Full Press Release Details
Roivant Reports Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2025, and Provides Business
BASEL, Switzerland and LONDON and
NEW YORK, May 29, 2025 - Roivant (Nasdaq: ROIV) today reported its financial results for the fourth quarter and fiscal year ended March 31, 2025, and provided a business update.
"I am incredibly proud of the progress we reported in the final quarter of this past fiscal year. Continued broad development of
brepocitinib, positive data from our myasthenia gravis study, and expansion of IMVT-1402 into new indications underscore our commitment to patients. We remain focused on building value in our late-stage clinical pipeline, and on continued
discipline on capital allocation across the portfolio," said Matt Gline, CEO of Roivant. "We look forward to a number of exciting milestones later this year, including the upcoming brepocitinib readout in DM."
In March 2025, Immunovant announced positive results from its batoclimab MG and CIDP studies. The potentially
registrational study in MG met its primary endpoint of change from baseline in Myasthenia Gravis Activities of Daily Living (MG-ADL) score in the AChR+ population at week 12, with the higher dose arm achieving a 5.6-point improvement (with 74% mean
IgG reduction) and the lower dose arm achieving a 4.7-point improvement (with 64% mean IgG reduction). Initial results from week 12 of Phase 2b CIDP study, demonstrated a mean improvement in the adjusted Inflammatory Neuropathy Cause and Treatment
(INCAT) disability score of 1.8 across batoclimab arms and an 84% responder rate in those patients who achieved an IgG lowering greater than 70%. In both batoclimab studies, deeper IgG reductions correlated with improved clinical outcomes across a
range of assessments and timepoints. Potentially registrational trials for IMVT-1402 in both MG and CIDP are actively enrolling.
In March 2025, Immunovant initiated a potentially registrational trial of IMVT-1402 in adult participants with active,
anti-citrullinated protein autoantibody (ACPA) positive D2T RA and a proof-of-concept study in CLE. Both indications represent potential first-in-class and best-in-class opportunities based on positive in-class competitor data (D2T RA) and
promising efficacy data from patients dosed with IMVT-1402 as part of an open-label case study program (CLE). Immunovant also announced that its IND cleared for a potentially registrational trial of IMVT-1402 in SjD, a potentially best-in-class
indication. The trial is expected to initiate in summer 2025.
Major Upcoming Milestones
Quarter and Fiscal Year Ended March 31, 2025 Financial Summary
Cash Position and Marketable Securities
As of March 31, 2025, the company had cash, cash equivalents, restricted
cash and marketable securities of approximately $4.9 billion.
Research and Development Expenses
Research and development (R&D) expenses increased by $37.7 million to $145.2 million for the three months ended March 31, 2025, compared to $107.6 million for the three months ended March 31, 2024. This increase was
primarily driven by increase in program-specific costs of $25.8 million and personnel-related expenses of $10.4 million.
The increase of $25.8 million in program-specific costs was primarily driven by an increase of $14.5 million related to the anti-FcRn franchise and $3.8 million
related to mosliciguat.
The increase of $10.4 million in personnel-related expenses was primarily driven by higher personnel-related expenses at Immunovant.
Non-GAAP R&D expenses were $135.1 million for the three months ended March 31, 2025, compared to $96.9 million for the three months ended March 31, 2024.
Research and development expenses increased by $110.5 million to $550.4 million for the year ended March 31, 2025, compared to $439.9 million for the year ended March 31, 2024, primarily due to increases in
program-specific costs of $78.5 million, personnel-related expenses of $22.9 million,
share-based compensation of $7.4 million and other expenses of $1.7 million.
The increase of $78.5 million in program-specific costs was primarily
driven by increases of $91.1 million related to the anti-FcRn franchise, reflecting the progression of our programs, and $15.4 million related to mosliciguat,
which was acquired during the year ended March 31, 2024. These increases were partially offset by a decrease in expense of $35.1 million related to RVT-3101, which was sold to Roche in December 2023.
The increase of $22.9 million in personnel-related expenses was primarily driven by higher personnel-related expenses at Immunovant as a result of higher
headcount and enhancement of capabilities to support Immunovant's strategic objectives as clinical activities progress.
Non-GAAP R&D expenses were $508.0 million for the year ended March 31, 2025, compared to $402.9 million for the year ended March 31, 2024. The non-GAAP
R&D expense includes the expense related to the Cash Bonus Program of $5.8 million for the year ended March 31, 2025 and $9.9 million for the year ended March 31, 2024.
General and Administrative Expenses
General and administrative (G&A) expenses increased by $39.0 million to
$147.1 million for the three months ended March 31, 2025, compared to $108.1 million for the three months ended March 31, 2024. The increase was
primarily driven by an increase in share-based compensation expense of $39.9 million, primarily due to the long-term equity incentive awards granted in July 2024 pursuant to the 2024 Senior Executive Compensation Program.
