Skip to main content
ROIV

Roivant Sciences Ltd.

Biopharma developer (SEC filing verified)·Phase 2·London, United Kingdom·CEO: Mr. Matthew Gline
NeurologyImmunologyCardiovascularRespiratoryDermatologyMusculoskeletal

ROIV evidence brief

What we can confirm

BioSniper Score:
6.6 / 10
Market Cap:
$29.63B
Cash Runway:
44.2 mo

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $29.63B · Cash Runway: 44.2 mo
BioSniper AIPage context preserved

Prepared research question

What matters most for ROIV—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ROIV

Roivant Sciences Ltd. (ROIV) is a biopharmaceutical company focused on accelerating the development and commercialization of therapies across autoimmune, pulmonary, and other indications, with a pipeline including brepocitinib, IMVT-1402, and mosliciguat.

Key risk: No approved products yet

6.6/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$29.63B

Cash Runway

44.2 mo

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates for Roivant Sciences Ltd..

AI OverviewAI overview is shown in English only.

Roivant Sciences Ltd. (ROIV) is a biopharmaceutical company focused on accelerating the development and commercialization of therapies across autoimmune, pulmonary, and other indications, with a pipeline including brepocitinib, IMVT-1402, and mosliciguat.

  • Cash & equivalents of $1,248.5M as of 2026-06-30 [sec]
  • Total revenue of $1.4M and net income of -$189.8M as of 2026-06-30 [sec]
  • Shareholders' equity of $4,231.3M as of 2026-06-30 [sec]
  • Brepocitinib NDA for dermatomyositis under FDA priority review with decision expected in 3Q 2026 [sec_mda · as of 2026-08-06]
  • Positive Phase 2 results for mosliciguat in pulmonary hypertension associated with interstitial lung disease reported in September 2026 [news · published 2026-09-13]

What works

  • Strong cash position of $1,248.5M as of 2026-06-30 provides runway for pipeline development and potential launches [sec]
  • Multiple late-stage pipeline assets with near-term catalysts, including brepocitinib FDA decision and mosliciguat Phase 2 data [sec_mda · as of 2026-08-06]
  • Immunovant financing of ~$550 million in December 2025 extends cash runway to potential launch of IMVT-1402 in Graves' disease [sec · filed 2026-07-29]

What to weigh

  • Net loss of $189.8M as of 2026-06-30 with minimal revenue of $1.4M, indicating heavy reliance on external funding [sec]
  • Expenses expected to increase substantially as the company funds clinical trials, manufacturing, and commercialization efforts [sec_mda · as of 2026-08-06]
  • Operating results may fluctuate significantly quarter-to-quarter depending on trial timing and R&D expenditures [sec_mda · as of 2026-08-06]

From the filings

Quoted directly from source documents.

  • Brepocitinib NDA under FDA priority review for dermatomyositis

    “FDA decision on brepocitinib in dermatomyositis | 3Q 2026”

    SEC MD&A · August 6, 2026

  • Positive Phase 2 results for mosliciguat

    “Roivant Sciences Ltd. (NASDAQ:ROIV) shares surged 18% on September 8 after the biotech company reported strong Phase 2 results for an experimental treatment for pulmonary hypertension.”

    News · September 13, 2026

Catalyst timeline

  • 2026-09-30 · FDA decision on brepocitinib in dermatomyositis — Priority review decision expected in 3Q 2026; approval would mark Roivant's first FDA-approved drug.
  • 2026-12-31 · Topline data from Phase 2 trial of mosliciguat in PH-ILD — Data expected in 2H 2026; positive results could advance the pulmonary hypertension program.
  • New mid/late-stage in-licensing announcements — Ongoing catalyst; Roivant plans to in-license multiple potentially category-leading drugs per year.
Risks & what to watch (3)›

Key risks

  • No approved products yet — Roivant has minimal revenue ($1.4M) and relies on pipeline success; no FDA-approved drug as of mid-2026 [sec]
  • Rising expenses — Expenses expected to increase substantially for clinical trials, manufacturing, and commercialization [sec_mda · as of 2026-08-06]
  • Clinical trial uncertainty — Operating results may fluctuate significantly depending on trial timing and outcomes [sec_mda · as of 2026-08-06]

What to watch

  • FDA decision on brepocitinib for dermatomyositis expected in 3Q 2026 [sec_mda · as of 2026-08-06]
  • Topline data from Phase 2 trial of mosliciguat in PH-ILD expected in 2H 2026 [sec_mda · as of 2026-08-06]
  • Potential launch of IMVT-1402 in Graves' disease, supported by Immunovant's extended cash runway [sec · filed 2026-07-29]
  • Ongoing in-licensing announcements for mid/late-stage pipeline growth [sec_mda · as of 2026-08-06]

Sources: News · SEC filings · SEC MD&A · Generated October 8, 2026 · How we verify sources →

Run Roivant Sciences Ltd. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Roivant Sciences Ltd. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway10.0

44.2 months

Financial Health9.9

D/E 0.09 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 2/Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal0.0

0 buys · 33 sells (180d)

Runway

Pipeline

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

437

Total value held

$14.41B

HolderSharesValue
fmr llc77,981,253$2.16B
morgan stanley51,828,325$1.44B
blackrock, inc.44,254,260$1.23B
qvt financial lp25,161,237$697.0M
ubs group ag22,619,472$626.6M
vanguard capital management llc20,680,572$572.9M
vanguard portfolio management llc19,838,698$549.5M
state street corp16,186,613$448.4M
adage capital partners gp, l.l.c.12,794,097$354.4M
goldman sachs group inc11,111,591$307.8M

Showing top 10 of 437 institutional holders of Roivant Sciences Ltd.. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
4.5%
Days to cover
4.8
Shares short
24,470,022
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ROIV short interest

Governance

Frequently asked questions

What is the AI investment thesis for Roivant Sciences Ltd.?

Roivant Sciences Ltd. (ROIV) is a biopharmaceutical company focused on accelerating the development and commercialization of therapies across autoimmune, pulmonary, and other indications, with a pipeline including brepocitinib, IMVT-1402, and mosliciguat.

What is Roivant Sciences Ltd.'s lead drug candidate?

Roivant Sciences Ltd.'s most advanced tracked candidate is imvt-1402 (Phase 2/Phase 3) for Difficult-to-Treat Rheumatoid Arthritis, Graves' Disease, Myasthenia Gravis, Chronic Inflammatory Demyelinating Polyneuropathy, Sjögren's Disease, Cutaneous Lupus Erythematosus.

Who is the CEO of Roivant Sciences Ltd.?

Mr. Matthew Gline is the chief executive officer of Roivant Sciences Ltd. (ROIV).

Where is Roivant Sciences Ltd. headquartered?

Roivant Sciences Ltd. (ROIV) is headquartered in London, United Kingdom.

What therapeutic areas does Roivant Sciences Ltd. focus on?

Roivant Sciences Ltd. develops therapies across Neurology, Immunology, Cardiovascular, Respiratory, Dermatology, Musculoskeletal.

923 active companies304,861 SEC filings22,725 clinical trials
Citation log window (7 days): 13,363 recorded LLM calls; 0 block events, 0 warning events. These counts do not measure factual accuracy or research quality.Computed at
How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.