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Astellas Pharma
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Country
Country
Japan
Address
Address
2-5-1, Nihonbashi-Honcho, Chuo-Ku, Tokyo 103-8411
Telephone
Telephone
+81-3-3244-3000

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Details:

Under the agreement, Astellas will have access to Invenra’s cutting-edge B-Body® bispecific antibody platform to support its focused research and development initiatives.


Lead Product(s): Undisclosed

Therapeutic Area: Technology Product Name: Undisclosed

Highest Development Status: Discovery PlatformProduct Type: Large molecule

Recipient: Invenra

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement April 09, 2024

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The collaboration is to Utilize CytomX’s Novel Probody® Technology Platform for CD3 Bispecific Targets for the treatment of cancer. CytomX and Astellas are also collaborating on additional conditionally activated TCB programs.


Lead Product(s): Undisclosed

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Large molecule

Recipient: CytomX Therapeutics

Deal Size: $1,680.0 million Upfront Cash: $80.0 million

Deal Type: Collaboration April 03, 2024

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Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda (pembrolizumab), a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.


Lead Product(s): Enfortumab Vedotin,Pembrolizumab

Therapeutic Area: Oncology Product Name: Padcev

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Pfizer Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 28, 2024

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Astellas' Vyloy (zolbetuximab), a CLDN 18.2 inhibitor has been approved in combination with chemotherapy for patients with HER2-negative, CLDN18.2 positive, unresectable, advanced or recurrent gastric cancer.


Lead Product(s): Zolbetuximab,Oxaliplatin,Calcium Folinate

Therapeutic Area: Oncology Product Name: VYLOY

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 26, 2024

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Xtandi (enzalutamide) becomes the first and only androgen receptor signaling inhibitor approved by the FDA for the treatment of patients with nonmetastatic castration-sensitive prostate cancer with high-risk BCR for metastasis.


Lead Product(s): Enzalutamide

Therapeutic Area: Oncology Product Name: Xtandi

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Pfizer Inc

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 22, 2024

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The clinical candidate is the first PROBODY® T-cell engaging bispecific (TCB) molecule under the alliance between CytomX and Astellas to progress into a GLP toxicology study.


Lead Product(s): Undisclosed

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: PreclinicalProduct Type: Large molecule

Recipient: CytomX Therapeutics

Deal Size: $1,680.0 million Upfront Cash: $80.0 million

Deal Type: Collaboration March 18, 2024

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Details:

Under the terms of the agreement, Ubiquigent will provide Nanna with access to its deubiquitylase (DUB) focused drug discovery platform to support the development of novel therapeutics for human disease targets selected by Nanna.


Lead Product(s): Undisclosed

Therapeutic Area: Oncology Product Name: Undisclosed

Highest Development Status: DiscoveryProduct Type: Small molecule

Recipient: Ubiquigent

Deal Size: Undisclosed Upfront Cash: Undisclosed

Deal Type: Agreement March 11, 2024

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Cresemba (isavuconazonium sulfate) is the prodrug of isavuconazole which is an azole antifungal indicated for the treatment of invasive aspergillosis and invasive mucormycosis.


Lead Product(s): Isavuconazonium Sulfate

Therapeutic Area: Infections and Infectious Diseases Product Name: Cresemba

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 11, 2024

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Veozah (fezolinetant) is a neurokinin 3 (NK3) receptor antagonist indicated for the treatment of moderate to severe vasomotor symptoms due to menopause.


Lead Product(s): Fezolinetant

Therapeutic Area: Obstetrics/Gynecology (Women’s Health) Product Name: Veozah

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 03, 2024

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Details:

Padcev (enfortumab vedotin-ejfv), a nectin-4 inhibitor ADC in combination with Keytruda (pembrolizumab), a PD-1 inhibitor. It is being evaluated for the treatment of locally advanced or metastatic urothelial cancer.


Lead Product(s): Enfortumab Vedotin,Pembrolizumab

Therapeutic Area: Oncology Product Name: Padcev

Highest Development Status: ApprovedProduct Type: Large molecule

Partner/Sponsor/Collaborator: Merck & Co

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 15, 2024

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