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BriaCell Adds Penn Medicine’s Abramson Cancer Center as Clinical Site in Pivotal Phase 3 Breast Cancer Study

Key Takeaway: BriaCell Therapeutics has announced the addition of Penn Medicine's Abramson Cancer Center as a clinical trial site for its pivotal Phase 3 study on Bria-IMT in advanced breast cancer. This follows the activation of other notable sites and reflects growing interest in the trial. The study aims to evaluate the efficacy of Bria-IMT combined with an immune checkpoint inhibitor against standard treatments.
Price reaction · baseline $4.08 (2026-05-12 close) · hit after-hours · 2 other BCTX headline(s) in the window, move may be shared
day 0 close · peak
+2.5%

Market Sentiment Analysis

POSITIVE FACTORS

  • BriaCell adds a prestigious clinical site, enhancing study credibility.
  • Increased interest from leading cancer centers boosts enrollment momentum.
  • FDA Fast Track designation indicates potential for addressing unmet medical needs.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+44%
120-day peak, hindsight
Typical move
14.8%
average across 8 past catalysts
Cash runway
~7 mo
Medium dilution risk
Lead asset
SV-BR-1-GM
Phase 3 · Breast Cancer

Full Press Release Details

• Other recently activated sites include Indiana University Melvin and Bren Simon Comprehensive Cancer Center, University of Virginia (UVA) Comprehensive Cancer Center, Baptist Health South Florida, and SCRI Oncology Partners
PHILADELPHIA and VANCOUVER, British Columbia, May 13, 2026 (GLOBE NEWSWIRE) -- BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXL) (TSX: BCT) (“BriaCell” or the “Company”), a clinical-stage biotechnology company developing novel immunotherapies to transform cancer care is pleased to announce the addition of Penn Medicine’s Abramson Cancer Center, an internationally recognized cancer center, as a clinical trial site in BriaCell’s ongoing pivotal Phase 3 clinical study (Bria-ABC).
BriaCell has received increased interest from leading cancer centers and continued enrollment momentum following theindependent inclusionof its Phase 3 clinical trial inNature Medicine’sarticle, “Eleven clinical trials that will shape medicine in 2026”. The Phase 3 Bria-ABC study is evaluating BriaCell’s lead clinical candidate, Bria-IMT™, in combination with an immune checkpoint inhibitor versus physician’s choice of treatment inadvancedbreastcancer.
“We are pleased to partner with Penn Medicine’s Abramson Cancer Center, a world-renowned cancer institute, as a clinical site in BriaCell’s Phase 3 study,” stated Dr. William V. Williams, BriaCell’s President & CEO. “We look forward to working with the cancer experts at Penn to offer the Bria-IMT regimen to patients with metastatic breast cancer with the goal of making a meaningful difference for patients who have not responded to prior therapies.”
“The addition of Penn Medicine’s Abramson Cancer Center supports our goal of expanding access to BriaCell’s novel immunotherapy regimen to patients with metastatic breast cancer across the greater Philadelphia region,” said Dr. Giuseppe Del Priore, BriaCell’s Chief Medical Officer.
Other recently activated sites include:
• Indiana University Melvin and Bren Simon Comprehensive Cancer Center, Indianapolis, IN
• University of Virginia (UVA) Comprehensive Cancer Center, Charlottesville, VA
• Baptist Health South Florida, Coral Gables, FL
• SCRI Oncology Partners, Nashville, TN
An interim analysis of the pivotal Phase 3 study will be conducted after 144 patient events, defined as deaths, have occurred. Overall survival (OS) is the primary endpoint. The study compares the Bria-IMT regimen in combination with an immune checkpoint inhibitor versus physician’s choice of treatment in patients with advanced metastatic breast cancer. The Bria-IMT combination regimen has received FDA Fast Track designation, reflecting its potential to address a serious unmet medical need.
For additional information on BriaCell’s pivotal Phase 3 study, please visit ClinicalTrials.govNCT06072612.

About BriaCell Therapeutics Corp.

BriaCell is a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care. More information is available athttps://briacell.com/.

Safe Harbor

This press release contains “forward-looking statements” that are subject to substantial risks and uncertainties. All statements, other than statements of historical fact, contained in this press release are forward-looking statements. Forward-looking statements contained in this press release may be identified by the use of words such as “anticipate,” “believe,” “contemplate,” “could,” “estimate,” “expect,” “intend,” “seek,” “may,” “might,” “plan,” “potential,” “predict,” “project,” “target,” “aim,” “should,” “will,” “would,” or the negative of these words or other similar expressions, although not all forward-looking statements contain these words. Forward-looking statements, including those about the addition of a new clinical site in the ongoing pivotal Phase 3 clinical study of Bria‑IMT, and expectations regarding patient enrollment, interim analysis timing and the potential clinical benefits of the Bria‑IMT combination regimen, are based on BriaCell’s current expectations and are subject to inherent uncertainties, risks, and assumptions that are difficult to predict. Further, certain forward-looking statements, such as those are based on assumptions as to future events that may not prove to be accurate. These and other risks and uncertainties are described more fully under the heading “Risks and Uncertainties” in the Company’s most recent Management’s Discussion and Analysis, under the heading “Risk Factors” in the Company’s most recent Annual Information Form, and under “Risks and Uncertainties” in the Company’s other filings with the Canadian securities regulatory authorities and the U.S. Securities and Exchange Commission, all of which are available under the Company's profiles on SEDAR+ atwww.sedarplus.caand on EDGAR atwww.sec.gov. Forward-looking statements contained in this announcement are made as of this date, and BriaCell Therapeutics Corp. undertakes no duty to update such information except as required under applicable law.
Neither the Toronto Stock Exchange nor its Regulation Services Provider (as that term is defined in the policies of the Toronto Stock Exchange) accepts responsibility for the adequacy or accuracy of this release.

Company Contact:William V. Williams, MDPresident & CEO1-888-485-6340info@briacell.com

Investor Relations Contact:investors@briacell.com

Frequently Asked Questions

What is the focus of BriaCell's Phase 3 study?

The study evaluates BriaCell's Bria-IMT in combination with an immune checkpoint inhibitor for advanced breast cancer.

Which new site was added to BriaCell's clinical trial?

Penn Medicine's Abramson Cancer Center has been added as a clinical trial site.

What is the primary endpoint of the Phase 3 study?

Overall survival (OS) is the primary endpoint of the study.

What designation has the Bria-IMT regimen received?

The Bria-IMT regimen has received FDA Fast Track designation.

How many patient events are needed for interim analysis?

An interim analysis will occur after 144 patient events, defined as deaths.

Last updated: May 13, 2026