Logotype for Akebia Therapeutics Inc

Akebia Therapeutics (AKBA) Q3 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Akebia Therapeutics Inc

Q3 2026 earnings summary

5 Nov, 2026

Executive summary

  • Q3 revenue fell 37% YoY to $36.9M, primarily as Auryxia sales declined amid generic competition; net loss was $14.4M versus $0.5M net income a year earlier.

  • Vafseo active patients reached ~11,500, up ~140% YoY, while Q3 revenue was $14.8M versus $14.3M; inventory reductions muted reported sales despite patient growth.

  • VOICE and VOCAL results strengthened vadadustat’s clinical and commercial case, with VOICE showing fewer hospitalizations and VOCAL meeting its hemoglobin non-inferiority endpoint.

  • Ebribafusp and praliciguat Phase II programs advanced; initial ebribafusp data are expected in 2027.

Financial highlights

  • Total revenue was $36.9M versus $58.8M in Q3 2025; product revenue was $34.8M versus $56.8M, and license, collaboration and other revenue was $2.1M versus $2.0M.

  • Q3 operating loss was $11.5M versus $4.4M operating income; net loss was $14.4M versus $0.5M net income, with diluted EPS of $(0.05) versus $0.00.

  • R&D expense rose to $16.2M from $14.9M; SG&A fell to $23.5M from $29.1M, and COGS declined to $6.4M from $9.4M.

  • 9M revenue was $139.6M versus $178.6M; net loss was $32.3M versus $6.9M net income, and operating cash flow was $(15.4)M versus $36.9M provided.

Outlook and guidance

  • Post-TDAPA pricing is expected within the ESA price range; higher Vafseo unit volume is expected in 2027, but revenue is expected to decline significantly versus 2026.

  • Vafseo access is expected to expand beyond TDAPA-only patients in 2027; the post-TDAPA period begins Jan. 1, with reimbursement through the dialysis bundle and expected annual treatment cost of $1,000–$1,500.

  • Customer inventory reductions are expected to continue at year-end 2026; DaVita’s gradual rollout is expected to begin in Q4 and become more significant in early 2027.

  • Cash and expected product, royalty, supply and license receipts are expected to fund the current plan for at least two years, contingent on refinancing the secured term loan; without refinancing, runway is at least 12 months from filing.

  • Initial ebribafusp Phase II data are expected in 2027; praliciguat data timing will be set as enrollment visibility improves.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more

Latest events from Akebia Therapeutics