ROIV 8-K
Roivant Sciences Ltd. (ROIV)
8-K
2025-05-29
For: 2025-05-29
View Original
Added on
April 08, 2026
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of report (Date of earliest event reported): May 29, 2025
(Exact Name of Registrant as Specified in Charter)
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| (State or Other Jurisdiction of Incorporation) | (Commission File Number) |
(I.R.S. Employer Identification No.) |
(Address of Principal Executive Offices, and Zip Code)
+44 207 400-3347
Registrant’s Telephone Number, Including Area Code
Not Applicable
(Former Name or Former Address, if Changed Since Last Report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
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Written communication pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
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Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
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Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
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Securities registered pursuant to Section 12(b) of the Act:
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Title of each class
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Trading Symbol(s)
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Name of each exchange on which registered
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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405 of this chapter) or Rule
12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2 of this chapter).
Emerging growth company ☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised
financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
| Item 2.02. |
Results of Operations and Financial Condition.
|
On May 29, 2025, Roivant Sciences Ltd. (the “Company”) issued a press release announcing its financial results for the fourth quarter and fiscal year ended March 31,
2025. A copy of the press release is attached as Exhibit 99.1 to this Current Report on Form 8-K.
The information set forth under this “Item 2.02. Results of Operations and Financial Condition” (including the exhibit thereto) shall not be deemed to be “filed” for the
purposes of Section 18 of the Securities Exchange Act of 1934, as amended, nor shall it be incorporated by reference in any filing made by the Company pursuant to the Securities Act of 1933, as amended, other than to the extent that such filing
incorporates by reference any or all of such information by express reference thereto.
| Item 9.01. |
Financial Statements and Exhibits.
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(d) Exhibits.
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Exhibit No.
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Description of Exhibit
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Press Release dated May 29, 2025
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104
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Cover Page Interactive Data File (embedded with Inline XBRL document)
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly
authorized.
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ROIVANT SCIENCES LTD.
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By:
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/s/ Keyur Parekh | |
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Name: Keyur Parekh
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Title: Authorized Signatory
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Dated: May 29, 2025
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Exhibit 99.1
Roivant Reports Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2025, and Provides Business
Update
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.
| • |
Brepocitinib program progressing well with rapid enrollment in non-infectious uveitis (NIU) Phase 3 study and first patients dosed in cutaneous sarcoidosis (CS)
proof-of-concept trial, with readouts expected in the first half of calendar year 2027 and second half of calendar year 2026, respectively
|
| • |
Brepocitinib’s VALOR Phase 3 study evaluating its use in patients with dermatomyositis
(DM) is fully enrolled and on track for topline data readout in the second half of calendar year 2025; Roivant and Priovant will host a live conference call and webcast at 1:00 p.m. ET on Tuesday,
June 17, 2025, for an investor event on brepocitinib
|
| • |
Immunovant’s new management team is focused on rapid clinical execution for the six announced indications for IMVT-1402, including a second potentially registrational
study in Graves’ disease (GD) and a potentially registrational study in Sjögren’s disease (SjD), both expected to start in summer 2025
|
| • |
LNP litigation against Moderna expanded to include international lawsuits in Canada, Japan, Switzerland and the UPC with first trials in these jurisdictions expected
in calendar year 2026
|
| • |
Roivant repurchased $1.3B of the company’s shares as of March 31, 2025, reducing outstanding shares by 14% from March 31, 2024
|
| • |
Roivant reported consolidated cash, cash equivalents, restricted cash and marketable securities of $4.9B at March 31, 2025, supporting cash runway into profitability
|
| • |
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 business update
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“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.”
