Genmab — Juli 2020
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future where forthcoming clinical trials use the subcutaneous formulation rather than traditional daraIV. For these reasons, and assuming FDA/EHA approval in the near future, we support the use of dara-SC
for both standard of care and investigational use moving forward. -
Super.
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Could be this one : https://www.clinicaltrials.gov/ct2/show/NCT03473730
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FDA grants Breakthrough Therapy Designation for Roche’s CD20xCD3 bispecific cancer immunotherapy mosunetuzumab recognising its potential in follicular lymphoma
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FDA grants Breakthrough Therapy Designation for Roche’s CD20xCD3 bispecific cancer immunotherapy mosunetuzumab recognising its potential in follicular lymphoma
This designation is based on results from the phase I/Ib GO29781 study that showed mosunetuzumab demonstrated high response rates and durable complete remissions in people with relapsed or refracto...
(www.roche.com)
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Flot rebound af Genmab. NOVO og ZEAL bliver stående på perronen.
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Det holdt nu ikke mange timer.
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Mcjean...du tjekker bare her. https://www.proinvestor.com/chathistory/-120/finanskalender
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Velbekommen.
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