Clinical Trial ResultsVYN202 showed clean safety and tolerability, with no adverse events associated with BET inhibition, encouraging further development in other serious autoimmune diseases.
FDA ApprovalThe FDA lifted the clinical hold on 0.25 and 0.5mg doses of VYN202 for female patients, offering encouraging proof-of-concept for VYN202 and highlighting its potential across various autoimmune indications.
Preclinical DataVYN202 has demonstrated promising preclinical data across multiple models of fibro-inflammatory disease and hematologic malignancies.