Recent Developments
| • |
Priovant: The first patients have
been dosed in the proof-of-concept trial in CS. Phase 3 trial for brepocitinib in NIU is actively enrolling and on track for topline readout in the first half of calendar year 2027.
|
| • |
Immunovant: In April 2025, Immunovant announced changes to its leadership team as part of a
broader strategic transition with Roivant increasing operational involvement and oversight of Immunovant. Eric Venker, M.D. was appointed as CEO of Immunovant, and Tiago Girao as CFO of Immunovant. Given the strength of its potential
best-in-class profile, IMVT-1402 is being developed in six announced indications, including potentially registrational trials
in Graves’ disease (GD), difficult-to-treat rheumatoid arthritis (D2T RA), myasthenia gravis (MG), chronic inflammatory demyelinating polyneuropathy (CIDP) and Sjögren’s disease (SjD), and a proof-of-concept trial in cutaneous lupus erythematosus (CLE).
|
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.
| • |
Genevant: In March 2025, Genevant and Arbutus filed five international lawsuits in Canada, Japan, Switzerland and the UPC, seeking to enforce patents protecting their innovative LNP technology against Moderna, Inc. and certain
affiliates. Together, the enforcement actions target alleged infringing activities in 30 countries.
|
| • |
Roivant: Roivant reported consolidated cash, cash equivalents, restricted cash and marketable securities of $4.9B at March 31, 2025. Roivant repurchased $1.3B of the company’s shares as of March 31, 2025, reducing
outstanding shares by 14% from March 31, 2024.
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Major Upcoming Milestones
| • |
Priovant plans to report topline
data from the ongoing Phase 3 trial of brepocitinib in DM in the second half of calendar year 2025 and topline data from the ongoing Phase 3 trial of brepocitinib in NIU in the first half of calendar year 2027. Topline results for the
Phase 2 trial in CS are expected in the second half of calendar year 2026. Roivant and Priovant will be hosting an upcoming investor event on brepocitinib at 1:00 p.m. ET on Tuesday, June 17, 2025.
|
| • |
Immunovant expects to report
batoclimab six-month remission data from the proof-of-concept study in GD in the summer of 2025 and Phase 3 thyroid eye disease (TED) data in the second half of calendar year 2025. Immunovant plans to initiate a potentially registrational
trial evaluating IMVT-1402 in SjD and a second potentially registrational trial in GD in the summer of 2025.
|
| • |
Pulmovant plans to report topline
data from the ongoing Phase 2 trial of mosliciguat in pulmonary hypertension associated with interstitial lung disease in the second half of calendar year 2026.
|
| • |
Genevant litigation against
Moderna continues to progress; the court has informed the parties that it plans to update the timing for the summary judgment phase and jury trial, previously scheduled for the second or third quarter of calendar year 2025 and September
2025, respectively.
|
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.
Selected Balance Sheet Data
(in thousands)
|
|
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.
About Roivant
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
forward-looking statements contained in Section 27A of the Securities Act and Section 21E of the Exchange Act.
Our forward-looking statements include, but are not limited to, statements regarding our or our management team’s expectations, hopes,
beliefs, intentions or strategies regarding the future, and statements that are not historical facts, including statements about the clinical and therapeutic potential of our product candidates, the availability and success of topline results from
our ongoing clinical trials and any commercial potential of our product candidates following applicable regulatory approvals. In addition, any statements that refer to projections, forecasts or other characterizations of future events, results or
circumstances, including any underlying assumptions, are forward-looking statements. Actual results may differ materially from those contemplated in these statements due to a variety of risks, uncertainties and other factors.
Although we believe that our plans, intentions, expectations and strategies as reflected in or suggested by those forward-looking
statements are reasonable, we can give no assurance that the plans, intentions, expectations or strategies will be attained or achieved. Furthermore, actual results may differ materially from those described in the forward-looking statements and
will be affected by a number of risks, uncertainties and assumptions, including, but not limited to, those risks set forth in the Risk Factors section of our filings with the U.S. Securities and Exchange Commission. Moreover, we operate in a very
competitive and rapidly changing environment in which new risks emerge from time to time. These forward-looking statements are based upon the current expectations and beliefs of our management as of the date of this press release, and are subject
to certain risks and uncertainties that could cause actual results to differ materially from those described in the forward-looking statements. Except as required by applicable law, we assume no obligation to update publicly any forward-looking
statements, whether as a result of new information, future events or otherwise.
Contacts:
Investors
Keyur Parekh
Media
Stephanie Lee