Rakhi Kumar
Ms. Kumar stepped down from her role effective February 20, 2025.
Highest-materiality recent filing
Roivant reports Q4 GAAP EPS $0.28 on Moderna settlement; IMVT-1402 D2T RA ACR20 72.7%
Q4 GAAP income from continuing ops $355.7M ($0.28 diluted EPS) vs loss of $252.4M ($0.29 loss) YoY; includes $770M gain on Moderna settlement.
Batoclimab TED Phase 3 misses endpoint; Roivant starts brepocitinib LPP trial; $4.3B cash
Preliminary cash, cash equivalents and marketable securities as of Mar 31, 2026: ~$4.3B.
Settlement resolves all US and international patent infringement litigation between Genevant/Arbutus and Moderna over LNP technology in COVID-19 and other mRNA vaccines.
FDA accepts brepocitinib NDA for dermatomyositis, grants Priority Review; PDUFA Q3 2026
FDA accepted NDA and granted Priority Review for brepocitinib in dermatomyositis; PDUFA target action date in Q3 2026.
Roivant's Genevant/Arbutus settles Moderna LNP patent suit for $950M upfront, plus $1.3B contingent
Moderna to pay $950M non-contingent by July 8, 2026; additional $1.3B if Federal Circuit affirms rejection of Section 1498 defense.
Roivant reports positive Phase 2 brepocitinib data in CS; Q3 loss $313.7M vs $208.9M
Phase 2 BEACON study: brepocitinib 45mg achieved 22.3-point CSAMI-A improvement vs 0.7 placebo (Δ21.6, p<0.0001).
Roivant accelerates key pipeline timelines; Immunovant raises $550M
Brepocitinib NDA filing in dermatomyositis expected early 2026; commercial launch early 2027.
Roivant Q2 net loss $113.5M; brepocitinib Phase 3 DM trial succeeds on all endpoints
Brepocitinib 30 mg met primary and all nine key secondary endpoints in Phase 3 VALOR DM study; NDA filing planned H1 2026.
Brepocitinib 30 mg achieved week-52 mean TIS 46.5 vs placebo 31.2 (p=0.0006); all 9 key secondary endpoints met.
Matthew Gline, Keith Manchester, Melissa Epperly re-elected as Class I directors; each received >72% of votes cast excluding broker non-votes.
Roivant reports ~80% durability and ~50% ATD-free remission in Graves' disease data
Of 21 patients in 6-month off-treatment follow-up, ~80% (17/21) maintained normal thyroid function.
Roivant Q1 loss widens to $0.33/share; completes $1.5B buyback, initiates new $500M program
GAAP loss from continuing ops $273.9M ($0.33/share) vs income $31.6M ($0.01) YoY; revenue $2.2M down from $8.0M.
Roivant Sciences authorizes $500M share repurchase program
New $500M buyback authorization effective June 24, 2025, in addition to prior $1.5B program now exhausted.
Roivant Q4 net loss widens to $206.5M; brepocitinib DM readout on track for H2 2025
Net loss attributable to Roivant of $206.5M ($0.29 loss per share) for Q4 FY2025, vs $151.1M loss ($0.19) a year ago.
Immunovant CEO Pete Salzmann retires; Eric Venker appointed; IMVT-1402 adds SjD and CLE indications
Pete Salzmann retired as Immunovant CEO and Director; Eric Venker (Roivant President & COO) appointed CEO; Tiago Girao named CFO.
Roivant enters consulting agreement with former CAO Rakhi Kumar for 18-month transition services
Rakhi Kumar stepped down as Chief Accounting Officer effective Feb 20, 2025; consulting agreement dated March 16, 2025.
Phase 3 MG study met primary endpoint with 5.6-point MG-ADL improvement at 12 weeks in high-dose batoclimab arm.
Roivant Sciences appoints Jennifer Humes as Principal Accounting Officer
Rakhi Kumar stepped down as Principal Accounting Officer and Chief Accounting Officer effective February 20, 2025.
Roivant Q3 loss $208.9M; cash $5.2B; launches brepocitinib Ph2 in sarcoidosis
Revenue $9.0M (-42% YoY); loss from continuing ops $208.9M vs. $5.1B income in prior year (Telavant gain).
