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DiaMedica Therapeutics Reports Full Year 2025 Financial Results and Provides Business Highlights

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DiaMedica Therapeutics Reports Full Year 2025 Financial Results and Provides Business Highlights MINNEAPOLIS--( BUSINESS WIRE)--DiaMedica Therapeutics Inc. (Nasdaq: DMAC), a clinical-stage biopharmaceutical company focused on developing novel treatments for preeclampsia (PE), fetal growth restriction (FGR), and acute ischemic stroke (AIS), today provided a business update and reported financial results for the year ended December 31, 2025. Management will host a conference call on Tuesday, March 31, 2026, at 8:00 AM Eastern Time / 7:00 AM Central Time to provide a business update and discuss full-year 2025 financial results.

“We continue to make meaningful progress across our clinical programs, highlighted by further advancement of the DM199 preeclampsia (PE) program. In the IST, enrollment continues in the expansion cohort for Part 1a, and we anticipate initiating Parts 2 and 3, which will evaluate participants with early-onset preeclampsia and fetal growth restriction. We are also preparing to initiate a DiaMedica-sponsored Phase 2 study in early-onset preeclampsia later this year. There remains a critical need for differentiated, well-tolerated therapies that can deliver clinically meaningful benefits, prolong pregnancy, and improve outcomes for both the mother and baby,” said Rick Pauls, President and Chief Executive Officer of DiaMedica Therapeutics. “We are encouraged by the momentum in our ReMEDy2 acute ischemic stroke trial, which is approaching 70% of the required enrollment for the planned interim analysis, and we remain on track to complete the interim analysis in the second half of 2026. This, combined with a strong cash position expected to fund operations through the second half of 2027, supports our continued focus on advancing DM199 through key clinical and regulatory milestones in 2026.”

Recent Corporate Highlights

Preeclampsia Phase 2 IST Clinical Development:

Early-Onset Preeclampsia Phase 2 DiaMedica Sponsored Trial:

Acute Ischemic Stroke ReMEDy2 Phase 2/3 Clinical Developments:

Financial Results Highlights for the Year Ended December 31, 2025

Conference Call and Webcast Information

DiaMedica Management will host a conference call and webcast to discuss its business update and full year 2025 financial results on Tuesday, March 31, 2026, at 8:00 AM Eastern Time / 7:00 AM Central Time:

Date:

Tuesday, March 31, 2026

Time:

7:00 AM CDT / 8:00 AM EDT

Web access:

https://app.webinar.net/bxPLk6nkE0q

Dial In:

(646) 357-8766

Conference ID:

4545194

Interested parties may access the conference call by dialing in or listening to the simultaneous webcast. Listeners should log on to the website or dial in 15 minutes prior to the call. The webcast will remain available for play back on the Company’s website, under investor relations - events and presentations, following the earnings call and for 12 months thereafter. A telephonic replay of the conference call will be available until April 7, 2026, by dialing (800) 770-2030 (US Toll Free) and entering the replay passcode: 4545194#.

About DiaMedica Therapeutics Inc.

DiaMedica Therapeutics Inc. is a clinical-stage biopharmaceutical company committed to improving the lives of people suffering from serious ischemic diseases with a focus on preeclampsia, fetal growth restriction and acute ischemic stroke. DiaMedica’s lead candidate, DM199, is the first pharmaceutically active recombinant (synthetic) form of the KLK1 protein, an established therapeutic modality in Asia for the treatment of acute ischemic stroke, preeclampsia, and other vascular diseases. For more information, visit the Company’s website at www.diamedica.com.

Cautionary Note Regarding Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995 and forward-looking information that are based on the beliefs of management and reflect management’s current expectations. When used in this press release, the words “anticipates,” “believes,” “continue,” “could,” “estimates,” “expects,” “intends,” “may,” “plans,” “potential,” “should,” or “will,” the negative of these words or such variations thereon or comparable terminology and the use of future dates are intended to identify forward-looking statements and information. Forward-looking statements and information in this press release include statements regarding the Company’s expectations regarding the timing, nature and requirements for regulatory applications and approvals, including its application for an IND for the study of DM199 as a treatment for preeclampsia and fetal growth restriction and its conducting a Phase 2 trial in these indications; ReMEDy2 trial enrollment and timing of interim analysis; anticipated clinical benefits and success of DM199 for the treatment of preeclampsia, fetal growth restriction and acute ischemic stroke; future R&D and G&A expenses and the Company’s projected cash runway. By their nature, forward-looking statements involve known and unknown risks, uncertainties and other factors which may cause actual results, performance or achievements, or other future events, to be materially different from any future results, performance or achievements expressed or implied by such forward-looking statements. Applicable risks and uncertainties include, among others, risks and uncertainties relating to the timing and outcomes of non-clinical studies; risks and uncertainties relating to the timing of studies and trials; risks and uncertainties relating to the clinical expansion into preeclampsia and associated trials; the risk that existing preclinical and clinical data may not be predictive of the results of ongoing or later clinical trials; DiaMedica’s plans to develop, obtain regulatory approval for and commercialize its DM199 product candidate for the treatment of preeclampsia, fetal growth restriction, and acute ischemic stroke and its expectations regarding the benefits of DM199; DiaMedica’s ability to conduct successful clinical testing of DM199 and within its anticipated parameters, site activations, enrollment numbers, costs and timeframes; the perceived benefits of DM199 over existing treatment options; the potential direct or indirect impact of hospital and medical facility staffing shortages, increased tariffs and worldwide global supply chain shortages on DiaMedica’s business and clinical trials, including its ability to meet its site activation and enrollment goals; DiaMedica’s reliance on collaboration with third parties to conduct clinical trials; DiaMedica’s ability to continue to obtain funding for its operations, including funding necessary to complete current and planned clinical trials and obtain regulatory approvals for DM199 for preeclampsia, fetal growth restriction, and acute ischemic stroke; and the risks identified under the heading “Risk Factors” in DiaMedica’s annual report on Form 10-K for the fiscal year ended December 31, 2024 filed with the U.S. Securities and Exchange Commission (SEC) and subsequent SEC reports. The forward-looking information contained in this press release represents the expectations of DiaMedica as of the date of this press release and, accordingly, is subject to change after such date. Readers should not place undue importance on forward-looking information and should not rely upon this information as of any other date. While DiaMedica may elect to, it does not undertake to update this information at any particular time except as required in accordance with applicable laws.

