News
18h
TipRanks on MSNAstraZeneca’s Phase III Breast Cancer Study: A Potential Game Changer?
AstraZeneca, in collaboration with Daiichi Sankyo, is conducting a Phase III clinical study titled A Phase III Study of Dato-DXd With or Without Durvalumab Compared With Investigator’s Choice of ...
1d
TipRanks on MSNAstraZeneca’s Promising Phase I Study on Advanced Solid Tumors: Key Insights for Investors
Take advantage of TipRanks Premium at 50% off! Unlock powerful investing tools, advanced data, and expert analyst insights to help you invest with confidence.
In August 2025, Seagen announced a studies how well tucatinib works for solid tumors that make either more HER2 or a ...
In August 2025, BioNTech SE organized a Phase II study in participants with untreated extended-stage small-cell lung cancer (ES-SCLC) (Cohort 1) or small-cell lung cancer (SCLC) which has progressed ...
MATTERHORN supports the global adoption of perioperative durvalumab plus FLOT as a new standard for patients with localized gastric and gastroesophageal junction adenocarcinoma,” said Yelena Y.
From immunotherapy to targeted agents, learn how innovative strategies are redefining outcomes in early-stage triple-negative ...
Urogen's Zusduri is the first non-surgical therapy to be approved for NMIBC, setting a new standard for the indication.
AstraZeneca (AZ) has announced that Imfinzi (durvalumab) in combination with Imjudo (tremelimumab) has been recommended by ...
Hepatocellular carcinoma remains a substantial global public health concern, disproportionately affecting low-income and middle-income countries, particularly in Africa.1 Its burden in Africa is ...
The supplemental Biologics License Application for the gastric/GEJ cancer indication is supported by data from the double-blind, placebo-controlled MATTERHORN trial.
The US Food and Drug Administration (FDA) has granted priority review to durvalumab for the treatment of patients with resectable, stage II-IVA gastric or gastroesophageal junction (GEJ) cancer.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results