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Hoffmann-La Roche","sponsor":"Halozyme Therapeutics","pharmaFlowCategory":"DU","amount":"Not Applicable","upfrontCash":"Not Applicable","newsHeadline":"Halozyme Announces Roche Receives European Commission Approval of Tecentriq\u00ae SC with ENHANZE\u00ae Representing the EU's First Subcutaneous PD-(L)1 Cancer Immunotherapy for Multiple Cancer Types","therapeuticArea":"Oncology","highestDevelopmentStatus":"Approved","country":"SWITZERLAND","productType":"Large molecule","productStatus":"Approved","date":"January 2024","url1":"","url2":"","graph1":"Large molecule","graph2":"F. Hoffmann-La Roche"}]

Find Approved Oncology Drugs in Clinical Development in SWITZERLAND

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            Tecentriq (atezolizumab) is a PDL-1 inhibitor monoclonal antibody, It is approved by EMA for the treatment of patients with previously treated locally advanced or metastatic non-small cell lung cancer (NSCLC).

            Lead Product(s): Atezolizumab

            Therapeutic Area: Oncology Product Name: Tecentriq

            Highest Development Status: Approved Product Type: Large molecule

            Partner/Sponsor/Collaborator: Halozyme Therapeutics

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable January 16, 2024

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            Pluvicto (lutetium Lu 177 vipivotide tetraxetan) is a prostate-specific membrane antigen (PSMA) which is approved for the treatment of PSMA-positive metastatic castration-resistant prostate cancer (mCRPC).

            Lead Product(s): Lutetium-177 Vipivotide Tetraxetan

            Therapeutic Area: Oncology Product Name: Pluvicto

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable January 05, 2024

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            Pluvicto™ (lutetium (177Lu) vipivotide tetraxetan) is an intravenous radioligand therapy, which is investigated for the treatment of PSMA-positive metastatic castration-resistant prostate cancer.

            Lead Product(s): Lutetium Lu 177 Vipivotide Tetraxetan)

            Therapeutic Area: Oncology Product Name: Pluvicto

            Highest Development Status: Approved Product Type: Peptide

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable October 23, 2023

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            Alecensa (alectinib) is a small molecule and act as ALK inhibitor, which is being investigated in PIII trial for people With ALK-positive early-stage lung cancer.

            Lead Product(s): Alectinib Hydrochloride

            Therapeutic Area: Oncology Product Name: Alecensa

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable October 18, 2023

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            ADSTILADRIN® (nadofaragene firadenovec-vncg) is the first and only FDA-approved intravesical gene therapy for the treatment of adult patients with high-risk Bacillus Calmette-Guérin (BCG)-unresponsive non-muscle invasive bladder cancer.

            Lead Product(s): Nadofaragene Firadenovec

            Therapeutic Area: Oncology Product Name: Adstiladrin

            Highest Development Status: Approved Product Type: Cell and Gene therapy

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable September 12, 2023

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            Tecentriq (atezolizumab) is a monoclonal antibody, binds with PD-L1, which is expressed on tumour cells and tumour-infiltrating immune cells, blocking its interactions with both PD-1 and B7.1 receptors. By inhibiting PD-L1, drug may enable the activation of T-cells.

            Lead Product(s): Atezolizumab

            Therapeutic Area: Oncology Product Name: Tecentriq

            Highest Development Status: Approved Product Type: Large molecule

            Partner/Sponsor/Collaborator: Halozyme Therapeutics

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable August 29, 2023

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            Under the agreement, Royalty Pharma is acquiring a 5.1 percentage royalty on net sales of Adstiladrin (nadofaragene firadenovec-vncg), a gene therapy developed as a treatment for adult patients with BCG-unresponsive NMIBC, in the United States.

            Lead Product(s): Nadofaragene Firadenovec-vncg

            Therapeutic Area: Oncology Product Name: Adstiladrin

            Highest Development Status: Approved Product Type: Cell and Gene therapy

            Partner/Sponsor/Collaborator: Royalty Pharma

            Deal Size: $500.0 million Upfront Cash: $300.0 million

            Deal Type: Agreement August 23, 2023

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            Zynlonta (loncastuximab tesirine-lpyl), an antibody-drug conjugate (ADC) targeting CD19, is approved by FDA and EU for the treatment of adult patients with relapsed or refractory (r/r) diffuse large B-cell lymphoma (DLBCL).

            Lead Product(s): Loncastuximab Tesirine

            Therapeutic Area: Oncology Product Name: Zynlonta

            Highest Development Status: Approved Product Type: Large molecule

            Partner/Sponsor/Collaborator: Overland Pharmaceuticals

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable July 24, 2023

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            Columvi (glofitamab) is an investigational CD20xCD3 T-cell-engaging bispecific antibody designed to target CD3 on the surface of T-cells and CD20 on the surface of B-cells. It is approved by EU for relapsed or refractory diffuse large B-cell lymphoma.

            Lead Product(s): Glofitamab,Obinutuzumab,Tocilizumab

            Therapeutic Area: Oncology Product Name: Columvi

            Highest Development Status: Approved Product Type: Large molecule

            Partner/Sponsor/Collaborator: Not Applicable

            Deal Size: Not Applicable Upfront Cash: Not Applicable

            Deal Type: Not Applicable July 11, 2023

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            The agreement aims to to develop and market an anti-cancer drug, Tasigna (nilotinib), a transduction inhibitor, used for treatment of chronic myeloid leukemia.

            Lead Product(s): Nilotinib

            Therapeutic Area: Oncology Product Name: Tasigna-Generic

            Highest Development Status: Approved Product Type: Small molecule

            Partner/Sponsor/Collaborator: Aurobindo Pharma

            Deal Size: Undisclosed Upfront Cash: Undisclosed

            Deal Type: Licensing Agreement June 23, 2023

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