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Hoth Therapeutics Announces it Has Successfully Completed Manufacturing Feasibility of the HT-KIT Drug Substance

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Hoth Therapeutics, Inc. (NASDAQ: HOTH) announced significant development milestones for its cancer therapeutic, HT-KIT, following its receipt of Orphan Drug Designation from the FDA on March 11, 2022. HT-KIT targets the proto-oncogene cKIT and has shown promise in preclinical studies by inducing apoptosis in neoplastic mast cells. The company has completed manufacturing feasibility of HT-KIT in collaboration with WuXi STA and aims to hold a Pre-IND meeting with the FDA by the end of 2022, indicating progress towards advancing its clinical development.

Positive
  • Received Orphan Drug Designation from the FDA for HT-KIT.
  • Completed manufacturing feasibility of HT-KIT in collaboration with WuXi STA.
  • Plans to hold a Pre-IND meeting with FDA by the end of 2022.
Negative
  • None.

NEW YORK, March 22, 2022 /PRNewswire/ -- Hoth Therapeutics, Inc. (NASDAQ: HOTH), a patient-focused biopharmaceutical company, today announced development updates for its cancer therapeutic, HT-KIT after receiving Orphan Drug Designation from the U.S. Food and Drug Administration (FDA) on March 11, 2022. HT-KIT is an antisense oligonucleotide that targets the proto-oncogene cKIT by inducing mRNA frame shifting. Preclinical studies have demonstrated that HT-KIT induces apoptosis of neoplastic mast cells and reduces metastasis associated with aggressive mastocytosis.

Hoth has successfully completed manufacturing feasibility of the HT-KIT drug substance in collaboration with WuXi STA.  Hoth plans to pursue a Pre-IND meeting with FDA by the end of 2022.

"With this important step now completed, Hoth has moved drug development into the later stage which will yield us our clinical formulation and allow us to hold our Pre-IND meeting with the FDA this year," stated Robb Knie, Chief Executive Officer of Hoth.

About HT-KIT

HT-KIT is a new molecular entity (NME) under development for treatment of mast cell derived cancers and anaphylaxis. HT-KIT was developed Dr. Glenn Cruse, Assistant Professor at North Carolina State University and shares the same molecular class as Hoth's current HT-004 drug. The HT-KIT drug is designed to more specifically target the receptor tyrosine kinase KIT in mast cells, which is required for the proliferation, survival and differentiation of bone marrow-derived hematopoietic stem cells. Mutations in the KIT pathway have been associated with several human cancers, such as gastrointestinal stromal tumors and mast cell-derived cancers (mast cell leukemia and mast cell sarcoma). Based on the initial proof-of-concept success, Hoth intends to initially target mast cell neoplasms for development of HT-KIT, which is a rare, aggressive cancer with poor prognosis.

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 skin toxicities associated with cancer therapy, mast-cell derived cancers and anaphylaxis, Alzheimer's Disease, atopic dermatitis and other indications. 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 Hoth may develop, and the labeling under any approval Hoth may obtain; the timing and costs of clinical trials, the timing and costs of other expenses; market acceptance of Hoth's products; the ultimate impact of the current Coronavirus pandemic, or any other health epidemic, on Hoth's business, its clinical trials, its research programs, healthcare systems or the global economy as a whole; Hoth's intellectual property; Hoth's reliance on third party organizations; Hoth's competitive position; Hoth's industry environment; Hoth's anticipated financial and operating results, including anticipated sources of revenues; Hoth's assumptions regarding the size of the available market, benefits of Hoth's products, product pricing, timing of product launches; management's expectation with respect to future acquisitions; statements regarding Hoth's goals, intentions, plans and expectations, including the introduction of new products and markets; and Hoth's 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 undue 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 Hoth believes that the expectations reflected in the forward-looking statements are reasonable, Hoth 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 of this press release. Consequently, forward-looking statements should be regarded solely as Hoth's current plans, estimates, and beliefs. Hoth cannot guarantee future results, events, levels of activity, performance or achievements. Hoth does not undertake and specifically declines any obligation to update 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.

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

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SOURCE Hoth Therapeutics, Inc.

FAQ

What is the latest update on Hoth Therapeutics' HT-KIT?

Hoth Therapeutics announced the successful completion of manufacturing feasibility for HT-KIT and plans to meet with the FDA by the end of 2022.

When did Hoth Therapeutics receive Orphan Drug Designation for HT-KIT?

Hoth Therapeutics received Orphan Drug Designation from the FDA on March 11, 2022.

What is HT-KIT developed for?

HT-KIT is developed for the treatment of mast cell derived cancers and anaphylaxis.

Who is collaborating with Hoth Therapeutics on HT-KIT manufacturing?

Hoth Therapeutics is collaborating with WuXi STA for the manufacturing of HT-KIT.

What are the future plans for HT-KIT's development?

Hoth Therapeutics plans to hold a Pre-IND meeting with the FDA by the end of 2022.

Hoth Therapeutics, Inc.

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