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Efficacy and safety of topical minocycline foam (FMX101 4%) in treatment of Chinese subjects with moderate-to-severe facial acne vulgaris: A phase 3, multi-centre, randomized, double-blind, vehicle-controlled study.

Yan LeWenlin YangJianyun LuJiang XianQing GuoChunyun HuangQing SunHuiping WangMingye BiHaiying WangSongmei GengBin YangAi-E XuYong CuiXiao-Yong ManYi ZhaoLitao ZhangLinfeng LiZhiqiang SongJin ChenHao ChengWei ZhuXiuping HanShanshan LiTong LinChunlei ZhangJiuhong LiYanling LiYangfeng DingLinda WangYuefang ZhuLeihong Flora Xiang
Published in: Journal of the European Academy of Dermatology and Venereology : JEADV (2024)
FMX101 4% treatment for 12 weeks could lead to significantly reduced ILC and nILC, and improved IGA treatment success rate in Chinese subjects with moderate-to-severe facial AV. It also showed a well acceptable safe and tolerability profile.
Keyphrases
  • double blind
  • placebo controlled
  • clinical trial
  • open label
  • early onset
  • phase iii
  • soft tissue
  • preterm birth