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Lunai Bioworks, Inc. Issues Letter to Shareholders

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Lunai Bioworks (NASDAQ:LNAI) says its Augusta AI platform is now commercial after 12 months of development and is in active negotiations with pharmaceutical and drug‑discovery partners. The company highlights three revenue engines: AI drug discovery (CNS and new oncology pilot), AI biodefense programs targeting government contracts, and an allogeneic dendritic cell immunotherapy with published preclinical tumor regressions and an LOI for licensing.

The release emphasizes faster target validation via high‑throughput in vivo testing, near‑term pilots that can expand to commercial relationships, and ongoing efforts to finalize biodefense funding and a pharma royalty partnership.

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Positive

  • Augusta AI platform declared commercial after 12 months of development
  • Oncology pilot using randomized Phase 2 metastatic colorectal cancer data
  • Published preclinical complete regression in pancreatic tumors (Vaccines, Nov 2025)
  • Received an LOI to license the allogeneic dendritic cell immunotherapy
  • Three distinct, revenue‑focused engines: AI drug discovery, biodefense, immunotherapy

Negative

  • Current collaborations described as pilots or negotiations, not finalized commercial contracts
  • Key revenue and timing metrics not disclosed, limiting near‑term financial visibility
  • Immunotherapy results are preclinical; clinical efficacy and regulatory pathways remain unproven
  • Biodefense commercialization depends on securing government contracts, which are uncertain

Market Reaction

-4.94% $0.80 2.6x vol
15m delay 7 alerts
-4.94% Since News
$0.80 Last Price
$0.67 $0.83 Day Range
-$1M Valuation Impact
$19M Market Cap
2.6x Rel. Volume

Following this news, LNAI has declined 4.94%, reflecting a moderate negative market reaction. Our momentum scanner has triggered 7 alerts so far, indicating moderate trading interest and price volatility. The stock is currently trading at $0.80. This price movement has removed approximately $1M from the company's valuation. Trading volume is elevated at 2.6x the average, suggesting increased selling activity.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Silver for real-time data.

Key Figures

Platform build period: last 12 months Phase of colon trial: Phase 2 Discovery timelines: over 2 years to under a year +3 more
6 metrics
Platform build period last 12 months Time taken to complete and commercialize AI platform
Phase of colon trial Phase 2 Randomized metastatic colorectal cancer survival trial dataset
Discovery timelines over 2 years to under a year Claimed reduction in pharma discovery program duration
Revenue engines three AI Drug Discovery, AI Bio-Defense, Immunotherapy
Parkinson’s subtypes three distinct types Newly announced Parkinson’s disease subtypes
Publication date Nov. 2025 Peer-reviewed Brief Report in Vaccines on DC immunotherapy

Market Reality Check

Price: $0.6624 Vol: Volume 156,999 vs 20-day ...
normal vol
$0.6624 Last Close
Volume Volume 156,999 vs 20-day average 158,869 (relative volume 0.99) shows typical activity into this update. normal
Technical Shares at 0.6624 are trading below the 200-day MA at 1.04, and remain far under the 52-week high of 1.66.

Peers on Argus

No peers from the Pharmaceutical Preparations sector were flagged in the momentu...

No peers from the Pharmaceutical Preparations sector were flagged in the momentum scanner, suggesting today’s modest 2.4% move reflects company-specific sentiment to the shareholder letter rather than a sector-wide rotation.

Historical Context

5 past events · Latest: Jan 27 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Jan 27 AI biodefense product Positive -2.0% Launch of Sentinel AI safeguard for blocking novel chemical weapon designs.
Jan 26 NIH AI expansion Positive -2.5% Completion of NIH STTR milestone and launch of AUD drug-discovery program.
Dec 18 AI partnership coverage Positive +4.7% Media feature highlighting Augusta platform and advancing AI partnership talks.
Dec 09 Parkinson’s subtyping Positive -8.7% Identification of three Parkinson’s subtypes and prioritized drug targets.
Nov 25 Oncology LOI & data Positive -15.0% First licensing LOI following complete tumor regression in cancer models.
Pattern Detected

Recent AI and oncology announcements have generally been positive in tone but were followed by mostly negative next-day price moves, indicating a pattern of selling into good news.

