Peter Salzmann
and as a member of the Company’s Board of Directors (the “Board”), effective April 18, 2025.
Highest-materiality recent filing
Immunovant posts $0.73/sh Q4 loss; IMVT-1402 hits 72.7% ACR20 in D2T RA at Week 16
IMVT-1402 in D2T RA: 72.7% ACR20, 54.5% ACR50, 35.8% ACR70 at Week 16; open-label, blinded assessors; safety well-tolerated.
Immunovant reports Q3 net loss of $110.6M; cash $994.5M; D2T RA trial fully enrolled
Net loss $110.6M ($0.61/sh) for Q3 FY26; non-GAAP net loss $97.5M.
Immunovant raises $550M via 26.2M share offering at $21.00/share
Gross proceeds ~$550M from 26.2M shares priced at $21.00/share.
Immunovant prices $550M stock offering; updates IMVT-1402 and batoclimab timelines
Underwritten common stock offering of ~$550M gross proceeds; Roivant Sciences to purchase shares; expected close Dec 12, 2025.
Immunovant CMO Michael Geffner departs; consulting through April 2026
Michael Geffner, M.D., M.B.A., ceased as Chief Medical Officer effective Nov 21, 2025.
Immunovant Q2 loss $126.5M; batoclimab TED readout delayed to H1 2026; cash $521.9M
Net loss $126.5M ($0.73/share) in fiscal Q2 ended Sep 30, 2025, vs $109.1M ($0.74) prior year.
80% (17/21) of uncontrolled Graves' patients maintained normal thyroid function six months after stopping batoclimab.
Immunovant Q4 FY2025 net loss $106.4M, cash $714M; new CEO Eric Venker
Net loss of $106.4M ($0.64/share) for Q4 FY2025, vs $75.3M ($0.52/share) a year ago.
Immunovant appoints new CEO/CFO, expands IMVT-1402 into Sjögren's and CLE
CEO Peter Salzmann retired; Eric Venker (Roivant President) appointed CEO, effective April 21.
Batoclimab meets MG Phase 3 primary endpoint; CIDP shows 84% responder rate with >70% IgG reduction
MG Phase 3: 680mg batoclimab arm achieved 5.6-point MG-ADL improvement vs 3.6 placebo (p<0.001).
Immunovant reports Q3 net loss $111.1M; cash $374.7M plus $450M placement
Net loss $111.1M ($0.76/sh) vs $51.4M ($0.36) y/y; R&D spend $94.5M up from $48.3M on IMVT-1402 prep.
Immunovant announces $450M PIPE at $20/share to advance pipeline
Agreed to sell 22.5M shares at $20/share to three institutional investors, including Roivant Sciences.
Five INDs cleared for IMVT-1402 across therapeutic areas including Graves' disease and rheumatoid arthritis.
High-dose batoclimab (680 mg SC weekly) achieved 76% response rate and 56% ATD-free response at week 12 in patients uncontrolled on antithyroid drugs.
Immunovant reports Q1 FY2025 net loss $87.2M; completes batoclimab MG enrollment
Net loss $87.2M ($0.60/share) vs $73.9M ($0.57) YoY; cash $560M as of June 30, 2024.
Net loss $75.3M ($0.52/sh) for Q4 FY2024 vs $59.4M ($0.46/sh) YoY; FY net loss $259.3M ($1.88/sh).
Immunovant reports Q3 net loss $51.4M; plans 4-5 registrational trials for IMVT-1402
Net loss of $51.4M ($0.36/share) vs $63.2M ($0.49) a year ago; cash & equivalents $691M.
Initial cohort in Phase 2 trial exceeded 50% response rate; response defined as normalization of T3/T4 without increasing ATD dose.
Four weekly 600 mg SC doses of IMVT-1402 reduced total IgG by mean 74%, similar to batoclimab's 76% at 680 mg.
Net loss of $58.7M ($0.45/share) for Sep Q, vs. $47.9M ($0.41) a year ago; wider loss on higher R&D.
Immunovant Prices $280M Public Offering; Roivant Commits $170M Private Placement
Public offering of 7,370,000 shares at $38.00/share; gross proceeds ~$280.1M.
Mean total IgG reduction of 63% after four weekly 300 mg SC doses of IMVT-1402 in Phase 1 MAD cohort.
