AbbVie’s Venclexta granted full US approval in AML
FDA approved therapy for newly-diagnosed acute myeloid leukaemia patients
Read Moreby Lucy Parsons | Oct 19, 2020 | News | 0
FDA approved therapy for newly-diagnosed acute myeloid leukaemia patients
Read Moreby Anna Smith | Mar 24, 2020 | News | 0
Roche also reported that safety for Venclexta/Venclyxto with azacitidine appeared consistent with the known safety profile of these medicines.
Read Moreby Anna Smith | Mar 25, 2019 | News | 0
US regulators have posted a safety statement warning of an increased risk of death for patients receiving AbbVie’s venetoclax with bortezomib and dexamethasone for melanoma patients.
Read Moreby Selina McKee | Mar 19, 2019 | News | 0
US regulators have placed a partial clinical hold on all trials assessing venetoclax for multiple myeloma after a higher than expected number of patient deaths.
Read Moreby Selina McKee | Jul 12, 2018 | News | 0
Roche group Genentech has filed an application to market Venclexta in the US for acute myeloid leukemia (AML).
Read Moreby Selina McKee | Jun 18, 2018 | News | 0
AbbVie has unveiled new data showing high and durable undetectable minimal residual disease rates in patients with chronic lymphocytic leukaemia treated with venetoclax in combination with rituximab.
Read Moreby Selina McKee | Jun 11, 2018 | News | 0
US regulators have approved a combination of AbbVie and Roche’s Venclexta in combination with Roche/Biogen’s Rituxan (rituximab) to treat chronic lymphocytic leukaemia (CLL) or small lymphocytic lymphoma (SLL).
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