Tenaya Therapeutics reported positive safety update and DSMB clearance to dose escalate to Cohort 2 in the MyPEAK-1 study. They remain on track to report early clinical data from the first three patients from Cohort 1 of this study in December. As of September 30, 2024, cash, cash equivalents and investments in marketable securities were $79.5 million.
Completed dosing of the first three patients at the 3E13 vg/kg dose (Cohort 1) in MyPEAK-1 clinical trial with no unexpected events or toxicities associated with study drug observed.
Implemented changes to the MyPEAK-1 protocol intended to support future development, including adding a baseline biopsy; expanding trial participant eligibility to include obstructive HCM patients and patients without implantable cardioverter defibrillators (ICDs).
TN-201 was granted rare pediatric disease designation by the U.S. Food and Drug Administration for the treatment of MYBPC3-associated HCM in individuals under the age of 18.
Entered into a $45 million credit facility with Silicon Valley Bank (SVB) in August 2024.
Tenaya estimates sufficient funds are available to support planned company operations into the second half of 2025.
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