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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) - Vimarsana News

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 ...

Merck and Eisai Provide Update on Two Phase 3 Trials Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Patients With Certain Types of Metastatic Non-Small Cell Lung Cancer - Vimarsana News

Merck and Eisai Provide Update on Two Phase 3 Trials Evaluating KEYTRUDA® (pembrolizumab) Plus LENVIMA® (lenvatinib) in Patients With Certain Types of Metastatic Non-Small Cell Lung Cancer

Merck , known as MSD outside of the United States and Canada, and Eisai today provided updates on two Phase 3 trials, LEAP-006 and LEAP-008, evaluating KEYTRUDA, Merck’s anti-PD-1 therapy, plus...

Valneva Reports Half Year 2023 Financial Results and Provides Corporate Updates -September 21, 2023 at 01:01 am EDT - Vimarsana News

Valneva Reports Half Year 2023 Financial Results and Provides Corporate Updates -September 21, 2023 at 01:01 am EDT

 Product sales more than doubled in the first half of 2023 to €69.7 million compared to €33.3 million in the first half of 2022 Driven by IXIARO® and DUKORAL® sales, both of which benefited...

European Commission Approves Pfizer's LITFULO™ for Adolescents and Adults With Severe Alopecia Areata | Region - Vimarsana News

European Commission Approves Pfizer's LITFULO™ for Adolescents and Adults With Severe Alopecia Areata | Region

NEW YORK--(BUSINESS WIRE)--Sep 19, 2023--

Labeling for Biosimilar and Interchangeable Biosimilar Products - Vimarsana News

Labeling for Biosimilar and Interchangeable Biosimilar Products

Labeling for Biosimilar and Interchangeable Biosimilar Products

Source: fda.gov