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Anixa Biosciences Reports Updated Positive Survival Observations from Ongoing Phase 1 Trial of Lira-cel Ovarian Cancer CAR-T Therapy

Rhea-AI Impact
(High)
Rhea-AI Sentiment
(Positive)

Anixa Biosciences (NASDAQ: ANIX) reported updated survival and safety observations from its ongoing Phase 1 trial of lira-cel, a CAR-T therapy for recurrent ovarian cancer.

Multiple patients have lived well beyond the typical three‑to‑four‑month median survival, and preliminary safety data show no dose‑limiting toxicities, ICANS or significant CRS in the first three dose cohorts.

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AI-generated analysis. Not financial advice.

Positive

  • Multiple patients survived beyond expected 3–4 month median, including one at 28 months
  • Three patients survived 18, 17 and 11 months and remain alive with follow-up
  • No dose-limiting toxicities observed in the first three dose cohorts
  • No ICANS or significant cytokine release syndrome reported to date
  • All significant adverse events reported as unrelated to lira-cel administration
  • Next cohort planned at ~3x prior dose with added lymphodepletion

Negative

  • None.

News Market Reaction – ANIX

+1.00%
1 alert
+1.00% News Effect
+$996K Valuation Impact
$100.58M Market Cap
0.0x Rel. Volume

On the day this news was published, ANIX gained 1.00%, reflecting a mild positive market reaction. This price movement added approximately $996K to the company's valuation, bringing the market cap to $100.58M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

Median expected survival: 3–4 months Longest observed survival: 28 months Patients >1 year survival: 3 patients +5 more
8 metrics
Median expected survival 3–4 months Typical outcome for trial population based on disease and prior therapy
Longest observed survival 28 months Single patient survival duration after lira-cel treatment
Patients >1 year survival 3 patients Survived 18, 17 and 17 months after treatment
Additional survival durations 11, 11, 8, 7 months Four more patients exceeding expected median survival
Next cohort dose change 3x higher dose Planned lira-cel dose versus previous cohort
Dose-limiting toxicities 0 DLTs Observed in first three lira-cel dose cohorts
ICANS events 0 cases Immune Effector Cell-Associated Neurotoxicity Syndrome observed to date
CRS events 0 significant cases Significant Cytokine Release Syndrome observed to date

Market Reality Check

Price: $2.90 Vol: Volume 76,080 is about 0....
low vol
$2.90 Last Close
Volume Volume 76,080 is about 0.63x the 20-day average of 119,993, showing subdued trading ahead of this update. low
Technical Shares at $3.00 are trading below the 200-day MA of $3.36 and sit about 45% under the 52-week high.

Peers on Argus

ANIX was modestly higher by 1.35% while closely ranked biotech peers showed mixe...
1 Down

ANIX was modestly higher by 1.35% while closely ranked biotech peers showed mixed moves, from -6.43% (SRZN) to +20.7% (PYXS). Only one peer (FATE, -3.18%) appeared in momentum scans, reinforcing that today’s clinical update looks stock-specific rather than a broad sector rotation.

Previous Clinical trial Reports

5 past events · Latest: Apr 01 (Positive)
Same Type Pattern 5 events
Date Event Sentiment Move Catalyst
Apr 01 Breast vaccine Phase 1 Positive +5.4% Final Phase 1 breast cancer vaccine results and move toward Phase 2 manufacturing.
Mar 30 Ovarian CAR-T presentation Neutral -2.0% Announcement of upcoming ovarian CAR-T Phase 1 trial presentation at oncology meeting.
Dec 11 Breast vaccine data Positive -25.4% Positive final Phase 1 breast cancer vaccine data with strong immune responses.
Oct 07 Trial completion Positive +26.5% Completion of final patient visit in Phase 1 breast cancer vaccine trial.
Sep 08 Ovarian CAR-T dosing Positive +0.3% Completion of fourth ovarian CAR-T cohort with higher dosing and survival beyond median.
Pattern Detected

Clinical-trial headlines have often been received positively but with occasional sharp divergences, especially around major breast cancer vaccine readouts.

Recent Company History

Across recent clinical trial announcements, Anixa has repeatedly reported encouraging early-stage oncology data. Breast cancer vaccine updates have shown primary endpoints met with strong immune responses, while ovarian CAR-T disclosures have highlighted dose escalation and survival beyond expectations. Market reactions have ranged from a +26.46% jump on trial completion to a -25.42% drop on positive Phase 1 data, underscoring inconsistent trading responses to otherwise constructive clinical progress.

Historical Comparison

+1.0% avg move · Clinical-trial headlines for ANIX over the past year saw an average move of about 0.97%, with reacti...
clinical trial
+1.0%
Average Historical Move clinical trial

Clinical-trial headlines for ANIX over the past year saw an average move of about 0.97%, with reactions ranging from steep gains to sharp selloffs on otherwise positive data.

