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VivoSim Appoints Arumugham (Ragoo) Raghunathan as Vice President of Global Sales

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VivoSim (Nasdaq: VIVS) appointed Dr. Arumugham (Ragoo) Raghunathan as Vice President of Global Sales, effective March 3, 2026, to lead commercial expansion from the Greater Boston area and deepen East Coast engagement. The hire targets growth in liver and GI toxicity NAM services, strategic partnerships, and scaled deployments across biopharma, CROs, and research institutions.

Dr. Raghunathan will focus on earlier de‑risking of drug candidates, advancing pilot-to-scale customer programs, and accelerating adoption of human-relevant liver and GI toxicity solutions.

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Positive

  • VP Global Sales hire dated Mar 3, 2026
  • Leadership based in Greater Boston to expand US East Coast reach
  • Commercial focus on liver and GI toxicity NAM services

Negative

  • None.

News Market Reaction – VIVS

-12.73%
2 alerts
-12.73% News Effect
-4.5% Trough Tracked
-$761K Valuation Impact
$5M Market Cap
0.4x Rel. Volume

On the day this news was published, VIVS declined 12.73%, reflecting a significant negative market reaction. Argus tracked a trough of -4.5% from its starting point during tracking. Our momentum scanner triggered 2 alerts that day, indicating moderate trading interest and price volatility. This price movement removed approximately $761K from the company's valuation, bringing the market cap to $5M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Quarterly revenue: $26,000 Quarterly net loss: $2.7 million Nine‑month net loss: $8.1 million +4 more
7 metrics
Quarterly revenue $26,000 Quarter ended Dec 31, 2025 (royalty income)
Quarterly net loss $2.7 million Quarter ended Dec 31, 2025
Nine‑month net loss $8.1 million First nine months of fiscal 2026
Cash balance $4.3 million Cash and equivalents at Dec 31, 2025
Prior cash balance $11.3 million Cash and equivalents at Mar 31, 2025
Negative operating cash flow $8.6 million Nine months ended Dec 31, 2025
ATM equity proceeds $1.8 million Raised under at-the-market program

Market Reality Check

Price: $1.92 Vol: Volume 148,866 is below t...
low vol
$1.92 Last Close
Volume Volume 148,866 is below the 20-day average of 255,346 (relative volume 0.58). low
Technical Price at 2.20 is slightly below the 200-day MA of 2.21 and 58.49% under the 52-week high.

Peers on Argus

Momentum scanner shows peers like RNAZ up 10.939999669790268% and INAB up 2.3499...
2 Up

Momentum scanner shows peers like RNAZ up 10.939999669790268% and INAB up 2.3499999195337296%, but the scanner flags this as a stock-specific move rather than a sector-wide trend.

Historical Context

3 past events · Latest: Feb 11 (Positive)
Pattern 3 events
Date Event Sentiment Move Catalyst
Feb 11 Data presentation plans Positive +0.0% Announced NAMkind liver and intestine validation data for Society of Toxicology meeting.
Jan 29 APAC distributor deal Positive +71.8% Named distributors in Korea and China to expand NAMkind toxicology service access.
Jan 06 CSO appointment Positive +4.6% Appointed new Chief Scientific Officer to lead NAMkind scientific strategy and biomarkers.
Pattern Detected

Recent news has been generally positive, with one commercial expansion headline coinciding with a strong move and leadership/scientific updates seeing more modest or flat reactions.

Recent Company History

Over the past few months, VivoSim has focused on expanding its NAMkind™ toxicology platform and strengthening leadership. A January 29, 2026 distributor deal for Korea and China coincided with a 71.76% move, while a January 6, 2026 CSO appointment saw a smaller 4.62% reaction. Validation data plans announced on February 11, 2026 did not move the stock. Today’s sales leadership hire fits this pattern of building out commercial and scientific capabilities.

Market Pulse Summary

The stock dropped -12.7% in the session following this news. A negative reaction despite this leader...
Analysis

The stock dropped -12.7% in the session following this news. A negative reaction despite this leadership hire would fit a backdrop of tight liquidity and continued losses. Recent filings show quarterly revenue of only $26,000 against a net loss of $2.7 million and cumulative nine‑month losses of $8.1 million, with cash down to $4.3 million. Even constructive news on commercialization or staffing may be weighed against going‑concern disclosures and significant operating cash burn of $8.6 million.

