Recent Updates
Recently added Catalysts
ROIV Positive Sentiment Score: 75/100

Roivant Reports Financial Results for the Fourth Quarter and Fiscal Year Ended

Key Takeaway: Roivant Sciences reported its financial results for the fourth quarter and fiscal year ending March 31, 2023. The company highlighted promising data from its RVT-3101 study in ulcerative colitis and positive outcomes from VTAMA's Phase 3 trials for atopic dermatitis. Despite showing revenue growth and substantial cash reserves, Roivant experienced increased R&D expenses and ongoing losses from operations. Additionally, the company welcomed Meghan FitzGerald to its Board of Directors, enhancing its governance as it progresses in immunological and inflammatory disease treatments.

Market Sentiment Analysis

POSITIVE FACTORS

  • Strong progress in RVT-3101 trials for ulcerative colitis with favorable data.
  • Positive topline results for VTAMA's Phase 3 trials indicate potential for a new treatment option.
  • Significant growth in VTAMA revenue with increased insurance coverage.

CONCERNS & RISKS

  • Increased losses from continuing operations compared to last year.
  • Higher research and development expenses could impact financials in the future.

Full Press Release Details

Roivant Reports Financial Results for the Fourth Quarter and Fiscal Year Ended March 31, 2023, and Provides Business
BASEL, LONDON, and NEW YORK, June 28, 2023 - Roivant (Nasdaq: ROIV) today reported its financial results for the fourth quarter and fiscal year ended March 31, 2023, and provided an update on the business.
Roivant's Chief Executive Officer, Matt Gline, noted: "I'm incredibly pleased with the progress we've made in recent months. Last week,
we reported RVT-3101 data from the chronic period of TUSCANY-2, our Phase 2b study in ulcerative colitis. These data surpassed our expectations, demonstrating improvement from the induction period at week 14 to the chronic period at week 56 across
all key efficacy endpoints for patients treated with the expected Phase 3 dose. In addition, earlier this spring we announced positive topline results for VTAMA's ADORING 1 and ADORING 2 Phase 3 trials in atopic dermatitis. The results reported
across both studies showed efficacy comparable to that of many systemic products, and we feel VTAMA has the potential to be a safe and efficacious topical option for adults and children as young as 2 years old. Finally, we reported strong growth in
VTAMA revenue this past quarter in psoriasis with over 75% of US commercial lives now covered. These recent developments, combined with our strong balance sheet, continue to support Roivant's growing leadership in the treatment of immunological and
inflammatory disease, and we are proud of our continued track record in clinical execution."
Major Upcoming Milestones
Matt Gline added: "I am incredibly pleased to welcome Meghan FitzGerald to our Board of Directors. Meghan's deep expertise in healthcare
and her extraordinary commitment to patients will be invaluable to Roivant's mission to accelerate the development and commercialization of medicines that matter."
Fourth Quarter and Fiscal Year Ended March 31, 2023,
As of March 31, 2023, the company had cash, cash equivalents and restricted cash of approximately $1.7 billion.
Research and Development Expenses
Research and development (R&D) expenses decreased by $3.2 million to $131.9 million for the three months ended March 31, 2023, compared
to $135.1 million for the year ended March 31, 2022, primarily due to decreases in share-based compensation of $11.9 million and other expenses of $3.7 million, partially offset by an increase in program specific costs of $12.3 million, largely
driven by the anti-FcRn franchise.
Non-GAAP R&D expenses were $126.0 million for the three months ended March 31, 2023, compared to $117.8 million for the three months
ended March 31, 2022.
R&D expenses increased by $42.2 million to $525.2 million for the year ended March 31, 2023, compared to $483.0 million for the year
ended March 31, 2022, primarily due to increases in program-specific costs of $45.8 million and personnel-related expenses of $28.1 million, partially offset by a decrease in share-based compensation of $32.8 million. The increase of $45.8 million
in program-specific costs largely reflects the progression of our programs and drug discovery, including the anti-FcRn franchise, RVT-2001, brepocitinib, and RVT-3101. The asset acquisitions of brepocitinib, RVT-2001, and RVT-3101 were completed in
