Skip to main content
ANTXNasdaq

AN2 Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 2·Menlo Park, CA, United States·CEO: Mr. Eric E. Easom
OncologyRespiratory

ANTX evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

What matters most for ANTX—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ANTX

AN2 Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing novel therapies for infectious diseases, with a lead candidate epetraborole targeting Mycobacterium abscessus and a drug discovery platform for other indications.

Key risk: No approved products or revenue

6.0/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$210.6M

Cash Runway

33.1 mo

Lead Asset

an2-502998 (Phase 1)

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 2 clinical trials · 1 catalyst for AN2 Therapeutics, Inc..

AI OverviewAI overview is shown in English only.

AN2 Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing novel therapies for infectious diseases, with a lead candidate epetraborole targeting Mycobacterium abscessus and a drug discovery platform for other indications.

  • Lead product candidate epetraborole is in Phase 2/3 clinical development for Mycobacterium abscessus lung disease [sec_mda · as of 2026-08-11].
  • Cash, cash equivalents, and investments of $44.3 million as of June 30, 2026, expected to fund operations for at least the next 12 months [sec_mda · as of 2026-08-11].
  • Net loss of $8.2 million for the quarter ended June 30, 2026 [latest reported financials].
  • Company has not yet demonstrated ability to complete pivotal trials, obtain regulatory approvals, or commercialize a product [sec_mda · as of 2026-08-11].
  • Pipeline is primarily early- to mid-stage, with no clinical proof of concept established for any product candidate [sec_mda · as of 2026-08-11].

What works

  • Cash runway of at least 12 months provides near-term operational stability [sec_mda · as of 2026-08-11].
  • Epetraborole targets a significant unmet need in Mycobacterium abscessus lung disease, a rare and difficult-to-treat infection [sec_mda · as of 2026-08-11].
  • Company has raised substantial capital through multiple offerings, including $40 million in March 2026, indicating ongoing investor support [sec_mda · as of 2026-05-11].

What to weigh

  • No product candidate has achieved clinical proof of concept or regulatory approval, making future success highly uncertain [sec_mda · as of 2026-08-11].
  • Company expects negative cash flows to increase significantly as it advances candidates through clinical development [sec_mda · as of 2026-05-11].
  • Substantial additional funding will be needed beyond the current cash runway to continue operations and planned activities [sec_mda · as of 2026-08-11].
  • Early-stage drug development carries inherent risks of translation from preclinical to human studies, which may prevent achieving meaningful clinical results [sec_mda · as of 2026-08-11].

From the filings

Quoted directly from source documents.

  • Cash runway of at least 12 months

    existing cash, cash equivalents, and investments will enable us to fund our operating expenses and capital expenditure requirements for at least the next 12 months.

    SEC MD&A · August 11, 2026

  • No clinical proof of concept established

    clinical proof of concept has not yet been established for any of our product candidates.

    SEC MD&A · August 11, 2026

  • Need for substantial additional funding

    we will need to obtain substantial additional funding in connection with our continuing operations and planned activities.

    SEC MD&A · August 11, 2026

  • Company has not demonstrated ability to commercialize

    we have not yet demonstrated an ability to successfully complete pivotal clinical trials, obtain regulatory approvals, manufacture a commercial product or arrange for a third party to do so on our behalf, or conduct sales and marketing activities necessary for successful commercialization.

    SEC MD&A · August 11, 2026

Catalyst timeline

  • 2027-12-31 · Phase2_Topline · leucyl-trna synthetase — Phase 2 Readout: leucyl-trna synthetaseTopline data from the Phase 2 trial of epetraborole (leucyl-tRNA synthetase inhibitor) in Mycobacterium abscessus lung disease will be a key efficacy and safety readout.
Risks & what to watch (4)

Key risks

  • No approved products or revenueCompany has no products approved for commercial sale and has not generated any revenue from product sales [sec_mda · as of 2026-08-11].
  • Clinical development uncertaintyEpetraborole and other candidates are in early- to mid-stage trials; failure to demonstrate safety/efficacy could halt programs [sec_mda · as of 2026-08-11].
  • Need for additional capitalCurrent cash may not be sufficient to complete all planned development; future fundraising may be dilutive or unavailable [sec_mda · as of 2026-08-11].
  • Regulatory and manufacturing risksCompany has no experience in regulatory approval or commercial manufacturing, which could delay or prevent product launch [sec_mda · as of 2026-08-11].

What to watch

  • Phase 2 topline data for epetraborole in Mycobacterium abscessus lung disease, expected by end of 2027 [upcoming catalysts].
  • Cash burn rate and any additional financing activities, as the company will need substantial funding beyond current runway [sec_mda · as of 2026-08-11].
  • Progress of preclinical and early-stage pipeline programs, which are key to long-term value but carry high uncertainty [sec_mda · as of 2026-08-11].
  • Regulatory interactions and IND filings for new candidates, which could impact development timelines [sec_mda · as of 2026-08-11].

Sources: SEC MD&A · Generated August 29, 2026 · How we verify sources →

Run AN2 Therapeutics, Inc. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available AN2 Therapeutics, Inc. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway9.2

33.1 months

Financial Health9.9

D/E 0.08 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 2/Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst Momentum2.0

1 upcoming, next in ~488d

Insider Signal1.5

0 buys · 5 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

46

Total value held

$48.3M

Showing top 10 of 46 institutional holders of AN2 Therapeutics, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
2.9%
Days to cover
2.6
Shares short
879,488
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ANTX short interest

Governance

Frequently asked questions

What is the AI investment thesis for AN2 Therapeutics, Inc.?

AN2 Therapeutics, Inc. is a clinical-stage biopharmaceutical company developing novel therapies for infectious diseases, with a lead candidate epetraborole targeting Mycobacterium abscessus and a drug discovery platform for other indications.

What is AN2 Therapeutics, Inc.'s lead drug candidate?

AN2 Therapeutics, Inc.'s most advanced tracked candidate is an2-502998 (Phase 1) for Chagas disease.

What is AN2 Therapeutics, Inc.'s next catalyst?

AN2 Therapeutics, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: leucyl-trna synthetase" — expected December 31, 2027.

Who is the CEO of AN2 Therapeutics, Inc.?

Mr. Eric E. Easom is the chief executive officer of AN2 Therapeutics, Inc. (ANTX).

Where is AN2 Therapeutics, Inc. headquartered?

AN2 Therapeutics, Inc. (ANTX) is headquartered in Menlo Park, CA, United States.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.