A Revolutionary
Way to Treat Cancer
10 million people died last year because the body does not easily recognize and kill cancer cells. However, the body is very good at killing diseases that it recognizes, such as measles. Our unique pre-clinical technology is designed to disguise cancer cells to look like measles and “tricks” the body into killing them.
  • $10.2 million in venture and crowdfunding previously raised. Our pre-clinical technology disguises cancer cells to look like well-immunized diseases, such as measles or chickenpox, activating immune memory so the body can attack them while leaving healthy cells unharmed.
    ‍
  • A world-class science team that has created multiple successful drugs that have gone to market.
    ‍
  • The global cancer immunotherapy market is expected to grow from $83 billion
in 2023 to $231 billion by 2031.*

Share Price
$2.25
Min Investment
$524.25
This Reg CF offering is made available through StartEngine Primary, LLC, a member of FINRA/SIPC. This investment is speculative, illiquid, and involves a high degree of risk, including the possible loss of your entire investment.
*Market projections are inherently uncertain and actual results may vary significantly.
$XXX,XXX.XX RAISED SO FAR
THE OPPORTUnity
A Universal Cancer
Treatment Platform
CancerVax is a pre-clinical biotech company developing a Universal Cancer Treatment Platform designed to target and eliminate cancer cells while leaving healthy cells unharmed. Our technology harnesses AI to DETECT, MARK, and KILL cancer cells by disguising them as known pathogens, like measles, to trigger a natural immune response.  Unlike most cancer drugs developed for a single cancer type, our platform is designed
to expand across multiple cancer indications.
Cancer Cell Detection​
A single injection contains billions of CancerVax nanoparticles.
Each nanoparticle is equipped with detectors to seek out cancer cells.
Step 1 Detection
The nanoparticles latch on to cells with matching surface protein.
Cancer Cell Marking
Cancer Cell Killing
*The graphics shown represent the Company's pre-clinical technology; FDA clearance is required before market use and may never be obtained.
Learn More About the future of cancer treatment
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THE PROBLEM
Cancer remains
one of the deadliest
diseases worldwide
Cancer claimed 10 million lives in 2023 alone (source: WHO). Traditional treatments like chemotherapy, radiation, and surgery come with severe side effects and inconsistent success rates. Despite advancements in immunotherapy, current therapies struggle to generate a strong or lasting immune response, leaving patients with limited options.

The body’s immune system is very good at killing foreign pathogens, such as the measles virus. Unfortunately, it’s not very good at killing cancer cells, because cancer cells were originally healthy cells. This is why cancer grows undetected by the immune system and is so hard to treat. 

OUR SOLUTION
CancerVax is pioneering a novel approach
Our pioneering approach tricks the immune system into identifying and attacking only cancer cells. Our technology is designed to force cancer cells to produce proteins that mimic those of well-immunized diseases, like measles or chickenpox. The immune system, already trained to fight these diseases, then rapidly eliminates the disguised cancer cells.  This innovative method leverages AI-powered detection and a
two-step targeting system, providing a precise and potentially
more effective treatment.
The two-step detection process shown is based on the Company's pre-clinical technology.
FDA clearance is required before market use and may never be obtained.
What Makes
CanceRVax Different
Traditional treatments like chemotherapy, radiation, and surgery involve long, difficult regimens that frequently damage healthy cells alongside cancerous ones, causing severe side effects and inconsistent outcomes for patients.  In contrast, modern immunotherapies like Keytruda (Merck) and Opdivo (Bristol Myers Squibb) attempt to activate the immune system but often produce only short-lived or weak responses.

CancerVax’s approach stands apart by not just stimulating the immune system but actively disguising cancer cells as a known pathogen. This method allows the immune system to respond immediately and aggressively, potentially leading to more effective and longer-lasting results than traditional immunotherapies.
OUR MARKET
Cancer is the second leading cause of death globally
With 1.95 million new cases diagnosed in the U.S. in 2023 (American Cancer Society). The global cancer immunotherapy market is projected to grow from $83 billion in 2023 to $231 billion by 2031* (Statista), reflecting increasing demand for innovative treatment options. CancerVax's platform approach
is designed to work across multiple cancer indications,
addressing one of the largest markets in medicine.
