Inhibrx Announces Participation in Upcoming Scientific Conferences

On November 4, 2025 Inhibrx Biosciences, Inc. (Nasdaq: INBX) ("Inhibrx" or the "Company"), a clinical-stage biopharmaceutical company with a pipeline of novel biologic therapeutic candidates, reported it will be presenting at the following upcoming scientific conferences:

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21st Annual Industry/Academia Precision Oncology & Radmed Symposium
November 5th, 2025 – La Jolla, California

Title: DR5 Agonist Clinical Data in Chondrosarcoma, Colorectal Cancer and Ewings Sarcoma
Format: Presentation
Presenters: Josep Garcia, PhD, Executive Vice President, Chief Clinical Development Officer, Inhibrx; Katelyn Willis, PhD, Director, Biotherapeutics, Inhibrx
Date: Wednesday, November 5th, 2025
Time: 4:45 PM Eastern Standard Time
Location: The Alexandria at Torrey Pines, La Jolla, California

Connective Tissue Oncology Society (CTOS) 2025 Annual Meeting
November 12th – 15th, 2025 – Boca Raton, Florida

Title: The Tetravalent Death Receptor 5 (DR5) Agonist ozekibart (INBRX-109) in Conventional Chondrosarcoma: Results from the Randomized, Registrational, Phase 2 ChonDRAgon Study
Lead Author: Robin L. Jones, MD – Medical Oncology, The Royal Marsden and Institute of Cancer Research
Format: Presentation
Date: Friday, November 14th, 2025
Time: 8:30 AM – 10:00 AM Eastern Standard Time
Location: The Boca Raton, Boca Raton, Florida

Society for NeuroOncology (SNO) 2025 Annual Meeting
November 19th – 23rd, 2025 – Honolulu, Hawaii

Title: The Tetravalent Death Receptor 5 (DR5) agonist ozekibart (INBRX-109) exhibits anti-tumor activity in GBM models as a monotherapy and in combination with TMZ
Format: Poster Presentation
Date: Saturday, November 22nd, 2025
Time: 4:45 pm – 6:00 PM Eastern Standard Time
Location: Hawaii Convention Center, Honolulu, Hawaii; Kamehameha Exhibit Hall II & III

The presentation and poster will be accessible through a link on the investors’ section of Inhibrx’s website at View Source upon commencement of each event.

(Press release, Inhibrx, NOV 4, 2025, View Source [SID1234659396])

BriaCell to Present Robust Anti-Cancer Activity of Bria-OTS+(TM) in Breast and Prostate Cancer Models

On November 4, 2025 BriaCell Therapeutics Corp. (Nasdaq: BCTX, BCTXW, BCTXZ) (TSX: BCT) ("BriaCell" or the "Company"), a clinical-stage biotechnology company that develops novel immunotherapies to transform cancer care, reported that the Company will be showing evidence of strong immune system engagement inducing potent anti-cancer cell activity of its next generation Bria-OTS+ platform in preclinical models at a poster presentation at the Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper) 40 th Anniversary Annual Meeting, to be held November 7-9, 2025, in National Harbor, MD. The details are listed below.

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Title: Redefining Cancer Vaccines: Bria-OTS+ Integrates Trained Innate Immunity and Adaptive Memory to Overcome Immune Resistance
Abstract Number: 353
Location: Prince George ABC Exhibit Halls, Gaylord National Resort and Convention Center
Date: Friday, November 7, 2025
Time : 12:15-1:45 PM, and 5:35-7 PM ET

"We are very excited with this opportunity to showcase the activity of our novel Bria-OTS+ platform which is designed to reinvigorate the body’s immune system to powerfully and selectively attack cancer cells while sparing normal tissues," commented Miguel A. Lopez-Lago, PhD, BriaCell’s Chief Scientific Officer.

"We will present extensive immune system activation and cytotoxicity data at the upcoming poster session on November 7, 2025. Our data further validates the promise of our personalized cancer immunotherapy platform in advancing new treatments for cancer," stated Dr. William V. Williams, BriaCell’s President and CEO. "We look forward to evaluating these encouraging results in upcoming clinical studies of Bria-BRES+ for breast cancer and Bria-PROS+ for prostate cancer, as we strive to bring new hope to patients with unmet medical needs."

