+1-786-628-7980
Sign Up/Sign In 
Inhibikase Therapeutics, Inc. a clinical-stage pharmaceutical company developing therapeutics to modify the course of Parkinson’s disease and related disorders, today announced dosing of the first patient in its Phase 2a study (‘201 trial’) evaluating IkT-148009, the Company’s novel Abelson Tyrosine Kinase, or c-Abl, inhibitor for the treatment of Parkinson’s disease.
“Dosing of the first patient in our Phase 2a ‘201’ trial represents a major milestone in the development of IkT-148009 for the treatment of Parkinson’s disease and related disorders,” commented Milton H. Werner, Ph.D., President and Chief Executive Officer. “Parkinson’s disease remains one of the most prevalent neurodegenerative disorders and affects nearly one million people in the U.S. annually. Our research continues to validate the critical role that c-Abl, a mechanistically defined target, plays in the initiation and progression of Parkinson’s disease, as well as the potential of IkT-148009 as a promising new approach to disease modification. Preclinical data in animal models of human PD suggested that functional recovery could be achieved in less than 8 weeks in animal.”
“We are excited to evaluate the safety and tolerability of IkT-148009 in a three-month dosing regimen, which may also have the potential to show preliminary benefits from IkT-148009 inhibition of c-Abl in patients. 12 of up to 40 planned sites have been opened, and as the summer vacation months pass, we anticipate seeing an uptick in screening rates and enrolling patients in this study as we seek to deliver on our mission to improve the lives of patients suffering from devastating neurodegenerative diseases,” concluded Dr. Werner.
The 201 trial is a 1:1:1:1 randomized, double-blind, twelve-week dosing trial that will measure the safety, tolerability and steady-state pharmacokinetics of IkT-148009 as primary endpoints. The trial will enroll approximately 120 patients with untreated Parkinson’s disease (Hoehn & Yahr < 3.0) who have not yet progressed to the need for symptomatic therapy. Patients will be treated at one of three randomized doses, either 50, 100 or 200 mg given once daily, or to a placebo dose. The trial will also measure a hierarchy of Parkinson’s-related disease assessments in the brain and gut as secondary or exploratory endpoints. The 201 trial is currently screening patients across 12 of a planned 40 sites in North America with additional site activations ongoing on a rolling basis.
For more information regarding the trial design please see www.clinicaltrials.gov (identifier: NCT05424276).
About IkT-148009
IkT-148009 is a selective c-Abl kinase inhibitor that uniquely inhibits c-Abl and the closely related Abl2/Arg enzyme without inhibition of other members of the Abl-kinase family, namely c-Kit or PDGFRa/b. It has nearly 25x the potency of the anticancer agent Imatinib against wild type c-Abl in enzyme inhibition assays. IkT-148009 has been designed to have a predictable low toxicity profile with the ability to cross the blood brain barrier and accumulate in the brain, features that were validated in animal models and extensive toxicology studies. The Company opened its first study site in its Phase 2a clinical trial to evaluate 12-week safety, tolerability and steady-state PK of IkT-148009 in untreated Parkinson’s patients on 23 May, 2022.
Company Contact:
Milton H. Werner, Ph.D.
President & CEO
678-392-3419
info@inhibikase.com
Investor Relations:
Alex Lobo
SternIR, Inc.
alex.lobo@sternir.com
