Eupraxia Pharmaceuticals' CEO Dr. James Helliwell to Participate in Webinar Event, "Eosinophilic Esophagitis: The Emerging Digestive Disorder Frequently Misdiagnosed", on November 15, 2024
Eupraxia Pharmaceuticals (TSX: EPRX) (NASDAQ: EPRX) announced that CEO Dr. James A. Helliwell will present at a Tribe Public Webinar focused on Eosinophilic Esophagitis (EoE), a digestive disorder affecting over 450,000 people in the United States. The presentation, titled 'Eosinophilic Esophagitis: The Emerging Digestive Disorder Frequently Misdiagnosed,' is scheduled for November 15, 2024, at 8:30 am PT / 11:30 am ET.
The event is open to public registration at EPRXNOV1524.TribePublic.com. Participants can submit questions in advance via email or during the event through ZOOM chat. The webinar will be hosted by Tribe Public's Managing Member, John F. Heerdink, Jr.
Eupraxia Pharmaceuticals (TSX: EPRX) (NASDAQ: EPRX) ha annunciato che il CEO Dr. James A. Helliwell presenterà un webinar pubblico di Tribe incentrato su Esogastroenterite Eosinofila (EoE), un disturbo digestivo che colpisce oltre 450.000 persone negli Stati Uniti. La presentazione, intitolata 'Esogastroenterite Eosinofila: Il Disturbo Digestivo Emergente Spesso Erroneamente Diagnosticato,' è prevista per il 15 novembre 2024, alle 8:30 PT / 11:30 ET.
L'evento è aperto alla registrazione pubblica su EPRXNOV1524.TribePublic.com. I partecipanti possono inviare domande in anticipo via email o durante l'evento attraverso la chat di ZOOM. Il webinar sarà ospitato dal Membro Gestore di Tribe Public, John F. Heerdink, Jr.
Eupraxia Pharmaceuticals (TSX: EPRX) (NASDAQ: EPRX) anunció que el CEO Dr. James A. Helliwell presentará en un webinar público de Tribe enfocado en Esofagitis Eosinofílica (EoE), un trastorno digestivo que afecta a más de 450,000 personas en los Estados Unidos. La presentación, titulada 'Esofagitis Eosinofílica: El Trastorno Digestivo Emergente Frecuentemente Mal Diagnosticado,' está programada para el 15 de noviembre de 2024, a las 8:30 a.m. PT / 11:30 a.m. ET.
El evento está abierto a la inscripción pública en EPRXNOV1524.TribePublic.com. Los participantes pueden enviar preguntas con anticipación por correo electrónico o durante el evento a través del chat de ZOOM. El webinar será presentado por el Miembro Gerente de Tribe Public, John F. Heerdink, Jr.
유프락시아 제약회사 (TSX: EPRX) (NASDAQ: EPRX)는 CEO인 제임스 A. 헬리웰 박사가 트라이브 공공 웨비나에서 호산구 식도염 (EoE)에 대한 발표를 할 것이라고 발표했습니다. 이 소화 장애는 미국에서 450,000명 이상에게 영향을 미칩니다. '호산구 식도염: 자주 잘못 진단되는 새로운 소화 장애'라는 제목의 발표는 2024년 11월 15일 오전 8:30 PT / 오전 11:30 ET로 예정되어 있습니다.
이 행사에는 EPRXNOV1524.TribePublic.com에서 공개 등록이 가능합니다. 참가자는 이메일로 미리 질문을 제출하거나 행사 동안 ZOOM 채팅을 통해 질문할 수 있습니다. 웨비나는 트라이브 퍼블릭의 관리 멤버인 존 F. 히어딩크 주니어가 주최합니다.
Eupraxia Pharmaceuticals (TSX: EPRX) (NASDAQ: EPRX) a annoncé que le PDG Dr. James A. Helliwell présentera lors d'un webinaire public de Tribe axé sur l'œsophagite éosinophile (EoE), un trouble digestif touchant plus de 450 000 personnes aux États-Unis. La présentation, intitulée 'L'œsophagite éosinophile : Le trouble digestif émergent souvent mal diagnostiqué,' est programmée pour le 15 novembre 2024, à 8h30 PT / 11h30 ET.
