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FDAsafety guidance77% confidence

FDA AP — BAXFENDY (ORIG)

Source: FDA

Why This Matters

Why this matters: sets a safety guidance precedent in the same sub-indication (cardiology) as United Therapeutics; the same agency is already in play for this signal, so precedent weight is higher.

Regulatory Analysis

Application NDA219878. Sponsor: ASTRAZENECA AB. Submission status: AP. Submission type: ORIG. Review priority: PRIORITY. Active ingredients: BAXDROSTAT.

Supporting Context

Therapeutic area
Pulmonary Arterial Hypertension · Prostacyclin Analog
Sub-indication
Hypertension

Related signal: FDA Accepts Supplement Application for Tyvaso (Treprostinil)

Source

View source document

Related Signal

Open signal — FDA Accepts Supplement Application for Tyvaso (Treprostinil)
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