- Hungary granted regulatory clearance to expand Hoth Therapeutics’ Phase 2 HT-001 trial into Europe.
- Interim analysis showed HT-001 met primary endpoint, with patients reaching ARIGA rash severity score ≤1 by week six.
- Program update reported zero dose reductions or discontinuations of EGFR inhibitor therapy during HT-001 treatment.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Hoth Therapeutics Inc. published the original content used to generate this news brief on April 01, 2026, and is solely responsible for the information contained therein.
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