Press Releases May 12, 2026 07:30 AM

BriaCell Phase 3 Bria-IMT™ Study Enrollment Surpasses 230 Patients

BriaCell enrolls over 230 patients in Phase 3 Bria-IMT trial for metastatic breast cancer, aiming for 2026 interim data

By Hana Yamamoto BCTX

BriaCell Therapeutics Corp. reports that over 230 patients have been enrolled in its pivotal Phase 3 Bria-ABC study testing Bria-IMT in combination with an immune checkpoint inhibitor for metastatic breast cancer. The study, which has FDA Fast Track designation, expects to report interim topline overall survival data in 2026, potentially supporting full approval of Bria-IMT. Continued strong site and patient interest enhances enrollment momentum.

BriaCell Phase 3 Bria-IMT™ Study Enrollment Surpasses 230 Patients
BCTX

Key Points

  • Enrollment in Phase 3 Bria-ABC study surpasses 230 patients with over 315 screened, demonstrating strong clinical and patient interest.
  • Bria-IMT combination regimen has FDA Fast Track designation, with topline interim data due in 2026 potentially supporting full drug approval.
  • The study's primary endpoint is overall survival, assessing Bria-IMT plus immune checkpoint inhibitor versus physician's choice in metastatic breast cancer treatment.
  • Impacted sectors include biotechnology, pharmaceuticals, and healthcare, specifically oncology therapeutics.
  • Over 315 patients screened and over 230 patients enrolled in BriaCell’s pivotal Phase 3 Bria-ABC study of Bria-IMT plus immune checkpoint inhibitor in metastatic breast cancer 
  • Enrollment momentum continues with strong clinical site and patient interest
  • Interim topline data expected in 2026
  • Positive interim overall survival results could support potential approval of Bria-IMT in metastatic breast cancer
  • BriaCell’s Bria-IMT combination regimen continues under FDA Fast Track designation

PHILADELPHIA and VANCOUVER, British Columbia, May 12, 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, announces that its pivotal Phase 3 Bria-ABC study has screened over 315 and enrolled over 230 patients. BriaCell anticipates reporting topline data in 2026.

BriaCell has received increased interest from leading cancer centers and continued enrollment momentum following the independent inclusion of its Phase 3 clinical trial in Nature Medicine’s article, “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 in advanced breast cancer.

The interim analysis will be conducted after 144 patient events, defined as deaths, have occurred. Overall survival (OS) is the primary endpoint, and positive results could support full approval of Bria-IMT in patients with metastatic breast cancer. The Bria-IMT combination regimen has received FDA Fast Track designation.

“Sustained and new interest from world class institutions and their patients continues to drive remarkable patient engagement,” stated Dr. William V. Williams, BriaCell’s President & CEO. “We remain on track to report the interim analysis in 2026 while continuing to enroll patients and advance preparations for potential commercialization, with the goal of bringing our novel immunotherapy regimen to patients with metastatic breast cancer as efficiently as possible.”

For additional information on BriaCell’s pivotal Phase 3 study, please visit ClinicalTrials.gov NCT06072612 .

About BriaCell Therapeutics Corp.

BriaCell is a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care. More information is available at https://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 ongoing patient enrollment in the pivotal Phase 3 clinical study of Bria‑IMT, the expected timing of interim analysis and topline data readout, and the potential for full approval and marketing authorization 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+ at www.sedarplus.ca and on EDGAR at www.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.

Contact Information

Company Contact:
William V. Williams, MD
President & CEO
1-888-485-6340
[email protected]

Investor Relations Contact:
[email protected]


Risks

  • Clinical trial risks include the possibility that interim data may not show positive overall survival benefit, delaying or preventing approval.
  • Enrollment and operational risks exist should patient recruitment slow or clinical sites face challenges, impacting trial timelines.
  • Regulatory risks surround the FDA approval process despite Fast Track status; full approval depends on positive efficacy and safety data.

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