Non-GAAP G&A expenses were $72.3 million for the three months ended March 31, 2025, compared to $72.9 million for the three months ended March 31, 2024.
General and administrative expenses increased by $175.3 million to $591.4 million for the year ended March 31, 2025, compared to $416.1 million for the year
ended March 31, 2024. This increase was primarily due to increases in share-based compensation expense of $84.6 million and personnel-related expenses of $79.6 million, largely as a result of long-term equity and one-time cash retention awards
from the 2024 Senior Executive Compensation Program.
Non-GAAP G&A expenses were $347.7 million for the year ended March 31, 2025, compared to $256.4 million for the year ended March 31, 2024. The non-GAAP
G&A expense includes the expense related to the Cash Bonus and 2024 Senior Executive Compensation Programs of $107.6 million for the year ended March 31, 2025 and $35.6 million for the year ended March 31, 2024.
(Loss) income from discontinued operations, net of tax
Income from discontinued operations, net of tax was $373.0 million for the
year ended March 31, 2025 and reflects the gain on sale of subsidiary interests resulting from the sale of our entire equity interest in our majority-owned
subsidiary, Dermavant, to Organon in October 2024, partially offset by Dermavant's net losses. Losses from discontinued operations, net of tax were $87.5 million
for the three months ended March 31, 2024 and $315.1 million for the year ended March 31, 2024, representing the financial results of Dermavant.
(Loss) income from continuing operations, net of tax
Loss from continuing operations, net of tax was $252.4 million for the three months ended March 31, 2025, compared to $95.0 million for the three months ended March 31, 2024. On a per common share basis, loss from continuing operations, net of tax was $0.29 and $0.08 for the three months ended March 31,
2025 and 2024, respectively. Non-GAAP loss from continuing operations, net of tax was $154.4 million for the three months ended March 31, 2025, compared to $99.8 million for the three months ended March 31, 2024.
Loss from continuing operations, net of tax was $729.8 million for the year ended March 31, 2025, compared to income from continuing operations, net of tax of approximately $4.5 billion for the year ended March 31, 2024. On a per common share basis, loss from continuing operations, net of tax was $0.75 for the year ended March 31, 2025. On a basic and diluted per common share
basis, income from continuing operations, net of tax was $5.95 and $5.61,
respectively, for the year ended March 31, 2024.
Non-GAAP loss from continuing operations was $623.9 million for the year ended March 31, 2025, compared to $541.9 million for the year ended March 31, 2024.
ROIVANT SCIENCES LTD.
Selected Balance Sheet Data
| March 31, 2025 | March 31, 2024 | |||||||
| Cash, cash equivalents and restricted cash | $ | 2,725,661 | $ | 6,506,189 | ||||
| Marketable securities | 2,171,480 | - | ||||||
| Total assets | 5,436,940 | 7,222,482 | ||||||
| Total liabilities | 249,742 | 773,953 | ||||||
| Total shareholders' equity | 5,187,198 | 6,448,529 | ||||||
| Total liabilities and shareholders' equity | 5,436,940 | 7,222,482 |
ROIVANT SCIENCES LTD.
Consolidated Statements of Operations
(in thousands, except share and per share amounts)
| Three Months Ended March 31, | Years Ended March 31, | |||||||||||||||
| 2025 | 2024 | 2025 | 2024 | |||||||||||||
| (Unaudited) | (Unaudited) | |||||||||||||||
| Revenue | $ | 7,570 | $ | 9,020 | $ | 29,053 | $ | 32,713 | ||||||||
| Operating expenses: | ||||||||||||||||
| Cost of revenues | 205 | 196 | 911 | 1,599 | ||||||||||||
