facial re-pigmentation, the company said.

Currently, there are no approved systemic drugs available to help stabilize the disease or restore skin color for the approximately 84% of patients with the non-segmental form of the disorder, AbbVie said.

Common side effects reported during the trials included acne and respiratory infections, with no new safety risks identified, it added.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

Most Discussed

  1. 1
     
     
     
     
  2. 2
     
     
     
     
  3. 3
     
     
     
     
  4. 4
     
     
     
     
  5. 5
     
     
     
     
  6. 6
     
     
     
     
  7. 7
     
     
     
     
  8. 8
     
     
     
     
  9. 9
     
     
     
     
  10. 10