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On May 14, 2025, the FDA granted accelerated approval to Emrelis (telisotuzumab vedotin) for treating adults with high c-Met protein overexpressing non-small cell lung cancer...
On May 14, 2025, the FDA approved belzutifan (Welireg) for treating adults and children aged 12 and older with locally advanced, unresectable, or metastatic pheochromocytoma...
The FDA has granted accelerated approval to the combination therapy of avutometinib and defactinib for treating KRAS-mutated recurrent low-grade serous ovarian cancer. This decision is...
Chimerix’s drug Dordaviprone has received FDA priority review for treating recurrent H3 K27M-mutant diffuse glioma. With a PDUFA date of August 18, 2025, it could...
Penpulimab-kcqx, developed by Akeso Biopharma, has received FDA approval for treating recurrent or metastatic non-keratinizing nasopharyngeal carcinoma. This PD-1 inhibitor marks a major advancement in...
Dr. Zhang Wei of Tsinghua University leads pioneering research in epigenetic-based immunotherapy for Diffuse Midline Glioma (DMG). His work integrates advanced diagnostics, precision medicine, and...
A groundbreaking case study reveals that epigenetic agent-based immunotherapy significantly regressed tumors in a patient with diffuse midline glioma (DMG), extending survival to 20 months....
Introduction In a stunning surprise that has stunned the international biotech industry, a tiny and micro business in Tianjin, China, has come up with an...
Gliomas Introduction Brain gliomas, especially aggressive types such as glioblastoma multiforme (GBM), have long been extremely challenging to treat because of their insensitivity to traditional...
China has become a leading destination for medical tourism, providing high-end treatment at 30-70% lower prices compared to Western nations. Ranging from state-of-the-art cancer treatments...
4th generation CAR T-cell therapy with IL-15 represents a groundbreaking advancement in cancer immunotherapy. By incorporating IL-15, these engineered T cells exhibit enhanced persistence, potency,...
On April 11, 2025, the Food and Drug Administration sanctioned nivolumab (Opdivo, Bristol Myers Squibb Company) in conjunction with ipilimumab (Yervoy, Bristol Myers Squibb Company)...
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