Hoth Therapeutics Inc. announced an expansion of its CLEER-001 Phase 2a clinical trial of HT-001, adding Regis Clinical Research in Miami, Florida as a new enrolling site to increase enrollment capacity. HT-001 is being studied for skin toxicities associated with EGFR inhibitor cancer therapy, for which the company noted there is no FDA-approved treatment option. The company reported interim trial data showing patients in the open-label cohort met the primary efficacy endpoint (ARIGA rash severity score of 1 or less) by week six, with no dose reductions or discontinuations of EGFR inhibitor therapy while on HT-001 and no dose-limiting toxicities observed to date; it also referenced a case study presented at the American Academy of Dermatology Annual Meeting showing complete lesion and symptom resolution after one week of twice-daily application. The announcement did not specify when a full trial readout will be presented.
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 via PR Newswire (Ref. ID: 202602241615PR_NEWS_USPR_____NY94862) on February 24, 2026, and is solely responsible for the information contained therein.
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