Thiogenesis Therapeutics, Corp. (TTI) Gets FDA IND Clearance for TTI-0102 in Cystinosis
Thiogenesis Therapeutics (TTI) received FDA clearance to test TTI-0102 in nephropathic cystinosis. The open-label pilot study at Emory will assess safety, tolerability, and pharmacokinetics in ~6 adults, with topline data expected in Q1 2027. This milestone aligns with the company's orphan-disease strategy, according to the company.


