Stock Markets January 22, 2026

Hoth Therapeutics Shares Advance Following Promising CLEER-001 Trial Interim Data

Positive early clinical outcomes reinforce HT-001’s potential in managing EGFR inhibitor-related side effects

By Marcus Reed HOTH
Hoth Therapeutics Shares Advance Following Promising CLEER-001 Trial Interim Data
HOTH

Hoth Therapeutics Inc's stock increased notably on positive interim findings from the open-label pharmacokinetic segment of its CLEER-001 trial assessing HT-001 in cancer patients undergoing EGFR inhibitor therapy. The results demonstrated full clinical response by Week 6 among evaluable participants, significant reductions in disease severity and pruritus, and good tolerability without unexpected safety concerns.

Key Points

  • Hoth Therapeutics' stock rose 5.7% following promising interim clinical trial results from the CLEER-001 study evaluating HT-001.
  • The trial showed 100% clinical response at Week 6 among evaluable patients, with disease severity reduced by approximately 50% as measured on the ARIGA scale.
  • HT-001 demonstrated favorable tolerability and meaningful improvements in oncology toxicity (34%) and patient-reported pruritus (37%), supporting its potential as a supportive-care option in EGFR inhibitor-treated cancer patients.

Shares of Hoth Therapeutics Inc (NASDAQ:HOTH) climbed 5.7% in early Thursday trading after the release of encouraging interim data from the company's ongoing CLEER-001 clinical study. This trial is examining the efficacy and safety of HT-001 in cancer patients who are being treated with epidermal growth factor receptor (EGFR) inhibitors.

In the pharmacokinetic cohort of the open-label trial, which centers on drug exposure and early clinical effects, all evaluable patients showed a clinical response by the sixth week. The severity of disease, as assessed by investigators, was reduced by about half compared to initial measurements. Specifically, scores on the ARIGA scale improved from an average baseline of 1.67 down to 0.83 at Week 6, with every participant achieving a low-severity disease classification.

Secondary outcomes further highlighted beneficial effects, with an approximate 34% improvement noted in oncology toxicity according to the Common Terminology Criteria for Adverse Events (CTCAE), alongside a roughly 37% decrease in patient-reported itching symptoms. The therapy demonstrated a favorable safety profile, with no unanticipated adverse events noted during the evaluation period.

EGFR-directed therapies remain a cornerstone treatment for several major cancers including lung, colorectal, and head-and-neck malignancies; however, their associated treatment-related toxicities often present challenges in maintaining uninterrupted therapy. HT-001 is designed as a supportive-care agent to alleviate these toxicities, thereby improving patient adherence to cancer treatment regimens.

Robb Knie, Chief Executive Officer of Hoth Therapeutics, highlighted the significance of these findings stating, "These results represent a meaningful milestone for HT-001." The company plans to continue the CLEER-001 trial to further evaluate pharmacokinetics, tolerability, and ongoing clinical benefits.

Risks

  • The CLEER-001 clinical trial is ongoing, so long-term efficacy and safety data for HT-001 are not yet available, reflecting inherent uncertainties in drug development.
  • While interim data are positive, results are derived from an open-label pharmacokinetic cohort, which may be subject to limitations compared to blinded, controlled studies.
  • Treatment-related toxicity management impacts cancer therapy adherence, but the efficacy of HT-001 in broader patient populations and different oncology contexts remains to be fully established.

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