Edesa Biotech reports fiscal results, updates on drug development, and government funding for ARDS treatment studies.

Quiver AI Summary

Edesa Biotech, Inc., a clinical-stage biopharmaceutical company, reported its financial results for the fiscal year ending September 30, 2024, highlighting a pivot in its drug development strategy. The company is shifting its focus to a U.S. government-funded study of its anti-TLR4 drug candidate, EB05 (paridiprubart), for treating Acute Respiratory Distress Syndrome (ARDS), while also amending a related Canadian project. Despite industry challenges, Edesa reduced its operating expenses by over 20%, resulting in a net loss of $6.2 million for the year, down from $8.4 million the previous year. The company also announced plans to manufacture its anti-CXCL10 drug, EB06, and is preparing a submission to the FDA for an investigational new drug application. Edesa's CEO emphasized the importance of government funding in strengthening the company's position for future financing and the expansion of its development pipeline.

Potential Positives

• The company has successfully pivoted its anti-TLR4 drug candidate, EB05, to a U.S. government-funded study, indicating strong backing from governmental institutions and potential for further development in a critical health area.
• Edesa Biotech received a third competitive government award that validates its TLR4 technology, showcasing recognition and support from federal entities.
• There was a significant financial improvement, with total operating expenses decreasing by over 20%, highlighting effective cost management and operational efficiency.
• The company reported a reduced net loss of $6.2 million for the fiscal year, a marked improvement from a $8.4 million loss in the previous year, indicating progress in financial health.

Potential Negatives

• Edesa reported a net loss of $6.2 million for the fiscal year, indicating ongoing financial challenges despite a reduction in operating expenses.
• The company's cash and cash equivalents dropped significantly from $5.36 million to $1.0 million, raising concerns about its liquidity and ability to fund future operations.
• Edesa has negative working capital of $0.2 million, which may limit its operational flexibility and ability to invest in ongoing projects.

FAQ

What are the recent developments at Edesa Biotech?

Edesa Biotech pivoted its anti-TLR4 drug candidate EB05 to a U.S. government-funded study for ARDS.

What financial results did Edesa report for the fiscal year 2024?

Edesa reported a net loss of $6.2 million, a decrease from $8.4 million in the previous year.

How much did Edesa reduce its operating expenses?

Total operating expenses decreased by $2.2 million to $7.0 million for the fiscal year ended September 30, 2024.

What is the timeline for Edesa's clinical trials?

Edesa anticipates topline results for its Phase 2 study could be available within 12 to 18 months following U.S. regulatory clearance.

How can investors meet Edesa's management?

Edesa management plans to participate in one-on-one meetings during JP Morgan week starting January 13, 2025, in San Francisco.

Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.

$EDSA Hedge Fund Activity

We have seen 4 institutional investors add shares of $EDSA stock to their portfolio, and 4 decrease their positions in their most recent quarter.

Here are some of the largest recent moves:

• CM MANAGEMENT, LLC added 20,000 shares (+22.2%) to their portfolio in Q3 2024
• CIBC WORLD MARKET INC. removed 10,770 shares (-100.0%) from their portfolio in Q3 2024
• GEODE CAPITAL MANAGEMENT, LLC added 2,590 shares (+14.2%) to their portfolio in Q3 2024
• TOWER RESEARCH CAPITAL LLC (TRC) removed 1,430 shares (-58.5%) from their portfolio in Q3 2024
• AVION WEALTH added 242 shares (+inf%) to their portfolio in Q3 2024
• FMR LLC removed 142 shares (-100.0%) from their portfolio in Q2 2024
• WELLS FARGO & COMPANY/MN removed 17 shares (-100.0%) from their portfolio in Q2 2024

To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.

Full Release

TORONTO, Dec. 13, 2024 (GLOBE NEWSWIRE) -- Edesa Biotech, Inc. (Nasdaq:EDSA), a clinical-stage biopharmaceutical company focused on developing host-directed therapeutics for immuno-inflammatory diseases, today reported financial results for the fiscal year ended September 30, 2024 and provided an update on its business.

During the fiscal year, the company pivoted the in-house development of its anti-TLR4 drug candidate, EB05 (paridiprubart), to a U.S. government-funded study investigating novel threat-agnostic host-directed therapeutics in patients with Acute Respiratory Distress Syndrome (ARDS). Given this opportunity, Edesa is also amending a development and drug manufacturing project for the same asset that is supported by the Government of Canada. The company said that the goal is to maximize synergies between the two government-funded projects. For its anti-CXCL10 program, Edesa intends to manufacture EB06 and submit related data to the U.S. Food and Drug Administration as part of an investigational new drug (IND) application. The manufacturing of clinical-grade drug batches and initiation of the patient enrollment is subject to funding. Edesa anticipates topline results for this Phase 2 study could be available within as few as 12 to 18 months following regulatory clearance in the U.S. The study is currently approved in Canada.

