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Under the agreement, Everest Medicines will transfer all development and commercialization rights to Gilead for Trodelvy® (sacituzumab govitecan), a first-in-class Trop-2 directed antibody-drug conjugate, in Greater China and South Korea, among Other Asian Markets.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: ApprovedProduct Type: Large molecule

Recipient: Everest Medicines

Deal Size: $455.0 million Upfront Cash: $280.0 million

Deal Type: Acquisition March 26, 2023

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In single-arm Phase 2 study, Trodelvy demonstrated an ORR of 33.3 percent and a median DoR of 7.7 months, as determined by local assessment, in 108 adult TNBC patients who had previously received a median of three prior systemic therapies in the metastatic setting.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable April 22, 2022

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Gilead gains Trodelvy, Immunomedics' lead ADC, is the first ADC the FDA has approved for the treatment of people with metastatic triple-negative breast cancer and is also the first FDA-approved anti-Trop-2 ADC.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Gilead Sciences

Deal Size: $21,000.0 million Upfront Cash: $15,000.0 million

Deal Type: Acquisition October 23, 2020

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Under the agreement, Immunomedics gains commercial rights for application of ProteoNic’s technology platform to the development of specified proprietary products from mammalian cells.


Lead Product(s): Recombinant protein

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: UndisclosedProduct Type: Large molecule

Recipient: ProteoNic

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Licensing Agreement October 20, 2020

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Trodelvy has shown encouraging activity in an early-stage study in brain cancers, including partial responses in small cohorts of patients with brain metastasis from breast cancer and recurrent glioblastoma.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: Phase IProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable October 12, 2020

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Trodelvy achieves a 27 percent overall response rate and a 5.9-month median duration of response in heavily-pretreated patients with metastatic urothelial cancer (mUC).


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: Phase IIIProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 19, 2020

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Results include partial responses in small cohort of patients with brain metastasis from breast cancer (BMBC) and recurrent glioblastoma (rGBM).


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: Phase IProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 18, 2020

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Acquisition provides Gilead with TrodelvyTM (sacituzumab govitecan-hziy), a first-in-class Trop-2 directed antibody-drug conjugate that was granted accelerated approval by the FDA for the treatment of adult patients with metastatic triple-negative breast cancer.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Gilead Sciences

Deal Size: $21,000.0 million Upfront Cash: $15,000.0 million

Deal Type: Acquisition September 13, 2020

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Collaboration aims to evaluate Trodelvy in combination with Tecentriq in patients with metastatic urothelial cancer and metastatic non-small cell lung cancer. Roche will be conducting two open-label, randomized Phase 1b/2 studies using its MORPHEUS platform.


Lead Product(s): Sacituzumab Govitecan,Atezolizumab

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: Phase I/ Phase IIProduct Type: Large molecule

Recipient: F. Hoffmann-La Roche

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Collaboration July 13, 2020

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Trodelvy significantly improved progression-free survival (PFS) and overall survival (OS) in previously-treated brain metastasis negative patients with advanced mTNBC.


Lead Product(s): Sacituzumab Govitecan

Therapeutic Area: Oncology Product Name: Trodelvy

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 06, 2020

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