This page shows the latest Adcetris news and features for those working in and with pharma, biotech and healthcare.
The trial compared Keytruda to Seattle Genetic’s antibody-drug conjugate Adcetris – a standard treatment for relapsed and refractory lymphoma. ... Merck’s drug beat Adcetris in terms of progression-free survival (PFS), according to an interim
Padcev is Seattle's second marketed drug after its lymphoma therapy Adcetris (brentuximab vedotin), which is expanding its business into the solid tumour category.
Approval comes well ahead of the FDA’s action date of 15 March, and gives ADC specialist Seattle its second marketed product after lymphoma therapy Adcetris (brentuximab vedotin), expanding its business ... That would drive a sizeable step up in
Seattle Genetics/Takeda’s classical Hodgkin lymphoma therapy Adcetris (brentuximab vedotin) and Roche’s Kadcyla (trastuzumab emtansine) for breast cancer.
did not achieve a complete response, with Adcetris reducing that measure by 23% compared to the control group. ... Crucially, Adcetris avoids the use of the chemotherapy drug bleomycin, which can be associated with severe and unpredictable toxicity.
months on Adcetris, as well as improvements in median progression-free survival (PFS) and overall response rate, and symptom burden. ... The approval of Adcetris in this setting brings a much needed, effective treatment option to patients living with CTCL
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In its 2019 reviews of Pfizer’s Vizimpro and Takeda’s Adcetris, NICE noted that EQ-5D “may not be sensitive to skin-related diseases” and may fail to fully capture ... Takeda, for example, used EQ- 5D in its Adcetris programme despite doubts
Adcetris (for Hodgkin Lymphoma), Entyvio (for ulcerative colitis and Crohn's Disease) and future compound Ninlaro (an oral protease inhibitor for relapsed/refractory multiple myeloma) which was approved by the FDA
This passion has seemingly been ignited further by the recent FDA approvals of Kadcyla (Genentech/ ImmunoGen) and Adcetris (Seattle Genetics) both following impressive clinic trials in HER2 breast cancer and lymphoma,
Even closer to market is Takeda's monoclonal antibody treatment for Hodgkin's Lymphoma, Adcetris (brentuximab vedotin), which was recommended for European approval in July and which Takeda expects to launch
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