*Market projections are inherently uncertain and actual results may vary significantly.
OUR PROGRESS
Our Early-Stage Validation
CancerVax is a pre-clinical biotech company with successful in-vitro test results. Our nanoparticle-based cancer vaccine technology is being developed in collaboration with leading scientific teams and biotech partners, including Cytiva and Charles River. We aim to complete pre-IND animal studies to determine toxicity and efficacy of the above cancer treatments in 2026.*
‍
  • Filed multiple provisional patent applications with the USPTO, including an international PCT application filed in 2025, to protect the core technology of the Universal Cancer Treatment Platform
    ‍
  • Designed several Smart mRNAs for targeting multiple cancer types​​
    ‍
  • Lab tests successfully validated Smart mRNAs can work in actual cancer cells (Q1 2025)​
    ‍
  • Complete therapeutic nanoparticles for the above cancer indications (Q3 2025)
    ‍
  • Planned Completion of pre-IND animal studies to determine toxicity and efficacy of the above cancer treatments (2026)**
 * There can be no assurance these studies will occur or that they will be successful.
 ** Forward-looking statements based on management’s current expectations. Actual results may differ. 

OUR TRACTION
achievements & recognition
OUR DEVELOPMENT PARTNERS
Cytiva, owned by Danaher (NYSE: DHR, ~$170B+ market cap), formerly Precision NanoSystems, is a global leader in advancing and accelerating therapeutics.
Charles River (NYSE: CRL, ~$10B+ market cap) provides essential products and services to help pharmaceutical and biotechnology companies, government agencies and leading academic institutions around the globe accelerate their research and drug development efforts.
TriLink BioTechnologies, a Maravai LifeSciences company (NASDAQ: MRVI, ~$1-2B) is a global leader in nucleic acid and mRNA solutions. TriLink delivers unrivaled chemical and biological experience, CDMO services, and high-quality readymade and custom materials, including its patented CleanCap® mRNA capping technology.
Crown Bioscience is a division of multinational JSR Corporation (TYO: 4185). JSR Life Sciences provides specialized technology, products, materials, and services to biopharmaceutical companies and life science researchers.
Axis Bio, a division of QIMA Life Sciences, is a preclinical contract research organisation with specialist capabilities in oncology, inflammation and respiratory diseases. Services range from in vitro efficacy and mechanistic studies, to in vivo target engagement, with each study tailored to the unique requirements of the client.
OUR TEAM
Byron Horton Elton
President, CEO and Principal Accounting Officer
Byron Elton has served as our director since December 16, 2022 and our President and CEO since February 1, 2024. Mr. Elton is an experienced media and marketing executive with a proven record in pioneering new business development strategies and building top-flight marketing organizations. Since June 2018, he has been President of Elton Enterprises, Inc., which is involved in the wellness, fitness and health sectors. Mr. Elton is also the owner of certain StretchLab franchises. He is a co-founder since June 2017 of Pardue Associates, operating monsho, a brand-centric, creative communications agency focused on delivering results. From 2013 to 2017, Mr. Elton was a partner of Clear Search, an executive search firm. Prior to that, from 2009 until 2013, Mr. Elton served as President and Chief Executive Officer of Carbon Sciences, Inc., a cleantech company developing a technology to convert earth destroying carbon dioxide into a useful form. Mr. Elton previously served as Senior Vice President of Sales for Univision Online from 2007 to 2008. Mr. Elton also served for eight years as an executive at AOL Media Networks from 2000 to 2007, where his assignments included Regional Vice President of Sales for AOL and Senior Vice President of E-Commerce for AOL Canada. His broadcast media experience includes leading the ABC affiliate in Santa Barbara, California from 1995 to 2000 and the CBS affiliate in Monterrey, California from 1998 to 1999, in addition to serving as President of the Alaskan Television Network from 1995 to 1999. Mr. Elton studied Advertising and Marketing Communications at Brigham Young University.
