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

(Moderate)
(Positive)

BriaCell (Nasdaq:BCTX) added Penn Medicine’s Abramson Cancer Center as a clinical site for its pivotal Phase 3 Bria-ABC study in advanced metastatic breast cancer.

The trial evaluates lead candidate Bria-IMT plus an immune checkpoint inhibitor versus physician’s choice, with overall survival as the primary endpoint and FDA Fast Track designation.

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Positive

  • Penn Medicine’s Abramson Cancer Center added as Phase 3 trial site
  • Multiple new U.S. cancer centers recently activated as trial sites
  • Pivotal Phase 3 Bria-ABC study in advanced metastatic breast cancer underway
  • Overall survival selected as primary endpoint for Bria-ABC trial
  • Bria-IMT combination regimen holds FDA Fast Track designation

Negative

  • Interim analysis only after 144 patient death events are recorded
  • Pivotal Phase 3 study ongoing with no efficacy results yet reported

News Market Reaction – BCTX

+2.45%
+2.45% Session close to close

In the May 13 session, BCTX gained 2.45%, reflecting a moderate positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement expands BriaCell’s pivotal Phase 3 Bria-ABC trial by adding Penn Medicine’s Abrams...
Analysis

This announcement expands BriaCell’s pivotal Phase 3 Bria-ABC trial by adding Penn Medicine’s Abramson Cancer Center and other leading institutions, reinforcing interest in the Bria-IMT plus checkpoint inhibitor regimen for advanced metastatic breast cancer. The study’s interim analysis after 144 patient events with overall survival as the primary endpoint remains a key future catalyst. Investors may track enrollment progress, upcoming data readouts, and how these align with prior clinical presentations and regulatory designations.

Key Figures

Interim analysis trigger: 144 patient events (deaths) Trial phase: Phase 3
2 metrics
Interim analysis trigger 144 patient events (deaths) Pivotal Phase 3 Bria-ABC study
Trial phase Phase 3 Bria-ABC advanced metastatic breast cancer study

Previous Clinical trial Reports

5 past events · Latest: May 07 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 07 Trial site expansion Positive -1.2% NYU Langone Perlmutter Cancer Center added to pivotal Bria-ABC Phase 3 study.
Apr 27 Conference data update Positive +3.9% Six metastatic breast cancer data presentations announced for ASCO 2026.
Apr 20 QoL & biomarker data Positive -9.3% Positive Phase 3 QoL and Phase 2 biomarker data presented at AACR 2026.
Dec 18 Nature Medicine feature Positive +3.2% Bria-IMT Phase 3 featured among trials that may shape medicine in 2026.
Dec 10 Survival data update Positive -7.9% Phase 2 survival and Phase 3 biomarker data presented at SABCS 2025.

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

Pattern Detected

Clinical-trial headlines have often seen mixed-to-negative next-day moves, with 3 of the last 5 clinical updates selling off despite positive scientific framing.

Recent Company History

Over the past several months, BriaCell has repeatedly highlighted progress in its Bria-IMT clinical program. Prior clinical-trial news included high-profile recognition in Nature Medicine, additions of major cancer centers as trial sites, ASCO and AACR data disclosures, and survival/biomarker updates. Market reactions to these clinically positive milestones were inconsistent, with both sharp gains and notable declines, underscoring that favorable scientific updates have not translated into reliably positive short-term price moves.