Recent Company History

Over the past few months, Lunai reported multiple AI and oncology milestones, including a biodefense safeguard launch on Jan 27, 2026, an NIH-supported AUD discovery program on Jan 26, 2026, and partnership-focused AI coverage in Dec 2025. Earlier, it disclosed new Parkinson’s subtypes and a licensing LOI after complete tumor regression data. Despite constructive narratives, four of the last five news days saw negative price reactions, so today’s shareholder letter arrives after a stretch of market skepticism toward similar positive updates.

Market Pulse Summary

This announcement outlines a completed commercial AI platform, three revenue-focused engines, and on...
Analysis

This announcement outlines a completed commercial AI platform, three revenue-focused engines, and ongoing negotiations in pharma and biodefense. In the past six months, similar AI, CNS, and oncology updates often preceded mixed or negative price reactions, including moves of -8.7% and -14.96%. Investors may focus on the transition from letters and pilots to concrete contracts, licensing deals, and clinical milestones, alongside the stock’s position well below its 200-day MA of 1.04.

Key Terms

in vivo, allogeneic, metastatic, phase 2
4 terms
in vivo medical
"Lunai rapidly tests its predictions in living systems using high-throughput in vivo models."
In vivo describes tests or experiments performed inside a living organism, such as an animal or human, to observe how a drug, device or biological process behaves in a real, functioning body. Investors care because in vivo results reveal safety, effectiveness and possible side effects that lab tests cannot, much like road-testing a prototype car in traffic rather than only on a bench — outcomes can strongly influence regulatory approval, clinical success and a company’s valuation.
allogeneic medical
"next-generation allogeneic dendritic cell (DC) immunotherapy achieved complete regression"
Allogeneic describes a process or material involving different individuals of the same species, such as cells, tissues, or organs donated from one person to another. It is important to investors because products or treatments based on allogeneic sources can enable scalable, off-the-shelf solutions, potentially reducing costs and increasing accessibility in healthcare and biotech industries.
metastatic medical
"metastatic pancreatic tumors in preclinical humanized mouse models"
Metastatic describes cancer that has spread from its original spot to other organs or tissues, like weeds moving from one garden bed into several others. For investors, metastatic disease matters because it often requires more complex, long-term treatments, larger clinical trials, and can drive demand for specialized drugs and diagnostics—factors that affect a drug’s development costs, regulatory risk, market size, and potential revenue.
phase 2 medical
"randomized Phase 2 metastatic colorectal cancer survival trial"
Phase 2 is the mid-stage clinical trial where a new drug or treatment is tested in a larger group of patients to see if it works and to keep checking safety after initial human testing. Think of it as a field test that proves whether a product actually delivers its promised benefit. Investors watch Phase 2 closely because its results strongly influence a medicine’s chances of reaching the market, the size of its potential sales, and the company’s valuation.

AI-generated analysis. Not financial advice.

SACRAMENTO, Calif. , Feb. 9, 2026 /PRNewswire/ --

Dear Shareholders,

We have completed our AI platform in the last 12 months and now it is commercial. Negotiations are moving forward with several pharmaceutical and drug discovery companies. Partnerships and collaborations are imminent. Why? -because Lunai Bioworks operates a closed loop AI system that is truly disruptive (and complementary) to current discovery platforms and that turns complex biology into real-world action in several ways with less cash burn and new revenue streams. Our Augusta platform starts with real biological signals from patients — genetic, molecular, and clinical data — and uses artificial intelligence to reverse-engineer diseases into biologically defined subgroups. Instead of asking, "What drug hits this target?" Lunai asks, "What biology is actually driving this subgroup of patients?"

Then comes the part most AI companies can't do.

Lunai rapidly tests its predictions in living systems using high-throughput in vivo models. That means its drug ideas aren't just computer outputs — they're biologically validated early, before hundreds of millions of dollars are spent. Our approach is designed to shorten pharmaceutical companies' current drug discovery programs from over 2 years to under a year, same them substantial money, and increase the probability of success.

In short:

Better data → smarter targets → earlier proof → lower risk.

