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Genmab Announces European Commission Approval of TEPKINLY® (epcoritamab) for Adults with Relapsed or

Company AnnouncementTEPKINLY® (epcoritamab) is the first and only subcutaneous bispecific antibody approved as a monotherapy for adult patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) after two or more lines of systemic therapyConditional marketing authorization approval from the Eur. ....

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AbbVie Announces European Commission Approval of TEPKINLY® (epcoritamab) for Adults with Relapsed or Refractory Diffuse Large B-cell Lymphoma

TEPKINLY® is the first and only subcutaneous bispecific antibody approved as a monotherapy for adult patients with relapsed or refractory diffuse large B-cell lymphoma after two or more lines of. ....

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Genmab Announces European Commission Approval of TEPKINLY® (epcoritamab) for Adults with Relapsed or Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)

Company Announcement TEPKINLY® is the first and only subcutaneous bispecific antibody approved as a monotherapy for adult patients with relapsed or refractory diffuse large B-cell lymphoma . ....

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Mirati Therapeutics Provides Update on Regulatory Review in the European Union of KRAZATI (adagrasib) for the Treatment of Advanced Non-Small Cell Lung Cancer (NSCLC) with a KRAS G12C Mutation

SAN DIEGO and ZUG, Switzerland, July 21, 2023 /PRNewswire/ Mirati Therapeutics, Inc.® , a commercial stage biotechnology company, today announced the European Medicine Agency s Committee for. ....

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Mirati Therapeutics (MRTX) Provides Update on Regulatory Review in EU of KRAZATI

Mirati Therapeutics (MRTX) Provides Update on Regulatory Review in EU of KRAZATI
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