Logotype for Beyond Air Inc

Beyond Air (XAIR) Q1 2027 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Beyond Air Inc

Q1 2027 earnings summary

13 Aug, 2026

Executive summary

  • Reported $1.8 million in revenue for the quarter ended June 30, 2026, matching the same period last year.

  • Focused on expanding commercial reach for LungFit PH, preparing for Gen 2 system launch pending FDA approval, and strengthening global infrastructure.

  • Entered a national group purchasing agreement with a major U.S. GPO, expanding access to nearly 2,000 hospitals and health systems.

  • Regained compliance with Nasdaq's minimum bid price requirement after a 1-for-20 reverse stock split.

  • International distribution network now covers over 45 countries, with regulatory milestones including CE mark approval in Europe.

Financial highlights

  • Revenue for the quarter ended June 30, 2026, was $1.8 million, flat year-over-year.

  • Gross margin improved to 13% from 9% year-over-year, marking the third consecutive quarter of positive gross profit.

  • R&D expenses decreased to $2.0 million from $3.1 million year-over-year.

  • SG&A expenses were $4.9 million, up from $4.7 million year-over-year.

  • Net loss attributable to common stockholders was $7.9 million, or $11.00 per share, compared to $7.7 million, or $30.67 per share, in the prior year.

Outlook and guidance

  • Reaffirmed 2026 revenue guidance of $8 million, representing ~15% growth over 2025, excluding Gen 2 LungFit PH revenue.

  • 2027 revenue guidance of $16–$18 million, over 110% growth at midpoint, includes Gen 2 LungFit PH launch, subject to FDA approval.

  • Management expects continued net losses and significant cash outflows for at least the next year, with substantial doubt about the ability to meet obligations without additional funding.

  • Confident in achieving H2 revenue targets due to a doubled pipeline and international wins.

  • Future capital needs depend on commercialization success, regulatory approvals, and clinical trial progress.

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