Immunovant Provides Corporate Updates and Reports Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2026
Rhea-AI Summary
Immunovant (Nasdaq: IMVT) reported fiscal Q4 and full-year 2026 results and key IMVT-1402 updates. In difficult-to-treat rheumatoid arthritis, Week 16 ACR20/50/70 response rates were 72.7%, 54.5% and 35.8%. A cutaneous lupus trial is fully enrolled, with topline data in 2H 2026. Cash and equivalents of $902.1 million are expected to fund development through potential IMVT-1402 launch in Graves’ disease. Batoclimab development was discontinued after two Phase 3 thyroid eye disease studies did not meet primary endpoints. Full-year net loss was $505.6 million, driven largely by higher IMVT-1402 R&D spending and batoclimab wind-down costs.
Positive
- IMVT-1402 D2T RA Week 16 ACR20/50/70 responses of 72.7%/54.5%/35.8%
- CLE IMVT-1402 proof-of-concept trial fully enrolled; topline data expected 2H 2026
- Potentially registrational IMVT-1402 trials in GD and MG with topline data targeted in 2027
- Cash and equivalents of $902.1 million as of March 31, 2026
- Cash runway projected through potential IMVT-1402 commercial launch in Graves’ disease
- Fiscal 2026 GAAP G&A expenses down slightly to $76.2 million; non-GAAP to $50.2 million
Negative
- Two Phase 3 batoclimab thyroid eye disease studies did not meet primary endpoint
- Batoclimab development discontinued across all indications, incurring $39.0 million contractual costs
- Fiscal Q4 2026 R&D expenses rose to $142.3 million from $93.7 million
- Fiscal 2026 full-year R&D expenses increased to $456.7 million from $360.9 million
- Fiscal Q4 2026 net loss widened to $147.9 million from $106.4 million
- Full-year 2026 net loss increased to $505.6 million from $413.8 million
News Market Reaction – IMVT
In the May 20 session, IMVT gained 35.26%, reflecting a significant positive market reaction. Argus tracked a peak move of +29.4% during that session. Our momentum scanner triggered 62 alerts that day, indicating high trading interest and price volatility. Trading volume was exceptionally heavy at 11.4x the daily average, suggesting very strong buying interest.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Previous Earnings Reports
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Feb 06 | Q3 2025 earnings | Positive | +12.4% | Earnings plus financing that lifted cash to $994.5M and advanced IMVT-1402. |
| Nov 10 | Q2 2025 earnings | Positive | +0.1% | Earnings update with $521.9M cash and encouraging Graves’ off‑treatment data. |
| Aug 11 | Q2 2025 earnings | Positive | -4.5% | Earnings and clinical progress alongside higher R&D and widening net loss. |
| May 29 | FY2025 results | Positive | +5.6% | FY2025 results with new leadership, strong $714M cash and IMVT-1402 plans. |
| Feb 06 | Q3 2024 earnings | Positive | -9.6% | Earnings showing expanded pipeline and higher R&D with widening net loss. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
Earnings updates with clinical progress and solid cash have produced mixed reactions, ranging from -9.55% to +12.43%, with a slight tilt toward positive alignment.
Over the past year, Immunovant’s earnings releases have consistently paired IMVT-1402 pipeline progress with detailed cash runway disclosures. Prior updates highlighted advancing registrational programs across GD, MG, CIDP, D2T RA and SjD, plus financings that lifted cash to as high as $994.5M. Price reactions have been mixed, with both rallies and selloffs. Today’s Q4/FY2026 update continues that pattern, combining robust IMVT-1402 efficacy data in D2T RA with a sizable cash balance of $902.1M and widening R&D-driven losses.
Key Terms
acr20 medical
acr50 medical
acr70 medical
das28-crp medical
dmards medical
open label medical
phase 3 medical
rule 10b5-1 trading plan regulatory
AI-generated analysis. How Rhea-AI works. Not financial advice.
- IMVT-1402 showed clinically meaningful response rates of
72.7% ACR20,54.5% ACR50 and35.8% ACR70 at Week 16 in the open label period of its trial in difficult-to-treat rheumatoid arthritis (D2T RA); Immunovant will provide further updates on this program in the second half of calendar year 2026 - IMVT-1402 proof-of-concept trial in cutaneous lupus erythematosus (CLE) fully enrolled with topline data expected in the second half of calendar year 2026
- All other clinical development timelines remain on track for IMVT-1402, including potentially registrational studies in Graves’ disease (GD), myasthenia gravis (MG), chronic inflammatory demyelinating polyneuropathy (CIDP) and Sjögren’s disease (SjD)
- Current cash balance provides runway to the potential launch of IMVT-1402 in GD
- Roivant will host a live conference call and webcast at 8:00 a.m. ET on Wednesday, May 20, 2026, to discuss these updates
DURHAM, N.C., May 20, 2026 (GLOBE NEWSWIRE) -- Immunovant, Inc. (Nasdaq: IMVT), a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases, today reported corporate updates and financial results for its fourth quarter and fiscal year ended March 31, 2026.
