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Roivant Sciences (ROIV) Q4 2026 earnings summary

Event summary combining transcript, slides, and related documents.

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Q4 2026 earnings summary

21 May, 2026

Executive summary

  • Achieved significant clinical and financial milestones in FY2026, including strong execution across the development portfolio and advancing late-stage pipeline assets.

  • IMVT-1402 demonstrated high ACR20/50/70 response rates (up to 73%, 55%, and 36%) in difficult-to-treat rheumatoid arthritis, with a consistent safety profile in a highly refractory population.

  • Brepocitinib received Breakthrough Therapy Designation for cutaneous sarcoidosis and is preparing for commercial launch in dermatomyositis by September 2026; new indication (LPP) announced and enrolling.

  • $2.25 billion global settlement reached with Moderna, with $950 million upfront expected in July 2026 and $1.3 billion contingent on litigation outcome.

  • Mosliciguat advanced as a differentiated inhaled therapy for PH-ILD, with Phase 2 topline data expected in H2 2026.

Financial highlights

  • Cash, cash equivalents, and marketable securities totaled $4.3 billion as of March 31, 2026, prior to Moderna settlement proceeds.

  • R&D expenses for FY26 were $681.8M, with G&A expenses at $610.5M; both increased year-over-year due to program expansion and litigation costs.

  • Gain on litigation settlement was $770.2M for FY26, reflecting Genevant's share of the Moderna settlement.

  • No debt on the balance sheet at fiscal year-end.

  • Active share repurchase program, with 3,956,362 shares repurchased for $110M in Q4 FY2026.

Outlook and guidance

  • Commercial launch of brepocitinib in dermatomyositis expected by end of September 2026, pending FDA approval.

  • Topline Phase 3 data for NIU and updates on IMVT-1402 and mosliciguat expected in H2 2026.

  • Multiple pivotal and proof-of-concept readouts anticipated by year-end 2027, including for IMVT-1402 in Graves' disease and myasthenia gravis.

  • Commercial launches and NDA/BLA filings anticipated across at least three indications by end of 2028.

  • Ongoing litigation and settlement payments, including $950M from Moderna, expected to impact cash flows in 2026.

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