Breaking
🇪🇺 EMA
Biotheryx BTX-9341 Phase 1A Results to Be Presented at ESMO Breast Cancer Congress 2026
NewsMay 5, 2026

Biotheryx BTX-9341 Phase 1A Results to Be Presented at ESMO Breast Cancer Congress 2026

Biotheryx announces Phase 1A dose escalation study results for BTX-9341, a CDK4/6 degrader for HR+/HER2- breast cancer treatment at ESMO 2026.

Dr. Lukas Schneider
Agenus Announces Q1 2026 Financial Report Date for Botensilimab and Balstilimab Cancer Programs
NewsMay 4, 2026

Agenus Announces Q1 2026 Financial Report Date for Botensilimab and Balstilimab Cancer Programs

Agenus will provide Q1 2026 financial results and corporate update on botensilimab and balstilimab cancer immunotherapy programs with regulatory timeline guidance.

Dr. Amina Farouk
Oncolytics Biotech Reports Durable Responses with Pelareorep in RAS-Mutant Colorectal Cancer Trial
NewsMay 4, 2026

Oncolytics Biotech Reports Durable Responses with Pelareorep in RAS-Mutant Colorectal Cancer Trial

Oncolytics Biotech announces sustained clinical benefit with pelareorep immunotherapy in patients with RAS-mutant, microsatellite-stable colorectal cancer.

Dr. Hannah O'Connor
Oncolytics Biotech Pelareorep Shows Durable Responses in RAS-Mutant Colorectal Cancer Trial
NewsMay 4, 2026

Oncolytics Biotech Pelareorep Shows Durable Responses in RAS-Mutant Colorectal Cancer Trial

Oncolytics Biotech reports sustained clinical benefit with pelareorep immunotherapy in second-line RAS-mutant MSS colorectal cancer patients.

Dr. Amina Farouk
Nuvation Bio's IBTROZI Generates $18.5M Revenue in Q1 2026, Shows Strong First-Line Adoption in ROS1+ NSCLC
NewsMay 4, 2026

Nuvation Bio's IBTROZI Generates $18.5M Revenue in Q1 2026, Shows Strong First-Line Adoption in ROS1+ NSCLC

Nuvation Bio reports $18.5M Q1 2026 revenue for IBTROZI (taletrectinib) with majority of 200 new patients being TKI-naïve ROS1+ NSCLC cases.

Prof. Marcus Webb
CAR-T Cell Therapy Europe: Clinical Trials, Safety & Market Access Insights
Analysishematological malignanciesMay 2, 2026

CAR-T Cell Therapy Europe: Clinical Trials, Safety & Market Access Insights

Discover the latest insights on CAR-T Cell Therapy in Europe, focusing on clinical trials, safety profiles, and market access for hematologic cancers.

Dr. Laura Bennett
Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins as Strategic Adviser for DCVax Cancer Vaccine Development
NewsMay 1, 2026

Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins as Strategic Adviser for DCVax Cancer Vaccine Development

Northwest Biotherapeutics names Dr. Annalisa Jenkins as Strategic Adviser to advance DCVax dendritic cell cancer vaccine platform with 25+ years biopharma experience.

Dr. Elena Rossi
FDA Advisory Committee Recommends AstraZeneca's TRUQAP for PTEN-Deficient Metastatic Prostate Cancer
NewsOncology - Prostate CancerMay 1, 2026

FDA Advisory Committee Recommends AstraZeneca's TRUQAP for PTEN-Deficient Metastatic Prostate Cancer

FDA's Oncologic Drugs Advisory Committee recognizes favorable benefit-risk profile for TRUQAP (capivasertib) in PTEN-deficient metastatic prostate cancer treatment.

Dr. Amina Farouk
Telix Pharmaceuticals' TLX101-Px (Pixlumi) Brain Cancer Imaging Drug Accepted for European Review
NewsMay 1, 2026

Telix Pharmaceuticals' TLX101-Px (Pixlumi) Brain Cancer Imaging Drug Accepted for European Review

Telix Pharmaceuticals' TLX101-Px (Pixlumi) glioma imaging drug enters 210-day European regulatory review after MAA acceptance, targeting brain cancer diagnosis.

Dr. Hannah O'Connor
Antibody-Drug Conjugates in Breast Cancer: Enhertu vs. Trodelvy in EU Market
AnalysisoncologyMay 1, 2026

Antibody-Drug Conjugates in Breast Cancer: Enhertu vs. Trodelvy in EU Market

This article compares Enhertu and Trodelvy, two leading antibody-drug conjugates, in their effectiveness for breast cancer treatment in the EU market.

Dr. Natalie Hughes
EMA Conditional Marketing Authorization: Linvoseltamab for RRMM in EU
AnalysisoncologyMay 1, 2026

EMA Conditional Marketing Authorization: Linvoseltamab for RRMM in EU

Linvoseltamab has received EMA's Conditional Marketing Authorization for treating relapsed/refractory multiple myeloma, offering new hope for patients in the EU.

Dr. Yuna Park
Bispecific Antibody Approvals in EU: Teclistamab & Elranatamab Review
AnalysisoncologyApr 30, 2026

Bispecific Antibody Approvals in EU: Teclistamab & Elranatamab Review

This article reviews the recent EU approvals of teclistamab and elranatamab, highlighting their significance in treating multiple myeloma.

Kenji Watanabe