Nearly 1,400 participants aged 12 to 64 received upadacitinib 15 mg, 30 mg, or placebo. All participants had alopecia areata affecting at least half their scalp.
Clinical Considerations
- Nearly half receiving 15 mg and over 54% receiving 30 mg achieved at least 80% scalp coverage.
- Complete scalp regrowth occurred in 13% and 23% of the respective treatment groups.
- Acne, upper respiratory infections, colds, and throat irritation represented the most frequently reported adverse events.
- The initial comparison covered 24 weeks, leaving treatment durability and long-term risk-benefit balance unresolved.
Practice Applications
- Recognize upadacitinib as an investigational alopecia option, not an approved indication.
- Interpret dose-response findings alongside systemic JAK inhibitor safety considerations.
- Consider adolescents within the studied population when evaluating future evidence.
- Monitor regulatory decisions and longer-term efficacy and safety results.
PATIENT EDUCATION
OBESITY/WEIGHT MANAGEMENT
EXERCISE/TRAINING
LEGAL MATTERS
GUIDELINES/RECOMMENDATIONS