Kinarus Therapeutics Announces Discontinuation of the Phase 2 KINETIC Study of KIN001 in Hospitalized COVID-19 Patients Following a Prespecified Interim Analysis of Efficacy and Safety
Safety data from KINETIC study indicate a favorable profile, with a balanced incidence of treatment-emergent adverse events (TEAEs) between study groups.
- Safety data from KINETIC study indicate a favorable profile, with a balanced incidence of treatment-emergent adverse events (TEAEs) between study groups.
- While it is disappointing that KIN001 has not shown sufficient signs of efficacy in the KINETIC study, it is important to remember that hospitalized COVID-19 patients have severe disease with highly complicated pathophysiology.
- For these reasons, we are continuing to study KIN001 as planned in KINFAST, a second Phase 2 study in ambulatory COVID-19 patients who are not hospitalized remarked Dr Fumeaux.
- Kinarus Therapeutics plans to study the potential of KIN001 as a treatment for wet Age-Related Macular Degeneration and Idiopathic Pulmonary Fibrosis.