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Jun 30, 2024

Roivant Sciences Q1 2025 Earnings Report

Roivant Sciences reported financial results for Q1 2025 and provided a business update.

Key Takeaways

Roivant Sciences reported a net income of $57.5 million for the quarter ended June 30, 2024, compared to a net loss of $327.8 million for the same period in 2023. VTAMA net product revenue was $18.4 million. The company's consolidated cash, cash equivalents, and restricted cash stood at $5.7 billion as of June 30, 2024.

Immunovant completed enrollment in batoclimab pivotal myasthenia gravis (MG) trial.

Brepocitinib development in non-infectious uveitis (NIU) is progressing to Phase 3.

VTAMA net product revenue was $18.4M for the first quarter ended June 30, 2024.

Roivant reported its consolidated cash, cash equivalents and restricted cash of $5.7B at June 30, 2024.

Total Revenue
$55.1M
Previous year: $21.6M
+155.0%
EPS
-$0.17
Previous year: -$0.38
-55.3%
R&D Expenses
$133M
Previous year: $125M
+6.5%
G&A Expenses
$149M
Previous year: $156M
-4.9%
Gross Profit
$48.6M
Previous year: $21.6M
+124.8%
Cash and Equivalents
$5.69B
Previous year: $1.45B
+292.7%
Free Cash Flow
-$194M
Previous year: -$250M
-22.6%
Total Assets
$6.5B
Previous year: $2.14B
+204.0%

Roivant Sciences

Roivant Sciences

Forward Guidance

Roivant anticipates several milestones in the coming quarters, including PDUFA action for VTAMA in atopic dermatitis in Q4 2024, topline data from the Phase 2 trial of namilumab for sarcoidosis in Q4 2024, and initiation of a Phase 3 program for brepocitinib in NIU in the second half of 2024.

Positive Outlook

  • Dermavant expects PDUFA action for VTAMA in atopic dermatitis in the fourth quarter of calendar year 2024.
  • Kinevant plans to report topline data from the ongoing Phase 2 trial of namilumab for the treatment of sarcoidosis in the fourth quarter of calendar year 2024.
  • Priovant plans to report topline data from the ongoing Phase 3 trial of brepocitinib in DM in the second half of calendar year 2025 and to initiate a Phase 3 program for brepocitinib in NIU in the second half of calendar year 2024.
  • Immunovant plans to have initiated 4-5 potentially registrational programs by March 31, 2025, and plans to have initiated studies in a total of 10 indications by March 31, 2026, for IMVT-1402.
  • Immunovant expects to have at least 3 IND applications active by the end of calendar year 2024.