Incyte to Present at Upcoming Investor Conferences

On April 29, 2026 Incyte (Nasdaq:INCY) reported that it will present at the following investor conferences during the month of May:

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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BofA Securities 2026 Health Care Conference on Wednesday, May 13, 2026 at 1:40 pm (PDT) and
RBC 2026 Global Healthcare Conference on Tuesday, May 19, 2026 at 10:30 am (EDT)

The presentations will be webcast live and can be accessed at Investor.Incyte.com and will be available for replay for 30 days.

(Press release, Incyte, APR 29, 2026, View Source [SID1234664916])

ME Therapeutics Provides Scientific Update on In Vivo CAR and Therapeutic mRNA Programs

On April 29, 2026 ME Therapeutics Holdings Inc. ("ME Therapeutics" or the "Company") (CSE: METX) (FSE: Q9T), a publicly listed biotechnology company developing novel cancer fighting drugs that reprogram and redirect immune cells to fight cancer, reported an update on recent advances within its in vivo CAR and therapeutic mRNA research and development programs.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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ME Therapeutics continues to advance its in vivo chimeric antigen receptor (CAR) pipeline. The lead candidate is a dual CD19/CD22-targeted CAR that combines the recently licensed CD22 nanobody asset with a clinically tested CD19 construct. The CAR mRNAs are continuing to be optimized for expression and function in both T cells and myeloid cells. In parallel, ME Therapeutics is testing lipid nanoparticle (LNP) formulations engineered for effective in vivo mRNA delivery to human T cells and macrophages. Following optimization of the CAR mRNAs, ME Therapeutics will develop the lead CAR into specific LNP formulations for testing in humanized mouse cancer models. The CD19/CD22 dual CAR program aims to target certain forms of leukemia, lymphoma and autoimmune disease indications.

Preclinical testing is also progressing for ME Therapeutics’ lead therapeutic mRNA candidate targeting the STING (Stimulator of Interferon Genes) pathway. Recent data demonstrate dose-dependent single agent efficacy of the candidate in a mouse colorectal cancer model. Two modified versions of the candidate have been optimized to enhance expression of STING in the tumour microenvironment to potentially further increase their safety and will now move forward for further testing. The STING program aims to target solid tumours such as certain forms of colorectal cancer that are currently underserved by other immuno-oncology drugs.

"We are excited by the latest preclinical progress and momentum behind our in vivo CAR and therapeutic mRNA programs, which both hold the promise of offering novel approaches for cancer patients who today have few treatment options," said Salim Dhanji, PhD, CEO of ME Therapeutics. "Our in vivo CD19/CD22-targeted CAR candidate has a potentially differentiated approach from the competition. Meanwhile, our therapeutic mRNA candidate targets STING, which is an important, highly validated pathway in many solid tumours that has been notoriously difficult to target using past approaches."

(Press release, ME Therapeutics, APR 29, 2026, View Source [SID1234664915])

Guardant Health to Participate in Upcoming Investor Conferences

On April 29, 2026 Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, reported the company will be participating in the following investor conferences.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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BofA Securities 2026 Healthcare Conference in Las Vegas, NV
Fireside chat on Tuesday, May 12th at 10:40 a.m. Pacific Time
William Blair 46th Annual Growth Stock Conference in Chicago, IL
Presentation on Tuesday, June 2nd at 9:20 a.m. Central Time
Jefferies 2026 Global Healthcare Conference in New York, NY
Fireside chat on Wednesday, June 3rd at 11:05 a.m. Eastern Time

Interested parties may access live and archived webcasts of the sessions on the "Investors" section of the company website at: www.guardanthealth.com.

