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XORTX To Have Type B Meeting With FDA Regarding Its Program For Gout Treatment, Stock Up

By RTTNews Staff Writer   ✉  | Published:  | Google News Follow Us  | Join Us
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XORTX Therapeutics Inc. (XRTX), Wednesday announced that the company has an upcoming Type B meeting with the US Food and Drug Administration regarding its XRx-026 program for the treatment of gout.

The XRx-026 program is developing XORLO, a proprietary formulation of oxypurinol to treat individuals suffering from gout, an inflammatory arthritis.

The purpose of this meeting will be to review the XRx-026 program and its readiness for submission of a New Drug Application to gain marketing approval for XORLOTM in the US using the FDA 505(b)2 development pathway.

The company stated that it will submit a type B meeting package to the FDA during the next week, with FDA communications expected by April 26, 2025.

The Type B meeting review will include review of chemistry, manufacturing, pharmacology, toxicology and clinical evidence regarding XRx-026 program.

Currently, XORTX's stock is moving up 5.78 percent, to $1.005 on the Nasdaq.

For comments and feedback contact: editorial@rttnews.com

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