Immunovant
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Immunovant (IMVT) investor relations material

Immunovant Q3 2026 earnings summary

Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
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Q3 2026 earnings summary6 Feb, 2026

Executive summary

  • Reported positive phase 2 results for brepocitinib in cutaneous sarcoidosis, with 100% of high-dose patients achieving clinically meaningful improvement and strong safety profile.

  • IMVT-1402 registrational trial in difficult-to-treat rheumatoid arthritis fully enrolled; topline data expected in H2 2026.

  • Multiple pipeline updates: NDA for brepocitinib in dermatomyositis submitted, phase 2B studies for IMVT-1402 in D2T-RA and mosliciguat in PH-ILD fully enrolled.

  • No product revenue to date; all activities are pre-commercial and centered on clinical development and regulatory progress.

  • $550 million raised in underwritten financing, extending cash runway to potential IMVT-1402 launch in Graves' disease.

Financial highlights

  • R&D expense for the quarter was $165M (GAAP), $147M (non-GAAP); G&A was $175M (GAAP), $71M (non-GAAP).

  • Net loss for Q3 FY2026 was $110.6M ($0.61 per share); non-GAAP net loss was $97.5M.

  • Cash and cash equivalents totaled $994.5M as of December 31, 2025, up from $714.0M at March 31, 2025, mainly due to a $550M equity raise.

  • Consolidated cash position remains strong at $4.5B, providing ample runway to profitability and flexibility for further investments.

  • Net loss for the nine months ended December 31, 2025 was $357.8M, up from $307.4M year-over-year.

Outlook and guidance

  • Pivotal phase 3 readout for brepocitinib in NIU expected in H2 2026; phase 3 in cutaneous sarcoidosis to start this year.

  • Topline data for IMVT-1402 in D2T RA and CLE expected in H2 2026; Graves' disease and MG data expected in 2027.

  • Existing cash is expected to fund operating expenses and capital requirements for announced indications through the potential commercial launch of IMVT-1402 in Graves' disease.

  • Multiple NDA and BLA filings anticipated, with several commercial launches possible in the next few years.

  • Anticipates continued net losses and significant R&D spending for the foreseeable future.

Brepo CS Phase III design considerations?
1402 D2T RA data: criteria for next study?
Capital allocation for internal vs. external R&D?
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Frequently asked questions

Immunovant, Inc. (IMVT) is a clinical-stage biopharmaceutical company focused on the development of innovative treatments for patients with autoimmune diseases. Leveraging advanced anti-FcRn technology, Immunovant aims to create targeted therapies designed to address the complex and variable nature of autoimmune conditions. The company's approach is centered on improving the lives of patients by developing treatments that can potentially modify or halt the autoimmune response without compromising the immune system's ability to fight infections. Immunovant's research pipeline includes promising investigational products that embody the company's commitment to advancing the field of immunology and providing new options for individuals affected by autoimmune diseases. The company is headquartered in New York, NY, and its shares are listed on the Nasdaq.

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