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FDA

Regulatory intelligence
FDAsafety guidance72% confidence

Janus Kinase (JAK) inhibitors: Drug Safety Communication - FDA Requires Warnings about Increased Risk of Serious Heart-related Events, Cancer, Blood Clots, and Death

Source: FDA

Why This Matters

Why this matters: sets a safety guidance precedent in the same sub-indication (liver cancer) as Alnylam Pharmaceuticals.

Regulatory Analysis

FDA is requiring revisions to the Boxed Warning, FDA’s most prominent warning, for Xeljanz/Xeljanz XR, Olumiant, and Rinvoq to include information about the risks of serious heart-related events, cancer, blood clots, and death.

Supporting Context

Therapeutic area
Oncology · Hepatocellular Carcinoma
Sub-indication
Liver Cancer

Related signal: Alnylam's ALN-BCAT Study in Hepatocellular Carcinoma Evaluates Safety and Efficacy

Source

View source document

Related Signal

Open signal — Alnylam's ALN-BCAT Study in Hepatocellular Carcinoma Evaluates Safety and Efficacy
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