Immunovant reports Q1 net loss of $73.9M; IMVT-1402 Phase 1 data on track for September 2023
Net loss $73.9M ($0.57/share) vs $40.4M ($0.35/share) in prior year; cash $330M funds ops into H2 2025.
Immunovant reports FY2023 net loss $211M; IMVT-1402 IND cleared, Phase 1 started
Net loss of $59.4M ($0.46/share) for Q4 FY2023 vs $47.2M ($0.41) a year ago.
Immunovant unveils next-gen FcRn inhibitor IMVT-1402; Q2 net loss $47.9M
IMVT-1402 observed in animal study to have best-in-class IgG reduction with minimal albumin/LDL impact.
Immunovant prices $75M stock offering at $6/share to fund IMVT-1402 development
Priced 12.5M shares at $6.00 per share; gross proceeds ~$75M before discounts.
Immunovant announces next-generation anti-FcRn IMVT-1402 with promising preclinical data
IMVT-1402 showed deep IgG lowering with minimal impact on albumin and LDL in animal studies.
Immunovant to start pivotal Phase 2b in CIDP in H2 2022; Phase 2 in Graves' Disease in early 2023
Pivotal Phase 2b trial of batoclimab in CIDP to start H2 2022; initial open-label results expected H1 2024.
Immunovant Q1 net loss $40.4M; initiates pivotal MG trial, TED trials on track
Net loss of $40.4M ($0.35/share) vs $30.5M ($0.31) YoY; R&D expenses up to $28.4M from $18.7M.
Immunovant gains FDA alignment for Phase 3 batoclimab trials in TED; reports FY2022 loss of $156.7M
FDA aligned on Phase 3 TED program: two placebo-controlled trials (100 patients each) initiating H2 2022; top-line data H1 2025.
Immunovant provides Phase 3 update for batoclimab in myasthenia gravis
Corporate webcast held Jan 5, 2022; presentation focuses on Phase 3 development of batoclimab.
Immunovant achieves FDA alignment to start Phase 3 trial for batoclimab in MG in 1H 2022
FDA Division of Neurology 1 agreed to move forward; Phase 3 for batoclimab in myasthenia gravis starts 1H 2022.
Immunovant enters $36M manufacturing deal with Samsung Biologics for batoclimab
Minimum purchase commitment estimated at $36M; PSA runs through Dec 31, 2029.
and as a member of the Company’s Board of Directors (the “Board”), effective April 18, 2025.
the Board appointed Robert Susman and Jacob Bauer to fill the vacancies on the Board created by the departure of each of Dr. Salzmann and Mr. Migausky
the Board appointed Robert Susman and Jacob Bauer to fill the vacancies on the Board created by the departure of each of Dr. Salzmann and Mr. Migausky
Peter Salzmann, M.D. retired from his roles as the Chief Executive Officer and principal executive officer of Immunovant, Inc. (the "Company" or "Immunovant"), effective April 20, 2025
On April 18, 2025, George Migausky, a member of Immunovant’s Board and Chair of the Audit Committee of the Board (the “Audit Committee”), resigned from the Board and the Audit Committee, effective immediately.
Also effective April 20, 2025, Renee Barnett ceased serving as the Chief Financial Officer (including the principal financial officer and principal accounting officer) of the Company.
Effective September 9, 2021, each of Frank M. Torti, M.D., Andrew Fromkin, Atul Pande, M.D. and Eric Venker, M.D. were elected as Series A preferred stock directors of Immunovant
Effective September 9, 2021, each of Frank M. Torti, M.D., Andrew Fromkin, Atul Pande, M.D. and Eric Venker, M.D. were elected as Series A preferred stock directors of Immunovant
On September 14, 2021, Renee Barnett was appointed the Chief Financial Officer of Immunovant, Inc. effective October 4, 2021.
Effective September 9, 2021, each of Frank M. Torti, M.D., Andrew Fromkin, Atul Pande, M.D. and Eric Venker, M.D. were elected as Series A preferred stock directors of Immunovant
Effective September 9, 2021, each of Frank M. Torti, M.D., Andrew Fromkin, Atul Pande, M.D. and Eric Venker, M.D. were elected as Series A preferred stock directors of Immunovant
Effective August 2, 2021, Dr. Frank M. Torti, age 42, Immunovant’s current Chairperson, was appointed Executive Chairperson.
Max materiality 0.90 · Median 0.68 · Most common event other_material