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Anixa Biosciences Reports Positive Data from Completed Breast Cancer Vaccine Phase 1 Trial and Positive Survival Observations from Ongoing CAR-T Phase 1 Trial at New York Academy of Sciences' Frontiers in Cancer Immunotherapy Symposium

(Positive)

Anixa Biosciences (NASDAQ: ANIX) reported updated clinical data for its breast cancer vaccine and ovarian cancer CAR‑T therapy presented at the New York Academy of Sciences' Frontiers in Cancer Immunotherapy symposium.

The completed Phase 1 breast cancer vaccine trial met all major primary endpoints, showed the vaccine was safe and well tolerated at the maximum tolerated dose, and induced protocol-defined immune responses in 74% of participants. The ongoing Phase 1 trial of ovarian cancer CAR‑T therapy lira-cel reported survival observations of multiple patients living over one year after treatment. Both programs are being developed with Cleveland Clinic and Moffitt Cancer Center, and presentations are available on Anixa's investor events webpage.

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AI-generated analysis. How Rhea-AI works. Not financial advice.

Positive

  • Breast cancer vaccine Phase 1 met all major primary endpoints
  • Vaccine generated protocol-defined immune responses in 74% of participants
  • Breast cancer vaccine was safe and well tolerated at maximum tolerated dose
  • Ongoing lira-cel Phase 1 shows multiple patients living over one year post-treatment
  • Clinical programs advanced with Cleveland Clinic and Moffitt Cancer Center collaborations

Negative

  • None.

News Market Reaction – ANIX

+6.49% 2.3x vol
15 alerts
+6.49% News Effect
+7.9% Peak Tracked
-13.6% Trough Tracked
+$5M Valuation Impact
$89.14M Market Cap
2.3x Rel. Volume

On the day this news was published, ANIX gained 6.49%, reflecting a notable positive market reaction. Argus tracked a peak move of +7.9% during that session. Argus tracked a trough of -13.6% from its starting point during tracking. Our momentum scanner triggered 15 alerts that day, indicating notable trading interest and price volatility. This price movement added approximately $5M to the company's valuation, bringing the market cap to $89.14M at that time. Trading volume was elevated at 2.3x the daily average, suggesting notable buying interest.

Data tracked by StockTitan Argus on the day of publication.

What This Means

The stock moved +6.5% in the session following this news. A strong positive reaction aligns with pri...
Analysis

The stock moved +6.5% in the session following this news. A strong positive reaction aligns with prior enthusiasm around Phase 1 data, where several clinical updates drove double‑digit moves. Ongoing ATM and shelf capacity and trial risk could still cap follow‑through if future data or financing disappoints.

Key Figures

Immune response rate: 74% Survival duration: over one year
2 metrics
Immune response rate 74% Phase 1 breast cancer vaccine trial participants with protocol-defined immune responses
Survival duration over one year Multiple lira-cel Phase 1 ovarian cancer patients living beyond one year post-treatment

Previous Clinical trial Reports

5 past events · Latest: May 11 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 11 Lira-cel survival update Positive +1.0% Phase 1 ovarian CAR-T data showing encouraging survival and clean safety profile.
Apr 01 Breast vaccine Phase 2 prep Positive +5.4% Positive Phase 1 breast vaccine results and selection of cGMP manufacturer for Phase 2.
Mar 30 Lira-cel trial presentation Neutral -2.0% Announcement of upcoming ovarian CAR-T Phase 1 trial presentation and study design overview.
Dec 11 Breast vaccine Phase 1 data Positive -25.4% Final Phase 1 breast vaccine data with endpoints met and 74% immune response rate.
Oct 07 Breast trial completion Positive +26.5% Completion of final patient visit in Phase 1 breast cancer vaccine trial funded by DoD.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Clinical trial updates have often led to positive moves, though one major selloff shows reactions can be volatile and inconsistent.

Historical Comparison

+1.1% avg move · Clinical-trial headlines have produced an average move of about 1.1% for ANIX across five events. To...
clinical trial
+1.1%
Average Historical Move clinical trial

Clinical-trial headlines have produced an average move of about 1.1% for ANIX across five events. Today’s Phase 1 updates appear less favorably received versus that generally positive historical response.

