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Stoke Therapeutics, Inc. (STOK)

Stoke Therapeutics, Inc. is an emerging biopharmaceutical company dedicated to developing innovative antisense oligonucleotide (ASO) therapies. Its primary focus is to target and address the fundamental causes of severe genetic disorders, particularly within the United States. The company employs its exclusive Targeted Augmentation of Nuclear Gene Output (TANGO) platform to engineer ASOs that precisely enhance protein expression. Stoke's most advanced candidate, STK-001, is currently progressing through Phase I/IIa clinical trials for Dravet syndrome, a severe and debilitating genetic epilepsy. Additionally, STK-002 is in the preclinical development stage for treating autosomal dominant optic atrophy. The company has also established a licensing and collaborative agreement with Acadia Pharmaceuticals Inc. to identify, develop, and market new RNA-based medicines for critical and rare genetic neurodevelopmental conditions impacting the central nervous system. Formerly known as ASOthera Pharmaceuticals, Inc., the company rebranded to Stoke Therapeutics, Inc. in May 2016. Founded in 2014, Stoke Therapeutics, Inc. maintains its headquarters in Bedford, Massachusetts.

Sector: Pharmaceutical Preparations

Industry: Biotechnology

Stoke Therapeutics, Inc. logo

Stoke Therapeutics, Inc.

NASDAQ:STOKHealthcare
-0.23%$26.29
AH$27.00+2.70%vs close
Mkt Cap$1.7B
Float54.4M
O/S64.53M
Vol
$ Vol
RVOL
Inst Own-
Earnings
Dilution
Upcoming Catalysts
  • STK-002READOUT
    Cash runway at this date: 5mo
    First half of 2027~34wPR
  • Cash runway at this date: 2mo
    Third quarter of 2027~47wPR
  • zorevunersenSUBMISSIONNDA PLANNED
    Cash runway at this date: -1mo
    Second half of 2027~60wPR
Pipeline3 lead-sponsored trials·2 active1 completed

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Status
Phase
  • Phase 3
    Active, not recruiting

    A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome

    zorevunersen

    Dravet Syndrome

    Enrollment
    170
    Start
    Jun 2025
    Primary Completion
    Mar 2027est.READOUT
    Completion
    Oct 2028est.
    NCT06872125
  • Phase 2
    Active, not recruiting

    An Open-Label Extension Study of STK-001 for Patients With Dravet Syndrome

    zorevunersen (STK-001)

    Dravet Syndrome

    Enrollment
    60
    Start
    Jan 2021
    Primary Completion
    Mar 2029est.
    Completion
    Mar 2029est.
    NCT04740476
  • Phase 1/2
    Completed

    An Open-Label Study to Investigate the Safety of Single and Multiple Ascending Doses in Children and Adolescents With Dravet Syndrome

    STK-001 - Single Ascending Doses, STK-001 - Multiple Ascending Doses

    Dravet Syndrome

    Enrollment
    62
    Start
    Jun 2020
    Primary Completion
    Nov 2023
    Completion
    Nov 2023
    NCT04442295