Edesa Biotech to Participate in Swiss Biotech Day

Rhea-AI Summary

Edesa Biotech, a clinical-stage biopharmaceutical company (NASDAQ:EDSA), will participate in the Swiss Biotech Day on April 24-25, 2023, in Basel, Switzerland. This event will feature a delegation of Canadian officials and industry leaders. Interested parties can schedule meetings using the conference system or contact Edesa directly via email.

Edesa focuses on innovative treatments for inflammatory and immune-related diseases. Their leading candidate, EB05 (Paridiprubart), is in a Phase 3 study for Acute Respiratory Distress Syndrome (ARDS). Additionally, Edesa is developing an sPLA2 inhibitor, EB01, for chronic Allergic Contact Dermatitis and plans to conduct a Phase 2 trial of EB06 for vitiligo. The company emphasizes the importance of regulatory approvals and the inherent risks associated with clinical trials.

TORONTO, ON / ACCESSWIRE / April 20, 2023 / Edesa Biotech, Inc. (NASDAQ:EDSA), a clinical-stage biopharmaceutical company focused on inflammatory and immune-related diseases, announced today that the company will join a Canadian delegation of officials and industry participating in Swiss Biotech Day on April 24-25, 2023 in Basel, Switzerland.

Attendees who are interested in meeting with the company can utilize the conference scheduling system or contact Edesa directly via email at investors@edesabiotech.com.

About Edesa Biotech

Edesa Biotech, Inc. (NASDAQ:EDSA) is a clinical-stage biopharmaceutical company developing innovative ways to treat inflammatory and immune-related diseases. The company's most advanced drug candidate is EB05 (Paridiprubart), a monoclonal antibody developed for acute and chronic disease indications that involve dysregulated innate immunity responses. Edesa is currently evaluating EB05 in a Phase 3 study as a potential treatment for Acute Respiratory Distress Syndrome (ARDS), a life-threatening form of respiratory failure. In addition, Edesa is developing an sPLA2 inhibitor, EB01, as a topical treatment for chronic Allergic Contact Dermatitis (ACD), a common occupational skin condition. The company has also received regulatory approval to conduct a Phase 2 trial of its EB06 monoclonal antibody as a treatment for vitiligo, a life-altering autoimmune disease that causes skin to lose its color in patches. Sign up for news alerts. Connect with us on Twitter and LinkedIn.

Edesa Forward-Looking Statements

This press release may contain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. Forward-looking statements may be identified by the use of words such as "anticipate," "believe," "plan," "estimate," "expect," "intend," "may," "will," "would," "could," "should," "might," "potential," or "continue" and variations or similar expressions. Readers should not unduly rely on these forward-looking statements, which are not a guarantee of future performance. There can be no assurance that forward-looking statements will prove to be accurate, as all such forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause actual results or future events to differ materially from the forward-looking statements. Such risks include: the ability of Edesa to obtain regulatory approval for or successfully commercialize any of its product candidates, the risk that access to sufficient capital to fund Edesa's operations may not be available or may be available on terms that are not commercially favorable to Edesa, the risk that Edesa's product candidates may not be effective against the diseases tested in its clinical trials, the risk that Edesa fails to comply with the terms of license agreements with third parties and as a result loses the right to use key intellectual property in its business, Edesa's ability to protect its intellectual property, the timing and success of submission, acceptance and approval of regulatory filings, and the impacts of public health crises. Many of these factors that will determine actual results are beyond the company's ability to control or predict. For a discussion of further risks and uncertainties related to Edesa's business, please refer to Edesa's public company reports filed with the U.S. Securities and Exchange Commission and the British Columbia Securities Commission. All forward-looking statements are made as of the date hereof and are subject to change. Except as required by law, Edesa assumes no obligation to update such statements.

CONTACT
Gary Koppenjan
Edesa Biotech, Inc.
(805) 488-2800
investors@edesabiotech.com

SOURCE: Edesa Biotech

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FAQ

What is Edesa Biotech's participation in Swiss Biotech Day 2023?

Edesa Biotech (NASDAQ:EDSA) will participate in Swiss Biotech Day on April 24-25, 2023, in Basel, Switzerland, alongside a delegation of Canadian officials and industry.

What drug candidates is Edesa Biotech developing?

Edesa Biotech is developing several drug candidates, including EB05 for Acute Respiratory Distress Syndrome, EB01 for chronic Allergic Contact Dermatitis, and EB06 for vitiligo.

What clinical trials is Edesa Biotech currently conducting?

Edesa Biotech is evaluating EB05 in a Phase 3 study for ARDS and has received regulatory approval for a Phase 2 trial of EB06 for vitiligo.

How can I contact Edesa Biotech during Swiss Biotech Day?

Interested parties can contact Edesa Biotech via their email at investors@edesabiotech.com or use the conference scheduling system.

What are the key risks mentioned in Edesa Biotech's press release?

Key risks include regulatory approval challenges, funding access, and the effectiveness of product candidates in clinical trials.