"This year, Edesa maintained its momentum despite the headwinds in the drug development sector, and we once again validated our TLR4 technology with a third competitive government award," said Par Nijhawan, MD, Chief Executive Officer of Edesa Biotech. "I have maintained my strategic support financially and I believe that our team can continue to advance and expand our development pipeline and partnerships."

Edesa's Chief Financial Officer Stephen Lemieux reported that financial results for the fiscal year benefited from prudent use of working capital and effective financial management, including a more than 20% decrease in operating expenses. "Following the end of the fiscal year, we strengthened our balance sheet, and with two governments now funding the advancement of our anti-TLR4 technology, we have improved our position for future financing, potential strategic arrangements as well as other opportunities to advance our pipeline."

Financial Results for the Fiscal Year Ended September 30, 2024

Total operating expenses decreased by $2.2 million to $7.0 million for the year ended September 30, 2024 compared to $9.2 million for the prior year:

• 
  Research and development expenses decreased by $1.9 million to $2.9 million for the year ended September 30, 2024 compared to $4.8 million for the prior year primarily due to decreased external research expenses related to the company's completed dermatitis study and a reduction in labor costs and noncash share-based compensation, which were partially offset by an increase in expenses related to manufacturing of paridiprubart.
  
• 
  General and administrative expenses decreased by $0.3 million to $4.1 million for year ended September 30, 2024 compared to $4.4 million for the prior year primarily due to a decrease in noncash share-based compensation, which was partially offset by an increase salaries and related costs.
  

Total other income was unchanged at $0.8 million for the years ended September 30, 2024 and September 30, 2023 as a $0.1 million increase in reimbursement funding from the Canadian government's Strategic Innovation Fund was offset by a $0.1 million decrease in interest income.

For the year ended September 30, 2024, Edesa reported a net loss of $6.2 million, or $1.93 per common share, compared to a net loss of $8.4 million, or $2.93 per common share, for the year ended September 30, 2023.

Working Capital

At September 30, 2024, Edesa had cash and cash equivalents of $1.0 million and negative working capital of $0.2 million. Subsequent to the fiscal year end, the company received $1.5 million in gross proceeds under a securities purchase agreement with an entity affiliated with Edesa's Chief Executive Officer and Founder, and $0.6 million in net proceeds, after deducting sales agent commissions, from common shares sold under an at-the-market offering program.

Calendar

Edesa management plans to participate in one-on-one meetings during JP Morgan week, which begins on January 13, 2025, in San Francisco, California. Attendees interested in meeting with management can request meetings through the conference organizers or by contacting Edesa directly at

investors@edesabiotech.com

.

About Edesa Biotech, Inc.

Edesa Biotech, Inc.

(Nasdaq: EDSA) is a clinical-stage biopharmaceutical company developing innovative ways to treat inflammatory and immune-related diseases. Its clinical pipeline is focused on two therapeutic areas: Medical Dermatology and Respiratory. In Medical Dermatology, Edesa is developing EB06, an anti-CXCL10 monoclonal antibody candidate, as therapy for vitiligo, a common autoimmune disorder that causes skin to lose its color in patches. Its medical dermatology assets also include EB01 (1.0% daniluromer cream), a Phase 3-ready asset developed for use as a potential therapy for moderate-to-severe chronic Allergic Contact Dermatitis (ACD), a common occupational skin condition. The company's most advanced Respiratory drug candidate is EB05 (paridiprubart), which is being evaluated in a U.S. government-funded platform study as a treatment for Acute Respiratory Distress Syndrome (ARDS), a life-threatening form of respiratory failure. The EB05 program has been the recipient of two funding awards from the Government of Canada to support the further development of this asset. In addition to EB05, Edesa is preparing an investigational new drug application (IND) in the United States for EB07 (paridiprubart) to conduct a future Phase 2 study in patients with pulmonary fibrosis. Sign up for

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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, including statements related to: Edesa's ability to pivot the in-house development of its anti-TLR4 drug candidate; the company's plans to amend its contribution agreement with the Government of Canada; the company's goal to maximize synergies between two government-funded projects; Edesa plans to manufacture EB06 and submit related data to the FDA as part of an IND application; the company's plans to manufacture clinical-grade drug and initiate patient enrollment; the company's plans to finance clinical and manufacturing activities; the company's estimate that topline results for its Phase 2 vitiligo study could be available within as few as 12 to 18 months following regulatory clearance; the company's belief that in 2024 it maintained its momentum despite the headwinds in the drug development sector and once again validated its TLR4 technology with a third competitive government award; the company's belief that its team can continue to advance and expand its development pipeline and partnerships; the company's belief that its fiscal year financial results benefited from prudent use of working capital and effective financial management; the company's belief that with two governments funding the advancement of its anti-TLR4 technology, it has improved its position for future financing, potential strategic arrangements and alternatives as well as other opportunities to advance its pipeline; and the company's timing and plans regarding its clinical studies in general. 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.