Sarepta Therapeutics earnings date
Sarepta Therapeutics (SRPT) Q3 2026 Earnings Report
MX:SRPT Q3 2026 EPS Results
- Actual EPS
- -MXN 5.02
- Consensus EPS
- MXN 1.47
- Beat/Miss
- Missed by -MXN 6.49
- One Year Ago EPS
- -MXN 33.48
MX:SRPT Q3 2026 Revenue Results
- Actual Revenue
- MXN 7.09B
- Expected Revenue
- MXN 6.55B
- Beat/Miss
- Beat by +MXN 542.52M
- YoY Revenue Growth
- -4.51%
Earnings Announcement Details
- Quarter
- Q3 2026
- Date
- 11/05/2026
- Time
- After Close
- Conference Call
- Thursday, November 5, 2026
Sarepta Therapeutics's next earnings date is estimated for March 3, 2027, based on past reporting schedules.
Q3 2026 Earnings Call Audio
Q3 2026 Earnings Slide Deck
Q3 2026 Earnings Call Summary
The call conveyed focused optimism, supported by stabilized ELEVIDYS demand, strong PMO performance, raised revenue guidance, positive pipeline data, upcoming DM1 and FSHD readouts, non-GAAP profitability, and nearly $1 billion of cash and investments. These positives were partially offset by year-over-year revenue declines driven by lower ELEVIDYS sales, significant take-or-pay charges and related gross-margin pressure, a third-quarter GAAP operating loss, the termination of ENVISION enrollment, and continued uncertainty around near-term ELEVIDYS growth and the non-ambulatory label.
Sarepta raised the low end of its 2026 total net product revenue guidance by $50 million and narrowed the range to $1.25 billion-$1.3 billion; ELEVIDYS revenue was $83 million in the third quarter and is expected in the fourth quarter to trend in line with Q3, while the PMO franchise is expected to remain strong. Full-year combined non-GAAP R&D and SG&A expense guidance was narrowed to between $800 million and $825 million. The company expects to submit an sBLA for the under-four population mid-next year, complete enrollment of ENDEAVOR Cohort eight by the end of this year and engage with FDA in Q1 2027, share DM1 and FSHD MAD data in the coming weeks, receive higher-dose data early next year, and generate Huntington’s disease proof-of-biology data sometime around mid-year next year.
- Raised 2026 Revenue GuidanceBased on strong PMO performance and stabilization in ELEVIDYS, Sarepta raised the low end of its 2026 total net product revenue guidance by $50 million and narrowed the range to $1.25 billion-$1.3 billion.
- Third-Quarter Commercial RevenueThird-quarter total net product revenue was approximately $324 million, including $83 million from ELEVIDYS and $240 million from the PMO franchise.
- ELEVIDYS Demand StabilizationELEVIDYS enrollment form activity in the third quarter was in line with the second quarter and above where the company started the year. Willingness to treat remained solid, and recent start form activity supported the current run rate.
- Durable ELEVIDYS Clinical EvidenceMore than 1,500 patients have been treated with ELEVIDYS. The company said three-year EMBARK results and data in eight to 12-year-old patients showing durable and clinically meaningful benefits over two years are resonating with physicians and families.
- Strong PMO and Exon-Skipping FranchiseNew patient enrollments for the exon-skipping franchise increased, while patient adherence continued to support stability in the commercial patient base. More than 1,800 patients worldwide have been treated with Sarepta's exon-skipping therapies, and EXONDYS 51 reached its 10-year U.S. approval anniversary.
- Progress Toward Under-Four ELEVIDYS SubmissionAn analysis of 26 patients treated at ages two and three demonstrated robust ELEVIDYS dystrophin expression and sarcolemma localization 12 weeks after infusion. Sarepta expects to submit a supplemental biologics license application for the under-four population in the middle of next year.
- Positive ELEVIDYS Safety-Mitigation DataPreliminary data from the phase IV ENDURE study showed treatment-related acute liver injury rates consistent with prior reports, with no acute liver injury events observed among the subset of participants who received prophylactic sirolimus.
- DM1 and FSHD Pipeline AdvancementSarepta expects to share multiple ascending dose datasets for its DM1 and FSHD programs in the coming weeks. The datasets are intended to evaluate dose, muscle exposure, target knockdown, downstream biological effects, safety, and exploratory functional measures.
- Encouraging siRNA Biological EvidenceThe company reported dose-dependent increases in plasma and muscle concentration, no evidence of saturation in muscle uptake, and the potential to achieve deeper target knockdown. In DM1, SRP-1003 demonstrated dose-dependent degradation of pathogenic DMPK mRNA in both the cytoplasm and nucleus and established correction of MBNL-dependent mis-splicing.
- Preparation for Registrational StudiesSarepta is preparing registrational studies for both DM1 and FSHD, including operational readiness and manufacturing initiation for planned phase III studies. The company intends to preserve flexibility between accelerated approval and traditional approval pathways.
- Pipeline and Regulatory Milestones AheadSarepta expects DM1 and FSHD multiple ascending dose data later this year, proof-of-biology data from its Huntington's disease program next year, and ENDEAVOR Cohort eight data next year. For Huntington's disease, preclinical studies demonstrated blood-brain barrier crossing and delivery to deep brain nuclei, with proof-of-biologic-activity data expected around mid-year.
- Completion of MIS51ON StudySarepta achieved last patient, last visit in the MIS51ON phase III dose-ranging study evaluating higher doses of EXONDYS 51.
- Non-GAAP Profitability and Cash GenerationSarepta reported a third-quarter non-GAAP operating profit of $23 million and said its base business generated nearly $300 million of cash year-to-date after adjusting for $250 million of collaboration payments to Arrowhead.
- Strengthened Liquidity and Balance SheetCash and investments increased by $54 million during the third quarter to nearly $1 billion, compared with $954 million at year-end 2025. Management said continued non-GAAP profitability, cash generation, and balance-sheet strength provide flexibility to invest in pipeline catalysts.
- Operating Expense DisciplineSarepta narrowed full-year 2026 combined non-GAAP R&D and SG&A expense guidance to $800 million-$825 million. Third-quarter non-GAAP R&D and SG&A expenses were $169 million, down 40% year-over-year.
MX:SRPT Earnings History
| Report Date | Fiscal Quarter | Forecast / EPS | Last Year's EPS | EPS YoY Change | Press Release |
|---|---|---|---|---|---|
| Mar 03, 2027 | 2026 (Q4) | -6.58- | -73.1 | ― | ― |
| Nov 05, 2026 | 2026 (Q3) | 1.47-5.02 | -33.48 | 85.00% (+28.46) | |
| Aug 05, 2026 | 2026 (Q2) | 4.04-0.93 | 35.15 | -102.65% (-36.08) | |
| May 06, 2026 | 2026 (Q1) | 18.1553.57 | -85.56 | 162.61% (+139.13) | |
| Feb 25, 2026 | 2025 (Q4) | -22.26-73.10 | 27.9 | -362.00% (-101.00) | |
| Nov 03, 2025 | 2025 (Q3) | -13.52-33.48 | 6.32 | -629.41% (-39.80) | |
| Aug 06, 2025 | 2025 (Q2) | 15.4835.15 | 1.3 | 2600.00% (+33.85) | |
| May 06, 2025 | 2025 (Q1) | -59.65-85.56 | 6.88 | -1343.24% (-92.44) | |
| Feb 26, 2025 | 2024 (Q4) | 35.0227.90 | 8.74 | 219.15% (+19.16) | |
| Nov 06, 2024 | 2024 (Q3) | -1.396.32 | -8.56 | 173.91% (+14.88) |
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.


