Edgewise Therapeutics (EWTX) Q1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2026 earnings summary
8 May, 2026Executive summary
Focused on late-stage clinical development for severe muscle diseases, with lead candidates sevasemten (muscular dystrophies) and EDG-7500 (hypertrophic cardiomyopathy) in multiple Phase 2 trials, and positive long-term data for sevasemten in Becker muscular dystrophy showing sustained stabilization up to 3.5 years.
Net loss increased to $49.0 million for Q1 2026 from $40.8 million in Q1 2025, reflecting higher R&D and G&A expenses.
Cash, cash equivalents, and marketable securities totaled $499.6 million as of March 31, 2026, expected to fund operations for at least 12 months.
Anticipates pivotal GRAND CANYON trial results for sevasemten in Becker in Q4 2026, with potential for first marketing application in H1 2027.
CIRRUS-HCM 12-week data for EDG-7500 in hypertrophic cardiomyopathy expected in Q2 2026, with Phase 3 initiation planned for H2 2026.
Financial highlights
Research and development expenses rose to $42.7 million in Q1 2026, up $5.9 million year-over-year, driven by later-stage clinical programs and increased headcount.
General and administrative expenses increased to $11.5 million, up $2.3 million year-over-year, mainly due to personnel and professional costs.
Interest income was $5.1 million, relatively flat year-over-year.
Net loss per share was $(0.46), compared to $(0.43) in Q1 2025.
Operating expenses for Q1 2026 were $54.1 million, up from $46.0 million in Q1 2025.
Outlook and guidance
Existing cash resources are projected to fund planned operating and capital expenditures through at least the next 12 months.
Anticipates continued increases in R&D and G&A expenses as clinical programs advance and organization scales for future commercialization.
GRAND CANYON top-line data for sevasemten in Becker expected in Q4 2026; marketing application planned for H1 2027.
CIRRUS-HCM 12-week Part D data for EDG-7500 in HCM due in Q2 2026; Phase 3 trial initiation in H2 2026.
Phase 2 trial for EDG-15400 in heart failure with preserved ejection fraction (HFpEF) expected to start in H2 2026.
Latest events from Edgewise Therapeutics
- Proxy covers director elections, auditor ratification, and executive pay, with strong governance focus.EWTX
Proxy filing23 Apr 2026 - Election of directors, auditor ratification, and executive pay vote set for June 2026 meeting.EWTX
Proxy filing23 Apr 2026 - 7500 advances toward Phase III in HCM, with Becker data showing disease stabilization.EWTX
Leerink Global Healthcare Conference 202611 Mar 2026 - Pivotal trial data expected in 2026–2027; Q4 net loss rose to $50.2M, cash at $530.1M.EWTX
Q4 202526 Feb 2026 - Phase III readouts and new cardiac programs drive momentum, with strong commercial readiness.EWTX
Guggenheim Securities Emerging Outlook: Biotech Summit 202612 Feb 2026 - EDG-7500 reduced LVOT gradients and NT-proBNP in HCM without lowering LVEF.EWTX
Study Update20 Jan 2026 - Pivotal data and strong financials drive late-stage muscle and cardiac disease programs.EWTX
44th Annual J.P. Morgan Healthcare Conference13 Jan 2026 - Sevasemten reduced muscle damage biomarkers and stabilized function in Becker phase 2 trial.EWTX
Status Update12 Jan 2026 - Sevasemten reduced muscle damage biomarkers and stabilized function in Becker muscular dystrophy.EWTX
Study Update12 Jan 2026