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Details:

Livtencity (maribavir), Phosphotransferase pUL97 inhibitor has been approved by the National Medical Products Administration of China for the treatment of adult patients with Post-transplant CMV Infection/Disease.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: LIVTENCITY

Highest Development Status: Phase IVProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 21, 2023

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LIVTENCITY (maribavir), an orally bioavailable anti-CMV compound, is the first and only antiviral agent that targets and inhibits the UL97 protein kinase and its natural substrates.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: Livtencity

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 19, 2022

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LIVTENCITY (maribavir), an orally bioavailable anti-CMV compound, is the first and only antiviral agent that targets and inhibits the UL97 protein kinase and its natural substrates.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: Livtencity

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 11, 2022

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Positive Opinion Based on Phase 3 SOLSTICE Study Demonstrating Maribavir (livtencity) Was Statistically Superior to Conventional Therapies at Study Week 8, for Primary Endpoint.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: Livtencity

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 16, 2022

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Data include exploratory analysis showing Livtencity treated patients with post-transplant cytomegalovirus infections/disease had reductions in hospitalizations (34.8%) and length of hospital stay (53.8%) compared to those treated with conventional antiviral therapies.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: Livtencity

Highest Development Status: ApprovedProduct Type: Small 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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LIVTENCITY (maribavir), an orally bioavailable anti-CMV compound, is the first and only antiviral agent that targets and inhibits the pUL97 protein kinase and its natural substrates.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: Livtencity

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable November 24, 2021

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The results of the SOLSTICE trial are promising and show that maribavir may help with post-transplant CMV viremia, including cases of drug-resistance for which there is an unmet need.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: SHP620

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: SHIRE LLC

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable May 21, 2021

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More than three times as many transplant recipients with confirmed resistant cytomegalovirus (CMV) infection at baseline receiving the investigational drug Maribavir achieved cmv viremia clearance compared to conventional antiviral therapies.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: TAK-620

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable March 15, 2021

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More than twice as many transplant recipients with R/R CMV infection/disease treated with maribavir achieved confirmed CMV viremia clearance at Study Week 8, the study’s primary endpoint, as compared to 23.9% of those on conventional antiviral therapies.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: TAK-620

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable February 12, 2021

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Phase 3 clinical trial evaluating the efficacy and safety of the investigational drug TAK-620 (maribavir), in the treatment of transplant recipients with refractory/resistant cytomegalovirus (CMV) infection met its primary endpoint.


Lead Product(s): Maribavir

Therapeutic Area: Infections and Infectious Diseases Product Name: TAK-620

Highest Development Status: Phase IIIProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable December 04, 2020

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