Tag-specific history shows steady progression: repeated positive Phase 1 breast vaccine readouts, movement toward Phase 2 manufacturing, and ongoing dose-escalation and survival updates for lira-cel in ovarian cancer.

Regulatory & Risk Context

Active S-3 Shelf · Short Interest: 3.2%
Shelf Active
Short Interest
3.2% of float
0% 15% 30%+
low as of 2026-05-29 Days to cover: 10.82

Reported short interest appears relatively low, suggesting limited squeeze potential but also less downside cushioning from short-covering during periods of selling pressure.

Active S-3 Shelf Registration 2025-09-10

An active Form S-3 shelf filed in 2025 allows Anixa to issue various securities over time, which, if utilized, could introduce future equity dilution despite no usage so far.

Key Terms

car-t, autologous t cells, chimeric receptor, follicle-stimulating hormone receptor, +1 more
5 terms
car-t medical
"Ovarian cancer CAR-T therapy, lira-cel, presentation highlights positive survival observations"
CAR-T is a type of cancer therapy that reprograms a patient’s own immune cells to seek and destroy specific cancer cells, like teaching guard dogs a new scent to track intruders. It matters to investors because CAR-T treatments can command high prices, drive strong revenue for successful developers, and carry regulatory and manufacturing risks that can sharply affect a company’s valuation and long-term growth prospects.
autologous t cells medical
"An infusion of Autologous T cells Genetically Engineered with a Chimeric Receptor"
Autologous T cells are a patient’s own immune cells taken out, sometimes modified or multiplied in a lab, and then returned to help fight disease. Think of it as customizing and strengthening a person’s own soldiers rather than bringing in outsiders; for investors this signals highly personalized, potentially powerful therapies but also complex manufacturing, higher costs, and regulatory hurdles that affect commercial scale and profitability.
chimeric receptor medical
"T cells Genetically Engineered with a Chimeric Receptor to Target the Follicle-Stimulating"
A chimeric receptor is an engineered protein made by stitching together parts from different natural receptors so a cell can recognize new signals or respond in new ways—think of attaching a new sensor to an existing machine. For investors, these receptors are central to many cutting‑edge therapies because they can reprogram cells to target disease; their success affects drug pipelines, regulatory reviews, manufacturing complexity, and the commercial potential of biotech companies.
follicle-stimulating hormone receptor medical
"to Target the Follicle-Stimulating Hormone Receptor in Patients with Recurrent Ovarian Cancer"
A protein on the surface of certain reproductive cells that binds follicle-stimulating hormone (FSH) and converts that signal into a cellular response, like a lock accepting a key or an antenna receiving a message. Drugs or tests that activate, block or measure this receptor can change fertility outcomes, hormone production or growth of some tumors, so it’s a common target for therapies and diagnostics that can create clinical progress and commercial value for investors.
maximum tolerated dose medical
"the vaccine was safe and well tolerated at the maximum tolerated dose based on safety"
Maximum tolerated dose is the highest amount of a substance, such as a medication or chemical, that can be used without causing unacceptable side effects or harm. It’s like finding the maximum speed you can drive without risking a ticket or accident. For investors, understanding this concept helps gauge how much risk or exposure is safe or sustainable in a given situation.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Breast cancer vaccine presentation includes final Phase 1 data showing all major primary endpoints were met and protocol-defined immune responses in 74% of participants

Ovarian cancer CAR-T therapy, lira-cel, presentation highlights positive survival observations from ongoing Phase 1 clinical trial

Presentations highlight Anixa's clinical progress and collaborations with leading cancer research institutions, including Cleveland Clinic and Moffitt Cancer Center

SAN JOSE, Calif., June 26, 2026 /PRNewswire/ -- Anixa Biosciences, Inc. ("Anixa" or the "Company") (NASDAQ: ANIX), a biotechnology company focused on the treatment and prevention of cancer, today announced that its two clinical-stage immunotherapy programs were presented at the New York Academy of Sciences' Frontiers in Cancer Immunotherapy symposium this week.