Lunia has established three revenue driven engines

A) AI Drug Discovery: enabling pharmaceutical companies to understand disease biology and design better clinical trials, so promising therapies reach patients faster. We have established new fully owned company technologies for royalty-based partnerships.  While we have been focused on CNS diseases today, we launched a new AI oncology pilot with a clinical-stage partner using our Augusta platform to re-analyze data from a randomized Phase 2 metastatic colorectal cancer survival trial—work that can expand into a broader commercial relationship. We validated the foundation for this project in our work for Northwell Health and J&J (Janssen) using real-world hospital data from severe COVID-19 patients to show that different patient subgroups experience very different outcomes. This program demonstrated that analyzing large clinical datasets can reveal which patients are most likely to benefit from specific treatments, reinforcing the value of Lunai's precision-medicine approach.

B) AI Bio-Defense discoveries: using AI to detect emerging chemical/biological threats, understand their effects quickly, and help identify effective antidotes and countermeasures. This initiative applied our same technology stack in reverse. We already understand chemical toxicity which we use to screen out potential new drugs. For biodefense we can use our data in combination with other large data sets to identify new chemical weapons, test antidotes in our closed loop in vivo system, and can then identify countermeasures.  Our goal is to monetize this program through government contracts.

C) Immunotherapy: we reported that its next-generation allogeneic dendritic cell (DC) immunotherapy achieved complete regression of both primary and metastatic pancreatic tumors in preclinical humanized mouse models, and that these results were published in a peer-reviewed Brief Report in the journal Vaccines (Nov. 2025). We have recieved an LOI to license the therapy and are currently in discussion with several other companies for licensing other parts of our oncology platform.

Path A: AI Drug Discovery — making clinical trials smarter and more likely to succeed

Despite billions spent every year, drug development still fails more than it succeeds — especially in brain diseases like Alzheimer's, Parkinson's, alcohol use disorder, and epilepsy. The traditional model is slow, expensive, and based largely on educated guesswork. Companies pick a target, design a drug, and hope it works in humans years later. Most don't. The reason that no drugs have worked for what call Alzheimer's and Parkinsons is that the "one-size-fits-all" drugs were doomed from the start because the assumption was wrong. Each category of these CNS diseases is defined by a collection of different biological subtypes. By standardizing human data, and then using AI to reverse engineer the disease, Lunai traces the biology of each subtype to the related genes and then discovers potential drugs of interest and test them in living systems. We did this for Supernus Pharmaceuticals (NASDAQ: SUPN) by identifying the right epilepsy subgroup for their lead candidate (SPN_817) phase 2 clinical trial. We have recently announced three distinct types of Parkinsons and are working towards commercial deals in Parkinsons and Alzheimer's.

We announced today that we are also applying our drug discovery platform to cancer through the launch of a new oncology collaboration with a clinical-stage partner to analyze data from a randomized Phase 2 metastatic colorectal cancer trial. Cancer trials are expensive and difficult, and many fail late because the right patients weren't identified early enough. What we're doing in the program announced today is straightforward to explain:

We're using Augusta to learn more from existing clinical trial data—combining patient clinical data, AI-derived imaging signals, and long-term outcomes—to identify which patients benefit most from a new colon cancer drug and why. 

Our technology platform identifies biologically meaningful subgroups that are designed to enable our partner to:

  • enroll the right patients,

  • choose the right endpoints,

  • size trials more accurately,

  • and reduce costly and time consuming late-stage risk in programs targeting FDA submissions.  

This engagement begins as a defined pilot, with a clear path to expand into a multi-study commercial relationship based on results. For Lunai, this is the kind of near-term work that can translate into repeatable revenue while proving out our approach in real-world datasets. 

Path B: AI Bio Defense discoveries, - prevention, response, and countermeasures when time matters

In parallel, Lunai has built a biodefense platform aimed at a hard problem: modern threats can spread quickly, and decision-makers often need answers when information is incomplete.

Our biodefense stack is designed to support the full lifecycle: 

Sentinel (Prevention): AI systems designed to help detect and prevent the misuse of chemical and biological knowledge before harm occurs. 

