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U.S. FDA Approves Tablet Formulation of BeOne's BRUKINSA® for All Approved Indications

1. ONC's BRUKINSA tablet formulation approved by the FDA for all indications. 2. BRUKINSA leads CLL patient starts and BTK inhibitor market share.

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FAQ

Why Very Bullish?

FDA approval enhances ONC's product pipeline and market position. Historical FDA approvals correlate with stock uptrends, e.g., recent approvals of peers like ABBV.

How important is it?

FDA approval is a significant catalyst for revenue growth and investor confidence. It also strengthens ONC's competitive stance in the BTK inhibitor market.

Why Short Term?

Immediate sales boosts expected post-FDA approval. Market reactions to similar drug approvals have shown short-term gains.

Related Companies

SAN CARLOS, Calif.--(BUSINESS WIRE)---- $ONC #BeOne--BeOne Medicines Ltd. (NASDAQ: ONC; HKEX: 06160; SSE: 688235), a global oncology company, today announced that the U.S. Food and Drug Administration (FDA) has approved a new tablet formulation of BRUKINSA® (zanubrutinib) for all five approved indications. BRUKINSA remains the leader in new chronic lymphocytic leukemia (CLL) patient starts across all lines of therapy in the U.S., and for the first time, has become the overall BTK inhibitor market share leader.

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