(Press release, BriaCell Therapeutics, NOV 4, 2025, View Source [SID1234659459])

Azalea Therapeutics Launches with $82 Million Financing to Redefine Precision Genomic Medicines by Engineering Cells Directly Inside Each Patient

On November 04, 2025 Azalea Therapeutics, Inc., a biotechnology company redefining precision genomic medicines in vivo, reported its official launch and completion of $82 million in seed and Series A financing to advance its proprietary Enveloped Delivery Vehicle (EDV) technology. The company’s mission is to engineer therapeutic cells with precision directly inside the patient, transforming how cell and gene therapies are created and delivered.

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Azalea’s EDV technology selectively targets cells, delivering transient CRISPR-Cas9 cargo to mediate programmable genome editing. Combining this with a highly efficient T cell-tropic AAV to deliver a promoterless homology-directed repair template enables programmable, site-specific large gene insertion at defined genomic sites within the T cell. This dual-vector platform provides multiple layers of precision by achieving cell- and genomic site-specific gene insertion under regulatory control of a native promoter, with the potential to increase durability, efficacy and safety. Azalea has utilized this approach to insert chimeric antigen receptor (CAR) genes under an endogenous, T cell-restricted promoter in vivo – enabling durable therapeutic benefit while eliminating the need for ex vivo manufacturing and lymphodepletion. Together, these advances enable precise engineering of functional CAR-T cells within a patient – a monumental advancement in the fields of cell and gene therapy.

"At Azalea, we are aiming to make cell therapy as simple as dosing a medicine," said Jenny Hamilton, Ph.D., co-founder, president and chief executive officer of Azalea Therapeutics. "By combining cell-selective delivery with site-specific genome integration, we can create potent and durable in vivo CAR-T and other cell-based therapies inside the body and extend the reach of genome engineering to many more patients."

The $82 million funding, which includes a recently closed $65 million Series A financing, was led by Third Rock Ventures, with participation from RA Capital Management, Yosemite, Sozo Ventures and select individual investors. Funds will be used to advance Azalea’s CD19-based in vivo CAR-T therapy for B cell malignancies and autoimmune diseases through IND-enabling studies and into the clinic, progress its BCMA-targeted in vivo CAR-T program for multiple myeloma and an undisclosed program for solid tumors, while exploring expansion of the platform to other cell types.

Currently based at UC Berkeley’s Bakar Bio Labs, Azalea grew out of collaborative research conducted at the Innovative Genomics Institute in Dr. Jennifer Doudna’s laboratory and in Dr. Justin Eyquem’s laboratory at UC San Francisco, as part of the Gladstone/UCSF Institute for Genomic Immunology. The early academic work was supported by philanthropic grants from the Yosemite team and the Parker Institute for Cancer Immunotherapy to support early de-risking, and Azalea’s company launch was supported by a $1 million non-dilutive award from the HS Chau Women in Enterprising Science program, which fosters the translation of breakthrough academic research into biotech startups.

Together with Dr. Hamilton, Azalea’s co-founders bring deep academic and translational expertise across genome engineering, synthetic biology and cell therapy, including:

Jennifer Doudna, Ph.D., the Li Ka Shing Chancellor’s Chair in Biomedical and Health Sciences and professor of molecular and cell biology at UC Berkeley, Howard Hughes Medical Institute Investigator, founder of the Innovative Genomics Institute and 2020 Nobel laureate in chemistry
Michael Fischbach, Ph.D., the Liu (Liao) Family Professor of Bioengineering at Stanford University, institute scholar of Stanford ChEM-H and director of the Stanford Microbiome Therapies Initiative
Justin Eyquem, Ph.D., associate professor of medicine in the Division of Hematology and Oncology at UCSF, affiliate investigator at Gladstone Institutes and member of the Parker Institute for Cancer Immunotherapy
"Azalea is advancing a powerful concept – delivering precision genome editing tools to specific cells inside the body," said Justin Eyquem, Ph.D. "The ability to directly engineer cells in vivo opens new possibilities for treating disease and for bringing genomic medicines to patients in a safer and more scalable way."

