• General Dermatology
  • Eczema
  • Chronic Hand Eczema
  • Alopecia
  • Aesthetics
  • Vitiligo
  • COVID-19
  • Actinic Keratosis
  • Precision Medicine and Biologics
  • Rare Disease
  • Wound Care
  • Rosacea
  • Psoriasis
  • Psoriatic Arthritis
  • Atopic Dermatitis
  • Melasma
  • NP and PA
  • Skin Cancer
  • Hidradenitis Suppurativa
  • Drug Watch
  • Pigmentary Disorders
  • Acne
  • Pediatric Dermatology
  • Practice Management
  • Prurigo Nodularis

Article

FDA removes screening, monitoring requirement for acne drug

Washington - The Food and Drug Administration (FDA) has removed a blood-screening and monitoring requirement for Aczone, a topical acne treatment manufactured by QLT USA, a unit of biotech company QLT Inc., Vancouver, British Columbia, the Associated Press reports.

Washington - The Food and Drug Administration (FDA) has removed a blood-screening and monitoring requirement for Aczone, a topical acne treatment manufactured by QLT USA, a unit of biotech company QLT Inc., Vancouver, British Columbia, the Associated Press reports.

Prior to the FDA’s action, patients using the drug had to be monitored for blood conditions, including a type of anemia. According to the company, recent post-marketing studies show no clinical evidence of anemia in patients who have used the drug.

Related Videos
E. James Song is featured in this video series.
E. James Song is featured in this video series.
Benjamin Lockshin, MD, FAAD, is featured in this series.
Benjamin Lockshin, MD, FAAD, is featured in this series.
Benjamin Lockshin, MD, FAAD, is featured in this series.
1 KOL is featured in this series.
2 KOLs are featured in this series.
1 KOL is featured in this series.
2 KOLs are featured in this series.
E. James Song is featured in this video series.
© 2024 MJH Life Sciences

All rights reserved.