India’s Tata Institute develops tablet for cancer recurrence prevention

India’s Tata Institute develops tablet for cancer recurrence prevention
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来源: Pharmaceutical Technology
The pro-oxidant tablet has shown a 30% effectiveness in preventing cancer. White Bear studio / Shutterstock.com.
India’s Tata Institute of Fundamental Research (TIFR) has announced the development of a new pro-oxidant tablet, combining resveratrol and copper (R+Cu), that has the potential to prevent the recurrence of cancer.
More than a decade of research at the Tata Memorial Centre has resulted in the creation of this tablet which will be priced at around Rs100 ($1.2), Indian media publication NDTV has reported.
The institute’s findings suggest that cancer cell remnants, known as cell-free chromatin particles (cfChPs), can induce cancer in healthy cells, leading to new tumour formation.
The R+Cu tablet, when ingested, produces oxygen radicals within the stomach.
These radicals are rapidly absorbed into the bloodstream, where they target and destroy cfChPs, hindering the process of metastasis—the spread of cancer cells to other body parts.
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India’s Tata Institute develops tablet for cancer recurrence prevention
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来源: Pharmaceutical Technology
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India’s Tata Institute develops tablet for cancer recurrence prevention
Preview
来源: Pharmaceutical Technology
The tablet also reduces the toxicity associated with chemotherapy and diminishes the overall side effects of cancer treatment by around 50%.
It has shown 30% effectiveness in preventing cancer.
Its potential extends to the treatment of cancers including pancreatic, oral and lung.
Tata Memorial Hospital senior cancer surgeon Dr Rajendra Badve stated: “Tata doctors were working on this tablet for almost a decade.
“The tablet is awaiting approval from the Food Safety and Standards Authority of India (FSSAI). TIFR scientists have applied to FSSAI to approve this tablet.
“This tablet will be available everywhere for just Rs100.”
The institute plans to make the tablet available from June/July 2024 for cancer patients following approval from the Indian regulator.
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