George Edwin Katibah
PhD, Chief Scientific Officer
Expert in the discovery, development, and translation of novel therapies across diverse therapeutic modalities Part of teams that developed the first-in-human drug candidates, including small molecule STING agonists and personalized cancer neoantigen vaccine Co-authored more than 16 scientific papers and inventor on 3 issued U.S. patents and multiple pending applications Formerly Director of Discovery Biology at RAPT Therapeutics Formerly Senior Scientist and Head of Biochemistry at Aduro Biotech B.S. in Plant Sciences from the University of California, Santa Cruz PhD in Molecular and Cell Biology from the University of California, Berkeley"
Adam Grant
PhD, Principal Scientist
An inventor of the Company’s Universal Cancer Treatment platform. Expert computational biologist using next generation sequencing data to identify new drug targets and biomarkers of response to cancer therapeutics/ Formerly Bioinformatician at Xenter Medical Technologies/Formerly Computational Scientist at RAPT Therapeutics. Invented software to improve cancer antigen detection. Invented a gene-signature approach to select treatment for breast cancer. Received his B.S in Bioinformatics from Brigham Young University. Received his PhD in Cancer Biology with an emphasis in Bioinformatics from the University of Arizona
Sumant Ramachandra
MD, PhD, MBA, Chief Scientific Advisor
Sumant Ramachandra serves as an Independent Director on the Board of Lyell Immunopharma (“Lyell”), following Lyell’s acquisition of ImmPACT Bio (“ImmPACT”) in October 2024. As CEO of ImmPACT from November 2021 until its acquisition, he led capital raises, secured clinical grants, and built a team that achieved FDA clearance for three Investigational New Drug (IND) applications, established manufacturing capabilities, and advanced multiple clinical studies. In addition, Dr. Ramachandra currently serves as an advisor to private equity funds on companies in the pharmaceuticals, biotechnology, and medical devices/software spaces. Previously, Dr. Ramachandra served as Chief Science, Technology, and Medical Officer at Baxter International, starting in June 2017. He was also appointed President of Baxter Pharmaceuticals in 2019. Prior to Baxter, he held the role of Senior Vice President, Head of Research & Development, at Pfizer Essential Health, and served as Chief Scientific Officer at Hospira from 2008 until Pfizer acquired Hospira in 2015. Earlier in his career, Dr. Ramachandra held senior roles at Pfizer and Merck & Co., specializing in oncology, global product development, medical affairs, business development, and clinical pharmacology. He began his medical career as an intern and resident physician at Massachusetts General Hospital, Harvard Medical School. Dr. Ramachandra earned his undergraduate degree in biochemistry, a PhD in experimental pathology (with a focus on chronic lymphocytic leukemia), and an MD from Rutgers University. He also holds an MBA from the Wharton School, University of Pennsylvania.
Gordon Ringold
PhD, Strategic Advisor
Dr. Gordon Ringold is currently CEO of Quadriga BioSciences, a clinical phase cancer biotech company developing a novel L-type Amino Acid Transporter 1 (LAT1) for delivering chemotherapeutic agents across the blood brain barrier and into rapidly growing cancer cells. He is also the Founder and Executive Chairman of Maxymune, a biopharma company developing differentiated treatments to transform the lives of those affected by serious immunological diseases. He is currently on the board of directors of Okava Pharmaceuticals. From 1997 to 2015, he served in various capacities as Co-Founder and/or CEO of Maxygen, SurroMed, Alexza, and Alavita. From 1991 to 2000, Dr. Ringold was CEO and Scientific Director of Affymax Research Institute (acquired by Glaxo in 1995) where he managed the development of novel technologies to accelerate the pace of drug discovery; prior to that he was VP and Director of the Institute for Cancer and Developmental Biology at Syntex Corporation (1986-1991). Dr. Ringold received his Ph.D. in the laboratory of Dr. Harold Varmus (University of California, San Francisco), before joining the Stanford University School of Medicine, Department of Pharmacology (1978-1987). While on the Stanford faculty he invented technologies for manufacturing of recombinant proteins in mammalian cells, now widely used for production of dozens of therapeutic products and received the John J. Abel Award as the best Pharmacologist in the US under the age of 35. Dr. Ringold is an alumnus of Crown College, University of California, Santa Cruz, 1972.