Recent Highlights and Upcoming Milestones:
The Company announced preliminary Week 16 (end of Period 1) results from the IMVT-1402 trial in D2T RA with ACR20, ACR50, and ACR70 response rates of
In calendar year 2027, topline data are expected across potentially registrational trials of IMVT-1402 in GD and MG.
In April 2026, we announced topline results from the two Phase 3 clinical studies evaluating batoclimab for adults with active, moderate-to-severe thyroid eye disease (TED), neither of which met the primary endpoint. The safety profile observed in these studies was consistent with prior batoclimab studies. Following these results, we discontinued further development of batoclimab across all indications to focus fully on IMVT-1402. Learnings from the batoclimab program, including clinical data, operational trial experience and relationships with investigators, have been and continue to be leveraged to inform the development of IMVT-1402.
Preliminary Results from IMVT-1402 Trial in D2T RA:
The trial evaluating IMVT-1402 in participants with D2T RA who have failed two or more prior mechanisms of advanced therapies (including biologic and targeted synthetic DMARDs) is currently ongoing. A total of 170 participants have been enrolled in the initial 16-week open label period (Period 1) of the study evaluating weekly subcutaneous (SC) dosing of IMVT-1402 600 mg. Participants achieving a response at Week 14 and Week 16 in Period 1 per the American College of Rheumatology response criteria 20 (ACR20) will be randomized in a 1:1:1 ratio to receive blinded treatment in Period 2 with either IMVT-1402 600 mg, IMVT-1402 300 mg or placebo, weekly SC for 12 weeks. The primary endpoint will assess the proportion of such participants who maintain the ACR20 response at Week 28. ACR20 response is defined as a ≥
At the completion of Period 1, 165 of the 170 patients were evaluable for ACR20 response. Of these patients,
Period 1 was conducted in an open-label setting, with joint assessments performed by independent assessors blinded to treatment status, which we believe reduces the potential for assessor bias in the response measures. IMVT-1402 was observed to be safe and well-tolerated in the study, and no new drug-related safety signals were identified. We anticipate providing further updates on this program in the second half of calendar year 2026.
Financial Highlights for Fiscal Fourth Quarter Ended March 31, 2026:
Cash Position: As of March 31, 2026, Immunovant’s cash and cash equivalents totaled approximately
R&D Expenses: Research and development expenses were
Non-GAAP R&D expenses were
G&A Expenses: General and administrative expenses were
Non-GAAP G&A expenses were
Net Loss: Net loss was
Common Stock: As of March 31, 2026, there were 203,940,353 shares of common stock issued and outstanding.
Financial Highlights for Fiscal Year Ended March 31, 2026:
R&D Expenses: Research and development expenses were
Non-GAAP R&D expenses were
G&A Expenses: General and administrative expenses were
Non-GAAP G&A expenses were
Net Loss: Net loss was
About DT2 RA
RA is a chronic progressive autoimmune disease that causes inflammation in the joints and surrounding tissues. Inadequate control of the joint inflammation associated with RA may result in irreversible joint erosions. The estimated prevalence of patients treated with biologic or targeted synthetic disease modifying anti-rheumatic drugs (“DMARDs”) in the U.S. is approximately 820,000, approximately
About Immunovant, Inc.
Immunovant, Inc. is a clinical-stage immunology company dedicated to enabling normal lives for people with autoimmune diseases. As a trailblazer in anti-FcRn technology, the Company is developing innovative, targeted therapies to meet the complex and variable needs of people with autoimmune diseases. For additional information on the Company, please visit immunovant.com.
Investor Conference Call Information
Roivant will host a live conference call and webcast at 8:00 a.m. ET on Wednesday, May 20, 2026, to discuss these updates.
To access the conference call by phone, please register online using this registration link. The presentation and webcast details will also be available under “Events & Presentations” in the Investors section of the Roivant website at https://investor.roivant.com/news-events/events. The archived webcast will be available on Roivant’s website after the conference call.
