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Sarepta Therapeutics (SRPT) investor relations material
Sarepta Therapeutics Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Business stabilized in Q1 2026 with improved commercial execution, expanded field reach, and increased physician engagement, especially for ELEVIDYS, which is positioned for renewed growth.
Achieved net income of $331.0 million for Q1 2026, a significant turnaround from a net loss of $447.5 million in Q1 2025, driven by collaboration revenue and cost reductions.
Over 1,300 patients treated with ELEVIDYS in commercial and clinical settings as of May 5, 2026.
Early clinical data from siRNA programs in FSHD and DM1 showed dose-dependent exposure, biomarker effects, and favorable tolerability, with additional readouts expected in the second half of 2026.
Profitable and cash-flow positive base business, with disciplined cost management and self-funded growth.
Financial highlights
Q1 2026 total revenues were $730.8 million, down 2% year-over-year, with net product revenue of $330.5 million and a 46% decline in product sales offset by a 200% increase in collaboration and other revenues.
GAAP operating profit was $358.4 million; non-GAAP operating profit was $397.7 million.
Cash and investments at quarter-end totaled $748.3 million, down from $953.8 million at year-end 2025.
Q1 2026 net income: $331.0 million GAAP, $385.4 million Non-GAAP; diluted EPS: $2.88 GAAP, $3.16 Non-GAAP.
Cost of sales was $108.8 million, down 21% year-over-year; gross margin on unit sales was 82%.
Outlook and guidance
Full-year 2026 revenue guidance reiterated at $1.2 billion–$1.4 billion, with combined non-GAAP R&D and SG&A expenses expected at $800–$900 million.
Expectation to remain profitable and grow cash balance for the remainder of 2026.
Commercial momentum for ELEVIDYS expected to build gradually, with greater visibility into improvement in late 2026 and 2027.
Management expects current cash and investments, plus operational inflows and credit facility access, to fund operations for at least the next 12 months.
- Proxy seeks approval for director elections, compensation, equity plans, and auditor ratification.SRPT
Proxy filing24 Apr 2026 - Virtual annual meeting on June 4, 2026, includes key votes on directors, pay, and auditor.SRPT
Proxy filing24 Apr 2026 - 2026 outlook: $954M cash, $1.2–$1.4B revenue guidance, stable franchises, Japan launch.SRPT
Q4 202512 Apr 2026 - SRP-1001 and SRP-1003 show strong early efficacy, safety, and muscle delivery, with phase III trials planned for 2027.SRPT
Study result25 Mar 2026 - 2026 revenue targets remain solid as clinical and commercial initiatives advance toward 2027.SRPT
TD Cowen 46th Annual Health Care Conference3 Mar 2026 - Two-year results confirm durable efficacy, safety, and muscle health benefits in Duchenne.SRPT
Status Update3 Feb 2026 - FDA expands ELEVIDYS approval for Duchenne patients 4+, with robust readiness and stable pricing.SRPT
Status Update3 Feb 2026 - Three-year data show ELEVIDYS provides durable, significant slowing of Duchenne progression.SRPT
Study result2 Feb 2026 - Q2 2024 revenue up 51% to $362.9M, led by ELEVIDYS; 2025 guidance $2.9–$3.1B.SRPT
Q2 20242 Feb 2026
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