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Wire

Sarepta's Elevidys Showing Signs of Stabilization as siRNA Pipeline Gains Importance, RBC Says

Sarepta Therapeutics' (SRPT) Elevidys for Duchenne muscular dystrophy shows near-term stabilization, while the company's $800 million to $900 million operating expense base provides reassuring visibility around cash flow positivity, RBC Capital Markets said in a Thursday note.The investment firm further said it does not view gene therapy competition as a major near-term threat, as management believes the US Food and Drug Administration is likely to require functional and randomized data from Regenxbio (RGNX) and Solid Biosciences (SLDB) rather than allow an accelerated approval pathway.Regarding Amondys and Vyondys, the company believes strong real-world data, positive elements from the Essence study and precedent from NS Pharma should support continued market access, helping sustain roughly $400 million in revenue over the next several years, RBC noted.The brokerage said the success of Sarepta's partnered siRNA programs for facioscapulohumeral muscular dystrophy and myotonic dystrophy type 1 is becoming increasingly important as competitive pressures could weigh on the company's exon-skipping franchise and, over the longer term, its gene therapy business.RBC said positive data from the programs in H2 could support the stock.The firm has a sector perform rating on the shares and a $19 price target.Price: $17.23, Change: $+0.27, Percent Change: +1.59%

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Wire

Sarepta's Elevidys Faces 'Little' Pressure After Regenxbio Data, Wedbush Says

Sarepta Therapeutics' (SRPT) Elevidys is put under a "little" pressure on Regenxbio's (RGNX) positive trial data in Duchenne muscular dystrophy, Wedbush Securities said in a note Friday.The note pointed to statistically significant correlation between microdystrophin expression and functional improvement in the trial of RGX-202, and should benefit all microdystrophin gene therapy programs/products."We see no other big impact on Elevidys," it said. "We do not believe that the relatively small patient number in RGNX's study allows for a fair comparison of microdystrophin expression."The report also said the regulatory pathway for RGX-202 remains to be defined.Wedbush kept its outperform rating and a $35 price target.Price: $18.12, Change: $-0.56, Percent Change: -3.00%

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Wire

Sarepta Therapeutics' Commercial Portfolio Alone Should Support Higher Valuation, Wedbush Says

Sarepta Therapeutics' (SRPT) commercial portfolio alone should support a higher valuation, while the company's clinical development programs should add further upside, Wedbush said in a Friday note.Wedbush sees quarterly Elevidys net revenue as in line with management's previous guidance and said that the company's reiterated 2026 total net product revenue guidance represents confidence that continued positive cash flow will be enough to fund the siRNA programs in the pipeline.Looking ahead, the brokerage said that Elevidys uptake should increase over time, with recent three-year data from the phase 3 Embark study supporting Elevidys' clinical benefit as well as the importance of early clinical intervention.Wedbush said that the DM1 and FSHD muscle diseases data in phase 1/2 studies in single ascending dose groups showed a strong safety profile with no dose limiting toxicities, and that the company expects to report data from multiple ascending dose groups of the studies by year-end.Additionally, the company's Huntington's Disease program is on track to dose the first patient in Q2 and Sarepta Therapeutics expects to confirm proof-of-biology with target gene-protein knockdown in early 2027, Wedbush said.The brokerage maintained the company's outperform rating with a $35 price target.Price: $20.10, Change: $-0.71, Percent Change: -3.39%

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Wire

Sarepta Therapeutics Seen Benefiting From New Elevidys Study, Better US Uptake in Second Half of 2026

Sarepta Therapeutics (SRPT) could benefit from Roche's new late-stage Elevidys study, stronger US demand in the second half of 2026, steady sales and possible regulatory progress for key exon-skipping drugs, Wedbush said in a note Friday.Roche's plan to start a new global phase 3 trial outside the US signals confidence in Elevidys and should not affect the therapy's US commercialization, though Elevidys revenue in the first half of 2026 could stay soft, the investment firm said.Wedbush said feedback from key opinion leaders points to better uptake in the second half of 2026 as doctors remain positive on Elevidys in ambulatory patients.Data due by the end of 2026 from non-ambulatory patients in Cohort 8 of the ENDEAVOR study could improve confidence in the drug's safety if the results are positive, according to the note.Wedbush maintained its outperform rating and $35 price target for Sarepta, adding that phosphorodiamidate morpholino oligomer sales should remain stable in 2026, with an update on filings for Amondys 45 and Vyondys 53 expected by the end of the second quarter.Price: $21.30, Change: $+0.13, Percent Change: +0.59%

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