Key Terms

in vitro, new approach methodologies (nams), cro/cdmo, drug-induced liver injury (dili)
4 terms
in vitro medical
"spheroid-based in vitro services to spearhead commercial growth"
In vitro describes laboratory tests performed on cells, tissues, or biological molecules outside a living body—literally “in glass,” such as in test tubes or dishes. For investors, in vitro results are an early sign that a drug or technology has a desired effect under controlled conditions, but they don’t guarantee it will work or be safe in animals or people; think of them as a prototype tested on a bench rather than in real-world use.
new approach methodologies (nams) medical
"provider of next-generation New Approach Methodologies (NAMs) for preclinical safety"
New approach methodologies (NAMs) are modern testing tools and strategies—such as computer models, advanced cell-based assays, and lab-grown tissues—that replace or supplement traditional animal tests to evaluate safety, toxicity, and biological activity of drugs, chemicals and products. For investors, NAMs can shorten development timelines, lower testing costs, and reduce regulatory uncertainty, much like switching from slow manual inspection to faster automated quality checks in a factory.
cro/cdmo technical
"pharmaceutical companies, CROs/CDMOs, and research institutions"
Contract Research Organizations (CROs) and Contract Development and Manufacturing Organizations (CDMOs) are outside companies that handle scientific testing, product development and large-scale production for drug and biotech firms. For investors, they matter because they let drug companies outsource costly lab work and manufacturing — similar to hiring a specialist contractor instead of building your own workshop — which can speed time to market, reduce capital needs and concentrate risk on partners’ capabilities.
drug-induced liver injury (dili) medical
"liver toxicity including drug-induced liver injury (DILI) risk—and GI toxicity"
Drug-induced liver injury (DILI) is liver damage caused by a medication, vaccine, supplement, or chemical that disrupts the liver’s normal filtering and processing functions—think of the liver as the body’s filter that becomes clogged or harmed by a product. It matters to investors because DILI can trigger clinical trial pauses, regulatory warnings, label changes, expensive monitoring, or market value swings for companies developing or selling the implicated product.

AI-generated analysis. Not financial advice.

Veteran business development leader with deep expertise in human-relevant NAM and spheroid-based in vitro services to spearhead commercial growth along the US East Coast, deepening VivoSim’s reach with biopharma innovators seeking human-relevant liver and GI toxicity solutions

SAN DIEGO, March 03, 2026 (GLOBE NEWSWIRE) -- VivoSim Labs, Inc. (Nasdaq: VIVS) (the “Company” or “VivoSim”), a provider of next-generation New Approach Methodologies (NAMs) for preclinical safety, today announced the appointment of Dr. Arumugham (Ragoo) Raghunathan, PhD as Vice President of Global Sales. Based in the Greater Boston area, Dr. Raghunathan will lead commercial expansion and secure strategic partnerships with biopharma innovators, established pharmaceutical companies, CROs/CDMOs, and research institutions. His focus will be on delivering VivoSim’s liver and gastrointestinal (GI) toxicity solutions for earlier de-risking of drug candidates and clearer feasibility decisions throughout the development process.

A seasoned executive, Dr. Raghunathan brings extensive experience building trusted, consultative relationships across drug discovery and advanced in vitro biology. He is recognized for bridging scientific and commercial stakeholders, structuring collaborative programs, and guiding customers from pilot studies to scaled deployments—particularly in complex, high-stakes areas such as safety assessment and translational decision-making.

“Ragoo builds and strengthens relationships through scientific rigor and a relentless emphasis on outcomes,” said Tony Lialin, Chief Commercial Officer of VivoSim. “He is the kind of leader customers instantly trust and recognize as a true long-term partner. He understands how discovery, DMPK, and safety teams operate under real-world timelines and constraints. As we accelerate adoption of our liver and GI tox services, Ragoo will be instrumental in helping partners generate clearer, earlier signals—so they can move forward with the best programs with confidence, maximizing both cost and time efficiency.”

Expanding Customer Impact Across Liver and GI Toxicology

Under Dr. Raghunathan’s leadership, VivoSim will intensify engagement with customers who need stronger human relevance and sharper predictivity in preclinical development, including:

  • Discovery and translational teams seeking earlier insight into toxicity liabilities while optimizing efficacy and chemical series
  • Preclinical safety, toxicology, and DMPK groups looking to improve go/no-go decision quality, candidate selection, and risk management
  • Biotech startups and emerging pharma aiming to conserve capital by reducing late-stage attrition
  • Large pharma portfolios requiring scalable, reproducible screening approaches across multiple programs
  • CROs/CDMOs and strategic partners integrating advanced in vitro safety services into broader development packages
  • Academic medical centers and research institutes studying mechanism, disease biology, and human-relevant endpoints

VivoSim’s portfolio supports safety assessment programs focused on liver toxicity   including drug-induced liver injury (DILI) risk—and GI toxicity, enabling teams to interrogate potential liabilities with models and readouts designed to better reflect human biology. This is particularly valuable for programs where traditional approaches can obscure or miss risk signals entirely.