Forward-Looking Statements
This press release contains forward-looking statements for the purposes of the safe harbor provisions under The Private Securities Litigation Reform Act of 1995 and other federal securities laws. The use of words such as “can,” “may,” “might,” “will,” “would,” “should,” “expect,” “believe,” “estimate,” “design,” “plan,” “intend,” and other similar expressions are intended to identify forward-looking statements. Such forward looking statements include statements regarding Immunovant’s progress towards developing IMVT-1402 across a broad range of indications; Immunovant’s expectations regarding the availability of results of clinical trials of IMVT-1402 and whether those results may be adequate to support registration; and the Company’s beliefs regarding the potential sufficiency of its cash runway. All forward-looking statements are based on estimates and assumptions by Immunovant’s management that, although Immunovant believes to be reasonable, are inherently uncertain. All forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those that Immunovant expected. Such risks and uncertainties include, among others: Immunovant may not be able to protect or enforce its intellectual property rights; initial results or other preliminary analyses or results of early clinical trials may not be predictive final trial results or of the results of later clinical trials; the timing and availability of data from clinical trials; the timing of discussions with regulatory agencies, as well as regulatory submissions and potential approvals; the continued development of Immunovant’s product candidates, including the number and timing of the commencement of additional clinical trials; Immunovant’s scientific approach, clinical trial design, indication selection, regulatory strategy, and general development progress; future clinical trials may not confirm any safety, potency, or other product characteristics described or assumed in this press release; any product candidate that Immunovant develops may not progress through clinical development or receive required regulatory approvals within expected timelines or at all; Immunovant’s product candidates may not be beneficial to patients, or even if approved by regulatory authorities, successfully commercialized; the potential impact of global factors, such as international trade tariffs, geopolitical tensions, and adverse macroeconomic conditions on Immunovant’s business operations and supply chain, including its clinical development plans and timelines; Immunovant’s business is heavily dependent on the successful development, regulatory approval, and commercialization of IMVT-1402; Immunovant is at various stages of clinical development for IMVT-1402; and Immunovant will require additional capital to fund its operations and advance IMVT-1402 through clinical development. These and other risks and uncertainties are more fully described in Immunovant’s periodic and other reports filed with the Securities and Exchange Commission (SEC), including in the section titled “Risk Factors” in Immunovant’s Annual Report on Form 10-K filed with the SEC on May 20, 2026, and Immunovant’s subsequent filings with the SEC. Any forward-looking statement speaks only as of the date on which it was made. Immunovant undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise.
| IMMUNOVANT, INC. Consolidated Statements of Operations (In thousands, except share and per share data) | |||||||||||||||
| Three Months Ended March 31, | Years Ended March 31, | ||||||||||||||
| 2026 | 2025 | 2026 | 2025 | ||||||||||||
| Operating expenses: | |||||||||||||||
| Research and development | $ | 142,287 | $ | 93,652 | $ | 456,660 | $ | 360,917 | |||||||
| General and administrative | 17,267 | 20,174 | 76,242 | 77,235 | |||||||||||
| Total operating expenses | 159,554 | 113,826 | 532,902 | 438,152 | |||||||||||
| Interest income, net | (8,056 | ) | (6,889 | ) | (25,330 | ) | (24,732 | ) | |||||||
| Other income, net | (798 | ) | (1,071 | ) | (2,181 | ) | (471 | ) | |||||||
| Loss before provision (benefit) for income taxes | (150,700 | ) | (105,866 | ) | (505,391 | ) | (412,949 | ) | |||||||
| Provision (benefit) for income taxes | (2,844 | ) | 583 | 215 | 891 | ||||||||||
| Net loss | $ | (147,856 | ) | $ | (106,449 | ) | $ | (505,606 | ) | $ | (413,840 | ) | |||
| Net loss per common share – basic and diluted | $ | (0.73 | ) | $ | (0.64 | ) | $ | (2.77 | ) | $ | (2.73 | ) | |||
