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Find Clinical Drug Pipeline Developments & Deals by Genmab
Through the Acquisition, Genmab will leverage the worldwide rights of three candidates in clinical development, including PRO1184 (rinatabart sesutecan) for the treatment of FRα-expressing platinum-resistant ovarian cancer.
Epkinly (epcoritamab) is an IgG1-bispecific antibody, being evaluated to-treat relapsed/refractory follicular lymphoma, which is designed to direct cytotoxic T cells selectively to elicit an immune response towards target cell types.
Tivdak (tisotumab vedotin-tftv) is a tissue factor (TF)-directed antibody drug conjugate. It is approved by USFDA for the treatment of cervical cancer.
Tivdak (tisotumab vedotin-tftv) is an antibody-drug conjugate (ADC) composed of Genmab’s human monoclonal antibody directed to tissue factor (TF) and Pfizer’s ADC technology. It is being evaluated in phase 3 studies for the treatment of recurrent or metastatic cervical cancer.
Epkinly (epcoritamab) is an IgG1-bispecific antibody created using Genmab's proprietary DuoBody® technology and administered subcutaneously. It is under clinical development for the treatment of relapsed/refractory follicular lymphoma.
Tivdak (tisotumab vedotin) is an antibody-drug conjugate, which is investigating in phase III and met its primary endpoint of overall survival for recurrent or metastatic cervical cancer compared to chemotherapy.
Tepkinly (epcoritamab) is an IgG1-bispecific antibody created using Genmab's proprietary DuoBody® technology, which is received approval from EU for Diffuse Large B-cell Lymphoma.
Epkinlytm (epcoritamab) is an IgG1-bispecific antibody created using Genmab's proprietary DuoBody® technology, which is received approval from EU for Diffuse Large B-cell Lymphoma.
TIVDAK (tisotumab vedotin) is an antibody-drug conjugate, which is investigating in phase III and met its primary endpoint of overall survival for recurrent or metastatic cervical cancer compared to chemotherapy.
Tepkinly (epcoritamab), if approved, would become the first and only subcutaneous bispecific antibody conditionally approved as a monotherapy in the European Union for the treatment of adult patients with R/R DLBCL and is approved by FDA with brand name Epkinly.
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