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Liver transplant is a critical treatment for cirrhosis due to alcoholism, providing an opportunity for recuperation for end-stage liver disease patients. Stringent eligibility criteria, such...
Living donor liver transplant (LDLT) is vital in the treatment of organ deficits, with improved success rates and shorter waiting periods. With increased cases of...
Following a liver transplant, it is important to take lifelong medicines to avoid organ rejection and control resultant conditions. This manual deals with important immunosuppressive...
On December 18, 2024, the Food and Drug Administration sanctioned ensartinib (Ensacove, Xcovery Holdings, Inc.) for adult patients with anaplastic lymphoma kinase (ALK)-positive locally...
The FDA has approved cosibelimab (iPDL1) for metastatic or locally advanced cutaneous squamous cell carcinoma (cSCC). This PD-L1 inhibitor demonstrated significant efficacy in clinical trials,...
The FDA has approved durvalumab (Imfinzi) for limited-stage small cell lung cancer (LS-SCLC), marking a significant advancement in treatment. This approval is based on clinical...
Astraeus asiaticus, an edible wild mushroom, has shown remarkable anticancer and antioxidant potential. Researchers identified key bioactive compounds that inhibit cervical, breast, and lung cancer...
The FDA has granted accelerated approval to Zenocutuzumab for non-small cell lung cancer and pancreatic cancer with NRG1 gene fusion. This bispecific antibody targets HER2...
The FDA has granted accelerated approval to Zanidatamab for previously treated, unresectable, or metastatic HER2-positive cancers. This bispecific antibody targets HER2 with enhanced precision, offering...
The FDA has approved Revumenib for relapsed or refractory acute leukemia with KMT2A translocation. This breakthrough treatment offers new hope for patients with limited options....
CAR T-cell therapy is revolutionizing cancer treatment, offering a highly personalized approach to fighting hematologic malignancies. Early intervention with this groundbreaking therapy can significantly improve...
On November 8, 2024, the Food and Drug Administration sanctioned obecabtagene autoleucel (Aucatzyl, Autolus Inc.), a CD19-targeted genetically engineered autologous CAR T cell therapy, for...
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