Roivant: Phase 2 namilumab study fails in sarcoidosis; development discontinued
Namilumab failed to meet the primary endpoint (proportion of subjects with a Rescue Event) in chronic active pulmonary sarcoidosis.
Roivant Q2 loss $236.8M; Dermavant deal closed; cash $5.4B; brepocitinib NIU data
Q2 loss from continuing ops $236.8M ($0.25 EPS); R&D $143.1M; G&A $202.9M up $114.3M YoY on retention awards.
Roivant subsidiary Dermavant acquired by Organon; merger closed Oct 28, 2024
Organon completed acquisition of Dermavant from Roivant on October 28, 2024, expanding dermatology portfolio.
Roivant sells Dermavant to Organon for up to $1.2B in cash plus royalties
Total consideration up to ~$1.2B: $175M at closing, $75M milestone on FDA approval for atopic dermatitis, up to $950M in net sales milestones.
Roivant's Dermavant to be acquired by Organon for $1.2B
Organon (OGN) will acquire Dermavant, a Roivant (ROIV) subsidiary, for $1.2B in cash and milestone payments.
Directors Ilan Oren, James Momtazee, Dr. Mayukh Sukhatme re-elected with 68%-92% of votes cast.
Phase 1b ATMOS in 38 PH patients: single dose of mosliciguat produced mean-max PVR reduction up to ~38%, exceeding ≥20% threshold.
Roivant/Immunovant: Phase 2a batoclimab 76% response in GD; pivotal IMVT-1402 trial by year end
High-dose batoclimab (680mg SC weekly) achieved 76% response rate and 56% ATD-free response in uncontrolled GD at week 12.
Roivant Q1 net income $57.5M, cash $5.7B; pipeline advances in MG, DM, NIU
Net income of $57.5M vs net loss of $327.8M YoY; diluted EPS $0.12 vs ($0.38).
Roivant reports FY2024 GAAP income from continuing ops $4.2B on $5.3B Telavant gain; Q4 loss $182.5M
Net product revenue from VTAMA (psoriasis) $75.1M for FY2024; over 385K prescriptions since launch.
Roivant subsidiary Dermavant renegotiates debt, reduces potential payments by over $300M
Dermavant caps RIPSA royalties at $6M/yr for FY2025-2027, reducing near-term cash outflow.
Roivant reports positive Phase 2 NIU data; authorizes $1.5B buyback, repurchases Sumitomo's 9% stake
Phase 2 NEPTUNE: brepocitinib 45mg arm had 29% Treatment Failure at week 24 (vs 44% for 15mg), best observed in NIU studies.
Roivant posts $5.1B net income on $7.1B Telavant sale to Roche; cash at $6.7B
Net income $5.1B ($6.37 basic EPS) vs loss of $384.9M a year ago, driven by $5.3B gain on Telavant sale.
Roivant files pro forma financials for $7.1B Telavant sale to Roche; gain of $5.3B
Roivant sold its 75% stake in Telavant to Roche for ~$7.1B cash plus $150M milestone for Phase 3 trial initiation.
Roivant reports positive Phase 2 batoclimab data in Graves' disease; response >50%
Initial cohort in Phase 2 trial of batoclimab in Graves' disease showed response rates meaningfully exceeding 50%.
Roivant closes $7.1B sale of Telavant to Roche; retains 75% ownership prior to closing
Total upfront cash consideration of approximately $7.1 billion paid to Telavant equity holders.
Roivant: IMVT-1402 600 mg Phase 1 data shows best-in-class potential; 74% IgG reduction
Four weekly SC doses of 600 mg IMVT-1402 reduced total IgG by mean 74%, similar to batoclimab's 76% reduction.
Roivant subsidiary Priovant's Phase 2 lupus study of oral brepocitinib fails primary endpoint
Oral brepocitinib did not meet primary endpoint of SRI-4 at Week 52 in moderate-to-severe active lupus.
Roivant reports Q2 net loss $331M; announces $7.1B Telavant sale to Roche
Net loss $331.1M ($0.40/share) vs $315.9M prior year; revenue $37.1M up from $12.5M.
Roche to acquire Telavant for $7.1B upfront; Roivant owns 75% stake
Roche pays $7.1B cash at closing plus $150M milestone for rights to RVT-3101 in US and Japan.