Historically, ANIX’s clinical-trial news has traced a path from Phase 1 breast cancer vaccine completion and final data toward a planned Phase 2, while ovarian CAR-T updates have advanced dose-escalation cohorts and highlighted patients living beyond expected survival benchmarks.

Regulatory & Risk Context

Active S-3 Shelf
Shelf Active
Active S-3 Shelf Registration 2025-09-10

ANIX has an effective Form S-3 shelf filed on 2025-09-10, allowing issuance of various securities including common and preferred stock, warrants, and units. The filing details net tangible book value of $0.46 per share as of July 31, 2025 and outlines potential dilution metrics and offering expenses, indicating flexibility to raise additional capital when needed.

Market Pulse Summary

This announcement highlights updated Phase 1 data for lira-cel, showing several recurrent ovarian ca...
Analysis

This announcement highlights updated Phase 1 data for lira-cel, showing several recurrent ovarian cancer patients living well beyond the usual 3–4 month median survival, including one at 28 months, with no dose-limiting toxicities, ICANS or significant CRS reported. In context of ANIX’s broader oncology pipeline and prior clinical updates, investors may watch upcoming higher-dose cohorts, survival durability, and any future capital-raising under the existing Form S-3 shelf.

Key Terms

car-t, follicle-stimulating hormone receptor, autologous t cells, chimeric receptor, +4 more
8 terms
car-t medical
"ongoing Phase 1 clinical trial of liraltagene autoleucel, or lira-cel, the Company's ... CAR-T therapy being developed"
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.
follicle-stimulating hormone receptor medical
"the Company's follicle-stimulating hormone receptor ("FSHR")-targeted CAR-T therapy"
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.
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
"autologous T cells genetically engineered with a chimeric receptor to target"
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.
intraperitoneal medical
"All doses have been administered successfully by the intraperitoneal ("IP") route."
A treatment or substance described as intraperitoneal is delivered into the peritoneal cavity, the fluid‑filled space lined by membranes inside the abdomen that surrounds the organs. For investors, this matters because the delivery route affects how quickly and evenly a drug acts, the risks and side effects, clinical trial designs, manufacturing and administration costs, and ultimately how practical and sellable a therapy may be compared with pills or injections given elsewhere in the body.
immune effector cell-associated neurotoxicity syndrome medical
"There have been no observations of Immune Effector Cell-Associated Neurotoxicity Syndrome ("ICANS")"
immune effector cell-associated neurotoxicity syndrome (ICANS) is a brain-related side effect that can occur after treatments that activate powerful immune cells, such as engineered cell therapies. It can cause confusion, speech problems, seizures or coma when the immune response unintentionally harms brain function; think of an overenthusiastic security system that starts damaging the house it’s protecting. Investors care because ICANS affects clinical trial results, regulatory approvals, product labeling, treatment adoption, monitoring costs and potential liability, all of which influence a therapy’s commercial value.
cytokine release syndrome medical
"or significant Cytokine Release Syndrome ("CRS")."
An intense immune overreaction in which the body's defense system releases a large surge of signaling proteins, causing fever, low blood pressure, breathing trouble or organ stress; imagine the immune system's alarm going into overdrive and flooding the body with emergency responders. Investors care because this side effect can slow or block regulatory approval, increase clinical trial costs and liabilities, limit how widely a therapy can be used, and therefore affect a drug's market value and sales potential.
lymphodepletion medical
"expected to evaluate a dose approximately three times higher ... and to include lymphodepletion with cyclophosphamide and fludarabine."
Lymphodepletion is a short medical treatment that lowers a patient’s lymphocytes, the immune cells that can interfere with certain cell-based therapies, to create a more supportive environment for the new therapy to work. Think of it like clearing a crowded garden bed before planting seeds: by temporarily reducing competing cells, the engineered therapy can take hold more effectively. Investors watch lymphodepletion because it affects clinical trial results, safety profiles, treatment adoption, and overall commercial potential.

AI-generated analysis. Not financial advice.

Multiple patients have survived substantially beyond expected median survival, including one
patient who survived 28 months and several patients who remain alive with continued follow-up

Lira-cel clinical trial featured in presentation at the International Society for Cell & Gene Therapy
2026 Annual Meeting

SAN JOSE, Calif., May 11, 2026 /PRNewswire/ -- Anixa Biosciences, Inc. ("Anixa" or the "Company") (NASDAQ: ANIX), a biotechnology company focused on the treatment and prevention of cancer, today announced updated positive survival observations from its ongoing Phase 1 clinical trial of liraltagene autoleucel, or lira-cel, the Company's follicle-stimulating hormone receptor ("FSHR")-targeted CAR-T therapy being developed for the treatment of recurrent ovarian cancer.

Updated data were presented on May 7, 2026, at the International Society for Cell & Gene Therapy ("ISCT") 2026 Annual Meeting by Cheryl Cox, MHA, Operations Director of the Cell Therapies and Gene Expression Engineering Facility at Moffitt Cancer Center. The 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," reviewed the trial design, objectives and current clinical status of Anixa's ongoing Phase 1 trial of lira-cel.