“VivoSim is building exactly what the market has been asking for: practical, human-relevant tools that give development teams a clearer view of tox-compatible candidates earlier in the process,” said Dr. Raghunathan. “In the Boston area and across the East Coast pharma clusters, there is enormous demand for better prediction of liver and GI liabilities—especially as drug modalities diversify and development timelines compress. I’m excited to help customers translate VivoSim’s science into concrete wins: smarter prioritization, fewer late-stage surprises, and faster progress to the clinic.”

In his role, Dr. Raghunathan will also support VivoSim’s broader business and strategic initiatives, including key account development, bespoke partnership plans, and customer success programs designed to move engagements from pilot studies to long-term collaborations.

About VivoSim Labs
VivoSim Labs, Inc. (“VivoSim” and the “Company”), is a pharmaceutical and biotechnology services company that is focused on providing testing of drugs and drug candidates in three-dimensional (“3D”) human tissue models of liver and intestine. The Company offers partners liver and intestinal toxicology insights using its new approach methodologies (“NAM”) models. The Company anticipates 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. VivoSim Labs operates from San Diego, CA. Visit www.vivosim.ai.

Forward-Looking Statements

Any statements contained in this press release that do not describe historical facts constitute forward-looking statements as that term is defined in the Private Securities Litigation Reform Act of 1995. Any forward-looking statements contained herein are based on current expectations but are subject to a number of risks and uncertainties. Forward-looking statements include statements regarding NAMKind™, including target turnaround time and its potential to help users de-risk their pipelines, avoid costly downstream failures, reduce rework, prioritize the right assets, move faster, save millions and reduce risk; VivoSim’s commercial presence across Asia-Pacific; the evaluation and acceptance of scientifically robust NAM-based evidence; the Company’s ability to capture growing demand in the in vitro toxicology testing market; demand for human-relevant toxicology; the market opportunity and market size of gastrointestinal in vitro models and toxicology services; and the Company’s scaling capacity to support expanding global demand and development needs. Such forward-looking statements are not guarantees of performance and actual actions or events could differ materially from those contained in such statements. These risks and uncertainties and other factors are identified and described in more detail in the Company’s filings with the SEC, including its Annual Report on Form 10-K filed with the SEC on June 5, 2025, as such risk factors are updated in its most recently filed Quarterly Report on Form 10-Q filed with the SEC on February 11, 2026. You should not place undue reliance on these forward-looking statements, which speak only as of the date that they were made. These cautionary statements should be considered with any written or oral forward-looking statements that the Company may issue in the future. Except as required by applicable law, including the securities laws of the United States, the Company does not intend to update any of the forward-looking statements to conform these statements to reflect actual results, later events, or circumstances or to reflect the occurrence of unanticipated events. 

Contact(s):
Investor Relations
info@vivosim.ai
VivoSim Labs, Inc.


FAQ

Who is VivoSim hiring as Vice President of Global Sales (VIVS) on March 3, 2026?

Dr. Arumugham (Ragoo) Raghunathan is the new Vice President of Global Sales. According to the company, he will be based in the Greater Boston area and lead commercial expansion, strategic partnerships, and customer programs focused on liver and GI toxicity services.

How will the VIVS hire affect VivoSim's commercial strategy on the US East Coast?

The appointment is intended to accelerate East Coast commercial growth and partner engagement. According to the company, Dr. Raghunathan will deepen relationships with biopharma, CROs, and research institutions to drive adoption of VivoSim's liver and GI toxicity NAM services.

What responsibilities will Dr. Raghunathan have at VivoSim (VIVS)?

He will lead global sales, key account development, and bespoke partnership plans. According to the company, responsibilities include moving engagements from pilot studies to scaled deployments and supporting customer success programs across discovery, safety, and DMPK teams.

Which customer segments will VivoSim target after the VIVS sales appointment?

VivoSim will intensify work with discovery, preclinical safety, biotech, large pharma, CROs, and academic centers. According to the company, the focus is on teams needing human-relevant liver and GI toxicity assessment to improve candidate selection and reduce late-stage surprises.

What specific VivoSim capabilities will the new VP of Sales promote for VIVS customers?

He will promote VivoSim's human-relevant NAMs for liver and GI toxicity risk assessment. According to the company, these services aim to provide earlier, clearer toxicity signals to improve go/no-go decisions and conserve development capital.
VivoSim Labs Inc

NASDAQ:VIVS

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VIVS Stock Data

5.74M
2.51M
Biotechnology
Biological Products, (no Diagnostic Substances)
Link
United States
SAN DIEGO