I-FDA Igunyaza Ukwelashwa Okusha Kwesihloko Se-Angiofibromas Yobuso

A BAMBA Ukukhululwa Kwamahhala | eTurboNews | eTN
Ibhalwe ngu Linda Hohnholz

Today the TSC Alliance® applauds the U.S. Food and Drug Administration’s (FDA’s) approval of HYFTOR™, which is the first FDA-approved topical treatment for facial angiofibromas in adults and children six years of age or older who have tuberous sclerosis complex (TSC). HYFTOR™, manufactured by Nobelpharma America, LLC, has Orphan Drug Status for this particular indication.      …

eTurboNews izindatshana ezababhalisi kuphela. Ukubhalisa kuyinto MAHHALA.
Ababhalisile bangena lapha Chofoza lapha ukuze ubhalise MAHHALA

LOKHO ONGAKUTHATHE KULESI SIHLOKO:

  • Food and Drug Administration’s (FDA’s) approval of HYFTOR™, which is the first FDA-approved topical treatment for facial angiofibromas in adults and children six years of age or older who have tuberous sclerosis complex (TSC).
  • HYFTOR™, manufactured by Nobelpharma America, LLC, has Orphan Drug Status for this particular indication.
  • eTurboNews izindatshana ezababhalisi kuphela.

<

Mayelana umbhali

Linda Hohnholz

Umhleli omkhulu we eTurboNews ezinze eTN HQ.

Yabelana ku...