Welcome to our dedicated page for Immunovant SEC filings (Ticker: IMVT), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Tracking Immunovant’s journey from discovery to late-stage trials means wading through pages of scientific jargon and cash-flow tables. The latest annual report details anti-FcRn antibody engineering, while every 8-K discloses clinical milestones that can move the share price overnight. If you have ever typed “Immunovant SEC filings explained simply� or “How do I read Immunovant’s quarterly earnings report 10-Q filing?� you know the challenge.
Stock Titan’s AI-powered analysis turns each document into clear, skimmable insights. Our platform highlights where the 10-K reveals batoclimab safety data, flags liquidity risks inside the 10-Q, and alerts you to “Immunovant insider trading Form 4 transactions� the moment they post to EDGAR. Need “Immunovant 8-K material events explained�? We annotate trial updates line-by-line, while real-time push notices track “Immunovant Form 4 insider transactions real-time� and upcoming votes on executive pay.
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Immunovant is a clinical-stage immunology company advancing two anti-FcRn antibodies, IMVT-1402 and batoclimab. For the quarter ended June 30, 2025 the company reported a net loss of $120.6 million versus $87.2 million a year earlier, driven by higher research and development ($101.2 million versus $75.5 million) and increased general and administrative expense ($26.0 million versus $18.8 million). Cash and cash equivalents totaled $598.9 million at quarter end, down from $714.0 million three months earlier, and cash used in operations was $117.4 million.
The company has initiated multiple potentially registrational IMVT-1402 trials across Graves disease, myasthenia gravis, CIDP, difficult-to-treat rheumatoid arthritis, Sj f6grens disease and a CLE proof-of-concept study, and expects a Graves disease readout in 2027. Batoclimab Phase 3 top-line results in thyroid eye disease are expected in the second half of 2025. Contractual commitments include an estimated $43.1 million remaining minimum purchase obligation to Samsung and potential milestone payments under the HanAll license up to $420.0 million (after $32.5 million previously paid).