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Pluvicto becomes the first PSMA-targeted intravenous radioligand therapy – combining a targeting compound or ligand with a therapeutic radionuclide or radioactive particle (in this case, lutetium-177) – to demonstrate clinical benefit in mCRPC patients before receiving taxane-based chemotherapy.
The green light for Pemazyre (pemigatinib) has been hailed by cholangiocarcinoma charity AMMF, which said it was a “major milestone” in the fight against the “Cinderella” cancer, which for years has been overlooked by drugdevelopers.
Roche’s drug is already FDA-approved as a monotherapy and in combination with Avastin (bevacizumab) and chemotherapy for previously-untreated NSCLC with high PD-L1 expression. Meanwhile, drugs targeting TIM-3, LAG3, VISTA and STING also coming through development.
After a string of disappointments including the failure of bintrafusp alfa , a drugdeveloped with Germany’s Merck KGaA in lung cancer, any approval is welcome news.
The availability of oral chemotherapy treatments would provide stomach cancer patients with the option of more efficacious drugs with improved tolerability in a more convenient dosage format” The poor clinical outcomes of stomach cancer make it a key target for drugdevelopment. New hope for stomach cancer patients.
PSMAfore, is a Phase III, open-label, multi-centre, 1:1 randomised study comparing the efficacy and safety of Pluvicto to a change in ARPI in 469 patients with PSMA–positive mCRPC. The PSMAfore study. Novartis is evaluating opportunities to investigate Pluvicto in earlier stages of prostate cancer.
President, Global DrugDevelopment and Chief Medical Officer, Novartis. For many of these patients, there are currently no targeted therapeutic options outside of the standard chemotherapy and ET. The risk of recurrence peaks within the first three years after initial diagnosis and continues over decades.
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