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scPharmaceuticals (SCPH) investor relations material
scPharmaceuticals Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Net revenue reached $16M in Q2 2025, up 99% year-over-year, driven by strong FUROSCIX demand, commercial execution, and expanded CKD indication.
20,200 FUROSCIX doses filled in Q2, a 117% increase year-over-year and 45% sequential growth, with cardiology and nephrology as key contributors.
Launch in nephrology in late April 2025 showed rapid prescriber uptake and higher doses per prescription.
Development of an 80mg/1mL autoinjector is underway, with sNDA submission on track for Q3 2025, aiming to reduce COGS and environmental impact.
FDA granted 3-year exclusivity for FUROSCIX, preventing approval of competing subcutaneous furosemide products until October 2025.
Financial highlights
Q2 2025 product revenues were $16M, up from $8.1M in Q2 2024; cost of product revenues rose to $5M from $2.3M.
Net loss for Q2 2025 was $18M, compared to $17.1M in Q2 2024; net loss per share was $0.34.
Cash and cash equivalents at June 30, 2025, were $40.8M, down from $75.5M at year-end 2024.
Gross margin for Q2 2025 was approximately 69%.
Operating expenses for Q2 2025 were $30.3M, up from $22.5M in Q2 2024, driven by increased R&D and SG&A costs.
Outlook and guidance
Anticipates continued growth in nephrology and IDN segments, with further acceleration in Q3 and Q4.
Expects fill rates and prescription volumes to increase through 2025, supported by lower patient co-pays and Medicare Part D redesign.
sNDA for the autoinjector on track for Q3 2025, expected to reduce COGS by ~75% and boost penetration.
Management expects continued operating losses as commercialization expands and R&D investment continues.
Existing cash and available funds expected to cover commitments for at least the next 12 months.
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