| Research and development (includes $9,652 and $9,761 of share-based compensation expense for the three months ended March 31, 2025 and 2024, respectively, and $39,780 and $32,400 for the years ended March 31, 2025 and 2024, respectively) | 145,238 | 107,555 | 550,413 | 439,909 | ||||||||||||
| Acquired in-process research and development | - | - | - | 26,450 | ||||||||||||
| General and administrative (includes $73,835 and $33,982 of share-based compensation expense for the three months ended March 31, 2025 and 2024, respectively, and $239,505 and $154,873 for the years ended March 31, 2025 and 2024, respectively) | 147,092 | 108,103 | 591,410 | 416,133 | ||||||||||||
| Total operating expenses | 292,535 | 215,854 | 1,142,734 | 884,091 | ||||||||||||
| Gain on sale of Telavant net assets | - | - | 110,387 | 5,348,410 | ||||||||||||
| (Loss) income from operations | (284,965 | ) | (206,834 | ) | (1,003,294 | ) | 4,497,032 | |||||||||
| Change in fair value of investments | (12,899 | ) | (15,907 | ) | (55,186 | ) | 47,973 | |||||||||
| Change in fair value of liability instruments | (14,124 | ) | (2,637 | ) | (15,756 | ) | 46,838 | |||||||||
| Gain on deconsolidation of subsidiaries | (3,108 | ) | (15,418 | ) | (3,108 | ) | (32,772 | ) | ||||||||
| Interest income | (54,624 | ) | (83,458 | ) | (258,375 | ) | (146,425 | ) | ||||||||
| Other expense, net | 2,844 | 11,317 | 10,721 | 13,562 | ||||||||||||
| (Loss) income from continuing operations before income taxes | (203,054 | ) | (100,731 | ) | (681,590 | ) | 4,567,856 | |||||||||
| Income tax expense (benefit) | 49,321 | (5,773 | ) | 48,174 | 21,503 | |||||||||||
| (Loss) income from continuing operations, net of tax | (252,375 | ) | (94,958 | ) | (729,764 | ) | 4,546,353 | |||||||||
| (Loss) income from discontinued operations, net of tax | - | (87,538 | ) | 373,030 | (315,147 | ) | ||||||||||
| Net (loss) income | (252,375 | ) | (182,496 | ) | (356,734 | ) | 4,231,206 | |||||||||
| Net loss attributable to noncontrolling interests | (45,900 | ) | (31,381 | ) | (184,753 | ) | (117,720 | ) | ||||||||
| Net (loss) income attributable to Roivant Sciences Ltd. | $ | (206,475 | ) | $ | (151,115 | ) | $ | (171,981 | ) | $ | 4,348,926 | |||||
| Amounts attributable to Roivant Sciences Ltd.: | ||||||||||||||||
| (Loss) income from continuing operations, net of tax | $ | (206,475 | ) | $ | (63,979 | ) | $ | (545,166 | ) | $ | 4,662,703 | |||||
| (Loss) income from discontinued operations, net of tax | - | (87,136 | ) | 373,185 | (313,777 | ) | ||||||||||
| Net (loss) income attributable to Roivant Sciences Ltd. | $ | (206,475 | ) | $ | (151,115 | ) | $ | (171,981 | ) | $ | 4,348,926 |
| Net (loss) income per common share, basic: | ||||||||||||||||
| (Loss) income from continuing operations, net of tax | $ | (0.29 | ) | $ | (0.08 | ) | $ | (0.75 | ) | $ | 5.95 | |||||
| (Loss) income from discontinued operations, net of tax | $ | - | $ | (0.11 | ) | $ | 0.51 | $ | (0.40 | ) | ||||||
| Net (loss) income | $ | (0.29 | ) | $ | (0.19 | ) | $ | (0.24 | ) | $ | 5.55 | |||||
| Net (loss) income per common share, diluted: | ||||||||||||||||
| (Loss) income from continuing operations, net of tax | $ | (0.29 | ) | $ | (0.08 | ) | $ | (0.75 | ) | $ | 5.61 | |||||
| (Loss) income from discontinued operations, net of tax | $ | - | $ | (0.11 | ) | $ | 0.51 | $ | (0.38 | ) | ||||||
| Net (loss) income | $ | (0.29 | ) | $ | (0.19 | ) | $ | (0.24 | ) | $ | 5.23 | |||||
| Weighted average shares outstanding: | ||||||||||||||||
| Basic | 707,298,861 | 802,859,062 | 725,395,624 | 783,248,906 | ||||||||||||
| Diluted | 707,298,861 | 802,859,062 | 725,395,624 | 831,049,444 |
ROIVANT SCIENCES LTD.
