Alpheus Medical Opens Enrollment in New Clinical Trial for Butterfly Glioblastoma

On October 8, 2026 Alpheus Medical, Inc., a private, clinical-stage biotechnology company, reported the initiation of a new clinical trial evaluating its investigational Porphyrin Metabolite Activation (PoMA) therapy in patients with butterfly glioblastoma (GBM), a particularly aggressive form of brain cancer that extends across the corpus callosum. In the Alpheus Butterfly trial (NCT07862647), patients with newly diagnosed butterfly GBM will receive PoMA therapy, which combines 5-aminolevulinic acid (5-ALA) with bilateral low-intensity defocused ultrasound. Patients must enroll before beginning standard chemoradiation therapy.

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"Patients with butterfly glioblastoma are among the most challenging patients we treat because of the tumor’s bilateral nature. Historically, many clinical trials have excluded this group, leaving patients with few options," said David Reardon, MD, Chief of the Division of Neuro-Oncology and Director of the Center for Neuro-Oncology at Dana-Farber Cancer Institute. "This tumor’s diffuse distribution requires us to think differently about treatment. Alpheus’ strategy is designed to address disease across both hemispheres while maintaining tumor selectivity, representing a potentially important new and targeted approach in this patient population."

Butterfly glioblastoma carries a median survival of three to six months in published research, and the tumor’s spread across the midline makes surgical resection difficult or impossible. Because the disease involves both hemispheres, these patients are frequently ineligible for glioblastoma trials that exclude bilateral or multifocal disease.

Alpheus’ investigational PoMA therapy combines a tumor-localizing drug with proprietary low-intensity defocused ultrasound. Following oral administration of 5-ALA, protoporphyrin IX (PpIX) preferentially accumulates in tumor cells and is subsequently activated using externally delivered ultrasound. The therapy is delivered while the patient is awake in an outpatient setting and is designed to be repeatable.

In the multi-center Butterfly study, PoMA therapy is administered alongside standard of care. The Dent Neurologic Institute in Buffalo, New York is currently enrolling patients with additional U.S. clinical centers expected in the coming months.

The company raised additional financing to support the Butterfly GBM study and continued development of PoMA therapy.

"Butterfly glioblastoma is a devastating diagnosis for patients who have very limited treatment options," said Vijay Agarwal, MD, Chief Executive Officer of Alpheus Medical. "We designed this study specifically around the characteristics of the disease and the ability of PoMA therapy to treat both hemispheres non-invasively. We want patients and physicians caring for them to know that this study is available, but they need to reach us early in their treatment journey."

About the Butterfly GBM Clinical Trial

The study (NCT07862647) will evaluate the safety and clinical activity of Alpheus Medical’s investigational PoMA therapy in patients with newly diagnosed butterfly glioblastoma. Patients must enroll before beginning chemoradiation treatment.

Patients, caregivers and clinicians seeking information about eligibility and participating clinical centers should visit www.BrainCancerTrial.com.

(Press release, Alpheus Medical, OCT 8, 2026, View Source [SID1234673290])

Datroway® Approved in China as First and Only TROP2 Directed Antibody
Drug Conjugate with Overall Survival Benefit for Treatment of Patients with
Metastatic Triple Negative Breast Cancer Who Are Not Candidates for PD1/PD-L1 Inhibitor Therapy

On October 8, 2026 Daiichi Sankyo reported that Datroway (datopotamab deruxtecan) has been approved in China for the treatment of adult patients with unresectable or metastatic triple negative breast cancer (TNBC) who are not candidates for PD-1/PD-L1 inhibitor therapy.

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Datroway is a specifically engineered TROP2 directed DXd antibody drug conjugate (ADC) discovered by Daiichi Sankyo (TSE: 4568) and being jointly developed and commercialized by Daiichi Sankyo and AstraZeneca (LSE/STO/NYSE: AZN).

The approval of Datroway by China’s National Medical Products Administration (NMPA) is based on results from the TROPION-Breast02 phase 3 trial, which were presented at the 2025 European Society for Medical Oncology Congress and subsequently published in Annals of Oncology.

In TROPION-Breast02, Datroway demonstrated a statistically significant 5.0 month improvement in median overall survival (OS) versus investigator’s choice of chemotherapy (hazard ratio [HR]=0.79; 95% confidence interval [CI]: 0.64-0.98; p=0.0291). Median OS was 23.7 months for patients treated with Datroway versus 18.7 months for those treated with chemotherapy. Datroway reduced the risk of disease progression or death by 43% compared to chemotherapy (HR=0.57; 95% CI: 0.47-0.69; p<0.0001) as assessed by blinded independent central review (BICR). Median progression-free survival (PFS) was 10.8 months for patients treated with Datroway versus 5.6 months for those treated with chemotherapy in patients with metastatic TNBC who are not candidates for PD1/PD-L1 inhibitor therapy. Datroway also was associated with more robust treatment responses compared to chemotherapy, with an objective response rate (ORR) of 63% versus 29% for those treated with chemotherapy.

