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Mar 31

Immunovant Q4 2025 Earnings Report

Reported financial results for the fourth quarter and fiscal year ended March 31, 2025

Key Takeaways

Immunovant reported a net loss of $106.4 million for the fourth quarter of fiscal year 2025, an increase from the $75.3 million net loss in the same period last year. This was primarily driven by increased research and development and general and administrative expenses.

Immunovant reported a net loss of $106.4 million for Q4 2025, compared to $75.3 million for Q4 2024.

Research and development expenses increased to $93.7 million in Q4 2025 from $66.1 million in Q4 2024.

General and administrative expenses rose to $20.2 million in Q4 2025 from $14.8 million in Q4 2024.

As of March 31, 2025, cash and cash equivalents were approximately $714 million.

Total Revenue
$0
Previous year: $1.5M
-100.0%
EPS
-$0.64
Previous year: -$0.52
+23.1%
R&D Expenses
$93.7M
Previous year: $66.1M
+41.8%
G&A Expenses
$20.2M
Previous year: $14.8M
+36.1%
Stock-Based Comp Expense
$11.7M
Previous year: $9.7M
+20.6%
Cash and Equivalents
$714M
Previous year: $635M
+12.4%

Immunovant

Immunovant

Forward Guidance

Immunovant is focused on advancing its clinical programs, including initiating potentially registrational trials for IMVT-1402 in Sjögren’s disease and a second trial in Graves’ disease in summer 2025. The company expects data readouts from other trials in the second half of 2025 and 2027.

Positive Outlook

  • Initiating potentially registrational trials for IMVT-1402 in Sjögren’s disease and a second trial in Graves’ disease in summer 2025.
  • Positive data reported from batoclimab trials in myasthenia gravis (MG) and chronic inflammatory demyelinating polyneuropathy (CIDP).
  • Potentially registrational trials for IMVT-1402 in MG and CIDP are actively enrolling.
  • Initiated a potentially registrational trial of IMVT-1402 in difficult-to-treat rheumatoid arthritis (D2T RA) and a proof-of-concept study in cutaneous lupus erythematosus (CLE) in March 2025.
  • Current cash balance provides runway for announced indications through GD readout expected in 2027.

Challenges Ahead

  • No specific negative forward guidance points were provided in the report.
  • Clinical trial results may not be predictive of final outcomes.
  • Timing and availability of data from clinical trials may vary.
  • Regulatory approvals may not be received within expected timelines or at all.
  • Product candidates may not be beneficial to patients or successfully commercialized.