Tenaya Therapeutics (TNYA) Proxy filing summary
Event summary combining transcript, slides, and related documents.
Proxy filing summary
23 Oct, 2026Executive summary
Special meeting set for Dec. 9, 2026; the sole proposal seeks authority for a discretionary 1-for-10 to 1-for-25 reverse split.
Nasdaq granted a compliance period through Jan. 25, 2027, requiring a closing bid of at least $1.00 for 10 consecutive business days.
Voting matters and shareholder proposals
Board unanimously approved the proposal on Sept. 17, 2026, and recommends FOR; approval requires votes cast FOR to exceed votes cast AGAINST.
Record date is Oct. 19, 2026; 227,928,240 common shares were outstanding, with one vote per share.
If approved, the board may choose a ratio within the 1-for-10 to 1-for-25 range or abandon implementation before the one-year anniversary of the meeting.
Board of directors and corporate governance
The board retains sole discretion over whether and when to implement the split and its ratio; no further stockholder action is required to implement or abandon it.
Latest events from Tenaya Therapeutics
- Q3 loss narrowed as TN-201 and TN-401 milestones approach, with cash runway into Q4 2027.TNYA
Q3 2026 - Stockholders to vote on a board-discretionary 1-for-10 to 1-for-25 reverse split.TNYA
Proxy filing - A discretionary 1-for-10 to 1-for-25 reverse split targets Nasdaq bid-price compliance.TNYA
Proxy filing - Durable clinical improvements and strong market interest drive pivotal planning for gene therapy assets.TNYA
H.C. Wainwright 28th Annual Global Investment Conference - Q4 will bring pivotal regulatory and clinical updates across all major heart disease programs.TNYA
Canaccord Genuity's 46th Annual Growth Conference - Q2 2026 net loss rose to $43.4M on impairment; cash runway extends through Q3 2027.TNYA
Q2 2026 - Durable efficacy and safety in gene therapy programs drive pivotal trial plans for 2026.TNYA
Jefferies Global Healthcare Conference 2026 - TN-201 gene therapy produced durable cardiac and symptomatic improvements in MYBPC3-HCM patients.TNYA
Study result - Gene therapy for MYBPC3-HCM shows safety, efficacy, and protocol-related FDA hold; timelines intact.TNYA
Status Update