"One of the greatest challenges in my clinical practice is treating patients at their first metastatic triple negative breast cancer diagnosis who are not candidates for immunotherapy since there has been limited treatment options available," said Zhimin Shao, MD, Director, Fudan University Cancer Institute and Breast Cancer, China, and lead investigator in China of the TROPION-Breast02 trial. "The approval of Datroway in China introduces an important new treatment option, which is supported by clinically meaningful improvements in overall survival and progression-free survival, and offers a significant advancement over the current standard of care."

The safety profile of Datroway (6 mg/kg) was evaluated in 319 patients with TNBC who received Datroway in TROPION-Breast02. The most common (20%) adverse reactions, including laboratory abnormalities, were stomatitis, increased amylase, nausea, alopecia, decreased hemoglobin, decreased white blood cells, constipation, decreased calcium, fatigue, decreased lymphocytes, decreased neutrophils, increased alanine aminotransferase, increased aspartate aminotransferase, dry eye, decreased albumin, vomiting, decreased sodium and increased blood alkaline phosphatase. Serious adverse reactions occurred in 5.6% of patients who received Datroway. Serious adverse reactions in more than 1% of patients who received Datroway included vomiting and anemia. One patient fatality was attributed to interstitial lung disease/pneumonitis.

"Patients with metastatic triple negative breast cancer continue to face a poor prognosis, particularly those who are not eligible for immunotherapy," said Michio Hayashi, China President, Daiichi Sankyo. "As the only TROP2 directed antibody drug conjugate approved in China with an overall survival benefit in this setting, Datroway offers a much-needed treatment option supported by robust clinical evidence for patients facing this aggressive disease. We are proud to bring this innovative medicine to more patients in China."

"There remains a critical need for innovative treatment options that can help improve outcomes based on the aggressive nature of triple negative breast cancer," said Mary Guan, General Manager, China Oncology Business, AstraZeneca. "This second approval for Datroway in China, and the first TROP2 directed antibody drug conjugate approved in this setting, expands its use into triple negative breast cancer and marks another important step in our commitment to addressing the diverse needs of patients across the breast cancer continuum. We will continue to advance innovation and help improve outcomes for more patients living with breast cancer."

Datroway (6 mg/kg) is approved in more than 35 countries/regions, including China, EU, Japan and the U.S. for the treatment of adult patients with unresectable or metastatic TNBC who are not candidates for PD-1/PD-L1 inhibitor therapy. Additional reviews are underway in Australia, Canada, Israel and Switzerland as part of Project Orbis.

About TROPION-Breast02

TROPION-Breast02 is a global, multicenter, randomized, open-label phase 3 trial evaluating the efficacy and safety of Datroway versus investigator’s choice of chemotherapy (paclitaxel, nab-paclitaxel, capecitabine, carboplatin or eribulin) in patients with previously untreated locally recurrent inoperable or metastatic TNBC for whom immunotherapy was not an option. This included patients whose tumors did not express PD-L1 as well as patients with PD-L1 expressing tumors who could not receive immunotherapy due to prior exposure in early-stage disease, comorbidities or immunotherapy not being accessible in their geography. Enrollment included patients with de novo or recurrent disease, regardless of disease-free interval, and those with poor prognostic factors such as stable brain metastases.

The dual primary endpoints of TROPION-Breast02 are OS and PFS as assessed by BICR. Secondary endpoints include PFS as assessed by investigator, ORR, duration of response, disease control rate, pharmacokinetics and safety.

TROPION-Breast02 enrolled 644 patients at sites in Africa, Asia, Europe, North America and South America. For more information visit ClinicalTrials.gov.

About Triple Negative Breast Cancer

TNBC accounts for approximately 15% of all breast cancer cases, with an estimated 365,000 diagnoses globally each year.1,2 In China, there are an estimated 56,000 diagnoses of TNBC each year. 1,2 TNBC is diagnosed more frequently in younger and premenopausal women, and is more prevalent in Black and Hispanic women.3,4,5 Metastatic TNBC is the most aggressive type of breast cancer and has one of the worst prognoses, with median OS of just 12 to 18 months and only about 15% of patients living five years following diagnosis.

While some breast cancers may test positive for estrogen receptors, progesterone receptors or overexpression of HER2, TNBC tests negative for all three.3 Due to its aggressive nature and absence of common breast cancer receptors, TNBC is characteristically difficult to treat.3 For patients with metastatic disease with PD-L1 expressing tumors, the addition of immunotherapy to chemotherapy has improved outcomes in the first-line setting.8,9 However, for approximately 70% of patients with metastatic TNBC who are not candidates for immunotherapy, chemotherapy was the standard first-line treatment. TROP2 is a protein broadly expressed in several solid tumors, including TNBC.11 TROP2 is associated with increased tumor progression and poor survival in patients with breast cancer.