Roivant Sciences raises ~$200M via registered direct offering of 19.6M shares at $10.21
Sold 19,600,685 common shares at $10.21 each for aggregate gross proceeds of ~$200.1 million.
SC doses of IMVT-1402 achieved peak IgG reductions similar to batoclimab with no decrease in serum albumin or increase in LDL-C.
Shareholders elect two Class II directors and ratify EY as auditor at 2023 AGM
Daniel Gold elected as Class II director with 480,335,783 votes for, 189,651,604 withheld.
Roivant completes redemption of outstanding warrants; most exercised for shares
20,061,507 public warrants exercised cashless for 5,005,531 common shares; 397 exercised for cash at $11.50.
Roivant sets warrant redemption FMV at $11.35; cashless exercise yields 0.2495 shares per warrant
Redemption Fair Market Value of $11.35 determined for outstanding public and private warrants.
Roivant reports Q1 net loss of $327.8M, VTAMA revenue $16.7M; cash $1.45B
Net loss $327.8M ($0.38/share) vs $353.8M ($0.48) YoY; non-GAAP net loss $211.5M.
Director Hiroshi Nomura resigns from Roivant board effective Aug 31, 2023
Hiroshi Nomura, Class III director, to resign from board effective August 31, 2023.
Roivant announces redemption of all outstanding warrants at $0.10 each, effective September 1, 2023
Redemption of all outstanding public and private warrants at $0.10 each; redemption date Sept 1, 2023, 5:00 p.m. NY time.
Corrected timeline for Immunovant's Phase 3 TED trials: topline data expected in H1 2025 (previously misstated).
VTAMA net product revenue $13.7M in Q4, $28.0M FY; 170k prescriptions since launch; 76% US commercial lives covered.
At expected Phase 3 dose, Clinical Remission 36% at week 56 vs 29% at week 14; Endoscopic Improvement 50% vs 36%.
Ms. Kumar stepped down from her role effective February 20, 2025.
The Company has appointed Jennifer Humes to serve as its Principal Accounting Officer and as Chief Accounting Officer of RSI from the Effective Date.
Rakhi Kumar stepped down from her role as the Principal Accounting Officer of Roivant Sciences Ltd. (the “Company”) and Chief Accounting Officer of the Company’s subsidiary, Roivant Sciences, Inc. (“RSI”) effective February 20, 2025 (the “Effective Date”).
On July 31, 2023, Hiroshi Nomura, a Class III director of Roivant Sciences Ltd. (the “Company”), informed the Company of his intention to resign from his role on the Company’s board of directors (the “Board”), effective August 31, 2023, to focus on other business affairs.
In addition, the Board has appointed Ilan Oren as Chairman of the Board.
On March 13, 2023, the Board of Directors (the “Board”) of Roivant Sciences Ltd. (the “Company”) appointed Meghan M. FitzGerald, DrPH, to serve as a Class II director of the Company and as a member of the Nominating and Governance Committee of the Board, effective as of that date, filling a vacancy on the Board.
Vivek Ramaswamy, a Class II director of Roivant Sciences Ltd. (the “Company”), stepped down from his role on the Company’s board of directors (the “Board”) effective immediately, to imminently pursue an outside opportunity.
On November 17, 2022, Dr. Andrew Lo, a Class II director of Roivant Sciences Ltd. (the “Company”), informed the Company of his decision to resign from his role on the Company’s board of directors (the “Board”) effective immediately, to focus on other ventures.
Also on September 15, 2022, the Board appointed Hiroshi Nomura to serve as a Class III director of the Board, effective September 16, 2022, filling the vacancy created by and concurrent with the resignation of Mr. Tada from the Board.
On September 15, 2022, Masayo Tada resigned as a director of the Company, effective September 16, 2022.
the previously announced resignation of Patrick Machado from the Board
On June 22, 2022, the Board of Directors (the “Board”) of the Company appointed Melissa Epperly to serve as a Class I director of the Board and as a member of the Audit Committee of the Board, effective June 29, 2022, filling the vacancy created by, and concurrent with, the previously announced resignation of Patrick Machado from the Board.
Max materiality 1.00 · Median 0.75 · Most common event other_material