(Press release, Guardant Health, APR 29, 2026, View Source [SID1234664914])

Assertio and Garda Mutually Agree to Extend Tender Offer Deadline

On April 29, 2026 Assertio Holdings, Inc. ("Assertio" or the "Company") (Nasdaq: ASRT), reported that it has reached a mutual agreement with Garda Therapeutics, Inc. ("Garda") to extend the deadline to commence the previously announced tender offer to acquire all outstanding shares of Assertio to May 4, 2026.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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As previously announced on April 8, 2026, Assertio has entered into a definitive agreement (the "Garda Agreement") to be acquired by Garda for $18.00 per share in cash, or a total cash consideration of $125.1 million, plus a contingent value right. The Garda Agreement includes a 20-day "window-shop" period. Under the terms of the window-shop provision, Assertio is free to engage with other parties who may provide superior value to shareholders. In the event the Board terminates the Garda Agreement in favor of a superior bid during the window-shop period, a reduced breakup fee would apply.

(Press release, Assertio Holdings, APR 29, 2026, View Source [SID1234664913])

Caris Life Sciences Publishes Study Validating Caris AI Insights for Temozolomide Benefit in Glioblastoma Patients

On April 29, 2026 Caris Life Sciences (NASDAQ: CAI), a leading, patient-centric, next-generation AI TechBio company and precision medicine pioneer, reported the development and peer-reviewed validation of a new predictive signature to inform therapy selection in glioblastoma (GBM) patients. The study, published in Neuro-Oncology Advances, describes the development and evaluation of the model in a cohort of more than 5,800 GBM patients. The Caris AI Insights in Glioblastoma is featured on the Caris Molecular Tumor Board Report, an innovative profiling report that provides additional insight into tumor biology and is available upon request with no additional tissue required when ordering MI Cancer Seek.

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Caris Life Sciences continues to advance precision oncology by integrating multimodal real-world datasets, available with its proprietary CodeAI platform, enabling the creation of Caris AI Insights, an engine that utilizes Whole Exome Sequencing (WES), Whole Transcriptome Sequencing (WTS), and clinical data to generate deeper biological understanding and more actionable insights for clinicians and researchers.

GBM is the most common and aggressive brain cancer, with patients typically surviving around 12 months despite treatment. Current treatments include surgery to remove the tumor, radiation and chemotherapy with temozolomide (TMZ). Unfortunately, nearly half of GBM patients do not respond to TMZ and many develop resistance that leads to recurrence. Determining whether TMZ will benefit the patient is a critical step in treatment and provides insight for developing new therapies for patients who do not respond favorably.

The novel signature, developed by Caris using multimodal molecular and clinical data, is an AI-derived model designed to infer O6-methylguanine-DNA methyltransferase (MGMT) promoter methylation status from NGS data. MGMT promoter methylation is an established biomarker associated with response to TMZ therapy in GBM patients that is commonly assessed using pyrosequencing. In the peer-reviewed validation study, the signature demonstrated high concordance with pyrosequencing-based MGMT assessment and improved discrimination of overall survival outcomes across MGMT-defined patient subgroups, while also addressing variability in MGMT classification associated with traditional testing methods. These findings show that Caris’ proprietary AI signature can complement existing testing approaches and provide additional clinical insight for isocitrate dehydrogenase (IDH)-wild type GBM patients treated with TMZ.

"The Caris AI Insights signature for GBM showcases Caris’ advanced AI capabilities in our pursuit of improving cancer patient outcomes," said Caris President David Spetzler, MS, PhD, MBA. "With peer-reviewed validation demonstrating strong concordance with traditional testing approaches and clearer prognostic stratification, we believe that this signature can complement existing testing methods to improve clinical insight for glioblastoma patients treated with TMZ."

The model was trained to predict MGMT promoter methylation status, as measured by a pyrosequencing assay, using tumor profiling data from the MI Cancer Seek NGS assay, which also has FDA-approved CDx indications. As reported in the study, the signature was developed using a clinico-genomic dataset of 5,841 patients and further evaluated in a prospective cohort of more than 3,400 cases. The model stratified patients into distinct survival groups based on the signature score, with higher scores associated with significantly longer overall survival in TMZ-treated patients.

(Press release, Caris Life Sciences, APR 29, 2026, View Source [SID1234664912])