AN2 Therapeutics, Inc., today announced topline results from its Phase 1b dose-ranging study of oral epetraborole. AN2 Therapeutics is developing epetraborole.
| MENLO PARK, Calif., Feb. 10, 2022 /PRNewswire/ -- AN2 Therapeutics, Inc., a clinical-stage biopharmaceutical company focused on developing treatments for rare, chronic, and serious infectious diseases with high unmet needs, today announced topline results from its Phase 1b dose-ranging study of oral epetraborole. AN2 Therapeutics is developing epetraborole as a once-daily, orally administered treatment for patients with non-tuberculous mycobacterial (NTM) lung disease, with an initial focus on treatment-refractory Mycobacterium avium complex (MAC) lung disease.
The Phase 1b double-blind, placebo-controlled, dose-ranging study was designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of oral epetraborole administered to healthy volunteers at doses ranging from 250 mg to 1,000 mg for 28 days. Results showed that epetraborole was generally well tolerated, with no severe or serious adverse events. PK was shown to be generally linear and predictable, consistent with previous studies. “We believe the Phase 1b results further validate data from previous studies with epetraborole and demonstrate that it is well tolerated when dosed for 28 days,” said Paul Eckburg, M.D., Chief Medical Officer of AN2 Therapeutics. “These results, coupled with data available from our non-clinical efficacy and chronic toxicology studies completed earlier this year, provide us with additional confidence in dose selection for our pivotal Phase 2/3 trial, which we plan to initiate in the first half of this year in patients with treatment-refractory MAC lung disease.” “Epetraborole has the potential to meet many of the characteristics of an ideal target product profile. It has demonstrated high levels of efficacy in animal models of NTM infection, it works via a novel mechanism of action, and is well tolerated with a once-daily oral treatment for patients with NTM lung disease. There is only one approved therapy in the United States for patients with pulmonary NTM, and patients and physicians need better options,” said Eric Easom, President and Chief Executive Officer of AN2 Therapeutics. “Novel oral antibiotics are urgently needed that have the potential to improve therapeutic efficacy, safety and tolerability for this underserved patient population.” For more information on the epetraborole Phase 1b study design, visit clinicaltrials.gov and search NCT04892641. About Epetraborole About AN2 Therapeutics, Inc.
SOURCE AN2 Therapeutics, Inc. |
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