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Vir Biotechnology Initiates Second Pivotal Trial in Its Global ECLIPSE Registrational Program for Chronic Hepatitis Delta

1. VIR has initiated ECLIPSE 2 Phase 3 trial for chronic hepatitis delta. 2. Trial compares tobevibart and elebsiran against bulevirtide monotherapy.

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Why Bullish?

The initiation of a Phase 3 trial typically boosts investor confidence and can lead to increased stock prices, as seen in other biotech companies like Gilead Sciences during similar clinical advancements.

How important is it?

The initiation of a pivotal trial signals a critical phase in Vir's product pipeline, which is likely to attract investors and analysts focused on biotechnology advances.

Why Long Term?

The outcomes of the ECLIPSE 2 trial will shape future revenue streams; positive results could significantly advance product development and revenue timelines, akin to Roche's progression with emerging therapies.

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SAN FRANCISCO--(BUSINESS WIRE)--Vir Biotechnology, Inc. (Nasdaq: VIR) today announced the enrollment of the first participant in the ECLIPSE 2 Phase 3 clinical trial, which is designed to compare the combination of tobevibart and elebsiran to continued bulevirtide monotherapy in participants with chronic hepatitis delta (CHD) who have not achieved undetectable hepatitis delta virus (HDV) RNA despite bulevirtide treatment. ECLIPSE 2 is one of three trials in Vir Biotechnology's registrational EC.

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