September 2021, November 2021, and November 2022, respectively. Increases in program-specific costs were partially offset by certain decreases, including $19.3 million for tapinarof, which was primarily due to the completion of ADORING 1 and
ADORING 2 phase 3 atopic dermatitis clinical trials during the year ended March 31, 2023. The increase of $28.1 million in personnel-related expenses largely reflects the progression of our programs, particularly the anti-FcRn franchise. The
decrease of $32.8 million in share-based compensation expense was primarily due to the achievement of the liquidity event vesting condition for certain equity instruments upon the closing of the Business Combination in September 2021, resulting in
the recognition of a one-time catch-up expense of $22.9 million relating to cumulative service rendered between the grant date of the respective awards and completion of the Business Combination and continued recognition of expense over the
requisite service periods.
Non-GAAP R&D expenses were $489.2 million for the year ended March 31, 2023, compared to $416.1 million for the year ended March 31,
Acquired In-Process Research and Development Expenses
There was no acquired in-process research and development (IPR&D) expense for the three months ended March 31, 2023. Acquired IPR&D
expenses were $1.5 million for the three months ended March 31, 2022.
Acquired IPR&D expenses decreased by $42.1 million to $97.7 million for the year ended March 31, 2023, compared to $139.9 million for
the year ended March 31, 2022. The decrease was primarily due to higher consideration for the purchase of IPR&D during the year ended March 31, 2022 as a result of consideration for the purchase of IPR&D of $82.1 million relating to the
acquisition of brepocitinib, a one-time milestone expense of approximately $39 million due to the achievement of a development milestone related to tapinarof, and consideration for the purchase of IPR&D of $14.1 million relating to the
acquisition of RVT-2001. Acquired IPR&D expenses for the year ended March 31, 2023, was driven by consideration for the purchase of IPR&D of $87.7 million relating to the
acquisition of RVT-3101 and the achievement of a development milestone relating to batoclimab, which resulted in a one-time milestone expense of $10.0 million.
Selling, General and Administrative Expenses
Selling, general and administrative (SG&A) expenses decreased by $13.5 million to $125.5 million for the three months ended March 31,
2023, compared to $139.0 million for the three months ended March 31, 2022. The decrease was primarily due to a decrease in share-based compensation of $40.0 million, partially offset by higher SG&A expenses at Dermavant as a result of the
commercial launch of VTAMA.
Non-GAAP SG&A expenses were $102.6 million for the three months ended March 31, 2023, compared to $77.3 million for the three months
ended March 31, 2022.
SG&A expenses decreased by $174.5 million to $600.5 million for the year ended March 31, 2023, compared to $775.0 million for the year
ended March 31, 2022. The decrease was primarily due to a decrease in share-based compensation expense of $314.6 million, partially offset by higher SG&A expenses at Dermavant as a result of the commercial launch of VTAMA. The decrease in
share-based compensation resulted from the achievement of the liquidity event vesting condition for certain equity instruments upon the closing of the Business Combination in September 2021, resulting in the recognition of a one-time catch-up
expense of $350.0 million for the year ended March 31, 2022, for cumulative service rendered between the grant date of the respective awards and completion of the Business Combination.
Non-GAAP SG&A expenses were $407.6 million for the year ended March 31, 2023, compared to $271.1 million for the year ended March 31,
Loss from Continuing Operations
Loss from continuing operations was $175.4 million for the three months ended March 31, 2023, compared to $291.3 million for the three
months ended March 31, 2022. On a per common share basis, loss from continuing operations was $0.20 for the three months ended March 31, 2023, and $0.39 for the three months ended March
31, 2022. Non-GAAP loss from continuing operations was $189.4 million for the three months ended March 31, 2023, compared to $187.7 million for the three months ended March 31, 2022.
Loss from continuing operations was approximately $1.2 billion for the year ended March 31, 2023, compared to $924.1 million for the year
