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Hoth Therapeutics Receives Approval to Commence Cohort 2 in Clinical Trial of BioLexa for the Treatment of Atopic Dermatitis Patients

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Hoth Therapeutics, Inc. (NASDAQ: HOTH) announced the Human Research Ethics Committee (HREC) approval to initiate Cohort 2 of the Phase 1b clinical trial for BioLexa Lotion, aimed at treating mild to moderate atopic dermatitis in Australia. The randomized, double-blind study will assess the safety and pharmacokinetics of BioLexa Lotion over 14 days in adult patients. Screening for Cohort 2 is set to begin this month, with the company's scientific advisors optimistic about BioLexa's potential in addressing global healthcare needs.

Positive
  • Received HREC clearance for Cohort 2 of the Phase 1b clinical trial.
  • Study to evaluate the safety and pharmacokinetics of BioLexa Lotion.
  • Cohort 2 aims to assess preliminary efficacy in treating atopic dermatitis.
Negative
  • None.

NEW YORK, Oct. 12, 2021 /PRNewswire/ -- Hoth Therapeutics, Inc. (NASDAQ: HOTH), a biopharmaceutical company, today announced that is has received Human Research Ethics Committee (HREC) clearance to commence cohort 2 of the Phase 1b clinical trial of BioLexa Lotion for the treatment of mild to moderate atopic dermatitis in Australia. 

BioLexa Trial Design:

  • Randomized, double-blind, parallel-design, placebo-controlled study.
  • Cohort 2 includes adult patients with mild to moderate atopic dermatitis.
  • The primary goal of the study is to evaluate the safety and characterize pharmacokinetics of topical BioLexa Lotion.
  • Participants will be treated twice daily with topical application directly on skin for 14 days
  • Preliminary efficacy will also be investigated in the atopic dermatitis patient cohort, including change in atopic dermatitis extent of involvement and severity using EASI, SCORAD, IGA as well as patient-centric quality of life assessments.

Receiving clearance for Cohort 2 is the next critical milestone in the Phase 1b clinical trial in Australia. Hoth's scientific advisors believe that Hoth's atopic dermatitis solution, BioLexa, represents a significant global opportunity and looks forward to advancing the treatment through the clinic.

The Company expects to start screening and enrolling the first subject(s) of Cohort 2 in October.

About BioLexa
BioLexa is a patented, proprietary antimicrobial topical formulation being developed for treatment of diseases mediated by Staphylococcal biofilms. Bacterial biofilms are specialized communities consisting of bacteria adhered to a surface (both biological and abiotic surfaces) and to other bacteria, and often with a protective extracellular matrix. Mature bacterial biofilms often result in chronic, recurrent infections that are difficult to treat due to the barrier effect of the biofilm that facilitates antibiotic resistance and avoiding immune system mechanisms. The BioLexa formulation is optimized to prevent Staphylococcal biofilm formation, keeping the bacteria in a more susceptible state to antimicrobial therapy. This novel mechanism of action has the potential to broadly treat clinical manifestations resulting from Staphylococcal biofilm formation.

About Hoth Therapeutics, Inc.
Hoth Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on developing new generation therapies for unmet medical needs. Hoth's pipeline development is focused to improve the quality of life for patients suffering from indications including atopic dermatitis, skin toxicities associated with cancer therapy, chronic wounds, psoriasis, asthma, acne, mast-cell derived cancers & anaphylaxis and pneumonia. Hoth has also entered into two different agreements to further the development of two therapeutic prospects to prevent or treat COVID-19.  To learn more, please visit https://ir.hoththerapeutics.com/

Forward-Looking Statement
This press release includes forward-looking statements based upon Hoth's current expectations which may constitute forward-looking statements for the purposes of the safe harbor provisions under the Private Securities Litigation Reform Act of 1995 and other federal securities laws, and are subject to substantial risks, uncertainties and assumptions. These statements concern Hoth's business strategies; the timing of regulatory submissions; the ability to obtain and maintain regulatory approval of existing product candidates and any other product candidates we may develop, and the labeling under any approval we may obtain; the timing and costs of clinical trials, the timing and costs of other expenses; market acceptance of our products; the ultimate impact of the current Coronavirus pandemic, or any other health epidemic, on our business, our clinical trials, our research programs, healthcare systems or the global economy as a whole; our intellectual property; our reliance on third party organizations; our competitive position; our industry environment; our anticipated financial and operating results, including anticipated sources of revenues; our assumptions regarding the size of the available market, benefits of our products, product pricing, timing of product launches; management's expectation with respect to future acquisitions; statements regarding our goals, intentions, plans and expectations, including the introduction of new products and markets; and our cash needs and financing plans. There are a number of factors that could cause actual events to differ materially from those indicated by such forward-looking statements. You should not place reliance on these forward-looking statements, which include words such as "could," "believe," "anticipate," "intend," "estimate," "expect," "may," "continue," "predict," "potential," "project" or similar terms, variations of such terms or the negative of those terms. Although the Company believes that the expectations reflected in the forward-looking statements are reasonable, the Company cannot guarantee such outcomes. Hoth may not realize its expectations, and its beliefs may not prove correct. Actual results may differ materially from those indicated by these forward-looking statements as a result of various important factors, including, without limitation, market conditions and the factors described in the section entitled "Risk Factors" in Hoth's most recent Annual Report on Form 10-K and Hoth's other filings made with the U. S. Securities and Exchange Commission. All such statements speak only as of the date made. Consequently, forward-looking statements should be regarded solely as Hoth's current plans, estimates, and beliefs. Investors should not place undue reliance on forward-looking statements. Hoth cannot guarantee future results, events, levels of activity, performance or achievements. Hoth does not undertake and specifically declines any obligation to update, republish, or revise any forward-looking statements to reflect new information, future events or circumstances or to reflect the occurrences of unanticipated events, except as may be required by applicable law.

Contact
Investor Contact:
LR Advisors LLC
Email: investorrelations@hoththerapeutics.com
www.hoththerapeutics.com
Phone: (678) 570-6791

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/hoth-therapeutics-receives-approval-to-commence-cohort-2-in-clinical-trial-of-biolexa-for-the-treatment-of-atopic-dermatitis-patients-301398082.html

SOURCE Hoth Therapeutics, Inc.

FAQ

What is the purpose of the BioLexa trial by Hoth Therapeutics?

The BioLexa trial aims to evaluate the safety and pharmacokinetics of BioLexa Lotion in treating mild to moderate atopic dermatitis.

When does Hoth Therapeutics expect to start screening for Cohort 2?

Hoth Therapeutics expects to start screening and enrolling the first subjects of Cohort 2 in October.

What is the significance of the HREC clearance for Hoth Therapeutics?

The HREC clearance allows Hoth Therapeutics to advance to Cohort 2 of its clinical trial, marking a crucial milestone in the development of BioLexa.

What are the expected outcomes of the BioLexa clinical trial?

Expected outcomes include evaluating the safety of BioLexa Lotion and determining preliminary effectiveness in reducing atopic dermatitis severity.

Hoth Therapeutics, Inc.

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