DiaMedica Therapeutics Inc.

Condensed Consolidated Statements of Operations and Comprehensive Loss

(In thousands, except share and per share amounts)

Year Ended December 31,

2025

2024

Operating expenses:

Research and development

$

24,614

$

19,057

General and administrative

9,783

7,624

Total operating expenses

34,397

26,681

Operating loss

(34,397

)

(26,681

)

Other income:

Other income, net

1,659

2,267

Total other income, net

1,659

2,267

Loss before income tax expense

(32,738

)

(24,414

)

Income tax expense

(28

)

(30

)

Net loss

(32,766

)

(24,444

)

Other comprehensive income

Unrealized gain on marketable securities

27

17

Comprehensive loss

$

(32,739

)

$

(24,427

)

Basic and diluted net loss per share

$

(0.70

)

$

(0.60

)

Weighted average shares outstanding – basic and diluted

46,980,777

40,404,681

DiaMedica Therapeutics Inc.

Condensed Consolidated Balance Sheets

(In thousands, except share amounts)

December 31,

2025

December 31,

2024

ASSETS

Current assets:

Cash and cash equivalents

$

15,647

$

3,025

Marketable securities

44,243

41,122

Prepaid expenses and other assets

481

227

Amounts receivable

258

236

Total current assets

60,629

44,610

Non-current assets:

Deferred offering costs

400

Operating lease right-of-use asset

197

279

Property and equipment, net

145

148

Deposits

1,308

Total non-current assets

742

1,735

Total assets

$

61,371

$

46,345

LIABILITIES AND EQUITY

Current liabilities:

Accounts payable

$

1,475

$

940

Accrued liabilities

3,545

4,347

Operating lease obligation

101

90

Finance lease obligation

11

13

Total current liabilities

5,132

5,390

Non-current liabilities:

Operating lease obligation, non-current

124

225

Finance lease obligation, non-current

4

12

Total non-current liabilities

128

237

Shareholders’ equity:

Common shares, no par value; unlimited authorized;

53,742,370 and 42,818,660 shares issued and outstanding, as of December 31, 2025 and 2024, respectively

Paid-in capital

228,829

180,697

Accumulated other comprehensive income

50

23

Accumulated deficit

(172,768

)

(140,002

)

Total shareholders’ equity

56,111

40,718

Total liabilities and shareholders’ equity

$

61,371

$

46,345

DiaMedica Therapeutics Inc.

Condensed Consolidated Statements of Cash Flows

(In thousands)

Year Ended December 31,

2025

2024

Cash flows from operating activities:

Net loss

$

(32,766

)

$

(24,444

)

Adjustments to reconcile net loss to net cash used in operating activities:

Share-based compensation

3,846

2,085

Amortization of discounts on marketable securities

(942

)

(1,343

)

Non-cash lease expense

82

75

Depreciation

43

39

Changes in operating assets and liabilities:

Prepaid expenses and other assets

(254

)

184

Amounts receivable

(22

)

133

Deposits

1,308

(1,308

)

Accounts payable

535

14

Accrued liabilities

(892

)

2,489

Net cash used in operating activities

(29,062

)

(22,076

)

Cash flows from investing activities:

Purchase of marketable securities

(59,278

)

(50,411

)

Maturities and sales of marketable securities

57,126

59,000

Purchase of property and equipment

(40

)

(25

)

Net cash provided by (used in) investing activities

(2,192

)

8,564

Cash flows from financing activities:

Proceeds from issuance of common shares, net of offering costs

43,282

11,747

Proceeds from the exercise of stock options

1,004

256

Principal payments on finance lease obligations

(10

)

(9

)

Deferred financing costs, net

(400

)

Net cash provided by financing activities

43,876

11,994

Net increase (decrease) in cash and cash equivalents

12,622

(1,518

)

Cash and cash equivalents at beginning of period

3,025

4,543

Cash and cash equivalents at end of period

$

15,647

$

3,025

Supplemental disclosure of cash flow information:

Cash paid for income taxes

$

28

$

26

Assets acquired under financing lease

$

$

30