Together with its distinguished scientific founders, Azalea is supported by leading biotech investors committed to advancing the company’s vision.

"Azalea is at the forefront of realizing in vivo CAR-T cell therapy – combining scientific excellence with bold execution to make precise in-patient cell engineering a reality," said Andrea van Elsas, Ph.D., board director of Azalea and partner at Third Rock Ventures. "The team is uniquely positioned to deliver on the promise of off-the-shelf genome engineering with curative intent and a clear path toward the clinic."

Azalea will present its latest data on Thursday, November 20th at the American Society of Gene and Cell Therapy (ASGCT) (Free ASGCT Whitepaper) Breakthroughs in Targeted In Vivo Gene Editing, taking place virtually and in San Diego.

Abstract Title: In vivo generation of TRAC CAR-T cells by leveraging enveloped delivery vehicles
Presenting Author: Jenny Hamilton, Ph.D., Azalea Therapeutics
Session 5: Oral Abstracts
Date/Time: Thursday, November 20, 2025 | 3:45 – 5:00 pm PST

Visit the ASGCT (Free ASGCT Whitepaper) Breakthroughs in Targeted In Vivo Gene Editing website to view the published abstracts.

Azalea’s leadership and board bring deep scientific, operational and investment expertise spanning genome engineering, cell therapy and company building:

Leadership
Jenny Hamilton, Ph.D. – co-founder, president and chief executive officer
Paul Westberg, MBA – chief business officer
Connor Tsuchida, Ph.D. – scientific co-founder
Abdullah Syed, Ph.D. – scientific co-founder

Board of Directors
Andrea van Elsas, Ph.D. – partner, Third Rock Ventures
Mary Lynne Hedley, Ph.D. – venture partner, Third Rock Ventures
Nandita Shangari, Ph.D. – managing director, RA Capital Management
Michael Fischbach, Ph.D. – professor of bioengineering, Stanford University
Justin Eyquem, Ph.D. – associate professor of medicine, UCSF
Jenny Hamilton, Ph.D. – co-founder and chief executive officer

Board Observers
Jennifer Doudna, Ph.D. – professor of molecular and cell biology at UC Berkeley
Reed Jobs, M.A. – investor, Yosemite
Jenna Hebert, Ph.D. – investment director, RA Capital Management

(Press release, Azalea Therapeutics, NOV 4, 2025, View Source [SID1234663808])

Calidi Biotherapeutics Announces Investor Event to be Held on Friday, November 7th at the 2025 SITC Annual Meeting

On November 4, 2025 Calidi Biotherapeutics, Inc. (NYSE American: CLDI) ("Calidi" or the "Company"), a clinical-stage biotechnology company pioneering the development of systemically delivered, targeted genetic medicines, reported that it will hold an investor event at the Society of Immunotherapy for Cancer (SITC) (Free SITC Whitepaper) Annual Meeting centered around the Company’s groundbreaking RedTail platform and its lead candidate, CLD-401.

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The presentation will take place at the SITC (Free SITC Whitepaper) Annual Meeting on Friday, November 7th from 8:30AM to 9:30AM in the National Harbor Room 15 at the Gaylord National Hotel and Convention Center in National Harbor, Maryland.

The presentation will also be live streamed: (View Source).

Speakers at the event will include:

· Dr. Dmitriy Zamarin of the Icahn Genomics Institute and the Precision Immunology Institute at The Tisch Cancer Institute at the Icahn School of Medicine at Mount Sinai. Dr. Zamarin is a world renowned expert in virotherapy. Dr. Zamarin is a member of Calidi’s Scientific Advisory Board (SAB).

· Dr. Antonio F. Santidrian, Chief Scientific Officer of Calidi, responsible for leading all of the Company’s research and development initiatives.

· Dr. John M. Wrangle, a thoracis medical oncologist at the Medical University of South Carolina (MUSC). Dr Wrangle is an expert on the clinical development of IL-15 superagonist. Dr. Wrangle is also a member of Calidi’s SAB.

· Dr. Travis Clifton, Chief Medical Officer of Calidi and a surgical oncologist with over 17 years of experience in drug development, early phase and translational clinical trials, and cancer immunotherapy.