Mark Davis
Senior Scientific Advisor
Mark M. Davis, PhD. is the Director of the Stanford Institute for Immunology, Transplantation and Infection (ITI), which has become an international leader in the development of transformative technologies and approaches to better understand the human immune system and its responses to infectious diseases and autoimmunity. He also serves as a Professor of Microbiology and Immunology at Stanford and is a Howard Hughes Medical Institute Investigator. Dr. Davis is well known for identifying the first T-cell receptor genes, which are responsible for T lymphocytes ability to “see” foreign pathogens, such as viruses, solving a major mystery in immunology at that time. He and his research group have made many subsequent discoveries about this type of molecule, demonstrating that T-cells are able to detect and respond to even a single molecule of their ligand-fragments of antigens bound to Major Histocompatibility Complex cell surface molecules. He also developed a novel way of labeling specific T lymphocytes according to the molecules that they recognize, and this procedure is now an important method in many clinical and basic studies of T-cell activity, as are other technologies developed by his group. According to research.com, Dr. Davis has authored over 680 publications with over 110,000 citations. He has received numerous awards and honors for his work, including memberships in the National Academy of Sciences, The National Academy of Medicine and the Royal Society.
George Kemble
Senior Scientific Advisor
George Kemble, PhD is a veteran biotech executive and scientist with a specialty focus in the areas of virology, vaccines and small molecule biologics. Dr. Kemble is currently the Chairman of the Board at Sagimet Biosciences Inc. (NASDAQ: SGMT), a clinical-stage biopharmaceutical company developing novel fatty acid synthase (FASN) inhibitors for cancer treatment, liver fibrosis, acne and other diseases. He joined Sagimet in August 2011 as its chief scientific officer and served as CEO from October 2015 until October 2022, when he transitioned to the role of executive chairman. In May 2025, Dr. Kemble moved into the role of non-executive Chair of the Board. At Sagimet, he directed medicinal chemistry, research, translational and CMC groups, and worked on several programs including the lead product candidate, denifanstat.Prior to Sagimet, Dr. Kemble served as the senior vice president of R&D and head of research at MedImmune, Inc., a subsidiary of AstraZeneca PLC. During his tenure, he was responsible for a large group of scientists dedicated to the research and development of programs across a number of therapeutic areas, including the launch of FluMist®, the first innovation in influenza vaccines in over 60 years. Dr. Kemble received a BS degree from the University of Santa Clara, a PhD from Stanford University and completed post-doctoral training at UCSF, where he worked on various human viruses.
Amit Indap
PhD, Scientific  Advisor
Expert in immuno-oncology involving mRNA vaccine development for cancer and COVID, CDx development using comprehensive genomic profiling of tumors, ctDNA analysis of clinical samples, NGS based antibody discovery, and single cell RNAseq analysis. Formerly Principal Scientist at Pfizer. Formerly Scientist at Good Start Genetics. Formerly Research Scientist at Human Longevity, Inc. Formerly Bioinformatics Scientist at Illumina. Formerly Senior Manager of Bioinformatics at Xencor. Received his B.S. in Molecular and Cellular Biology and minor in Computer Science From University of Arizona. Received his M.S. degree in bioinformatics from Medical College of Wisconsin. Received his PhD in Biology from Boston College
Jonathan Lakey
PhD, Scientific  Advisor
An inventor of the famous “Edmonton Protocol” for treating Type 1 diabetes. Extensive experience in the fields of oncology, stem cells, and organ transplantation. Currently Professor Emeritus at University of California, Irvine. Formerly Postdoctoral Fellow, Cryobiology Research Institute Indiana University Indianapolis. Formerly Postdoctoral Fellow, Clinical tissue banking University of Washington. Formerly Postdoctoral Fellow, Tissue banking/cryopreservation University of Alberta. Published over 495 scientific papers, 45 books, and over 500 scientific abstracts. Advisor to many biotech companies. Received his BS in Zoology/Animal Biology from University of Alberta. Received his MS in Zoology/Animal Biology from University of Alberta. Received his PhD of Islet transplantation, diabetes, and medical devices from University of Alberta
Matthew Spear