Reconciliation of GAAP to Non-GAAP Financial Measures
(unaudited, in thousands)
| Three Months Ended March 31, | Years Ended March 31, | |||||||||||||||||||
| Note | 2025 | 2024 | 2025 | 2024 | ||||||||||||||||
| (Loss) income from continuing operations, net of tax | $ | (252,375 | ) | $ | (94,958 | ) | $ | (729,764 | ) | $ | 4,546,353 | |||||||||
| Adjustments: | ||||||||||||||||||||
| Research and development: | ||||||||||||||||||||
| Share-based compensation | (1 | ) | 9,652 | 9,761 | 39,780 | 32,400 | ||||||||||||||
| Depreciation and amortization | (2 | ) | 446 | 873 | 2,593 | 4,590 | ||||||||||||||
| General and administrative: | ||||||||||||||||||||
| Share-based compensation | (1 | ) | 73,835 | 33,982 | 239,505 | 154,873 | ||||||||||||||
| Depreciation and amortization | (2 | ) | 937 | 1,176 | 4,204 | 4,860 | ||||||||||||||
| Gain on sale of Telavant net assets | (3 | ) | - | - | (110,387 | ) | (5,348,410 | ) | ||||||||||||
| Other: | ||||||||||||||||||||
| Change in fair value of investments | (4 | ) | (12,899 | ) | (15,907 | ) | (55,186 | ) | 47,973 | |||||||||||
| Change in fair value of liability instruments | (5 | ) | (14,124 | ) | (2,637 | ) | (15,756 | ) | 46,838 | |||||||||||
| Gain on deconsolidation of subsidiaries | (6 | ) | (3,108 | ) | (15,418 | ) | (3,108 | ) | (32,772 | ) | ||||||||||
| Estimated income tax impact from adjustments | (7 | ) | 43,237 | (16,650 | ) | 4,261 | 1,385 | |||||||||||||
| Adjusted loss from continuing operations, net of tax (Non-GAAP) | $ | (154,399 | ) | $ | (99,778 | ) | $ | (623,858 | ) | $ | (541,910 | ) |
| Three Months Ended March 31, | Years Ended March 31, | |||||||||||||||||||
| Note | 2025 | 2024 | 2025 | 2024 | ||||||||||||||||
| Research and development expenses | $ | 145,238 | $ | 107,555 | $ | 550,413 | $ | 439,909 | ||||||||||||
| Adjustments: | ||||||||||||||||||||
| Share-based compensation | (1 | ) | 9,652 | 9,761 | 39,780 | 32,400 | ||||||||||||||
| Depreciation and amortization | (2 | ) | 446 | 873 | 2,593 | 4,590 | ||||||||||||||
| Adjusted research and development expenses (Non-GAAP) | $ | 135,140 | $ | 96,921 | $ | 508,040 | $ | 402,919 |
| Three Months Ended March 31, | Years Ended March 31, | |||||||||||||||||||
| Note | 2025 | 2024 | 2025 | 2024 | ||||||||||||||||
| General and administrative expenses | $ | 147,092 | $ | 108,103 | $ | 591,410 | $ | 416,133 | ||||||||||||
| Adjustments: | ||||||||||||||||||||
| Share-based compensation | (1 | ) | 73,835 | 33,982 | 239,505 | 154,873 | ||||||||||||||
| Depreciation and amortization | (2 | ) | 937 | 1,176 | 4,204 | 4,860 | ||||||||||||||
| Adjusted general and administrative expenses (Non-GAAP) | $ | 72,320 | $ | 72,945 | $ | 347,701 | $ | 256,400 |
Notes to non-GAAP financial measures:
(1) Represents non-cash share-based compensation expense.
(2) Represents non-cash depreciation and amortization expense.
(3) Represents a one-time gain on the sale of Telavant net assets to Roche in December 2023 and a gain on the achievement of a one-time
milestone in June 2024.
(4) Represents the unrealized (gain) loss on equity investments in unconsolidated entities that are accounted for at fair value with changes in value
reported in earnings.
(5) Represents the change in fair value of liability instruments, which is non-cash and primarily includes the unrealized (gain) loss relating to the
measurement and recognition of fair value on a recurring basis of certain liabilities.
(6) Represents the one-time gain on deconsolidation of subsidiaries.
(7) Represents the estimated tax effect of the adjustments.
Investor Conference Call Information
Roivant will host a live conference call and webcast at 8:00 a.m. ET on Thursday, May 29, 2025, to report its financial results for the fourth quarter and
fiscal year ended March 31, 2025, and provide a corporate update.
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.
Roivant (Nasdaq: ROIV) is a biopharmaceutical company that aims to improve
the lives of patients by accelerating the development and commercialization of medicines that matter. Roivant's pipeline includes brepocitinib, a potent small molecule inhibitor of TYK2 and JAK1 in development for the treatment of
dermatomyositis, non-infectious uveitis and cutaneous sarcoidosis; IMVT-1402 and batoclimab, fully human monoclonal antibodies targeting FcRn in development across several IgG-mediated autoimmune indications; and mosliciguat, an inhaled sGC
activator in development for pulmonary hypertension associated with interstitial lung disease. We advance our pipeline by creating nimble subsidiaries or "Vants" to develop and commercialize our medicines and technologies. Beyond therapeutics,
Roivant also incubates discovery-stage companies and health technology startups complementary to its biopharmaceutical business. For more information, visit https://roivant.com.
Roivant Forward-Looking Statements
This press release contains forward-looking statements. Statements in this press release may include statements that are not historical
facts and are considered forward-looking within the meaning of Section 27A of the Securities Act of 1933, as amended (the "Securities Act"), and Section 21E of the Securities Exchange Act of 1934, as amended (the "Exchange Act"), which are usually
identified by the use of words such as "anticipate," "believe," "continue," "could," "estimate," "expect," "intends," "may," "might," "plan," "possible," "potential," "predict," "project," "should," "would" and variations of such words or similar
expressions. The words may identify forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. We intend these forward-looking statements to be covered by the safe harbor provisions for