Pfizer FDA Tuesday, November 6, 2012 0.00 Neutral

FDA Approves XELJANZ — Pfizer Laboratories Div Pfizer Inc

FDA approved XELJANZ (tofacitinib citrate) from Pfizer Laboratories, a new oral treatment for rheumatoid arthritis, paving the way for the company to capture a significant share of the JAK inhibitor market. This pivotal approval marked a strategic advancement for Pfizer, expanding its oncology pipeline by diversifying its portfolio into immunology and strengthening its competitive position against both established and emerging rivals.

View original filing at SEC.gov →
AI-generated summary for informational purposes only. Always verify against the original filing. Not investment advice. BriefTape is not a registered investment adviser.

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