Compugen to Participate in a Fireside Chat at the H.C. Wainwright 3rd Annual AI Based Drug Discovery & Development Conference

On October 6, 2026 Compugen Ltd. (NASDAQ: CGEN) (TASE: CGEN) a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery powered by AI, reported that management will participate in a fireside chat at the H.C. Wainwright 3rd Annual AI Based Drug Discovery & Development Conference, being held virtually on October 8-9, 2026.

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The fireside chat will be held on Thursday, October 8, 2026, at 9:30 AM ET. A live webcast of the presentation will be available on the events page of the Investor Relations section of Compugen’s website at www.cgen.com. A replay will be available following the live event.

(Press release, Compugen, OCT 6, 2026, View Source;Wainwright-3rd-Annual-AI-Based-Drug-Discovery–Development-Conference/default.aspx [SID1234673232])

Phio Pharmaceuticals to Present at The Global Markets Virtual Forum October 8, 2026

On October 6, 2026 Phio Pharmaceuticals Corp. (NASDAQ: PHIO), a clinical-stage biotechnology company developing cancer therapeutics based on its proprietary INTASYL siRNA gene-silencing platform, reported that Robert Bitterman, President and Chief Executive Officer, reported it will present INTASYL siRNA therapeutic platform, its differentiated delivery approach, and the Company’s strategic direction at The Global Markets Virtual Forum hosted by www.VirtualInvestorConferences.com (VIC) on October 8th, 2026.

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"The Global Markets Virtual Forum offers a unique forum to highlight Phio’s differentiated siRNA therapeutic platform, which is designed to enhance immune-cell function in solid tumors and has demonstrated a strong safety profile," said Robert Bitterman, President and Chief Executive Officer of Phio Pharmaceuticals.

Presentation Details:

DATE: October 8th, 2026

TIME: 12:40 PM (EDT)

LINK: Phio Pharmaceuticals Corp. (NASDAQ: PHIO)

Availability for 1×1 Meetings: Robert Bitterman will be available for 1×1 meetings and can be scheduled with the link below:

DATE TIME
Thursday October 8, 2026 11:45 AM-2:15 PM (EDT)
Friday October 9, 2026 Noon – 4:30 PM (EDT)
Monday October 12, 2026 9 AM -1 PM (EDT)
LINK for 1×1 meetings: Event Details

This will be a live, interactive online event where investors are invited to ask the company questions in real-time. If attendees are not able to join the event live on the day of the conference, an archived webcast will also be made available after the event.

It is recommended that online investors pre-register and run the online system check to expedite participation and receive event updates.

Learn more about the event at www.virtualinvestorconferences.com

(Press release, Phio Pharmaceuticals, OCT 6, 2026, View Source [SID1234673220])

Personalis, Inc. entered into an Agreement and Plan of Merger (the “Merger Agreement”) with Tempus AI, Inc.

On October 6, 2026 Personalis, Inc., a Delaware corporation ("Personalis" or the "Company"), reported to have entered into an Agreement and Plan of Merger (the "Merger Agreement") with Tempus AI, Inc., a Nevada corporation ("Tempus" or "Parent"), Aviary Development, Inc., a Delaware corporation and a direct, wholly owned subsidiary of Parent ("Merger Sub I"), and Toucan Development, LLC, a Nevada limited liability company and a direct, wholly owned subsidiary of Parent ("Merger Sub II"). The Merger Agreement provides that, on the terms and subject to the conditions set forth in the Merger Agreement, Merger Sub I will merge with and into the Company (the "First Merger"), with the Company surviving the First Merger as a direct, wholly owned subsidiary of Parent, and immediately thereafter, the Company will merge with and into Merger Sub II (the "Second Merger" and, together with the First Merger, the "Mergers"), with Merger Sub II surviving as a direct, wholly owned subsidiary of Parent. Capitalized terms used but not otherwise defined herein have the meanings ascribed to them in the Merger Agreement. In connection with the Merger Agreement, Tempus filed with the U.S. Securities and Exchange Commission (the "SEC") a preliminary Registration Statement on Form S-4 on August 31, 2026 and Amendment No. 1 thereto on October 2, 2026, each of which includes a proxy statement of the Company and a prospectus of Tempus.

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Expiration of HSR Waiting Period

Consummation of the Mergers is subject to customary closing conditions, including, but not limited to, the expiration or early termination of the waiting period applicable to the consummation of the Mergers under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, as amended and the rules and regulations promulgated thereunder (the "HSR Act"). Pursuant to the Merger Agreement, the Company and Parent each filed a Premerger Notification and Report Form under the HSR Act with the Antitrust Division of the U.S. Department of Justice and the U.S. Federal Trade Commission with respect to the Mergers on July 31, 2026. On August 31, 2026, Parent voluntarily withdrew its Notification and Report Form, and Parent refiled its Notification and Report Form on September 2, 2026, which started a new statutory thirty (30)-day waiting period under the HSR Act. The waiting period applicable to the Mergers under the HSR Act expired at 11:59 p.m., Eastern time, on October 2, 2026.

The closing of the Mergers is subject to receipt of the Company Stockholder Approval at the Company Stockholders Meeting and satisfaction or waiver of the other closing conditions specified in the Merger Agreement. The Company Stockholders Meeting to consider and vote on, among other matters, the adoption of the Merger Agreement will be held virtually on a date and at a time to be determined and announced.