About Datroway

Datroway (datopotamab deruxtecan; datopotamab deruxtecan-dlnk in the U.S. only) is a TROP2 directed ADC. Designed using the proprietary DXd ADC Technology of Daiichi Sankyo, Datroway is one of seven DXd ADCs in the oncology pipeline of Daiichi Sankyo, and one of the most advanced programs in AstraZeneca’s ADC scientific platform. Datroway is comprised of a humanized anti-TROP2 IgG1 monoclonal antibody, developed in collaboration with Sapporo Medical University, attached to a number of topoisomerase I inhibitor payloads (an exatecan derivative, DXd) via tetrapeptide-based cleavable linkers.

Datroway (6 mg/kg) is approved in more than 35 countries/regions worldwide for the treatment of adult patients with unresectable or metastatic TNBC who are not candidates for PD-1/PD-L1 inhibitor therapy based on the results from the TROPION-Breast02 trial.

Datroway (6 mg/kg) is approved in more than 45 countries/regions worldwide for the treatment of adult patients with unresectable or metastatic HR positive, HER2 negative (IHC 0, IHC 1+ or IHC 2+/ISH-) breast cancer who have received prior endocrine-based therapy and chemotherapy for unresectable or metastatic disease based on the results from the TROPION-Breast01 trial.

Datroway (6 mg/kg) is approved in Brazil, Russia, Singapore and the U.S. for the treatment of adult patients with locally advanced or metastatic EGFR-mutated non-small cell lung cancer (NSCLC) who have received prior EGFR-directed therapy and platinum-based chemotherapy, based on the results from TROPION-Lung05 and TROPION-Lung01 trials. Continued approval for this indication in the U.S. may be contingent upon verification and description of clinical benefit in a confirmatory trial.

About the Datroway Clinical Development Program

A comprehensive global clinical development program is underway with more than 20 trials evaluating the efficacy and safety of Datroway across multiple cancers, including NSCLC, TNBC and urothelial cancer. The program includes eight phase 3 trials in lung cancer, five phase 3 trials in breast cancer, one phase 3 trial and one phase 2/3 trial in urothelial cancer evaluating Datroway as a monotherapy and in combination with other cancer treatments in various settings.

(Press release, Daiichi Sankyo, OCT 8, 2026, View Source [SID1234673289])

BioLineRx and Hemispherian Announce Two GLIX1 Presentations at the 31st Society for Neuro-Oncology (SNO) Annual Meeting & Education Day

On October 8, 2026 BioLineRx Ltd. (NASDAQ: BLRX) (TASE: BLRX), a clinical-stage biopharmaceutical company pursuing life-changing therapies in oncology and rare diseases, and Hemispherian AS, a clinical-stage oncology company developing novel small molecule therapeutics, reported that two abstracts featuring GLIX1 will be presented at the 31st Society for Neuro-Oncology (SNO) Annual Meeting & Education Day, taking place November 12-15 in Philadelphia, Pennsylvania.

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The presentations will highlight preclinical research evaluating GLIX1 across multiple glioblastoma models, as well as the design of the ongoing Phase 1/2a clinical trial evaluating GLIX1 in patients with recurrent or progressive high-grade glioma and other solid tumors.

Presentation Details:

Title: GLIX1, a TET2 activator targeting DNA damage response: potent anti-tumor activity across multiple glioblastoma models; orthotopic CDX models and a subcutaneous TMZ-resistant PDX model
Presenter: Dr. Adam Robertson, Ph.D., Chief Scientific Officer, Hemispherian AS
Abstract code: EXTH-31
Format: Poster presentation
Date/time: Friday, November 13, 2026, 7:30-9:30 p.m. EST
Location: Pennsylvania Convention Center, Exhibit Halls D and E

Title: Phase 1/2a study of GLIX1, a novel first-in-class oral TET2 activator, for the treatment of recurrent or progressive high-grade glioma
Presenter: Ditte Primdahl, MD, Northwestern University Feinberg School of Medicine
Abstract code: CTNI-25
Format: Poster presentation
Date/time: Friday, November 13, 2026, 7:30-9:30 p.m. EST
Location: Pennsylvania Convention Center, Exhibit Halls D and E

(Press release, BioLineRx, OCT 8, 2026, View Source [SID1234673288])

Armenia Grants First Marketing Authorizations for Agenus’ BOT+BAL in Previously Treated MSS Metastatic Colorectal Cancer

On October 8, 2026 Agenus Inc. (Nasdaq: AGEN), a leader in immuno-oncology innovation, reported that the Ministry of Health of the Republic of Armenia has granted marketing authorizations for Botvymo (botensilimab, BOT) and Evamplix (balstilimab, BAL), each approved for use in combination with the other for the treatment of adult patients with microsatellite stable (MSS) metastatic colorectal cancer (mCRC) without active liver metastases who have previously received available standard therapies. These are the first marketing authorizations for either medicine anywhere in the world. The approvals are expected to benefit patients in Armenia as well as patients who travel to Armenia for treatment under the care of Armenian oncologists.

