Catalyst Wire Dossier Catalyst Wire Dossier
FDA approval · 2021-07-28

FDA Approved: SOLIQUA 100/33 — Supplemental Application (Sanofi-Aventis U.S. LLC)

View source ↗

Summary

The FDA approved a supplemental application for Soliqua 100/33, a fixed-ratio combination of insulin glargine and lixisenatide, submitted by Sanofi-Aventis U.S.…

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

Drugs mentioned

  • SOLIQUA 100/33 (INSULIN GLARGINE AND LIXISENATIDE)

Snippet

SUPPL AP for SOLIQUA 100/33 (INSULIN GLARGINE AND LIXISENATIDE)