"We are excited to hold our first investor event," said Eric Poma, PhD, Chief Executive Officer. "We believe CLD-401 and the RedTail platform represent important breakthroughs in the area of genetic medicine, and we look forward to updating the investment community on our progress."

Calidi is currently conducting IND-enabling studies for CLD-401 and anticipates submitting an Investigational New Drug (IND) application by the end of 2026. The company is also actively pursuing strategic partnerships to accelerate clinical development and broaden the impact of its RedTail platform.

(Press release, Calidi Biotherapeutics, NOV 4, 2025, View Source [SID1234659347])

Merck Enters into Research and Development Funding Agreement with Blackstone Life Sciences for Sacituzumab Tirumotecan (sac-TMT)

On November 4, 2025 Merck (NYSE: MRK), known as MSD outside of the United States and Canada, reported that the company has entered into an agreement to receive funds managed by Blackstone Life Sciences ("Blackstone") for the development of sacituzumab tirumotecan (sac-TMT), an investigational antibody-drug conjugate (ADC) targeting trophoblast cell-surface antigen 2 (TROP2), a protein found on the surface of various cancer cells. Merck is currently evaluating sac-TMT in 15 global Phase 3 clinical trials spanning six tumor types, including breast, endometrial and lung cancers.

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"This agreement positions Merck to harness the potential of sac-TMT, a promising ADC candidate targeting TROP2, while we continue to advance our broad and expansive pipeline," said Caroline Litchfield, chief financial officer, Merck. "We are making important investments to drive patient impact and revenue growth, and to sustain our business for the future while remaining disciplined towards maintaining an appropriate financial profile."

Under the terms of the agreement, Blackstone will pay Merck $700 million (which is non-refundable, subject to termination provisions provided for in the agreement) to fund a portion of the development costs for sac-TMT expected to be incurred throughout 2026. In return, Blackstone is eligible to receive low-to-mid single-digit royalties on net sales of sac-TMT across all approved indications in Merck’s marketing territories contingent upon receipt of regulatory approval in the U.S. for first-line treatment of triple-negative-breast cancer based on findings of the TroFuse-011 clinical trial.

"Sac-TMT is an innovative asset that has the potential to improve patient care across many forms of cancer," said Dr. Nicholas Galakatos, global head, Blackstone Life Sciences. "We are excited to be collaborating with Merck to realize the full value of this high priority product and contribute to our partner’s revenue growth by leveraging our scale capital and expertise."

Sac-TMT is being developed as part of an exclusive license and collaboration agreement with Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd., a holding subsidiary of Sichuan Kelun Pharmaceutical Co, Ltd. ("Kelun-Biotech"), which is unchanged by this agreement with Blackstone. Merck will retain decision-making authority and control over the development, manufacturing, and commercialization of sac-TMT; Blackstone will not receive any rights to sac-TMT.

About sacituzumab tirumotecan (sac-TMT)

Sac-TMT is an investigational ADC that consists of three components: 1) a TROP2-targeting monoclonal antibody, sacituzumab, 2) a cytotoxic payload from the topoisomerase 1 inhibitor class, and 3) a novel, irreversible but hydrolyzable linker, which joins the monoclonal antibody and the cytotoxic payload leveraging proprietary linker conjugation technology. The average drug-to-antibody ratio of sac-TMT is 7.4. TROP2 is highly expressed in a variety of epithelial-derived tumors and can promote tumor cell proliferation, invasion and metastasis. TROP2 ADCs specifically target TROP2-expressing tumor cells to deliver cytotoxic effects and have shown encouraging anti-tumor activity in clinical studies.

Sac-TMT was developed by Kelun-Biotech. Kelun-Biotech (6990.HK) is a holding subsidiary of Kelun Pharmaceutical (002422.SZ), which focuses on the R&D, manufacturing, commercialization and global collaboration of innovative biological drugs and small molecule drugs. Under a collaboration agreement, Kelun-Biotech has granted Merck the exclusive rights to develop, manufacture and commercialize sac-TMT in all territories outside of Greater China (which includes Mainland China, Hong Kong, Macau and Taiwan).

(Press release, Merck & Co, NOV 4, 2025, View Source [SID1234659363])