ended March 31, 2022. On a per common share basis, loss from continuing operations was $1.58 for the year ended March 31, 2023, and $1.26 for the year ended March 31, 2022. Non-GAAP
loss from continuing operations was $924.3 million for the year ended March 31, 2023, compared to $784.2 million for the year ended March 31, 2022.
ROIVANT SCIENCES LTD.
Selected Balance Sheet Data
March 31, 2023 March 31, 2022
Cash, cash equivalents and restricted cash $ 1,692,115 $ 2,074,034
Total assets 2,389,604 2,585,129
Total liabilities 782,017 523,695
Total shareholders' equity 1,607,587 2,038,943
Total liabilities, redeemable noncontrolling interest and shareholders' equity 2,389,604 2,585,129
ROIVANT SCIENCES LTD.
Consolidated Statements of Operations
(in thousands, except share and per share amounts)
Three Months Ended March 31, Years Ended March 31,
2023 2022 2023 2022
(Unaudited) (Unaudited)
Revenues:
Product revenue, net $ 13,657 $ - $ 28,011 $ -
License, milestone and other revenue 13,719 9,223 33,269 55,286
Revenue, net 27,376 9,223 61,280 55,286
Operating expenses:
Cost of revenues 4,175 459 13,128 8,966
Research and development (includes $4,366 and $16,294 of share-based compensation expense for the three months ended March 31, 2023 and 2022, respectively, and $30,914 and $63,735 of share-based compensation expense for the years ended March 31, 2023 and 2022, respectively) 131,857 135,077 525,215 483,035
Acquired in-process research and development - 1,517 97,749 139,894
Selling, general and administrative (includes $20,832 and $60,865 of share-based compensation expense for the three months ended March 31, 2023 and 2022, respectively, and $186,603 and $501,221 of share-based compensation expense for the years ended March 31, 2023 and 2022, respectively) 125,510 138,973 600,506 775,033
Total operating expenses 261,542 276,026 1,236,598 1,406,928
Loss from operations (234,166 ) (266,803 ) (1,175,318 ) (1,351,642 )
Change in fair value of investments (32,462 ) 72,909 20,815 87,291
Gain on sale of investment - - - (443,754 )
Change in fair value of debt and liability instruments (12,031 ) (44,101 ) 78,001 (3,354 )
Gain on termination of Sumitomo Options - - - (66,472 )
Gain on deconsolidation of subsidiaries - (5,041 ) (29,276 ) (5,041 )
Interest income (14,284 ) (170 ) (32,184 ) (369 )
Interest expense 8,575 1,475 27,968 7,041
Other income, net (4,748 ) (399 ) (15,808 ) (3,237 )
Loss from continuing operations before income taxes (179,216 ) (291,476 ) (1,224,834 ) (923,747 )
Income tax expense (3,793 ) (163 ) 5,190 369
Loss from continuing operations, net of tax (175,423 ) (291,313 ) (1,230,024 ) (924,116 )
Income from discontinued operations, net of tax 114,561 - 114,561 -
Net loss (60,862 ) (291,313 ) (1,115,463 ) (924,116 )
Net loss attributable to noncontrolling interests (27,245 ) (21,251 ) (106,433 ) (78,854 )
Net loss attributable to Roivant Sciences Ltd. $ (33,617 ) $ (270,062 ) $ (1,009,030 ) $ (845,262 )
Amounts attributable to Roivant Sciences Ltd.:
Loss from continuing operations, net of tax $ (148,178 ) $ (270,062 ) $ (1,123,591 ) $ (845,262 )
Income from discontinued operations, net of tax 114,561 - 114,561 -
Net loss attributable to Roivant Sciences Ltd. $ (33,617 ) $ (270,062 ) $ (1,009,030 ) $ (845,262 )
Basic and diluted net (loss) income per common share:
Basic and diluted loss from continuing operations $ (0.20 ) $ (0.39 ) $ (1.58 ) $ (1.26 )
Basic and diluted income from discontinued operations $ 0.15 $ - $ 0.16 $ -
Basic and diluted net loss per common share $ (0.05 ) $ (0.39 ) $ (1.42 ) $ (1.26 )
Basic and diluted weighted average shares outstanding:
Basic 742,541,052 692,623,282 712,791,115 669,753,458
Diluted 742,541,052 692,623,282 712,791,115 669,753,458
ROIVANT SCIENCES LTD.
Reconciliation of GAAP to Non-GAAP Financial Measures
(unaudited, in thousands)
Three Months Ended March 31, Years Ended March 31,
Note 2023 2022 2023 2022
Loss from continuing operations, net of tax $ (175,423 ) $ (291,313 ) $ (1,230,024 ) $ (924,116 )
Adjustments:
Cost of revenues
Amortization of intangibles (1) 2,298 - 7,468 -
Share-based compensation (2) 37 - 95 -
Research and development:
Share-based compensation (2) 4,366 16,294 30,914 63,735
Depreciation and amortization (3) 1,539 943 5,097 3,244
Selling, general and administrative:
Share-based compensation (2) 20,832 60,865 186,603 501,221
Depreciation and amortization (3) 2,116 763 6,292 2,688
Other:
Change in fair value of investments (4) (32,462 ) 72,909 20,815 87,291
Gain on sale of investment (5) - - - (443,754 )
Change in fair value of debt and liability instruments (6) (12,031 ) (44,101 ) 78,001 (3,354 )
