Source: Pharamceutical Technology

Ocelot Bio: FDA grants Orphan Drug status to Ocelot's hepatorenal syndrome therapy

A placebo-controlled, randomised, multicentre Phase II trial of OCE-205 is underway in patients with HRS-AKI. The post FDA grants Orphan Drug status to Ocelot's hepatorenal syndrome therapy appeared first on Pharmaceutical Technology.

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Est. Annual Revenue
$100K-5.0M
Est. Employees
1-25
Katherine Vega Stultz's photo - President & CEO of Ocelot Bio

President & CEO

Katherine Vega Stultz

CEO Approval Rating

90/100

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