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Botensilimab is a multifunctional, Fc-enhanced anti-CTLA-4 antibody designed to activate innate and adaptive antitumor immune responses, including in tumors that have historically responded poorly to conventional immunotherapy. Balstilimab is an anti-PD-1 antibody designed to sustain antitumor T-cell activity.

The approvals are effective as of October 2, 2026. They follow a rigorous review by Armenia’s regulatory authorities of the complete registration dossier, submitted in the international Common Technical Document format used under Eurasian Economic Union rules. The review covered product quality and manufacturing (chemistry, manufacturing and controls), nonclinical data, clinical efficacy and safety data, and the pharmacovigilance system and risk management plan. BOT and BAL were separately submitted and approved for use as a combination regimen. Under the approved product information, Botvymo is administered at 75 mg intravenously every 6 weeks for up to 4 doses, in combination with Evamplix at 240 mg intravenously every 2 weeks for up to 2 years or until disease progression or unacceptable toxicity.

Each marketing authorization is conditional and valid for one year and is renewable based on the clinical updates that Agenus will provide to the Armenian regulator each year.

"Armenia is the first country in the world to grant marketing approval for BOT+BAL," said Garo H. Armen, PhD, Chairman and Chief Executive Officer of Agenus. "The evidence behind this decision has been published in peer-reviewed journals and presented at major cancer conferences, and it has consistently pointed to clinical benefit for patients with metastatic colorectal cancer. We thank Armenia’s health authorities for the depth and care of their review. Patients who have exhausted standard treatments now have a new option, and we are proud to bring it to them."

Clinical Evidence Supporting the Approvals

The Armenian approvals were based on the totality of clinical evidence for BOT+BAL in MSS mCRC, including mature results from the fully enrolled MSS mCRC patient cohort from the Phase 1b C-800-01 study and data from the randomized Phase 2 C-800-25 study. Results from this clinical program have been published in peer-reviewed journals, including Nature Medicine and Clinical Cancer Research, and presented at major oncology congresses, including the ASCO (Free ASCO Whitepaper) Gastrointestinal Cancers Symposium. The efficacy and safety data supporting the approvals are summarized in the approved product information for Botvymo and Evamplix.

Regional Opportunities

Following the Armenian approvals, Agenus will evaluate the potential to seek marketing authorizations for BOT+BAL in the MSS metastatic colorectal cancer setting in other Eurasian Economic Union member countries.

Access to BOT+BAL Outside Armenia

The Armenian marketing authorizations apply within the territory of Armenia.

In France, the national Autorisation d’Accès Compassionnel (AAC) program provides fully reimbursed, hospital-based access to BOT+BAL for eligible patients with MSS metastatic colorectal cancer without active liver metastases, platinum-resistant or platinum-refractory ovarian cancer, and certain advanced soft-tissue sarcomas. In a growing number of other countries, BOT+BAL is available through physician-initiated named-patient programs under local regulations. BAP Pharma serves as Agenus’ global partner for the French AAC pathway and named-patient access programs.

Physicians seeking information about authorized access pathways can visit the Patient Access section of our corporate website.

Important Safety Information

The approved product information for Botvymo and Evamplix includes warnings and precautions for immune-mediated adverse reactions, including colitis and diarrhea, hepatitis, pneumonitis, endocrinopathies, nephritis, myocarditis and pancreatitis, as well as infusion-related reactions. Healthcare professionals in Armenia should consult the approved product information before prescribing.

(Press release, Agenus, OCT 8, 2026, View Source [SID1234673287])

Lantern Pharma to Present at the ThinkEquity Conference in NYC on October 15th, 2026

On October 8, 2026 Lantern Pharma Inc. (NASDAQ: LTRN), an artificial intelligence ("AI") company developing targeted and transformative cancer therapies using its proprietary RADR AI and machine learning ("ML") platform with multiple clinical stage drug programs, reported that Lantern management will be presenting at the ThinkEquity Conference on Thursday, October 15, 2026, at 3:30 p.m. ET at the Mandarin Oriental in New York, NY.

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Webcast Link: https://event.summitcast.com/view/GXv6JAoMEphytK6ggozCk7/VS4pGMrvkgq2xwHrNQevWX
Conference Registration Link: View Source

Lantern Pharma management will be available for one-on-one meetings held throughout the conference.

(Press release, Lantern Pharma, OCT 8, 2026, View Source [SID1234673286])