Immunovant/$IMVT

1D1W1MYTD1Y5YMAX

About Immunovant

Immunovant Inc is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. Its focus is on developing IMVT-1402, a potential inhibitor of the neonatal fragment crystallizable receptor (FcRn), to address autoimmune diseases driven by high levels of pathogenic immunoglobulin G (IgG) antibodies. FcRn is involved in preventing the degradation of IgG antibodies, and inhibition of FcRn has been shown to reduce levels of total IgG and pathogenic IgG antibodies. The Company operates in a single operating segment and has one reportable segment, which includes all activities related to the discovery, development and manufacturing of its product candidates.
Ticker
$IMVT
Sector
Health
Primary listing
NASDAQ
Employees
315

Immunovant Metrics

BasicAdvanced
$6.9B
-
-$2.82
0.81
-

What the Analysts think about Immunovant

Analyst ratings (Buy, Hold, Sell) for Immunovant stock.
Analyst projections of the future price of Immunovant stock.

Bulls say / Bears say

IMVT-1402 produced encouraging early results in difficult-to-treat rheumatoid arthritis, with Week 16 ACR20, ACR50 and ACR70 response rates of 72.7%, 54.5% and 35.8%. No new drug-related safety signals were identified, although the data came from an open-label period. (Immunovant)
The same asset is being advanced across six autoimmune indications, with potentially registrational Graves’ disease and myasthenia gravis readouts expected in 2027 and CIDP and Sjögren’s disease data expected in 2028. This gives successful development in one indication the potential to support a broader multi-product franchise. (Immunovant)
Immunovant reported $797.8 million of cash and cash equivalents at 30 June 2026, which it believes provides runway to a potential Graves’ disease launch. That reduces the immediate need for a dilutive capital raise while several important clinical catalysts are still ahead. (Immunovant)
IMVT-1402 failed to achieve statistical significance on the primary endpoint in its 57-patient cutaneous lupus trial, and Immunovant is stopping development in that indication. The result weakens confidence that the FcRn mechanism will translate consistently across autoimmune diseases. (GlobeNewswire)
Immunovant has also discontinued batoclimab after two Phase 3 thyroid eye disease trials missed their primary endpoint, incurring $39 million in contractual costs. The failure highlights clinical and commercial risk for a company whose second-generation drug remains unapproved. (Fierce Biotech)
The company is loss-making and spending heavily to advance a single lead programme: quarterly R&D expense rose to $142.6 million and net loss reached $153.2 million. Its $797.8 million cash balance is expected to fund only the potential Graves’ disease launch, not development and commercialisation across every planned indication, increasing longer-term financing and dilution risk. (Immunovant, Immunovant)
Data summarised monthly by Lightyear AI. Last updated on 23 Sept 2026.

Immunovant Financial Performance

Revenues and expenses
Income statement
QuarterlyAnnual
Q3 24
QoQ growth
Revenue
Net income
Profit margin

Immunovant Earnings Performance

Company profitability
Earnings per share
QuarterlyAnnual
Q4 23
Q1 24
Q2 24
Q3 24
Q4 24
Actual
Expected
Surprise

Funds containing Immunovant

AllUSDGBPEUR
Data displayed above is indicative only and its accuracy or completeness is not guaranteed. Actual execution price may vary. Past performance is not indicative of future results. Your return may be affected by currency fluctuations and applicable fees and charges. Capital at risk.
Real-time US market data is sourced from the IEX order book provided by Polygon. After-hours US market data is 15 minutes delayed and may differ significantly from the actual tradable price at market open.