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Enveric Biosciences CEO Issues Letter to Shareholders

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Enveric Biosciences (NASDAQ: ENVB) has announced strategic updates through a CEO letter to shareholders. The company has repositioned to focus on developing EB-003, their lead non-hallucinogenic neuroplastogenic drug candidate for anxiety, depression, and addiction disorders. Recent data shows EB-003's ability to bind to the 5-HT2A receptor and induce neuroplasticity without significant hallucinatory effects.

The company completed several licensing agreements in 2024-2025, including partnerships with Aries Science & Technology, MycoMedica Life Sciences, and Restoration Biologics. Enveric recently secured new U.S. patents for their EVM301 series and unveiled the EVM401 Series of mescaline-inspired drug candidates.

Financially, Enveric completed a public offering raising approximately $5 million in gross proceeds after implementing a reverse stock split. The company is now preparing for EB-003's Investigational New Drug (IND) application and subsequent Phase 1 clinical trials.

Enveric Biosciences (NASDAQ: ENVB) ha annunciato aggiornamenti strategici attraverso una lettera del CEO agli azionisti. L'azienda si è riposizionata per concentrarsi sullo sviluppo di EB-003, il loro principale candidato farmaco neuroplastogenico non allucinogeno per disturbi d'ansia, depressione e dipendenza. Dati recenti mostrano la capacità di EB-003 di legarsi al recettore 5-HT2A e indurre neuroplasticità senza effetti allucinatori significativi.

L'azienda ha completato diversi accordi di licenza nel 2024-2025, inclusi partenariati con Aries Science & Technology, MycoMedica Life Sciences e Restoration Biologics. Enveric ha recentemente ottenuto nuovi brevetti negli Stati Uniti per la loro serie EVM301 e ha svelato la serie EVM401 di candidati farmaci ispirati alla mescalina.

Dal punto di vista finanziario, Enveric ha completato un'offerta pubblica raccogliendo circa $5 milioni di proventi lordi dopo aver implementato uno split azionario inverso. L'azienda si sta ora preparando per la domanda di Nuovo Farmaco Investigativo (IND) per EB-003 e per i successivi studi clinici di Fase 1.

Enveric Biosciences (NASDAQ: ENVB) ha anunciado actualizaciones estratégicas a través de una carta del CEO a los accionistas. La empresa se ha reposicionado para centrarse en el desarrollo de EB-003, su principal candidato a fármaco neuroplastogénico no alucinógeno para trastornos de ansiedad, depresión y adicción. Los datos recientes muestran la capacidad de EB-003 para unirse al receptor 5-HT2A e inducir neuroplasticidad sin efectos alucinatorios significativos.

La empresa completó varios acuerdos de licencia en 2024-2025, incluidas asociaciones con Aries Science & Technology, MycoMedica Life Sciences y Restoration Biologics. Enveric recientemente aseguró nuevas patentes en EE. UU. para su serie EVM301 y presentó la serie EVM401 de candidatos a fármacos inspirados en la mescalina.

Desde el punto de vista financiero, Enveric completó una oferta pública recaudando aproximadamente $5 millones en ingresos brutos después de implementar una división de acciones inversa. La empresa se está preparando ahora para la solicitud de Nuevo Medicamento Investigacional (IND) para EB-003 y los posteriores ensayos clínicos de Fase 1.

엔베릭 바이오사이언스(나스닥: ENVB)는 CEO의 주주 서한을 통해 전략적 업데이트를 발표했습니다. 이 회사는 불안, 우울증 및 중독 장애를 위한 주요 비환각성 신경가소성 약물 후보인 EB-003 개발에 집중하기 위해 재편성되었습니다. 최근 데이터는 EB-003이 5-HT2A 수용체에 결합하고 상당한 환각 효과 없이 신경가소성을 유도할 수 있는 능력을 보여줍니다.

회사는 2024-2025년 동안 Aries Science & Technology, MycoMedica Life Sciences 및 Restoration Biologics와의 파트너십을 포함하여 여러 라이선스 계약을 체결했습니다. 엔베릭은 최근 EVM301 시리즈에 대한 미국 특허를 확보하고 메스칼린에서 영감을 받은 약물 후보의 EVM401 시리즈를 공개했습니다.