PhD, Scientific  Advisor
Expert in guiding the development and commercialization of new drugs, therapies, and biotech products as Chief Development Officer and Chief Medical Officer of biotech companies. Dr. Spear has been working in oncology and gene therapy research and development for over 30 years. Currently Chief Development Officer / Chief Medical Officer at Denovo Biopharma. Formerly Associate Professor on the faculty of the USC Keck School of Medicine, and the UCSD Medical School / UCSD Cancer Center where he managed a clinical practice, drug discovery/gene therapy research, and clinical trial programs for cancer. Formerly led multiple oncology clinical development programs at Pfizer. Formerly served as Chief Medical Officer and Senior Vice-President at Nereus Pharmaceuticals. Formerly Head of Oncology and Head of Biotherapeutics at Sunovion Pharmaceuticals. Formerly Vice-President at Incyte and Sangamo Therapeutics. Formerly Chief Medical Officer at Poseida Therapeutics developing multiple CAR-T cell and gene therapy products. Received a B.A. degree from the Johns Hopkins University. Received his M.D. degree from Stanford University
Steven Warner
PhD, Scientific  Advisor
Specializes in small molecule drug discovery, new screening platforms in drug discovery, and translational research focusing on cancer therapeutics. He is an expert in the discovery of novel cancer agents and has played integral roles in moving multiple compounds into clinical trials. Currently Senior VP and Head of US Research at Sumitomo Pharma America. Formerly Manager of Discovery Biology at SuperGen. Formerly Senior Manager of Drug Discovery at Huntsman Cancer Institute. Formerly VP of Drug Discovery at Tolero Pharmaceuticals. Received his B.S. in Biology from Brigham Young University. Received his PhD in Pharmaceutical Sciences from the University of Arizona
Carla Jo Miller
Controller and Director
Carla Miller has served as our director since August 2021 and was appointed as our Controller on February 1, 2024. Ms. Miller is an accounting and business manager with years of experience working for and consulting to technology and financial services companies. Since 2009, she has been the Business Manager of Digital Locations, Inc., a publicly traded company focused on wireless communication. Prior to that, she was an Accounting Manager at Hub International Insurance, a provider of property, casualty, risk management, life and health, employee benefits, investment, and wealth management products and services across North America. Ms. Miller graduated from Platt College in St. Joseph, MO where she studied Accounting and Business Management."
Bradford Douglas Pearce
Director
Brad Pearce’s professional journey is marked by diverse achievements across sports, business, and leadership. Mr. Pearce was appointed Director of the Board of CancerVax on October 2, 2024. Since February 2025, Mr. Pearce has served on the Board of the Southern California Junior Tennis Foundation. In July 2024, Mr. Pearce expanded his business pursuits by becoming a Managing Director at Two Harbors Capital, an investment fund. Since 2020, Mr. Pearce has served as Vice President of Marketing for a leading US staffing firm. His strategic insights contributed significantly to the company's growth, helping revenue surge from $300 million to nearly $1 billion by the end of 2024. From 2000 to 2019 Mr. Pearce served as the Head Men’s Tennis Coach at Brigham Young University (BYU). During his nearly two-decade tenure, he elevated the program to national prominence, leading the team to numerous accolades and securing the unique achievement of endowing all scholarships in the men’s tennis program, a first in college sports. Mr. Pearce’s career began as a professional tennis player from 1986 to 1995, during which he secured 10 titles, earned a US Davis Cup appearance, defeated six former world #1 players, and made a notable run to the Wimbledon singles quarterfinals. After retiring from professional tennis, Brad transitioned into the technology and sales and marketing sectors, working for various firms from 1996 to 1999. Mr. Pearce’s career progression illustrates his ability to thrive in diverse fields, leveraging his competitive spirit, leadership skills, and strategic thinking across both sports and business.
Andrew Lewis Van Noy
Chief Operations Officer
Andrew Van Noy is a seasoned executive having been CEO of multiple companies in both the public and private markets. His operational expertise includes fundraising, marketing, business management and investor relations. He joined the company in February of 2024.
