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Final Data From the Phase 3 MYR301 Study Demonstrated Longer Treatment With Bulevirtide Was Associated With Sustaining Undetectability After Stopping Treatment

1. Gilead's MYR301 study shows 36% maintained virologic suppression after treatment. 2. Bulevirtide, a first-in-class drug, shows promise for chronic hepatitis delta.

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Why Bullish?

The positive results from the MYR301 study could enhance GILD's market position significantly, similar to past success with hepatitis drugs like Harvoni, which contributed to a notable rise in stock value post-approval.

How important is it?

The successful virologic suppression indicates potential for long-term treatment solutions, strengthening investor confidence and driving demand for GILD's stock.

Why Long Term?

The sustained efficacy of bulevirtide may expand GILD's market share in chronic hepatitis treatments over the years, similar to how long-term treatments for HIV expanded their product lines.

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FOSTER CITY, Calif.--(BUSINESS WIRE)--Gilead Sciences Inc. (Nasdaq: GILD) today announced final results from the pivotal Phase 3 MYR301 study revealing that 36% (23 out of 64) of adults living with chronic hepatitis delta virus (HDV) treated with the first-in-class entry inhibitor bulevirtide at either a 2 mg or 10 mg dose maintained virologic suppression for almost two years after stopping treatment after achieving undetectable HDV RNA at end of treatment (EOT). In participants who sustained u.

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