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FINTEPLA® (fenfluramine) oral solution is a prescription medication approved in the U.S. and Europe, and under regulatory review in Japan, for the treatment of seizures associated with Dravet syndrome in patients two years of age and older.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: UCB Pharma S.A

Deal Size: $1,900.0 million Upfront Cash: $1,900.0 million

Deal Type: Acquisition March 07, 2022

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FINTEPLA (fenfluramine) is approved by the FDA and European Commission for the treatment of seizures associated with Dravet syndrome and is in development in Japan for the treatment of seizures associated with Dravet syndrome.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

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 04, 2022

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The transaction will broaden and build upon UCB's role as a leader in rare forms of epilepsy after adding FINTEPLA® to UCB's existing product line and complementing existing medicines and expanding clinical development pipeline of epilepsy.


Lead Product(s): Fenfluramine Hydrochloride

Therapeutic Area: Neurology Product Name: Fintepla

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: UCB Pharma S.A

Deal Size: $1,900.0 million Upfront Cash: $1,900.0 million

Deal Type: Acquisition January 19, 2022

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The submission is based on the results of Phase 3, which met its primary objective in demonstrating that patients in the FINTEPLA (Fenfluramine) achieved a 64.8% greater reduction in mean monthly convulsive seizures compared to the placebo group.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

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 21, 2021

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In the long-term trial, FINTEPLA was generally well tolerated with no observed valvular heart disease or pulmonary hypertension.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

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 September 30, 2021

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sNDA is supported by Phase 3 Study 1601 for FINTEPLA® (fenfluramine) for treatment of seizures associated with Lennox-Gastaut Syndrome to FDA. FINTEPLA is approved by the FDA and European Commission for treatment of seizures associated with Dravet syndrome.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: PPD

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable September 28, 2021

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Zogenix plans to submit a new drug application (J-NDA) for FINTEPLA in Japan for the treatment of seizures associated with Dravet syndrome by year end.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Nippon Shinyaku

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable August 26, 2021

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Across studies, FINTEPLA has been generally well-tolerated, with no observed cases of pulmonary arterial hypertension (PAH) or valvular heart disease (VHD). The most common adverse events were reported as decreased appetite, fatigue, diarrhea, and pyrexia.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

Highest Development Status: ApprovedProduct Type: Small molecule

Partner/Sponsor/Collaborator: Not Applicable

Deal Size: Not Applicable Upfront Cash: Not Applicable

Deal Type: Not Applicable July 21, 2021

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The new program supports physician access to FINTEPLA in other parts of the world, where local regulations allow, including European countries where reimbursement has not yet been established.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

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 27, 2021

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More LGS study patients treated with FINTEPLA (fenfluramine) showed improvement in each of the BRIEF 2 indexes that have been used to assess behavior, emotion, and cognitive function in intractable epilepsy and other developmental conditions.


Lead Product(s): Fenfluramine

Therapeutic Area: Neurology Product Name: Fintepla

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 April 22, 2021

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