The presentations highlighted Anixa's breast cancer vaccine, being developed in collaboration with Cleveland Clinic, which recently completed a Phase 1 clinical trial in which all major primary endpoints were met and protocol-defined immune responses were generated in 74% of participants, and Anixa's ovarian cancer CAR-T therapy, liraltagene autoleucel, or lira-cel, which is being evaluated in an ongoing Phase 1 clinical trial in collaboration with Moffitt Cancer Center.

Both presentations may be accessed on the Events page of Anixa Biosciences' website: https://ir.anixa.com/events.

"Presenting both of our clinical-stage immunotherapy programs at this symposium was an important opportunity to highlight the progress of our pipeline and the strength of the collaborations supporting these programs," said Dr. Amit Kumar, Chairman and CEO of Anixa Biosciences. "Our breast cancer vaccine and ovarian cancer CAR-T therapy are being advanced with leading clinical and scientific institutions, and we believe these presentations underscore the potential of Anixa's approach to treating and preventing cancer."

The Company's breast cancer vaccine presentation, titled "Phase I Trial of an Alpha-Lactalbumin (aLA) Vaccine for Breast Cancer," was given by Dr. Emily Esakov Rhoades, FDA/IND Trial Program Manager, Cleveland Clinic Cancer Institute. The presentation reported final Phase 1 findings for the investigational vaccine, including that all major primary endpoints were met, the vaccine was safe and well tolerated at the maximum tolerated dose based on safety and tolerability, and protocol-defined immune responses were elicited in 74% of trial participants.

The Company's lira-cel presentation, titled "A Phase I Clinical Trial of an Infusion of Autologous T cells Genetically Engineered with a Chimeric Receptor to Target the Follicle-Stimulating Hormone Receptor in Patients with Recurrent Ovarian Cancer," was given by Dr. Pamela D. Garzone, Chief Development Officer of Anixa Biosciences. The presentation reported the clinical trial design and objectives, as well as the current status of Anixa's ongoing Phase 1 clinical trial of lira-cel, including survival observations of multiple patients living over one year past treatment.

About Anixa's Breast Cancer Vaccine
Anixa's breast cancer vaccine represents a novel approach to the prevention and treatment of breast cancer. The vaccine is based on immunizing against human α-lactalbumin, a protein associated with lactation that is highly expressed in certain types of breast cancer. This "retired" protein vaccine strategy aims to selectively prime the immune system to prevent tumor formation while avoiding harm to normal tissue.

About Lira-cel, Anixa's CAR-T Therapy for Recurrent Ovarian Cancer
Liraltagene autoleucel, or lira-cel, uniquely targets the follicle-stimulating hormone receptor (FSHR), which is selectively expressed on ovarian and testis cells, tumor vasculature, and certain cancer cells, but not in other healthy tissue. The ongoing Phase 1 trial (ClinicalTrials.gov NCT05316129) is enrolling adult women with recurrent ovarian cancer who are platinum resistant and have progressed after at least two prior therapies.

About Anixa Biosciences, Inc.
Anixa is a clinical-stage biotechnology company focused on the treatment and prevention of cancer. Anixa's therapeutic portfolio consists of liraltagene autoleucel, or lira-cel, an ovarian cancer immunotherapy being developed in collaboration with Moffitt Cancer Center, which uses a novel type of CAR-T, known as chimeric endocrine receptor-T cell (CER-T) technology. This technology is differentiated from other cell therapies as the natural ligand of the FSHR receptor, FSH, binds to the FSHR receptor on the tumor cell instead of an antibody fragment. Moffitt is a world leader in cancer immunotherapy treatments, pioneering next-generation cell therapies such as CAR-T, and tumor infiltrating lymphocytes (TILs) to harness the power of the immune system. The Company's vaccine portfolio includes vaccines being developed in collaboration with Cleveland Clinic to treat and prevent breast cancer and ovarian cancer, as well as additional cancer vaccines to address many intractable cancers, including high incidence malignancies in lung, colon, and prostate. These vaccine technologies focus on immunizing against "retired" proteins that have been found to be expressed in certain forms of cancer. The breast and ovarian cancer vaccines were developed at Cleveland Clinic and exclusively licensed to Anixa. Cleveland Clinic is entitled to royalties and other commercialization revenues from the Company related to these vaccine technologies. Anixa's unique business model of partnering with world-renowned research institutions on all stages of development allows the Company to continually examine emerging technologies in complementary fields for further development and commercialization. To learn more, visit www.anixa.com or follow Anixa on LinkedIn, X, Facebook and YouTube.

