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Roivant Sciences Ltd.

39.57

+0.07000.18%

Post-market: 39.830.2600+0.66%19:40 EDT

Volume:6.18M

Turnover:245.93M

Market Cap:28.59B

PE:-84.19

High:40.45

Open:39.77

Low:39.17

Close:39.50

52wk High:42.50

52wk Low:13.93

Shares:722.41M

Float Shares:581.00M

Volume Ratio:0.79

T/O Rate:1.06%

Dividend:- -

Dividend Rate:- -

EPS(TTM):-0.4700

EPS(LYR):-0.5400

ROE:-8.52%

ROA:-16.48%

PB:6.76

PE(LYR):-73.28

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Overview Company News Filings

Roivant Sciences - Mosliciguat Shows Lower Cough Incidence than Placebo in Phocus Study

THOMSON REUTERS

Roivant Sciences Ltd - Mosliciguat Observed to be Well Tolerated with a Favorable Safety Profile

THOMSON REUTERS

Roivant Sciences Ltd - Study Also Met Its Secondary Endpoints at Week 16

THOMSON REUTERS

Roivant to Present Phase 2 PHocus Mosliciguat Topline Data in PH-ILD at ERS Congress Sept. 8, 2026

Immunovant Holds Annual Stockholder Meeting with 96% Shares Represented

J.P. Morgan Reaffirms Their Buy Rating on Roivant Sciences (ROIV)

Roivant Sciences President, Immunovant CEO Eric Venker Disposes of Common Shares Worth $7.15 Million

NASD Most Active Issues

Immunovant Director Atul Pande Disposes of 1,500 Common Shares Worth $64,905

Roivant Sets Price for New Rare Disease Drug Lisraya at $35,000 a Month

Lisraya is Commercially Available NOW - Roivant Presentation

THOMSON REUTERS

Roivant Sciences Exec Says Lisraya Will be Available at List Price of $35,000 for a 30-Day Supply

THOMSON REUTERS

Roivant Sciences Price Target Maintained with a $41.00/Share by HC Wainwright & Co.

Roivant Sciences Gets FDA Approval for LISRAYA in Dermatomyositis; Shares Rise

MT Newswires Live

Priovant Therapeutics - Lisraya NOW Available in the U.S.

THOMSON REUTERS

Priovant Announces FDA Approval of Lisraya™ (Brepocitinib) for Adults with Dermatomyositis; NOW Available in the U.S.

THOMSON REUTERS

US FDA Approves Roivant-Priovant's Skin Disease Drug

FDA Approves First Oral Drug Indicated to Treat Dermatomyositis in Adults

FDA: Lisraya is the First FDA-Approved Oral Treatment Option for Patients with Dermatomyositis

THOMSON REUTERS

Roivant Says JAMA Dermatology Publishes Phase 3 VALOR Data Showing Brepocitinib Improves Dermatomyositis Skin Outcomes

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