Recent Updates
Recently added Catalysts
BCTX Positive Sentiment Score: 85/100

BriaCell Announces FDA-Authorized Expanded Access Policy for Metastatic Breast Cancer Patients

Key Takeaway: BriaCell Therapeutics Corp. has received FDA authorization for an Expanded Access Policy (EAP) that allows metastatic breast cancer patients to access the Bria-IMT™ treatment beyond its pivotal Phase 3 clinical trial. This policy is part of the requirements for BriaCell's Fast Track designation, aimed at patients in need of novel therapies. Company executives highlighted the potential of Bria-IMT™ to provide hope to patients and families affected by breast cancer, which remains a leading cause of cancer death among American women.

Market Sentiment Analysis

POSITIVE FACTORS

  • FDA authorization of the Expanded Access Policy for Bria-IMT™ is expected to help metastatic breast cancer patients in need.
  • Bria-IMT™ may provide a treatment option for patients who have failed multiple prior therapies.
  • The EAP will expand access to potential lifesaving treatment beyond the pivotal Phase 3 trial.
  • BriaCell aims for Bria-IMT™ to become a new standard of care for metastatic breast cancer.

Full Press Release Details

FDA has authorized the Expanded Access Policy (EAP) to help metastatic breast cancer patients in need for novel treatments
Expanded access policy will provide potential lifesaving Bria-IMT™ to those cancer patients in need beyond the scope of BriaCell’s pivotal Phase 3 clinical trial.
PHILADELPHIA and VANCOUVER, British Columbia, Sept. 18, 2024 (GLOBE NEWSWIRE) -- BriaCell Therapeutics Corp. (NASDAQ: BCTX, BCTXW) (TSX: BCT) (“BriaCell” or the “Company”), a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care, is pleased to announce U.S. FDA (FDA) authorization of an Expanded Access Policy (EAP) for metastatic breast cancer (MBC) patients.
FDA requires BriaCell to have an EAP policy, as a condition of granting BriaCell’s Fast Track designation, and to help MBC cancer patients in need of novel treatments. The EAP provides access to cancer patients beyond the scope of BriaCell’s pivotal Phase 3 trial (ClinicalTrials.gov as NCT06072612) to receive treatment with the Bria-IMT™ regimen.
“FDA authorization for the EAP highlights its awareness of the safety and efficacy profile of Bria-IMT™ and patients’ need to access such a novel treatment. While we are conducting our pivotal Phase 3 trial of Bria-IMT™ regimen with an immune checkpoint inhibitor, Bria-IMT™ may provide a treatment option for cancer patients in need,” stated Dr. William V. Williams, BriaCell’s President and CEO. “Despite numerous approved drugs, breast cancer remains the second leading cause of cancer death in American women. With our novel immunotherapy, we expect to bring hope to patients and families suffering from this deadly disease.”
“Given the recently reported impressive survival and clinical benefit of Bria-IMT™ regimen in metastatic breast cancer patients who failed multiple prior treatments, more patients would be able to benefit from the EAP with BriaCell’s novel immunotherapy approach,” stated Giuseppe Del Priore, MD, MPH, BriaCell’s Chief Medical Officer. “We hope that our novel immunotherapy will become a new standard of care for metastatic breast cancer patients.”
For additional information on BriaCell’s EAP program, please visit: https://briacell.com/eap/.
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/.
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. Further, certain forward-looking statements, including statements about the Company's belief of the therapeutic potential of Bria-IMT™ for metastatic breast cancer patients, 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.
William V. Williams, MD
Investor Relations Contact:

Frequently Asked Questions

What is the Expanded Access Policy (EAP)?

The EAP allows metastatic breast cancer patients access to Bria-IMT™ outside the Phase 3 trial.

Why was the EAP authorized for BriaCell?

The FDA authorized the EAP to provide novel treatment options for MBC patients in need.

What is Bria-IMT™?

Bria-IMT™ is a novel immunotherapy developed by BriaCell for treating metastatic breast cancer.

Who can benefit from the EAP?

Metastatic breast cancer patients who have exhausted other treatment options can benefit.

What is BriaCell's goal with their immunotherapy?

BriaCell aims to establish its immunotherapy as a new standard of care for MBC patients.

Last updated: Sep 18, 2024