| Weighted-average common shares outstanding – basic and diluted | 203,709,320 | 166,732,686 | 182,421,233 | 151,573,553 | |||||||||||
| IMMUNOVANT, INC. Consolidated Balance Sheets (In thousands, except share and per share data) | |||||||
| March 31, | |||||||
| 2026 | 2025 | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 902,110 | $ | 713,971 | |||
| Accounts receivable | 1,133 | 2,084 | |||||
| Prepaid expenses and other current assets | 42,763 | 51,180 | |||||
| Income tax receivable | 2,813 | 427 | |||||
| Total current assets | 948,819 | 767,662 | |||||
| Operating lease right-of-use assets | 72 | 98 | |||||
| Property and equipment, net | 443 | 844 | |||||
| Other assets | 7,680 | 7,618 | |||||
| Total assets | $ | 957,014 | $ | 776,222 | |||
| Liabilities and Stockholders’ Equity | |||||||
| Current liabilities: | |||||||
| Accounts payable | $ | 7,541 | $ | 17,656 | |||
| Accrued expenses | 96,634 | 50,748 | |||||
| Current portion of operating lease liabilities | 72 | 98 | |||||
| Due to Roivant Sciences Ltd. | 175 | 273 | |||||
| Total current liabilities | 104,422 | 68,775 | |||||
| Total liabilities | 104,422 | 68,775 | |||||
| Commitments and contingencies | |||||||
| Stockholders’ equity: | |||||||
| Series A preferred stock, par value | — | — | |||||
| Preferred stock, par value | — | — | |||||
| Common stock, par value | 20 | 16 | |||||
| Additional paid-in capital | 2,596,971 | 1,945,495 | |||||
| Accumulated other comprehensive income | 730 | 1,459 | |||||
| Accumulated deficit | (1,745,129 | ) | (1,239,523 | ) | |||
| Total stockholders’ equity | 852,592 | 707,447 | |||||
| Total liabilities and stockholders’ equity | $ | 957,014 | $ | 776,222 | |||
| IMMUNOVANT, INC. Reconciliation of GAAP to Non-GAAP Financial Measures (Unaudited, in thousands) | |||||||||||
| Three months ended March 31, | |||||||||||
| Note | 2026 | 2025 | |||||||||
| Net loss: | $ | (147,856 | ) | $ | (106,449 | ) | |||||
| Adjustments | |||||||||||
| Research and development: | |||||||||||
| Stock-based compensation | (1 | ) | 6,280 | 6,469 | |||||||
| General and administrative: | |||||||||||
| Stock-based compensation | (1 | ) | 4,861 | 5,218 | |||||||
| Estimated income tax impact from adjustments | (332 | ) | (150 | ) | |||||||
| Adjusted net loss (Non-GAAP) | $ | (137,047 | ) | $ | (94,912 | ) | |||||
| Three months ended March 31, | |||||||||
| Note | 2026 | 2025 | |||||||
| Research and Development Expenses | $ | 142,287 | $ | 93,652 | |||||
| Adjustments: | |||||||||
| Stock-based compensation | (1 | ) | 6,280 | 6,469 | |||||
| Adjusted research and development expenses (Non-GAAP) | $ | 136,007 | $ | 87,183 | |||||
| Three months ended March 31, | |||||||||
| Note | 2026 | 2025 | |||||||
| General and Administrative Expenses | $ | 17,267 | $ | 20,174 | |||||
| Adjustments: | |||||||||
| Stock-based compensation | (1 | ) | 4,861 | 5,218 | |||||
| Adjusted general and administrative expenses (Non-GAAP) | $ | 12,406 | $ | 14,956 | |||||
(1) Represents non-cash stock-based compensation expense
| Year Ended March 31, | |||||||||||
| Note | 2026 | 2025 | |||||||||
| Net loss: | $ | (505,606 | ) | $ | (413,840 | ) | |||||
| Adjustments | |||||||||||
| Research and development: | |||||||||||
| Stock-based compensation | (1 | ) | 29,712 | 27,014 | |||||||
| General and administrative: | |||||||||||
| Stock-based compensation | (1 | ) | 26,012 | 22,473 | |||||||
| Estimated income tax impact from adjustments | (62 | ) | (378 | ) | |||||||
| Adjusted net loss (Non-GAAP) | $ | (449,944 | ) | $ | (364,731 | ) | |||||
| Year Ended March 31, | |||||||||
| Note | 2026 | 2025 | |||||||
| Research and Development Expenses | $ | 456,660 | $ | 360,917 | |||||
| Adjustments: | |||||||||
| Stock-based compensation | (1 | ) | 29,712 | 27,014 | |||||
| Adjusted research and development expenses (Non-GAAP) | $ | 426,948 | $ | 333,903 | |||||
| Year Ended March 31, | |||||||||
| Note | 2026 | 2025 | |||||||
| General and Administrative Expenses | $ | 76,242 | $ | 77,235 | |||||
| Adjustments: | |||||||||
| Stock-based compensation | (1 | ) | 26,012 | 22,473 | |||||
| Adjusted general and administrative expenses (Non-GAAP) | $ | 50,230 | $ | 54,762 | |||||
(1) Represents non-cash stock-based compensation expense
Contacts:
Investors
Keyur Parekh
keyur.parekh@roivant.com
Media
Stephanie Lee
stephanie.lee@roivant.com