재무적으로 엔베릭은 역주식 분할을 시행한 후 약 $5 백만의 총 수익을 올리며 공개 제안을 완료했습니다. 이 회사는 현재 EB-003의 임상시험용 신약 신청(IND) 및 이후 1상 임상 시험을 준비하고 있습니다.

Enveric Biosciences (NASDAQ: ENVB) a annoncé des mises à jour stratégiques par le biais d'une lettre du PDG aux actionnaires. L'entreprise s'est repositionnée pour se concentrer sur le développement de EB-003, leur principal candidat médicament neuroplastogénique non hallucinogène pour les troubles de l'anxiété, de la dépression et de la dépendance. Des données récentes montrent la capacité d'EB-003 à se lier au récepteur 5-HT2A et à induire la neuroplasticité sans effets hallucinatoires significatifs.

L'entreprise a conclu plusieurs accords de licence en 2024-2025, y compris des partenariats avec Aries Science & Technology, MycoMedica Life Sciences et Restoration Biologics. Enveric a récemment obtenu de nouveaux brevets aux États-Unis pour sa série EVM301 et a dévoilé la série EVM401 de candidats médicaments inspirés de la mescaline.

Sur le plan financier, Enveric a complété une offre publique levant environ $5 millions de recettes brutes après avoir mis en œuvre une division d'actions inversée. L'entreprise se prépare maintenant à la demande de Nouveau Médicament Investigational (IND) pour EB-003 et aux essais cliniques de Phase 1 qui suivront.

Enveric Biosciences (NASDAQ: ENVB) hat strategische Updates durch einen CEO-Brief an die Aktionäre angekündigt. Das Unternehmen hat sich neu ausgerichtet, um sich auf die Entwicklung von EB-003, ihrem führenden nicht-halluzinogenen neuroplastogenen Arzneimittelkandidaten für Angstzustände, Depressionen und Suchterkrankungen, zu konzentrieren. Aktuelle Daten zeigen die Fähigkeit von EB-003, an den 5-HT2A-Rezeptor zu binden und Neuroplastizität ohne signifikante halluzinatorische Effekte zu induzieren.

Das Unternehmen hat im Zeitraum 2024-2025 mehrere Lizenzvereinbarungen abgeschlossen, darunter Partnerschaften mit Aries Science & Technology, MycoMedica Life Sciences und Restoration Biologics. Enveric hat kürzlich neue US-Patente für ihre EVM301-Serie gesichert und die EVM401-Serie von meskalin-inspirierten Arzneimittelkandidaten vorgestellt.

Finanziell hat Enveric eine öffentliche Angebot abgeschlossen und etwa $5 Millionen an Bruttoeinnahmen erzielt, nachdem eine Umkehraktienaufteilung durchgeführt wurde. Das Unternehmen bereitet sich nun auf den Antrag auf ein Investigational New Drug (IND) für EB-003 und die anschließenden Phase-1-Studien vor.

Positive
  • Secured multiple licensing agreements generating potential non-dilutive revenue
  • Raised $5M in gross proceeds through recent public offering
  • Obtained new U.S. patents for EVM301 and EVM401 series
  • Demonstrated EB-003's ability to bind to 5-HT2A receptor without hallucinatory effects
  • Advanced EB-003 toward IND application and Phase 1 trials
Negative
  • Challenging fundraising environment over past two years
  • Required reverse stock split implementation
  • No revenue-generating products in market yet
  • Still in pre-clinical development phase

CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Enveric Biosciences (NASDAQ: ENVB) (“Enveric” or the “Company”), a biotechnology company dedicated to the development of novel neuroplastogenic small-molecule therapeutics for the treatment of anxiety, depression, and addiction disorders, today announced that Joseph Tucker, Ph.D., CEO and Director, has issued a Letter to Shareholders to provide an update on the Company’s development program and recent events. The full text of the letter follows.

A MESSAGE FROM OUR CHIEF EXECUTIVE OFFICER

To Our Valued Shareholders,

This is a very exciting time in the growth and evolution of Enveric. We have successfully completed a strategic reshaping of the company to focus our business and development operations towards the advancement of EB-003 as our lead product. We believe EB-003 offers Enveric the greatest opportunity to drive shareholder value given its potential to be a first-in-class neuroplastogenic molecule that could address multiple, difficult-to-treat neuropsychiatric indications. We additionally recently unveiled an exciting new series of drug candidates in our pipeline, the EVM401 Series.

