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Access earnings results, analyst expectations, report, slides, earnings call, and transcript.
The earnings call highlights a fourfold revenue increase and a significant reduction in net loss, suggesting improved financial performance. The company is expanding its market presence with QUELIMMUNE and has a substantial market opportunity in adult AKI. Despite some regulatory and competitive risks, the management's optimistic outlook on faster approvals and pipeline growth is encouraging. The Q&A session revealed active engagement in clinical trials and expansion in pediatric sites, supporting a positive sentiment. Overall, the financial improvements and strategic positioning point to a potential 2% to 8% stock price increase.
Revenue $293,000 (up from $68,000 in Q4 2024 and $0 in Q1 2024), a fourfold increase driven by greater adoption of QUELIMMUNE therapy from existing customers.
Operating Expenses $4.1 million (up from $3.9 million in Q1 2024), primarily due to increased spending for the commercial launch and growing enrollment in the NEUTRALIZE-AKI trial, partially offset by reduced G&A expenses.
Net Loss $3.7 million (down from $12.7 million in Q1 2024), reflecting improved revenue performance and cost management.
Cash Position Approximately $5.3 million at the end of Q1 2025, indicating a strengthened balance sheet with the addition of new capital.
QUELIMMUNE Therapy Revenue: Achieved a fourfold increase in revenue compared to Q4 2024, totaling $293,000 in Q1 2025.
QUELIMMUNE Adoption: Increased adoption of QUELIMMUNE therapy among existing customers, with all existing customers purchasing during the quarter.
New Customer Acquisition: Added another prestigious nationally recognized Children's Hospital to QUELIMMUNE customer list.
SCD Therapy Pipeline: Received two new breakthrough device designations from the FDA for SCD therapy, expanding pipeline indications.
Pediatric AKI Market Opportunity: Estimated at $100 million annually in the U.S. for approximately 4,000 pediatric AKI patients.
Adult AKI Market Opportunity: Estimated at $4.5 billion annually in the U.S. for over 200,000 adult AKI patients.
NEUTRALIZE-AKI Trial Enrollment: Reached 50% enrollment milestone with 100 patients enrolled.
Cost Management: Lower sequential operating expenses while pushing forward NEUTRALIZE-AKI trial.
Commercial Strategy: Focus on acquiring new customers for QUELIMMUNE and expanding into the adult AKI market.
Future Plans: Anticipate filing a PMA for adult AKI indication in 2026.
Regulatory Issues: The company is navigating the FDA approval process for its QUELIMMUNE therapy and the NEUTRALIZE-AKI trial, which includes a post-approval surveillance registry that requires additional IRB approval, potentially delaying adoption.
Supply Chain Challenges: The company anticipates that sales will be lumpy in the initial phase of the QUELIMMUNE launch, indicating potential supply chain or distribution challenges as they scale up production and distribution.
Market Competition: The company faces competition in the adult AKI market, which is significantly larger than the pediatric market, with over 200,000 adults affected annually, highlighting the need for effective differentiation.
Clinical Trial Risks: The NEUTRALIZE-AKI trial's slow enrollment rate poses a risk to timely completion, and the independent Data Safety Monitoring Board (DSMB) could recommend stopping the trial for futility or adjusting the sample size if results are not as expected.
Financial Risks: The company reported a net loss of $3.7 million in Q1 2025, indicating ongoing financial challenges as they invest in commercialization and clinical trials.
Economic Factors: The overall economic environment could impact hospital budgets and willingness to adopt new therapies, affecting the company's growth and revenue projections.
QUELIMMUNE Customer Base Growth: The primary goal for 2025 is to grow the customer base for QUELIMMUNE therapy, with a focus on increasing adoption in pediatric medical facilities.
NEUTRALIZE-AKI Trial Progress: The NEUTRALIZE-AKI trial for adult patients has reached 50% enrollment, with plans to file a PMA for this indication in 2026.
Market Opportunity for Adult AKI: The adult AKI market represents a potential $4.5 billion annual opportunity in the U.S., with over 200,000 patients affected.
Breakthrough Device Designations: The company has received breakthrough device designations for five indications, expanding the potential market for SCD therapy.
Commercial Strategy: The strategy includes targeting the top 50 pediatric sites in the U.S. for QUELIMMUNE adoption and leveraging experiences from pediatric customers for adult AKI.
Q1 2025 Revenue: Revenue for Q1 2025 was $293,000, a fourfold increase from Q4 2024.
Future Revenue Expectations: Sales are expected to be lumpy initially but should trend upwards as more hospitals adopt QUELIMMUNE.
Operating Expenses: Operating expenses for Q1 2025 were $4.1 million, with a focus on commercial launch and trial enrollment.
Net Loss: Net loss for Q1 2025 was $3.7 million, down from $12.7 million in Q1 2024.
Cash Position: The company ended Q1 2025 with approximately $5.3 million in cash.
Quarterly Revenue: Revenue for the first quarter of 2025 was $293,000 compared to approximately $68,000 in the fourth quarter of 2024.
Net Loss: Net loss for the first quarter of 2025 declined to $3.7 million compared to a loss of $12.7 million in Q1 of 2024.
Market Opportunity for Adult AKI: The total market opportunity in the U.S. is approximately $4.5 billion.
Market Opportunity for Pediatric AKI: Estimated to be about $100 million total annual U.S. market opportunity based on a pediatric AKI population of approximately 4,000 patients.
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