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BioNTech Pact and Stock Sale Infuse Autolus With $600M for Its Cell Therapies - Vimarsana News

BioNTech Pact and Stock Sale Infuse Autolus With $600M for Its Cell Therapies

Autolus will apply the capital to its CAR T-cell therapy currently under FDA review in cancer and in early clinical development in lupus. Meanwhile, BioNTech will gain access to Autolus’s cell therapy manufacturing assets as well as technologies that could support the R&D of in vivo therapies and antibody drug conjugates.

Indigenous CAR-T cell therapy now available for commercial use: 'first' patient declared free of cancer | Mumbai News - Vimarsana News

Indigenous CAR-T cell therapy now available for commercial use: 'first' patient declared free of cancer | Mumbai News

Developed by ImmunoAct, IIT Bombay and Tata Memorial Hospital, the therapy has been administered to 15 patients in India. Three of them have successfully achieved cancer remission. Dr Gupta, the first commercial patient to be declared free of cancer, speaks of his experience exclusively to The Indian Express

Beyond chemotherapy: Navigating the promise and perils of CAR-T therapy in pediatric cancer - Vimarsana News

Beyond chemotherapy: Navigating the promise and perils of CAR-T therapy in pediatric cancer

Upon hearing the phrase ‘cancer treatment’, the first word that can typically spring to mind is chemotherapy – a primary therapy which uses powerful chemicals to destroy rapidly growing cancer cells in the body.

North Carolina: FDA warning of secondary cancer risk tied to CAR T cell therapy, officials say - Vimarsana News

North Carolina: FDA warning of secondary cancer risk tied to CAR T cell therapy, officials say

The FDA suggests people participating in clinical trials with these therapies are monitored for the rest of their lives for any new cancerous cells.

Source: wxii12.com
FDA Calls for New Safety Warning for the Class of CAR T Cancer Therapies - Vimarsana News

FDA Calls for New Safety Warning for the Class of CAR T Cancer Therapies

Two months after announcing an inquiry into reports of new cancers in patients treated with CAR T-cell therapies, the FDA is directing makers of these therapies to add new safety warnings to product labels describing this risk. Companies have 30 calendar days to comply.