The EB-003 Value Proposition

At Enveric, we believe that in order to maximize the possibility of achieving regulatory approval and widespread market acceptance, the hallucinatory effect of psychedelic-inspired drug candidates must be reduced or eliminated completely. The June 2024 Advisory Committee for Lykos Therapeutics’ MDMA-assisted therapy spotlighted some of the challenges facing first generation psychedelic molecules undergoing development for neuropsychiatry indications. In particular, the concerns around separating placebo effect from drug efficacy can present significant hurdles to regulatory approval, since in the presence of hallucinations it will not be possible to keep the patients blinded to the treatment assigned.

Based on these and other factors, Enveric made the strategic decision in early 2024 to elevate our non-hallucinogenic neuroplastogen drug candidate, EB-003, to be the Company’s lead product candidate. We are focusing our resources to EB-003’s development and the EVM401 Series pipeline compounds. Beyond streamlining the regulatory review and approval process, minimizing hallucinations should also strengthen our case in seeking an outpatient treatment label, which we believe would have a significant impact on patient, healthcare provider, and health care system acceptance of EB-003.

EB-003: An Orally Bioavailable, Brain-Delivered Neuroplastogen

In 2024, we generated data that demonstrated EB-003’s ability to bind to the 5-HT2A receptor and induce neuroplasticity, the hypothesized mechanism of action for neuroplastogens. We also demonstrated EB-003 does not elicit a significant head twitch response (“HTR”) in mice. HTR is a behavioral model used to predict the likelihood of a drug candidate to induce hallucinations when administered to humans. We next produced preclinical data that confirmed EB-003 has the potential to be delivered orally and to penetrate the brain at levels anticipated to elicit the desired therapeutic effect.

We are now focused on completing the studies required for EB-003’s Investigational New Drug (“IND”) application. Once we have a pre-IND meeting with the U.S. Food and Drug Administration (“FDA”), we should be poised to advance EB-003 into Phase 1 clinical trials.

Building Additional Value from Our Portfolios of Patented Technologies

We were pleased to enter into two licensing agreements during 2024, deriving additional value from our portfolio of patented product candidates. We entered into agreements with Aries Science & Technology, which plans to develop and market Enveric’s patented product for radiation dermatitis, and MycoMedica Life Sciences, which intends to develop and market Enveric’s patented drug candidate, EB-002, for neuropsychiatric disorders.

This business development momentum has continued into 2025. We recently entered into two additional licensing agreements with Restoration Biologics, which expects to develop and market Enveric’s patented Cannabinoid-COX-2 conjugate compounds for use in treating joint disease. We believe that out-licensing our non-core assets has the potential to generate non-dilutive revenue and build shareholder value.

We continue to strengthen and expand the intellectual property estate for our lead drug candidate, EB-003, and for additional new technologies that emerge from our discovery process. We were recently granted several additional U.S. patents for our EVM301 series of neuroplastogenic molecules, as well as for our now out-licensed EVM201 series, including EB-002.

Recently, we were pleased to receive a U.S. patent for a new series of mescaline-inspired drug candidates, which the company has unveiled as the first patent protecting its EVM401 Series. We will be revealing more in the future about this new group of drug candidates.

Positioning Enveric for Long-Term Growth

Enveric is at the forefront of the new field of neuroplastogens focused on providing entirely new treatment options for patients with neuropsychiatric disorders, an area of medicine that has been without substantial innovation for many years. Our goal is ambitious, but we are energized by the potential of EB-003 to be a first-in-class neuroplastogen designed to promote neuroplasticity, without inducing hallucinations.

The past two years have presented a challenging fundraising environment for innovative drug development companies, including Enveric. Recognizing this, we elected to streamline and manage operations to conserve our financial resources until the capital markets environment became more receptive to innovative drug development. We are hopeful that the markets are beginning to show signs of improvement, which is why we recently effected a reverse stock split and closed a public offering of common stock and warrants, raising approximately $5 million in gross proceeds; our first offering of this type in approximately two years.

As 2025 is underway, we believe the Company is well positioned to cement its leadership role in the industry by advancing the development of our innovative drug candidate, EB-003, for the treatment of neuropsychiatric conditions. We eagerly look forward to advancing toward clinical trials and ultimately receiving regulatory approval, so we can bring EB-003, and later our EVM401 Series candidates, to the market in support of our twin goals of improving the lives of patients and generating value for our shareholders.

