AN2 Therapeutics Announces FDA Clearance to Proceed with 90-Patient Investigator-Initiated Trial (IIT) of Epetraborole in Patients with M. abscessus Lung Disease
AN2 aims to advance oral treatment option for patients currently reliant on complex, off-label IV therapies
Led by nontuberculous mycobacteria (NTM) expert Dr.
Patient enrollment expected to be initiated in 1Q 2026
“Current treatment for M. abscessus relies on off-label, complex intravenous drug regimens that are difficult to tolerate, provide modest efficacy and are burdensome to patients,” said
“The IND clearance is a significant milestone as we evaluate epetraborole as potentially the first FDA-approved therapy for patients with M. abscessus,” said
About the IIT of epetraborole in M. abscessus
This investigator-initiated, proof-of-concept study is a randomized, double-blind, placebo-controlled, multicenter, prospective trial to assess the efficacy, safety, and pharmacokinetics of epetraborole in patients with M. abscessus.
The study will enroll approximately 90 patients across 10-15 sites in the
About
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including, but not limited to, statements regarding the potential of epetraborole to treat M. abscessus and to show efficacy as an oral therapy or once-daily therapy; statements regarding conducting future trials, including pivotal trials; the design and implementation of trials, including the anticipated number of sites and patients in the planned IIT; and epetraborole’s potential in early-stage, treatment-naïve patients. Forward-looking statements are based on AN2’s current expectations and involve risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include, among others, risk inherent in IITs, including reliance on third-party investigators and institutions for study conduct, availability and timing of external funding and operational support, site activation and retention, patient identification and enrollment pace, screen-failure rates, protocol adherence, and limited control over trial execution and data quality; the translation of preclinical data to outcomes in clinical trials; the ability to successfully initiate and complete clinical studies, obtain regulatory approvals, and commercialize any resulting products; the timing and success of clinical trials; the unmet need and market opportunity in M. abscessus; and other risks described in AN2’s filings with the Securities and Exchange Commission, including under the heading “Risk Factors” in AN2’s most recent quarterly report on Form 10-Q and other filings. AN2 undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise, except as required by law.
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Company Contact:
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l.day@an2therapeutics.com
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ir@an2therapeutics.com
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