All FDA drug approvals

FDA approval · Drugs@FDA

IMAAVYnipocalimab-aahu

BLA761430 ·

FDA approved the original biologics license application for IMAAVY on April 29, 2025, sponsored by JANSSEN BIOTECH. FDA classed that submission a new molecular entity, which makes it the first approval of nipocalimab-aahu in any product. FDA has approved 1 efficacy supplement on the application since, the most recent on August 24, 2026.

Application
BLA761430
Sponsor
JANSSEN BIOTECH
Original approval
Review
priority review
Submission class
Type 1 - New Molecular Entity
Active ingredient
nipocalimab-aahu

Products under this application

Ingredient and strengthFormRouteMarketing status
nipocalimab-aahu 1200MG/6.5ML(185MG/ML)INJECTABLEINJECTIONPrescription
nipocalimab-aahu 300MG/1.62ML(185MG/ML)INJECTABLEINJECTIONPrescription

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

ApprovedSupplementReview
S-2priority

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

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