(Press release, Personalis, OCT 6, 2026, View Source [SID1234673218])

PDS Biotech to Host Key Opinion Leader Event on PDS0301 for the Treatment of Advanced Colorectal Cancer with Liver Metastases

On October 6, 2026 PDS Biotechnology Corporation (Nasdaq: PDSB) ("PDS Biotech" or the "Company"), a late-stage immunotherapy company focused on transforming how the immune system targets and kills cancers, reported that the Company will host a virtual key opinion leader (KOL) event featuring Jonathan M. Hernandez, M.D, an Investigator with Surgical Oncology Program at the National Cancer Institute’s Center for Cancer Research. Dr. Hernandez will join company management to discuss clinical outcomes from the PDS0301 Phase 2 trials for the treatment of advanced liver-associated cancers, with a focus on the metastatic colorectal cancer (mCRC) cohort. The event will provide an overview of the PDS0301 trial in patients with second and third line unresectable microsatellite stable (MSS) or mismatch repair-proficient (pMMR) colorectal liver metastases. These MSS patients constitute the majority of mCRC, a population in which immunotherapy has been mostly ineffective.

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PDS0301 is an investigational IL-12 immunocytokine designed using an antibody that binds to necrotic DNA that is found within tumors. PDS0301 specifically targets and delivers the IL-12 into the tumor to promote T cell and natural killer (NK) cell infiltration into the tumor, as well as localized anti-tumor activation of both T cells and NK cells.

A live question and answer session will follow the formal presentations.

Register & Attend

Date:
Thursday, October 15, 2026
Time:
8:00 AM ET
Registration:
Click Here

Jonathan M. Hernandez, M.D., Investigator, Surgical Oncology Program, NCI/CCR

Dr. Hernandez graduated from medical school with honors from the University of Florida and completed general surgery training at the University of South Florida. During his residency, Dr. Hernandez spent two years at the Moffitt Cancer Center and Research Institute interrogating molecular diagnostics for liver metastases and miRNA-mediated mechanisms of metastatic spread. Following residency, Dr. Hernandez completed fellowship training in both surgical oncology and hepatopancreatobiliary surgery at Memorial Sloan Kettering Cancer Center. During his fellowships, Dr. Hernandez spent an additional two years in dedicated basic research studying metastatic colonization as a scholar in the Cell Biology Program of the Sloan Kettering Institute and as a visiting investigator in the Cell and Developmental Biology Department of Weill Medical College of Cornell University. The Hernandez lab studies hepatic metastases and has been the home to twenty surgical residents since its establishment at the NIH in 2016. Dr. Hernandez has authored over 175 peer-reviewed publications and has contributed book chapters in numerous authoritative surgical texts.

(Press release, PDS Biotechnology, OCT 6, 2026, View Source [SID1234673217])

NUCLIDIUM Announces First Patient Imaged in Phase 2 Study Evaluating 61Cu-NU101 Diagnostic in Patients with Metastatic Prostate Cancer

On October 6, 2026 NUCLIDIUM AG, a clinical-stage radiopharmaceutical company, reported that the first patient has been successfully imaged in a Phase 2 clinical trial evaluating the diagnostic accuracy and safety of the Company’s 61Cu-NU101 radiotracer in patients with metastatic prostate cancer. 61Cu-NU101 is a positron emission tomography (PET) imaging agent that effectively combines high-radiopure Copper-61 with a targeting peptide to specifically bind to Prostate-Specific Membrane Antigen (PSMA), an established biomarker for prostate cancer. 61Cu-NU101 is the diagnostic component of NUCLIDIUM’s NU101 theranostic program for metastatic prostate cancer, paired with the 67Cu-NU101 therapeutic.

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"PSMA-targeted PET is currently the best method of imaging metastatic prostate cancer, and we are always striving to do better. In a phase 1 trial, we showed that 61Cu-NU101 was safe and able to detect additional lesions in 50% of patients compared to the currently most sensitive imaging agents", said Dr. Gary Ulaner, MD, PhD, Chair of Molecular Imaging and Therapy at the Hoag Family Cancer Institute and Professor of Radiology at the University of Southern California. "These data supported the opening of our phase 2 trial, which is statistically powered to compare against currently available imaging agents and uses pathology as the reference standard of truth."

The investigator-initiated, non-randomized Phase 2 trial will enroll approximately 34 patients with biopsy-confirmed metastatic prostate cancer at clinical sites in the United States. Patients will receive a single intravenous dose of 61Cu-NU101, followed by PET/CT imaging at 1 and 4 hours post-dose. The primary endpoint will evaluate the sensitivity of tumor lesion detection of 61Cu-NU101 compared to an 18F-based, FDA-approved PSMA-targeting radiotracer. Secondary endpoints include a sensitivity comparison to CT and bone scans, and safety evaluation.

"The supportive Phase 1 diagnostic data and differentiated clinical profile reinforce our belief in the best-in-class potential of NU101 as a next-generation copper-based radiotheranostic for prostate cancer. Importantly, progress in our diagnostic program will inform and strengthen our therapeutic development strategy, enabling our true radiotheranostic approach of direct diagnosis to treatment conversion. The initiation of this Phase 2 trial represents an important step in executing our broad and robust development plan, with multiple clinical trials expected over the coming months and expansion into new cancer patient populations," said Thomas Reiner, PhD, CSO of NUCLIDIUM.

NUCLIDIUM’s 61Cu-NU101 program can be manufactured in 5 minutes at room-temperature, allowing for on-demand preparation and seamless integration into existing hospital infrastructure. These manufacturing advantages, coupled with the longer half-life, delayed imaging capability and beneficial tumor-to-background ratio, further underscore the benefits of this copper-based approach compared with alternative radioligands. Phase 1 data previously presented at the Society of Nuclear Medicine & Molecular Imaging (SNMMI) 2025 Annual Meeting highlight the favorable clinical profile of 61Cu-NU101.

(Press release, NUCLIDIUM, OCT 6, 2026, View Source [SID1234673216])