Key Terms

immune checkpoint inhibitor, overall survival (OS), Fast Track designation, metastatic breast cancer, +1 more
5 terms
immune checkpoint inhibitor medical
"The Phase 3 Bria-ABC study is evaluating Bria-IMT™ in combination with an immune checkpoint inhibitor..."
An immune checkpoint inhibitor is a type of medicine that helps the body's immune system recognize and attack cancer cells more effectively. It works by blocking certain signals that cancer uses to hide from immune defenses, allowing the immune system to target tumors. This breakthrough has led to new cancer treatments, making immune checkpoint inhibitors an important area of growth and innovation in the healthcare industry.
overall survival (OS) medical
"Overall survival (OS) is the primary endpoint."
Overall survival (OS) is the length of time from the start of a treatment or clinical study until death from any cause, essentially measuring how long patients live after a therapy begins. Investors watch OS because it is the most direct evidence a treatment extends life; stronger OS results can drive regulatory approvals, wider use and higher revenue expectations, much like sales figures proving a product actually works.
Fast Track designation regulatory
"The Bria-IMT combination regimen has received FDA Fast Track designation..."
Fast track designation is a status the U.S. Food and Drug Administration grants to drugs intended to treat serious conditions and address an unmet medical need. It gives the developer more frequent communication with the FDA and can allow parts of the application to be reviewed on a rolling basis, and it may pave the way to priority review or accelerated approval. It can shorten development timelines, though it does not guarantee approval.
metastatic breast cancer medical
"...patients with metastatic breast cancer with the goal of making a meaningful difference..."
Metastatic breast cancer is breast cancer that has spread beyond the breast and nearby lymph nodes to other organs, such as bones, liver, lungs or brain. For investors it matters because these advanced-stage cases often require long-term, complex and costly treatments, drive demand for specialty drugs and diagnostics, and influence regulatory approvals, pricing negotiations and the long-term revenue potential of companies developing therapies aimed at slowing spread or improving quality of life. An everyday analogy: it’s like a weed that has taken root in multiple beds rather than just one garden patch, requiring broader and more sustained effort to manage.
ClinicalTrials.gov regulatory
"For additional information ... please visit ClinicalTrials.gov NCT06072612."
clinicaltrials.gov is a publicly accessible U.S. government database that lists details, timelines and status updates for medical studies testing drugs, devices or procedures. For investors it acts like a public calendar and scoreboard—showing when trials start, are delayed, or report results—so it helps gauge a company’s development progress, regulatory risk and potential value impact before official earnings or approvals are announced.

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

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  • 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 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.

“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.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 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+ 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
info@briacell.com

Investor Relations Contact:
investors@briacell.com


FAQ

What did BriaCell (BCTX) announce about Penn Medicine on May 13, 2026?

BriaCell announced Penn Medicine’s Abramson Cancer Center joined as a clinical site in its pivotal Phase 3 Bria-ABC breast cancer study. According to BriaCell, this supports expanding access to its Bria-IMT immunotherapy regimen for metastatic breast cancer patients.

What is the Bria-ABC pivotal Phase 3 breast cancer study for BriaCell (BCTX)?

Bria-ABC is a pivotal Phase 3 trial in advanced metastatic breast cancer evaluating Bria-IMT plus an immune checkpoint inhibitor versus physician’s choice. According to BriaCell, overall survival is the primary endpoint, with an interim analysis after 144 death events.

How many events trigger the interim analysis in BriaCell’s (BCTX) Phase 3 study?

The interim analysis is planned after 144 patient events, defined as deaths. According to BriaCell, this analysis will assess overall survival for patients receiving the Bria-IMT regimen plus an immune checkpoint inhibitor compared with physician’s choice treatment.

Which other cancer centers have joined BriaCell’s (BCTX) Bria-ABC Phase 3 trial?

Recently activated sites include Indiana University Melvin and Bren Simon Comprehensive Cancer Center, UVA Comprehensive Cancer Center, Baptist Health South Florida, and SCRI Oncology Partners. According to BriaCell, these centers support broader access to the Bria-IMT regimen in metastatic breast cancer.

What is Bria-IMT in BriaCell’s (BCTX) Phase 3 breast cancer trial?

Bria-IMT is BriaCell’s lead clinical candidate used with an immune checkpoint inhibitor in the Bria-ABC Phase 3 study. According to BriaCell, the combination regimen has received FDA Fast Track designation for advanced metastatic breast cancer.

Where can investors find details on BriaCell’s (BCTX) Bria-ABC Phase 3 trial?

Details on the Bria-ABC pivotal Phase 3 study are available under identifier NCT06072612 on ClinicalTrials.gov. According to BriaCell, this listing provides protocol information for the Bria-IMT combination regimen in advanced metastatic breast cancer.

Why is FDA Fast Track designation important for BriaCell’s (BCTX) Bria-IMT regimen?

FDA Fast Track designation indicates Bria-IMT may address a serious unmet medical need in metastatic breast cancer. According to BriaCell, this status can facilitate development and expedite review of the Bria-IMT combination regimen in the Bria-ABC Phase 3 trial.