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ProQR Therapeutics (PRQR) reported its first-quarter 2025 results, revealing a net loss of €10.1 million (€0.10 per share), a 31% increase from the prior-year period. While the financials highlight the challenges of advancing a high-risk biotech pipeline, the company’s progress in its RNA editing platform and near-term clinical milestones suggest a compelling long-term narrative for investors.
The loss stems primarily from a 32% year-over-year jump in research and development (R&D) expenses to €12.3 million, driven by the acceleration of its lead candidate, AX-0810, into clinical development. However, ProQR’s robust cash position of €132.4 million as of March 2025—projected to sustain operations through mid-2027—provides critical runway to execute its ambitious pipeline.

ProQR’s Axiomer platform, which leverages ADAR-mediated RNA editing, is its crown jewel. The lead candidate, AX-0810, targets NTCP (sodium taurocholate cotransporting polypeptide), a protein implicated in cholestatic liver diseases such as progressive familial intrahepatic cholestasis (PFIC). The program is on track for a Clinical Trial Application (CTA) filing in Q2 2025, with initial safety and pharmacokinetic data in healthy volunteers expected by late 2025.
This milestone is pivotal: successful human data could validate the Axiomer platform’s ability to modulate NTCP and reduce bile acid accumulation—a breakthrough for patients with limited treatment options.
Beyond AX-0810, ProQR’s pipeline includes:
- AX-2402 (Rett Syndrome): Targets MECP2 mutations, with clinical candidate selection in 2025 and trials planned for 2026.
- AX-2911 (PNPLA3-related hepatic steatosis): A metabolic disease program targeting non-alcoholic fatty liver disease (NAFLD), also advancing toward clinical trials.
- AX-1412 (cardiovascular diseases): Optimized for GalNAc delivery, with updates expected mid-2025.
While ProQR’s net loss has expanded, its cash management remains disciplined. General and administrative (G&A) expenses were held steady at €3.2 million, and the company’s €132.4 million cash balance reflects a deliberate prioritization of R&D over short-term profitability.
A key revenue source is its collaboration with Eli Lilly, which delivered a $1.0 million milestone in Q1 2025. The partnership, which includes up to 10 initial targets, could expand to 15, triggering a $50 million opt-in payment—a potential lifeline if trials succeed.
Investing in ProQR is inherently speculative. The company’s fate hinges on AX-0810’s clinical data, expected in Q4 2025. If the program falters, the entire pipeline’s credibility—and valuation—could crumble. Additionally, ProQR’s cash burn rate (€15.8 million in operating cash used in Q1) underscores the need for future funding or partnerships to extend beyond mid-2027.
ProQR’s Q1 results reflect the trade-off between near-term losses and long-term potential. The company’s RNA editing platform is years ahead of competitors in clinical development, and AX-0810’s upcoming data could unlock transformative value.
Key Data Points to Watch:
- AX-0810 CTA submission (Q2 2025): A regulatory hurdle that, if cleared, validates ProQR’s operational execution.
- AX-0810 clinical data (Q4 2025): The first proof-of-concept for Axiomer’s safety and efficacy in humans.
- Lilly partnership expansion: A $50 million opt-in payment would significantly bolster ProQR’s cash position.
ProQR is a classic “all-in” biotech story: high risk, but with outsized upside if its RNA editing platform delivers. The Q1 net loss of €10.1 million is a direct cost of advancing its pipeline, and the €132.4 million cash runway buys time to execute. Investors should weigh the 31% rise in R&D spend against the €918,000 milestone revenue and upcoming clinical catalysts.
If AX-0810’s data in late 2025 meets expectations, ProQR could emerge as a leader in RNA therapeutics, justifying its valuation. Until then, this is a stock for those comfortable with high volatility and the possibility of binary outcomes. For now, the data—and the Axiomer platform—are what matter most.
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