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Chimerix Pursues FDA Approval for Dordaviprone
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Chimerix Pursues FDA Approval for Dordaviprone

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Chimerix ( (CMRX) ) has shared an update.

Chimerix announced plans to submit a new drug application for dordaviprone, targeting recurrent H3 K27M-mutant diffuse glioma, aiming for accelerated FDA approval by the end of 2024. The company has engaged with the FDA extensively and achieved significant program milestones, including substantial enrollment in the Phase 3 ACTION study. If approved, this could position Chimerix as a leader in treating this aggressive form of glioma, potentially impacting market dynamics and offering new hope for patients with no current approved therapies.

More about Chimerix

Chimerix, Inc. operates in the pharmaceutical industry, focusing primarily on developing innovative therapeutics for cancer treatment. The company is notably working on novel compounds like dordaviprone and ONC206 targeting specific mutations in gliomas and central nervous system tumors, with a market focus on unmet medical needs such as rare pediatric diseases.

YTD Price Performance: -10.08%

Average Trading Volume: 509,936

Technical Sentiment Consensus Rating: Strong Buy

Current Market Cap: $77.79M

See more data about CMRX stock on TipRanks’ Stock Analysis page.

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