Sincerely,
Joseph Tucker, Ph.D.
CEO and Director
Enveric Biosciences

About Enveric Biosciences

Enveric Biosciences (NASDAQ: ENVB) is a biotechnology company dedicated to the development of novel neuroplastogenic small-molecule therapeutics for the treatment of depression, anxiety, and addiction disorders. Leveraging its unique discovery and development platform, the Psybrary™, which houses proprietary information on the use and development of existing and novel molecules for specific mental health indications, Enveric seeks to develop a robust intellectual property portfolio of novel drug candidates. Enveric’s lead molecule, EB-003, is a potential first-in-class neuroplastogen designed to promote neuroplasticity, without inducing hallucinations, in patients suffering from difficult-to-address mental health disorders. Enveric is focused on advancing EB-003 towards clinical trials for the treatment of neuropsychiatric disorders while out-licensing all other novel, patented Psybrary™ drug candidates to third-party licensees advancing non-competitive market strategies for patient care. Enveric is headquartered in Naples, FL with offices in Cambridge, MA and Calgary, AB Canada. For more information, please visit www.enveric.com.

Forward-Looking Statements

This press release contains forward-looking statements and forward-looking information within the meaning of applicable securities laws. These statements relate to future events or future performance. All statements other than statements of historical fact may be forward-looking statements or information. Generally, forward-looking statements and information may be identified by the use of forward-looking terminology such as “plans,” “expects” or “does not expect,” “proposes,” “budgets,” “explores,” “schedules,” “seeks,” “estimates,” “forecasts,” “intends,” “anticipates” or “does not anticipate,” or “believes,” or variations of such words and phrases, or by the use of words or phrases which state that certain actions, events or results may, could, should, would, or might occur or be achieved. Forward-looking statements may include statements regarding beliefs, plans, expectations, or intentions regarding the future and are based on the beliefs of management as well as assumptions made by and information currently available to management. Actual results could differ materially from those contemplated by the forward-looking statements as a result of certain factors, including, but not limited to, the ability of Enveric to: successfully outlicense patented PsybraryTM drug candidates to third-party licensees; negotiate and finalize definitive agreements based on any of its out-licensing term sheets and for licensees to perform pursuant to the terms thereof; finalize and submit its IND filing to the U.S. Food and Drug Administration; carry out successful clinical programs; achieve the value creation contemplated by technical developments; avoid delays in planned clinical trials; establish that potential products are efficacious or safe in preclinical or clinical trials; establish or maintain collaborations for the development of therapeutic candidates; obtain appropriate or necessary governmental approvals to market potential products; obtain future funding for product development and working capital on commercially reasonable terms; scale-up manufacture of product candidates; respond to changes in the size and nature of competitors; hire and retain key executives and scientists; secure and enforce legal rights related to Enveric’s products, including patent protection; identify and pursue alternative routes to capture value from its research and development pipeline assets; continue as a going concern; and manage its future growth effectively.

A discussion of these and other factors, including risks and uncertainties with respect to Enveric, is set forth in Enveric’s filings with the Securities and Exchange Commission, including Enveric’s Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Enveric disclaims any intention or obligation to revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.

Investor Relations

Tiberend Strategic Advisors, Inc.

David Irish

(231) 632-0002

dirish@tiberend.com

Media Relations

Tiberend Strategic Advisors, Inc.

Casey McDonald

(646) 577-8520

cmcdonald@tiberend.com

Source: Enveric Biosciences

FAQ

What is the main focus of Enveric Biosciences (ENVB) development program in 2025?

ENVB is focusing on advancing EB-003, a non-hallucinogenic neuroplastogenic drug candidate for anxiety, depression, and addiction disorders, toward IND application and Phase 1 clinical trials.

How much funding did ENVB raise in their recent public offering?

ENVB raised approximately $5 million in gross proceeds through a public offering of common stock and warrants.

What key licensing agreements did ENVB secure in 2024-2025?

ENVB secured agreements with Aries Science & Technology, MycoMedica Life Sciences, and Restoration Biologics for various patented compounds.

What are the potential advantages of ENVB's EB-003 over traditional psychedelic treatments?

EB-003 is designed to promote neuroplasticity without inducing hallucinations, potentially enabling easier regulatory approval and outpatient treatment options.

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