Lyra Therapeutics Announces Positive Topline Results of Pharmacokinetic Study of LYR-210 in Patients with Chronic Rhinosinusitis
(Nasdaq: LYRA), a clinical-stage therapeutics company leveraging its proprietary XTreo platform to enable precise, sustained, and local delivery of medications to the ear, nose and throat (ENT) passages and other diseased tissues, today announced positive topline results from the companys pharmacokinetic (PK) study of LYR-210.
- (Nasdaq: LYRA), a clinical-stage therapeutics company leveraging its proprietary XTreo platform to enable precise, sustained, and local delivery of medications to the ear, nose and throat (ENT) passages and other diseased tissues, today announced positive topline results from the companys pharmacokinetic (PK) study of LYR-210.
- The clinical study was a 56-day open label, multi-center, U.S. study of the PK and safety of LYR-210 in adult subjects with chronic rhinosinusitis (CRS).
- MF blood plasma levels observed during the PK study support LYR-210s ability to deliver consistent and steady dosing over the entire treatment period.
- This was the first U.S. study of LYR-210 and it was fully enrolled across four sites in 11 weeks.