L'événement est ouvert à l'inscription publique sur EPRXNOV1524.TribePublic.com. Les participants peuvent soumettre des questions à l'avance par email ou pendant l'événement via le chat ZOOM. Le webinaire sera animé par John F. Heerdink, Jr., membre gérant de Tribe Public.
Eupraxia Pharmaceuticals (TSX: EPRX) (NASDAQ: EPRX) hat angekündigt, dass CEO Dr. James A. Helliwell bei einem öffentlichen Webinar von Tribe präsentieren wird, das sich auf eosinophile Ösophagitis (EoE) konzentriert, eine Verdauungsstörung, die über 450.000 Menschen in den Vereinigten Staaten betrifft. Die Präsentation mit dem Titel 'Eosinophile Ösophagitis: Die aufkommende Verdauungsstörung, die häufig falsch diagnostiziert wird,' ist für den 15. November 2024, um 8:30 Uhr PT / 11:30 Uhr ET angesetzt.
Die Veranstaltung ist für die öffentliche Registrierung unter EPRXNOV1524.TribePublic.com geöffnet. Die Teilnehmer können im Voraus Fragen per E-Mail einreichen oder während der Veranstaltung über den ZOOM-Chat stellen. Das Webinar wird von John F. Heerdink, Jr., dem Geschäftsführer von Tribe Public, geleitet.
- None.
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- EoE affects more than 450,000 people in
the United States and has been identified by the American Gastroenterological Association as rapidly increasing in both incidence and prevalence - Registration for the webinar now open to the public by visiting EPRXNOV1524.TribePublic.com
The event is scheduled to begin at 8:30 am PT / 11:30 am ET on Friday, November 15, 2024.
To register to join the complimentary event, please visit Tribe Public at:
EPRXNOV1524.TribePublic.com
Once registered, participants may begin forwarding their questions for Dr. Helliwell to Tribe Public at research@tribepublic.com, or share their questions via the ZOOM chat feature during the event. Tribe Public's Managing Member, John F. Heerdink, Jr., will host the event and relay all questions to management.
About Eosinophilic Esophagitis
Eosinophilic Esophagitis ("EoE") is an inflammatory-mediated disease in which white blood cells migrate into and become trapped in the esophagus, creating pain and difficulty with swallowing food. According to market research from Clearview Healthcare Partners, EoE affects more than 450,000 people in
About Eupraxia Pharmaceuticals Inc.
Eupraxia is a clinical-stage biotechnology company focused on the development of locally delivered, extended-release products that have the potential to address therapeutic areas with high unmet medical need. DiffuSphere™, a proprietary, polymer-based micro-sphere technology, is designed to facilitate targeted drug delivery of both existing and novel drugs. The technology is designed to support extended duration of effect and delivery of drugs in a hyper-localized fashion, targeting only the tissues that physicians are wanting to treat. We believe the potential for fewer adverse events may be achieved through the precision targeting and the stable and flat delivery of the active ingredient when using the DiffuSphere™ technology, versus the peaks and troughs seen with more traditional drug delivery methods. The precision of Eupraxia's DiffuSphere™ technology platform has the potential to augment and transform existing FDA-approved drugs to improve their safety, tolerability, efficacy and duration of effect. The potential uses in therapeutic areas may go beyond pain and inflammatory gastrointestinal disease, where Eupraxia currently is developing advanced treatments, to also be applicable in oncology, infectious disease and other critical disease areas.