CancerVax Terms
Overview
SHARE PRICE
$2.25
Valuation CAP
$109.44M
Deadline1
Sep 14, 2026 at 11:59 PM PDT
Funding Goal2
$20K – $3.94M
Breakdown
Min Investment
$524.25
Offering Type
Equity
MAX INVESTMENT
$3,935,533.50
Shares Offered
Common Stock
Min Number of Shares Offered
8,888
Max Number of Shares Offered
1,749,126
Maximum Number of Shares Offered subject to adjustment for bonus shares.  See bonus info below.
PERKS
earn bonus shares*
Your belief in our vision deserves more, and in recognition of that support, we are extending a limited-time package of premium perks.
Loyalty Bonus: Investors in CancerVax as of May. 1, 2026 at 12:59 AM MDT, including individuals waitlisted in our offering that ended on April 30, 2026, will receive 20% bonus shares.
Time-Based Perks (Available for the First 14 Days of the Offering Only):
$1,000+
EARLY Tier 1
Invest $1,000 or more within the first 14 days and receive 10% bonus shares.
Invest
$2,500+
EARLY Tier 2
Invest $2,500 or more within the first 14 days and receive 12% bonus shares.
Invest
$5,000+
EARLY Tier 3
Invest $5,000 or more within the first 14 days and receive 15% bonus shares.
Invest
$10,000+
EARLY Tier 4
Invest $10,000 or more and receive 18% bonus shares.
Invest
$25,000+
EARLY Tier 5
Invest $25,000 or more and receive 22% bonus shares.
Invest
$50,000+
EARLY Tier 6
Invest $50,000 or more and receive 25% bonus shares.
Invest
Amount-Based Perks (Available  Throughout the Offering):
$1,000+
Tier 1
Invest $1,000 or more and receive 5% bonus shares.
Invest
$2,500+
Tier 2
Invest $2,500 or more and receive 7% bonus shares.
Invest
$5,000+
Tier 3
Invest $5,000 or more and receive 10% bonus shares.
Invest
$10,000+
Tier 4
Invest $10,000 or more and receive 12% bonus shares.
Invest
$25,000+
Tier 5
Invest $25,000 or more and receive 15% bonus shares.
Invest
$50,000+
Tier 6
Invest $50,000 or more and receive 18% bonus shares.
Invest
$100,000+
Tier 7
Invest $100,000 or more and receive 20% bonus shares.
Invest
Mid-Campaign Flash Perks:
$2,500+
Day 35–40
Invest $2,500 or more and receive 8% bonus shares.
Invest
$2,500+
Day 60–65
Invest $2,500 or more and receive 8% bonus shares.
Invest
*In order to receive perks from an investment, one must submit a single investment in the same offering that meets the minimum perk requirement. Bonus shares from perks will not be granted if an investor submits multiple investments that, when combined, meet the perk requirement. All perks occur when the offering is completed.

Crowdfunding investments made through a self-directed IRA cannot receive non-bonus share perks due to tax laws. The Internal Revenue Service (IRS) prohibits self-dealing transactions in which the investor receives an immediate, personal financial gain on investments owned by their retirement account. As a result, an investor must refuse those non-bonus share perks because they would be receiving a benefit from their IRA account.

The 10% StartEngine Venture Club Bonus

This means eligible StartEngine shareholders will receive a 10% bonus for any shares they purchase in this offering. For example, if you buy 100 shares of Common stock at $2.25/ share you will receive 110 shares of Common Stock, meaning you'll own 110 shares for $225. Fractional shares will not be distributed and share bonuses will be determined by rounding down to the nearest whole share.

This 10% Bonus is only valid during the investor's eligibility period. Investors eligible for this bonus will also have priority if they are on a waitlist to invest and the company surpasses its maximum funding goal. They will have the first opportunity to invest should room in the offering become available if prior investments are canceled or fail.

Investors will receive the highest single bonus they are eligible for among the bonuses based on either the amount invested or the time of offering elapsed (if any). Eligible investors will also receive the Venture Club bonus and the Loyalty Bonus in addition to the aforementioned bonus.