FDA Clears IND Application for Phase II Pulmonary Arterial Hypertension Trial
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FDA Clears IND Application for Phase II Pulmonary Arterial Hypertension Trial

According to a story from news.cision.com, the US Food and Drug Administration (FDA) has cleared the investigational new drug (IND) application for CS1, an investigational drug being developed by the…

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Approval Application for ANCA-Associated Vasculitis Drug Amended by Developer
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Approval Application for ANCA-Associated Vasculitis Drug Amended by Developer

According to a story from ANCA Vasculitis News, the biopharmaceutical company ChemoCentryx has recently made an amendment to its approval application for its investigational therapy. This therapy, called avacopan, is…

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Rare Classroom: Narcolepsy
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Rare Classroom: Narcolepsy

Welcome to the Rare Classroom, a new series from Patient Worthy. Rare Classroom is designed for the curious reader who wants to get informed on some of the rarest, most…

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This Antiphospholipid Syndrome Patient Felt Relief When the FDA Approved COVID Boosters
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This Antiphospholipid Syndrome Patient Felt Relief When the FDA Approved COVID Boosters

According to a story from Ebene Magazine, the US Food and Drug Administration (FDA) officially authorized that immunocompromised people could receive a third booster shot of the COVID-19 vaccine. This…

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