Eupraxia's EP-104GI is currently in a Phase 1b/2a trial, the RESOLVE trial, for the treatment of EoE. EP-104GI is administered as an injection into the esophageal wall, providing local delivery of drug. This is a unique treatment approach for EoE. Eupraxia also recently completed a Phase 2b clinical trial (SPRINGBOARD) of EP-104IAR for the treatment of pain due to knee osteoarthritis. The trial met its primary endpoint and three of the four secondary endpoints. In addition, Eupraxia is developing a pipeline of later and earlier-stage long-acting formulations. Potential pipeline indications include candidates for other inflammatory joint indications and oncology, each designed to improve on the activity and tolerability of currently approved drugs. For further details about Eupraxia, please visit the Company's website at: www.eupraxiapharma.com.
About Tribe Public LLC
Tribe Public LLC is a
Notice Regarding Forward-looking Statements and Information
This news release includes forward-looking statements and forward-looking information within the meaning of applicable securities laws. Often, but not always, forward-looking information can be identified by the use of words such as "plans", "is expected", "expects", "suggests", "scheduled", "intends", "contemplates", "anticipates", "believes", "proposes", "potential" or variations (including negative and grammatical variations) of such words and phrases, or state that certain actions, events or results "may", "could", "would", "might" or "will" be taken, occur or be achieved. Forward-looking statements in this news release include statements regarding Tribe Public's webinar event; the Company's product candidates, including their expected benefits to patients with respect to safety, tolerability, efficacy and duration; the results gathered from studies and trials of Eupraxia's product candidates; the potential for the Company's technology to impact the drug delivery process; potential market opportunity for the Company's products, and potential pipeline indications. Such statements and information are based on the current expectations of Eupraxia's management, and are based on assumptions, including but not limited to: future research and development plans for the Company proceeding substantially as currently envisioned; industry growth trends, including with respect to projected and actual industry sales; the Company's ability to obtain positive results from the Company's research and development activities, including clinical trials; and the Company's ability to protect patents and proprietary rights. Although Eupraxia's management believes that the assumptions underlying these statements and information are reasonable, they may prove to be incorrect. The forward-looking events and circumstances discussed in this news release may not occur by certain dates or at all and could differ materially as a result of known and unknown risk factors and uncertainties affecting Eupraxia, including, but not limited to: risks and uncertainties related to the Company's limited operating history; the Company's novel technology with uncertain market acceptance; if the Company breaches any of the agreements under which it licenses rights to its product candidates or technology from third parties, the Company could lose license rights that are important to its business; the Company's current license agreement may not provide an adequate remedy for its breach by the licensor; the Company's technology may not be successful for its intended use; the Company's future technology will require regulatory approval, which is costly and the Company may not be able to obtain it; the Company may fail to obtain regulatory approvals or only obtain approvals for limited uses or indications; the Company's clinical trials may fail to demonstrate adequately the safety and efficacy of its product candidates at any stage of clinical development; the Company may be required to suspend or discontinue clinical trials due to side effects or other safety risks; the Company completely relies on third parties to provide supplies and inputs required for its products and services; the Company relies on external contract research organizations to provide clinical and non-clinical research services; the Company may not be able to successfully execute its business strategy; the Company will require additional financing, which may not be available; any therapeutics the Company develops will be subject to extensive, lengthy and uncertain regulatory requirements, which could adversely affect the Company's ability to obtain regulatory approval in a timely manner, or at all; the impact of health pandemics or epidemics on the Company's operations; the Company's restatement of its consolidated financial statements, which may lead to additional risks and uncertainties, including loss of investor confidence and negative impacts on the Company's common share price; and other risks and uncertainties described in more detail in Eupraxia's public filings on SEDAR+ (sedarplus.ca) and EDGAR (sec.gov). Although Eupraxia has attempted to identify important factors that could cause actual actions, events or results to differ materially from those described in forward-looking statements and information, there may be other factors that cause actions, events or results to differ from those anticipated, estimated or intended. No forward-looking statement or information can be guaranteed. Except as required by applicable securities laws, forward-looking statements and information speak only as of the date on which they are made and Eupraxia undertakes no obligation to publicly update or revise any forward-looking statement or information, whether as a result of new information, future events or otherwise.
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SOURCE Eupraxia Pharmaceuticals Inc.
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