Immunovant (IMVT) Up 3% as Q3 Earnings Top, Pipeline in Focus

Immunovant (IMVT) Up 3% as Q3 Earnings Top, Pipeline in Focus

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Immunovant, Inc. IMVT reported fiscal third-quarter 2024 net loss of 36 cents per share, narrower than the Zacks Consensus Estimate of a loss of 44 cents. The reported figure is also narrower than the year-ago quarter's loss of 49 cents per share.

Currently, Immunovant does not have any approved product in its portfolio. As a result, it is yet to generate revenues.

Quarter in Detail

Research and development (R&D) expenses totaled $48.3 million, up 14.2% from the year-ago quarter’s reported figure. The year-over-year rise can be attributed to increased operational costs and R&D activities for batoclimab and IMVT-1402 programs. The uptick was partially offset by decreased batoclimab program-specific expenses.

General and administrative expenses amounted to $13.2 million, up 11.9% on a year-over-year basis. The rise was primarily due to an increase in personnel-related expenses, legal and other professional fees, market research and information technology costs.

As of Dec 31, 2023, Immunovant had a cash balance of $691 million compared with $269.9 million as of Sep 30, 2023.

The company’s stock rose 3.4% in the last trading session as the investors cheered the better-than-expected fiscal third-quarter financial results. Shares of IMVT have skyrocketed 97.4% in the past year against the industry’s 11.7% decline.

Zacks Investment Research
Zacks Investment Research


Image Source: Zacks Investment Research

Pipeline Update

Immunovant is developing its lead pipeline candidate, batoclimab, as a subcutaneous injection to treat autoimmune indications, including myasthenia gravis (MG), thyroid eye disease (TED), chronic inflammatory demyelinating polyneuropathy (CIDP) and Graves’ disease (GD). Several mid-late-stage studies are currently ongoing to evaluate batoclimab for these indications.

During the reported quarter, the company announced positive top-line results from the initial cohort of patients in an ongoing 24-week phase II study of batoclimab in patients with GD. Per the data readout, treatment with the candidate observed more than 50% clinically meaningful response rates.

Immunovant expects to report top-line data from the phase III study of batoclimab to treat MG in the second half of calendar 2024. Data readout from the phase III program for TED is expected in the first half of calendar 2025. Initial data from the phase IIb study in CIDP is expected to be reported in the second or third quarter of 2024.

The company is also developing another candidate IMVT-1402, a next-generation FcRn inhibitor,as a subcutaneous injection in an early-stage study for the treatment of immunoglobulin G (IgG)-mediated autoimmune diseases. The phase I study is evaluating the safety, tolerability and pharmacodynamic profiles of subcutaneously administered IMVT-1402.