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VIVS

VivoSim Labs, INC.

Biopharma developer (SEC filing verified)·Phase 2·San Diego, CA, United States·CEO: Douglas Jay Cohen
ImmunologyInfectious DiseaseMetabolic

VIVS evidence brief

What we can confirm

BioSniper Score:
2.6 / 10
Market Cap:
$3.8M
Cash Runway:
1.6 mo

What it means

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

What to watch

Market Cap: $3.8M · Cash Runway: 1.6 mo
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · VIVS

VivoSim Labs, Inc. (VIVS) is a biotechnology company that shifted from clinical-stage drug development (FXR314 for IBD) to a service model centered on proprietary 3D human tissue models (NAMkind™) for preclinical safety testing, with a cash position of $1.7M as of June 30, 2026 and an accumulated deficit of $357.3M.

Key risk: Cash runway

2.6/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$3.8M

Cash Runway

1.6 mo

Lead Asset

fxr314 (Phase 2)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate for VivoSim Labs, INC..

Similar companies

AI OverviewAI overview is shown in English only.

VivoSim Labs, Inc. (VIVS) is a biotechnology company that shifted from clinical-stage drug development (FXR314 for IBD) to a service model centered on proprietary 3D human tissue models (NAMkind™) for preclinical safety testing, with a cash position of $1.7M as of June 30, 2026 and an accumulated deficit of $357.3M.

  • Cash and cash equivalents of $1.7M as of June 30, 2026, with an accumulated deficit of $357.3M [sec_mda · as of 2026-08-12].
  • Total revenue of $0.0M and net income of -$1.3M for the latest reported period as of June 30, 2026 [sec].
  • Shareholders' equity of -$2.3M as of June 30, 2026 [sec].
  • Company pivoted from clinical-stage development of FXR314 in IBD to a service model using NAMkind™ 3D human tissue models for preclinical safety testing [sec · filed 2026-07-31].
  • Presented new drug toxicity data at EUROTOX 2026 demonstrating predictive superiority in liver and gastrointestinal safety [news · published 2026-09-16].

What works

  • Proprietary NAMkind™ platform achieved 87.5% sensitivity and 100% specificity in liver toxicity prediction, which the company describes as 'world's best' [sec · filed 2026-07-31].
  • Company has demonstrated ability to discern antibody toxicity from payload toxicity in ADCs, opening a major new market [news · published 2026-03-24].
  • FDA announcement on April 10, 2025 to refine animal testing requirements in favor of non-animal NAM methods may accelerate adoption of the company's models [sec · filed 2026-07-31].

What to weigh

  • Company has zero revenue ($0.0M) and a net loss of -$1.3M as of June 30, 2026 [sec].
  • Accumulated deficit of $357.3M as of June 30, 2026, indicating significant historical losses [sec_mda · as of 2026-08-12].
  • Shareholders' equity is negative at -$2.3M as of June 30, 2026 [sec].
  • Cash and cash equivalents of only $1.7M as of June 30, 2026, with restricted cash of $0.1M, suggesting limited runway [sec_mda · as of 2026-08-12].

From the filings

Quoted directly from source documents.

  • Cash position and accumulated deficit

    “As of June 30, 2026, we had cash and cash equivalents of approximately $1.7 million, restricted cash of approximately $0.1 million and an accumulated deficit of $357.3 million.”

    SEC MD&A · August 12, 2026

  • Platform performance metrics

    “we believe at 87.5% is a world's best. Importantly, the specificity was 100%, meaning that none of the compounds tested that are not liver toxic were incorrectly identified as having liver toxicity issues by the platform.”

    SEC filings · July 31, 2026

  • Pivot from drug development to service model

    “Prior to March 2025, we were a clinical stage biotechnology company that was focused on developing FXR314 in inflammatory bowel disease ("IBD"), including ulcerative colitis ("UC"), based on demonstration of clinical promise in 3D human tissues as well as strong preclinical data.”

    SEC filings · July 31, 2026

  • FDA regulatory tailwind for NAM methods

    “We anticipate accelerated adoption of human tissue models following the U.S. Food and Drug Administration ("FDA") announcement on April 10, 2025 to refine animal testing requirements in favor of these non-animal NAM methods.”

    SEC filings · July 31, 2026

Risks & what to watch (4)›

Key risks

  • Cash runway — Only $1.7M cash as of June 30, 2026, with zero revenue, raising concerns about near-term liquidity [sec_mda · as of 2026-08-12].
  • Negative equity — Shareholders' equity of -$2.3M as of June 30, 2026 indicates liabilities exceed assets [sec].
  • Revenue generation — No revenue reported ($0.0M) as of June 30, 2026, meaning the service model has not yet generated sales [sec].
  • Accumulated deficit — Accumulated deficit of $357.3M as of June 30, 2026 reflects sustained historical losses [sec_mda · as of 2026-08-12].

What to watch

  • Adoption of NAMkind™ platform by pharmaceutical companies following FDA's April 2025 guidance on non-animal methods [sec · filed 2026-07-31].
  • Ability to convert pipeline of bespoke service contracts into revenue, given zero revenue as of June 30, 2026 [sec].
  • Progress of FXR314 pipeline candidate, which remains listed as Phase 2 for IBD and MASH [pipeline].
  • Cash burn rate and any new financing or partnership announcements given limited cash runway [sec_mda · as of 2026-08-12].

Sources: News · Pipeline · SEC filings · SEC MD&A · Generated October 6, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash Runway0.4

1.6 months

Financial Health0.5

OCF -$3M · Net income -$1M

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth3.3

1 candidate

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Pipeline

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

24

Total value held

$140K

Showing top 10 of 24 institutional holders of VivoSim Labs, INC.. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
1.8%
Days to cover
0.8
Shares short
52,788
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 →

VIVS short interest

Governance

Frequently asked questions

What is the AI investment thesis for VivoSim Labs, INC.?

VivoSim Labs, Inc. (VIVS) is a biotechnology company that shifted from clinical-stage drug development (FXR314 for IBD) to a service model centered on proprietary 3D human tissue models (NAMkind™) for preclinical safety testing, with a cash position of $1.7M as of June 30, 2026 and an accumulated deficit of $357.3M.

What is VivoSim Labs, INC.'s lead drug candidate?

VivoSim Labs, INC.'s most advanced tracked candidate is fxr314 (Phase 2) for Inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn's disease (CD); metabolic function-associated steatohepatitis (MASH).

Who is the CEO of VivoSim Labs, INC.?

Douglas Jay Cohen is the chief executive officer of VivoSim Labs, INC. (VIVS).

Where is VivoSim Labs, INC. headquartered?

VivoSim Labs, INC. (VIVS) is headquartered in San Diego, CA, United States.

What therapeutic areas does VivoSim Labs, INC. focus on?

VivoSim Labs, INC. develops therapies across Immunology, Infectious Disease, Metabolic.

923 companies304,841 SEC filings22,639 clinical trials100% citation-verification pass rate (7d)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.