Gain on termination of Sumitomo Options (7) - - - (66,472 )
Gain on deconsolidation of subsidiaries (8) - (5,041 ) (29,276 ) (5,041 )
Estimated income tax impact from adjustments (9) (704 ) 942 (294 ) 313
Adjusted loss from continuing operations, net of tax (Non-GAAP) $ (189,432 ) $ (187,739 ) $ (924,309 ) $ (784,245 )
Three Months Ended March 31, Years Ended March 31,
Note 2023 2022 2023 2022
Research and development expenses $ 131,857 $ 135,077 $ 525,215 $ 483,035
Adjustments:
Share-based compensation (2) 4,366 16,294 30,914 63,735
Depreciation and amortization (3) 1,539 943 5,097 3,244
Adjusted research and development expenses (Non-GAAP) $ 125,952 $ 117,840 $ 489,204 $ 416,056
Three Months Ended March 31, Years Ended March 31,
Note 2023 2022 2023 2022
Selling, general and administrative expenses $ 125,510 $ 138,973 $ 600,506 $ 775,033
Adjustments:
Share-based compensation (2) 20,832 60,865 186,603 501,221
Depreciation and amortization (3) 2,116 763 6,292 2,688
Adjusted selling, general and administrative expenses (Non-GAAP) $ 102,562 $ 77,345 $ 407,611 $ 271,124
Notes to non-GAAP financial measures:
(1) Represents non-cash amortization of intangible assets associated with milestone payments made in connection with regulatory
(2) Represents non-cash share-based compensation expense.
(3) Represents non-cash depreciation and amortization expense, other than amortization of intangible assets associated with milestone
payments made in connection with regulatory approvals.
(4) Represents the unrealized loss (gain) on equity investments in unconsolidated entities that are accounted for at fair value with
changes in value reported in earnings.
(5) Represents a one-time gain on sale of investment resulting from the merger of Datavant and CIOX Health in July 2021.
(6) Represents the change in fair value of debt and liability instruments, which is non-cash and primarily includes the unrealized loss
relating to the measurement and recognition of fair value on a recurring basis of certain liabilities.
(7) Represents the one-time gain on termination of the options held by Sumitomo Pharma Co., Ltd. to purchase Roivant's ownership
interest in certain Vants (the "Sumitomo Options").
(8) Represents the one-time gain on deconsolidation of subsidiaries.
(9) 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. EST on Wednesday, June 28, 2023, to report its financial results for the fourth quarter and fiscal year ended March 31, 2023, and provide a business update.
To access the conference call by phone, please register online using this registration
link. A webcast of the call 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 is a commercial-stage biopharmaceutical company that aims to improve the lives of patients by accelerating the development and
commercialization of medicines that matter. Today, Roivant's pipeline is concentrated in inflammation and immunology and includes VTAMA, a novel topical approved for the treatment of psoriasis and in development for the treatment of atopic
dermatitis; batoclimab and IMVT-1402, fully human monoclonal antibodies targeting the neonatal Fc receptor ("FcRn") in development across several IgG-mediated autoimmune indications; and RVT-3101, an anti-TL1A antibody in development for ulcerative
colitis and Crohn's disease, in addition to several other therapies in various stages of clinical development. 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 www.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 products and product candidates, the availability and success of topline
results from our ongoing clinical trials and any commercial potential of our products and product candidates. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including

Frequently Asked Questions

What financial results did Roivant report for Q4 2023?

Roivant reported a revenue increase to $61.3 million for the fiscal year ending March 31, 2023.

How did Roivant's R&D expenses change in 2023?

R&D expenses rose to $525.2 million for the year ending March 31, 2023, primarily due to increased program-specific costs.

What is Roivant's cash position as of March 31, 2023?

As of March 31, 2023, Roivant had approximately $1.7 billion in cash and cash equivalents.

Who joined Roivant's Board of Directors recently?

Meghan FitzGerald joined Roivant's Board of Directors, adding her extensive healthcare expertise.

What was Roivant's loss from continuing operations in 2023?

The loss from continuing operations was approximately $1.2 billion for the year ended March 31, 2023.

Last updated: Jun 28, 2023