This page shows the latest classical Hodgkin's lymphoma news and features for those working in and with pharma, biotech and healthcare.
Tyvyt’s major rival is Merck &Co’s Keytruda (pembrolizumab), which holds approvals across a range of NSCLC indications. ... Tyvyt has also been approved in China for the treatment of relapsed or refractory classical Hodgkin’s lymphoma (cHL).
BeiGene's PD-1 inhibitor tislelizumab was approved in China last week for use in classical Hodgkin’s lymphoma patients who have already received at least two prior lines of treatment. ... The country’s national medicines regulator – the Chinese
MCL is an aggressive type of non-Hodgkin’s lymphoma (NHL) for which Brukinsa also claimed a breakthrough designation from the FDA earlier this year. ... BeiGene is also developing PD-1 inhibitor tislelizumab – which has been filed for approval in
The US regulator awarded the status for zanubrutinib as a second-line treatment for mantle cell lymphoma (MCL), an aggressive type of non-Hodgkin’s lymphoma for which the drug also ... In addition to zanubrutinib, BeiGene is also developing PD-1
1 inhibitor tislelizumab for relapsed/refractory classical Hodgkin’s lymphoma. ... The current pace of development of the biotech ecosystem in China is remarkable,” said Simon To, Chi-Med’s chairman.
Tyvyt (sintilimab) was jointly developed by Innovent and partner Eli Lilly in China and was approved by the National Medical Products Administration (NMPA) for relapsed or refractory classical Hodgkin's lymphoma ... The home-grown PD-1 inhibitors join
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One of the best known pharma leaders in China, Dr Wu’s most recent achievement was to build Pfizer into one of the top multinational firms in China. ... CDA). The company is filing first for patients with relapsed/refractory classical Hodgkin’s
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