elzonris

Generic: tagraxofusp-erzs

elzonris: developed by 1 company · 1 FDA decision. Updated within the last hour.

Development Pipeline (1)

FDA Decisions

Approval1 INDICATIONS AND USAGE ELZONRIS is indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and in pediatric patients 2 years and older. ELZONRIS is a CD123-directed cytotoxin indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and in pediatric patients 2 years and older ( 1 )(STML)

Frequently asked questions

Who is developing elzonris?

elzonris is being developed by STEMLINE THERAPEUTICS INC.

What is elzonris's latest FDA decision?

The most recent tracked FDA decision for elzonris is Approval for 1 INDICATIONS AND USAGE ELZONRIS is indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and in pediatric patients 2 years and older. ELZONRIS is a CD123-directed cytotoxin indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and in pediatric patients 2 years and older ( 1 ), dated December 21, 2018.

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