Forward-Looking Statements
Statements that are not historical fact may be considered forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Forward-looking statements are not statements of historical facts, but rather reflect Anixa's current expectations concerning future events and results. We generally use the words "believes," "expects," "intends," "plans," "anticipates," "likely," "will" and similar expressions to identify forward-looking statements. Such forward-looking statements, including those concerning our expectations, involve risks, uncertainties and other factors, some of which are beyond our control, which may cause our actual results, performance or achievements, or industry results, to be materially different from any future results, performance, or achievements expressed or implied by such forward-looking statements. These risks, uncertainties and factors include, but are not limited to, those factors set forth in "Item 1A - Risk Factors" and other sections of our most recent Annual Report on Form 10-K as well as in our Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. We undertake no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. You are cautioned not to unduly rely on such forward-looking statements when evaluating the information presented in this press release.

Contact:
Mike Catelani
President, COO & CFO
mcatelani@anixa.com
408-708-9808

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/anixa-biosciences-reports-positive-data-from-completed-breast-cancer-vaccine-phase-1-trial-and-positive-survival-observations-from-ongoing-car-t-phase-1-trial-at-new-york-academy-of-sciences-frontiers-in-cancer-immunotherapy-symp-302811349.html

SOURCE Anixa Biosciences, Inc.

FAQ

What Phase 1 results did Anixa Biosciences (NASDAQ: ANIX) report for its breast cancer vaccine?

Anixa reported that its Phase 1 breast cancer vaccine trial met all major primary endpoints and showed safety at the maximum tolerated dose. According to Anixa, protocol-defined immune responses were observed in 74% of participants, supporting continued clinical development with Cleveland Clinic.

How effective was Anixa's breast cancer vaccine in generating immune responses in the Phase 1 trial?

Anixa reported protocol-defined immune responses in 74% of breast cancer vaccine trial participants. According to Anixa, the completed Phase 1 study also met all major primary endpoints and showed the investigational alpha-lactalbumin vaccine was safe and well tolerated at the maximum tolerated dose.

What survival observations were reported for Anixa's ovarian cancer CAR-T therapy lira-cel Phase 1 trial?

Anixa reported survival observations of multiple lira-cel Phase 1 patients living over one year after treatment. According to Anixa, the ongoing trial of this autologous CAR-T therapy in recurrent ovarian cancer is being conducted with Moffitt Cancer Center and continues to enroll and evaluate patients.

What is lira-cel in the Anixa (ANIX) ovarian cancer program and how is it being tested?

Lira-cel is Anixa's autologous T cell therapy genetically engineered with a chimeric receptor targeting follicle-stimulating hormone receptor. According to Anixa, it is under evaluation in an ongoing Phase 1 clinical trial for patients with recurrent ovarian cancer at Moffitt Cancer Center.

How did Anixa describe the safety profile of its breast cancer vaccine in the Phase 1 study?

Anixa indicated the breast cancer vaccine was safe and well tolerated at the maximum tolerated dose in Phase 1. According to Anixa, all major primary endpoints were met and predefined immune responses occurred in 74% of participants, supporting further investigation.

Where can investors access Anixa Biosciences' June 2026 cancer immunotherapy presentations?

Investors can access Anixa’s breast cancer vaccine and lira-cel CAR-T presentations on the Events page of its investor relations website. According to Anixa, these materials summarize Phase 1 trial design, primary endpoints, safety findings, immune responses, and survival observations from ongoing and completed studies.