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01

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : The start of dosing in the ACTION Study, designed to serve as a single registration trial and will evaluate the efficacy and safety of VPA-985 (lixivaptan), a nonpeptide selective vasopressin V2 receptor antagonist, in a broad group of ADPKD patients.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

February 24, 2022

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

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02

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : Decision is based on reassessment of commercial potential of VPA-985 (lixivaptan) as potential best-in-class therapy for patients with ADPKD, following recent observation of alanine aminotransferase and aspartate aminotransferase elevations in ALERT Stud...

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

February 06, 2022

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Inapplicable

Deal Size : Inapplicable

Deal Type : Inapplicable

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03

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : Lixivaptan (VPA-985) is an orally active and selective vasopressin receptor V2 antagonist, with IC50 values of 1.2 and 2.3 nM for human and rat V2, respectively.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

May 27, 2021

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Morgan Stanley

Deal Size : $330.0 million

Deal Type : Public Offering

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04

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : Centessa Pharmaceuticals portfolio consists of four clinical stage programs, including two that are in late-stage clinical development. Palladio Biosciences, a subsidiary of Centessa, is developing lixivaptan, an oral non-peptide of kidney diseases.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

February 16, 2021

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : General Atlantic

Deal Size : $250.0 million

Deal Type : Series A Financing

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05

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : The ALERT Study, designed to assess the safety of lixivaptan in autosomal dominant polycystic kidney disease (ADPKD) patients who previously discontinued therapy with tolvaptan due to liver toxicity, is currently recruiting patients in the United States.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

November 17, 2020

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Centessa Pharmaceuticals

Deal Size : Inapplicable

Deal Type : Inapplicable

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06

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : The presentation will include the results of more than 12 months of safe treatment with lixivaptan in this study, which was conducted as an expanded access clinical study under an IND.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Inapplicable

October 20, 2020

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Centessa Pharmaceuticals

Deal Size : Inapplicable

Deal Type : Inapplicable

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07

BePharma
Not Confirmed
BePharma
Not Confirmed

Details : Proceeds from the financing will fund Palladio’s Phase 3 ALERT Study and advance operations.

Product Name : VPA-985

Product Type : Other Small Molecule

Upfront Cash : Undisclosed

September 25, 2020

Lead Product(s) : Lixivaptan

Therapeutic Area : Genetic Disease

Highest Development Status : Phase III

Sponsor : Samsara BioCapital

Deal Size : $20.0 million

Deal Type : Series B Financing

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