Pathfinder (Response): rapid assessment of emerging threats—predicting potential toxicity, affected organ systems, and mechanisms of action. 

CounterAct (Countermeasures): identifying and validating antidotes, including rapid repurposing of approved drugs and development of novel countermeasures where none exist. 

Our objective is to help the U.S. and allied stakeholders prepare for elevated geopolitical risk, including the possibility of chemical weapons deployment, and to support evaluation, regulatory pathways, and potential stockpiling of effective countermeasures. 

We are actively in negotiation's with Government programs and with private-sector partners given the urgency and national security alignment of this work, and we intend to share more details in the near term.  

How these two paths fit together

Both efforts rely on the same core idea: AI should not just generate hypotheses, - we have put AI to work owning serious patents and IP today, so it delivers usable answers:

  • In healthcare: answers and tools that improve trial design and reduce development risk.

  • In biodefense: answers and tools that improve prevention, readiness, response, and treatment options under pressure.

What we're focused on next (near-term milestones)

Over the coming period, our focus is to:

  1. Advance late-stage commercial discussions across clinical data analytics, precision trial design, and biology-driven discoveries. 

  2. Finalizing biodefense funding conversations and defining the roadmap for Sentinel, Pathfinder, and CounterAct.  

  3. Complete a big new pharma Royalty partnership program on in-house immunotherapy technologies. 

We know many of you have read several Lunai announcements recently. The message we want to leave you with is simple: Lunai has established three immediately scalable revenue generating engines; AI powered drug discovery for CNS diseases and cancer and AI Bio Defense discoveries and tools, each designed for real-world impact, and each capable of creating long-term value and partnerships when implemented and executed with discipline; - our high level focus is driven by one thing only - creating value for our Shareholders. We are trying to fix one of the most expensive problems in medicine using a model that aligns perfectly with how drug development is evolving. When it executes, the gap between what it is today and what it could become is exactly how shareholder value is created.

Thank you for your continued support and confidence in Lunai's mission for a safer and better future for all. 

Sincerely,

David Weinstein

Chief Executive Officer

Lunai Bioworks, Inc. 

Forward-Looking Statements

This press release contains forward-looking statements, including statements regarding potential clinical impact, therapeutic benefit, development timelines, partnering strategy, and commercial value. These statements are subject to risks and uncertainties that may cause actual results to differ materially. Lunai Bioworks undertakes no obligation to update forward-looking statements, except as required by law.

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/lunai-bioworks-inc-issues-letter-to-shareholders-302682738.html

SOURCE Lunai Bioworks Inc.

FAQ

What does Lunai Bioworks (LNAI) announce about the Augusta AI platform on Feb 9, 2026?

The company says Augusta is commercial after 12 months and entering partner negotiations. According to Lunai Bioworks, Augusta uses patient genetic, molecular, and clinical data plus in vivo validation to create biologically defined subgroups for drug discovery and trial design.

How will Lunai Bioworks' LNAI oncology pilot affect metastatic colorectal cancer trials?

Lunai Bioworks says the pilot analyzes randomized Phase 2 trial data to identify responders and refine endpoints. According to Lunai Bioworks, the goal is to improve patient selection, endpoint choice, and trial sizing to reduce late‑stage failure risk and costs.

What evidence does LNAI provide for its immunotherapy program and licensing prospects?

Lunai Bioworks reports preclinical complete regression of primary and metastatic pancreatic tumors and a Nov 2025 Vaccines publication. According to Lunai Bioworks, it has received an LOI to license the therapy and is discussing additional licensing opportunities.

What are Lunai Bioworks' plans for its AI biodefense business (LNAI)?

The company plans Sentinel, Pathfinder, and CounterAct modules for prevention, rapid response, and countermeasures development. According to Lunai Bioworks, it intends to monetize biodefense through government contracts and private‑sector partnerships aligned with national security needs.

Does Lunai Bioworks (LNAI) report commercial revenues or timelines for partner deals?

The release cites active negotiations and pilots but does not disclose concrete revenue figures or binding contract timelines. According to Lunai Bioworks, pilots have clear paths to expand into multi‑study commercial relationships if results validate the approach.
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