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DiaMedica Therapeutics Inc. Common Stock/$DMAC

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About DiaMedica Therapeutics Inc. Common Stock

DiaMedica Therapeutics Inc is a clinical-stage biopharmaceutical company. The company is engaged in developing treatment for ischemic diseases with two main clinical programs focused on acute ischemic stroke (AIS) and preeclampsia (PE). Its main product candidate DM199 (rinvecalinase alfa) is a recombinant form of human tissue kallikrein-1, which is a synthetic version of the naturally occurring protease enzyme kallikrein-1 and a rhKLK1 undergoing clinical development studies in both AIS and PE. The other product candidate in the company's pipeline is DM300, its patented recombinant human ulinastatin, a broad-spectrum serine protease inhibitor, being developed as a potential therapy for severe acute pancreatitis.
Ticker
$DMAC
Sector
Health
Primary listing
NASDAQ
Employees
35

DMAC Metrics

BasicAdvanced
$487M
-
-$0.72
0.97
-

What the Analysts think about DMAC

Analyst ratings (Buy, Hold, Sell) for DiaMedica Therapeutics Inc. Common Stock stock.
Analyst projections of the future price of DiaMedica Therapeutics Inc. Common Stock stock.

Bulls say / Bears say

In a small Phase 2 pre-eclampsia cohort, DM199 produced sizeable reductions in maternal blood pressure, with systolic pressure remaining below 160 mmHg over 24 hours. This is an encouraging early clinical signal for the lead programme. (DiaMedica Therapeutics)
DM199 is also being tested in early-onset fetal growth restriction, a condition with no approved drug treatment. The first two trial cohorts are enrolled, and results are due at a November event, creating another near-term data catalyst. (DiaMedica Therapeutics, DiaMedica Therapeutics)
The Phase 2/3 stroke study has passed 85% of the 200-participant threshold for its planned interim analysis, with about 70 sites active. The analysis, expected in early 2027, is a major catalyst for the programme. (DiaMedica Therapeutics)
ReMEDy2 enrolment has been slower than expected, and the interim review may stop the study for futility or lead to a much larger trial of up to 728 participants. Further delays could increase costs and defer a decisive read-out. (U.S. Securities and Exchange Commission)
The pre-eclampsia result comes from a small, open-label, single-centre, single-arm proof-of-concept study, so it cannot establish that DM199 caused the improvement. Larger and more rigorous trials must confirm the apparent benefit. (U.S. Securities and Exchange Commission, DiaMedica Therapeutics)
DiaMedica remains loss-making and used $17.2 million in operating cash in the first half of 2026. Although it expects cash to last through 2027, it says substantial additional funding will be needed to advance development, creating financing and potential dilution risk. (U.S. Securities and Exchange Commission)
Data summarised monthly by Lightyear AI. Last updated on 20 Oct 2026.

DMAC Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

DMAC Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing DMAC

Funds
Fund name
Fund size
$DMAC weighting
SPDR Russell 2000 US Small Cap€R2US
$5.3B0.01%
SPDR Russell 2000 US Small Cap£R2SC
$5.3B0.01%
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