Several trial participants have lived significantly beyond their median expected survival of three to four months, based on disease stage and prior therapy history. One patient survived 28 months following treatment, three patients have survived greater than one year following treatment, at 18, 17 and 17 months, respectively, and four additional patients have survived 11, 11, 8 and 7 months, respectively. Three of the patients who reached 18, 17 and 11 months, respectively, remain alive, and one additional patient who was treated more recently is also currently alive.

Preliminary safety observations presented at ISCT include:

  • No dose-limiting toxicities ("DLTs") have been encountered in the first three dose cohorts.
  • All doses have been administered successfully by the intraperitoneal ("IP") route.
  • There have been no observations of Immune Effector Cell-Associated Neurotoxicity Syndrome ("ICANS") or significant Cytokine Release Syndrome ("CRS").
  • All significant adverse events observed to date have been unrelated to lira-cel administration.

Dr. Amit Kumar, Chairman and Chief Executive Officer of Anixa, stated, "The updated survival observations from this ongoing Phase 1 trial continue to be encouraging, particularly given the advanced disease status and limited treatment options for patients with recurrent ovarian cancer. While this remains an early-stage study, lira-cel has continued to demonstrate a favorable preliminary safety profile, with no dose-limiting toxicities, ICANS or CRS observed in the first three dose cohorts. We believe these findings support continued dose escalation and clinical evaluation."

Dr. Kumar continued, "We look forward to treating patients in the next dose cohort, which is expected to evaluate a dose approximately three times higher than the previous cohort and to include lymphodepletion with cyclophosphamide and fludarabine. This approach may create a more favorable environment for CAR-T cell expansion, persistence and activity."

About Lira-cel, Anixa's CAR-T Therapy for Recurrent Ovarian Cancer
Liraltagene autoleucel, or lira-cel, is Anixa's investigational autologous CAR-T therapy designed to target the follicle-stimulating hormone receptor ("FSHR"), which Anixa believes represents a unique CAR-T target in ovarian cancer. FSHR is selectively expressed on ovarian cells, tumor vasculature and certain cancer cells, but not in most healthy tissue. The ongoing Phase 1 trial (ClinicalTrials.gov Identifier: NCT05316129) is enrolling adult women with recurrent ovarian cancer who have progressed after at least two prior therapies.

The trial is designed to evaluate the safety and tolerability of lira-cel, determine the maximum tolerated dose, and assess preliminary evidence of clinical activity.

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-updated-positive-survival-observations-from-ongoing-phase-1-trial-of-lira-cel-ovarian-cancer-car-t-therapy-302767413.html

SOURCE Anixa Biosciences, Inc.

FAQ

What did Anixa Biosciences (NASDAQ: ANIX) report from its Phase 1 lira-cel ovarian cancer trial on May 11, 2026?

Anixa Biosciences reported updated survival and safety observations from its ongoing Phase 1 trial of lira-cel in recurrent ovarian cancer. According to Anixa, several patients have lived beyond expected median survival, and early safety data show no dose-limiting toxicities, ICANS or significant CRS.

How have survival outcomes compared to expected median survival in Anixa’s lira-cel Phase 1 ovarian cancer trial (ANIX)?

Patients in Anixa’s lira-cel trial have lived beyond the typical three-to-four-month median survival expectation. According to Anixa, one patient survived 28 months, three patients exceeded one year, and several additional patients reached 7–18 months, with some still alive under continued follow-up.

What preliminary safety results were observed in the Phase 1 lira-cel CAR-T trial for recurrent ovarian cancer?

Preliminary safety data indicate a favorable early profile for lira-cel in recurrent ovarian cancer. According to Anixa, no dose-limiting toxicities, ICANS or significant cytokine release syndrome have been seen in the first three dose cohorts, and significant adverse events were reported as unrelated to lira-cel.

How is lira-cel administered in Anixa Biosciences’ Phase 1 ovarian cancer study?

Lira-cel is being administered by the intraperitoneal route in the Phase 1 trial. According to Anixa, all doses across the first three cohorts have been successfully delivered intraperitoneally, supporting this localized administration approach for patients with recurrent ovarian cancer enrolled in the study.

What are the next steps for Anixa’s lira-cel Phase 1 trial in recurrent ovarian cancer?

The next trial cohort will evaluate a higher lira-cel dose and add lymphodepletion. According to Anixa, this cohort is expected to test a dose about three times higher than the previous cohort and include cyclophosphamide and fludarabine to support CAR-T expansion and persistence.

How many long-term survivors have been reported in Anixa’s lira-cel ovarian cancer trial so far?

Several patients have shown longer-term survival following lira-cel treatment. According to Anixa, one patient survived 28 months, three survived more than one year (18, 17 and 17 months), and four additional patients survived 7–11 months, with multiple individuals still alive under follow-up.