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Stoke Therapeutics stockholders elect three Class I directors at 2026 annual meeting
Elected G. Clare Kahn, Ph.D. (49,722,339 for), Adrian Krainer, Ph.D. (36,531,612 for), and Julie Anne Smith (43,500,649 for) as Class I directors.
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Stoke reports Q1 net loss $50M; new 4-year OLE data supports zorevunersen disease-modifying potential
Net loss $50.0M ($0.79/share) vs prior-year net income $112.9M; revenue $6.2M down from $158.6M due to 2025 Biogen license revenue.
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Stoke Therapeutics appoints Clare Kahn, Ph.D. to Board, increases size to ten
Board expanded to 10 directors; Kahn appointed as Class I director effective April 3, 2026.
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Stoke Therapeutics dismisses KPMG, appoints Ernst & Young as auditor
On March 23, 2026, Audit Committee dismissed KPMG as independent registered public accounting firm.
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Stoke Therapeutics awards CEO Ian F. Smith $697K discretionary bonus for 2025
Discretionary bonus of $697,125 for CEO Ian F. Smith, equal to full target bonus for 2025.
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Stoke Therapeutics enters $85.5M lease for 98,500 sq ft Waltham HQ/lab through 2038
New lease with NWALP PHOP Property Owner LLC for 98,500 sq ft at 245 Fifth Avenue, Waltham, MA.
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Stoke Therapeutics accelerates EMPEROR enrollment, expects Phase 3 data in mid-2027, cash $391.7M
Enrollment of 150 patients in Phase 3 EMPEROR study expected to complete in Q2 2026, accelerated from prior timeline.
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Stoke and Biogen present data supporting zorevunersen's disease-modifying potential for Dravet syndrome
Propensity score weighted analysis shows statistically significant reductions in major motor seizure frequency at 6 months (70mg loading dose) vs natural history.
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Stoke Q3 net loss $38.3M ($0.65/sh); Phase 3 EMPEROR >20 randomized
Net loss $38.3M ($0.65/sh) vs $26.4M ($0.47) in Q3 2024; revenue $10.6M vs $4.9M.
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Stoke Therapeutics appoints Ian F. Smith as permanent CEO; interim role since March 2025
Ian F. Smith, 59, appointed CEO effective Oct 6, 2025; served as interim CEO since March 19, 2025.
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Stoke Therapeutics to hold annual Say-on-Pay votes through 2031 based on stockholder vote
Stockholders voted in favor of one-year frequency for advisory Say-on-Pay votes at June 3 annual meeting.
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Stoke Q2 net loss $23.5M; Phase 3 EMPEROR dosed, 3-year OLE data show durability
Net loss $23.5M ($0.40/sh) for Q2 2025 vs $25.7M loss in Q2 2024; H1 net income $89.4M from Biogen collaboration.
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First patient dosed in Phase 3 EMPEROR study of zorevunersen for Dravet syndrome by Stoke and Biogen
First patient dosed in global Phase 3 EMPEROR study of zorevunersen for Dravet syndrome.
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Stoke/Biogen present zorevunersen Phase 3 EMPEROR analysis showing cognition/behavior improvements at Week 68
Analysis of patients on EMPEROR-like regimen (2x70mg loading + 2x45mg maintenance) showed cognition/behavior improvements at Week 68.
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Stoke Therapeutics initiates Phase 3 EMPEROR study of zorevunersen; first US sites in May 2025
Initiated Phase 3 EMPEROR study of zorevunersen; first U.S. sites activated in May 2025.
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Stoke Therapeutics shareholders elect three Class III directors at 2025 annual meeting
Edward M. Kaye, Seth L. Harrison, and Arthur O. Tzianabos elected as Class III directors with ~29.2M votes each.
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Stoke Therapeutics Q1 2025 net income $112.9M; advances zorevunersen Phase 3 with Biogen
Net income $112.9M ($1.90 diluted EPS) in Q1 2025 vs net loss $26.4M ($0.57 per share) in Q1 2024.
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Stoke Therapeutics CEO Kaye steps down; Ian Smith named interim; FY 2024 net loss $89M
CEO Edward Kaye steps down March 19; Ian F. Smith appointed Interim CEO; Arthur Tzianabos named Interim Executive Chair.
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Stoke and Biogen enter $165M upfront collaboration for zorevunersen (Dravet syndrome)
Stoke receives $165M upfront; eligible for up to $385M in milestones and low-double-digit to high-teen royalties.
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Stoke announces global regulatory alignment for Phase 3 study of zorevunersen in Dravet syndrome
Aligned with FDA, EMA, and PMDA for Phase 3 EMPEROR; study to start mid-2025, data by end of 2027.
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Stoke Therapeutics receives FDA Breakthrough Therapy Designation for zorevunersen in Dravet syndrome
FDA granted Breakthrough Therapy Designation for zorevunersen to treat Dravet syndrome with a confirmed SCN1A mutation.
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Stoke Therapeutics Q3 net loss $26.4M; FDA lifts partial clinical hold on zorevunersen; STK-002 Phase 1 delayed
Cash, equivalents, and marketable securities $269.2M as of Sep 30, 2024.
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Stoke Therapeutics settles shareholder derivative lawsuit; $590K in fees, governance reforms
Mootness fee of $175,000 paid to resolve certain director compensation claims; company denies wrongdoing.
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Stoke Therapeutics Q2 net loss $25.7M; FDA lifts partial clinical hold on zorevunersen
FDA removed Partial Clinical Hold on zorevunersen for Dravet syndrome; planning Phase 3 registrational study.
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Stoke Therapeutics COO steps down; Huw Nash remains as Chief Business Officer
Huw Nash, Ph.D., stepped down as COO effective June 18, 2024, by mutual agreement with the company.
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Stoke Therapeutics shareholders elect three Class II directors, ratify KPMG as auditor
Elected Jennifer C. Burstein, Arthur A. Levin, Ph.D., and Ian F. Smith as Class II directors for three-year terms.
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Stoke Therapeutics Q1 net loss $26.4M; STK-001 data supports disease modification
Net loss $26.4M ($0.57/share) vs $22.5M ($0.53) YoY; cash $178.6M at March 31, plus $120.3M net from April follow-on offering.
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Stoke Therapeutics names Thomas Leggett CFO; Stephen Tulipano resigns
Thomas Leggett appointed CFO effective May 7, 2024; previously CFO at Affinia Therapeutics and Black Diamond Therapeutics.
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Stoke Therapeutics prices $125M public offering of common stock and pre-funded warrants
Priced 5,555,557 shares at $13.50/share and pre-funded warrants for 3,703,730 shares at $13.4999.
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Stoke Therapeutics reports 2023 net loss $104.7M; cash $201.4M to fund to end 2025
Cash, equivalents & marketable securities $201.4M as of Dec 31, 2023; expected to fund operations through end of 2025.
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Stoke reports STK-001 data: 85% median seizure reduction at 3 months; FDA allows 70mg dosing
Phase 1/2a: 70mg (2-3 doses) showed median 85% reduction in convulsive seizure frequency at 3 months (n=10) and 74% at 6 months (n=9) after last dose.