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Details:
CVL-751 (tavapadon) is the first and only D1/D5 receptor partial agonist, which is being studied as a once-daily treatment for patients with parkinson’s disease.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: CVL-751
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable April 18, 2024
Details:
Cerevel will present data demonstrating consistent clinical pharmacology across a wide range of doses of tavapadon in several Phase 1 clinical trials, supporting its potential as a promising next-generation treatment for Parkinson’s disease.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: CVL-751
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable March 31, 2022
Details:
Cerevel Therapeutics' lead drug Tavapadon was rationally designed as an orally-bioavailable, once-daily partial agonist that selectively targets dopamine D1/D5 receptor subtypes with the goal of balancing meaningful motor activity with a favorable tolerability profile.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: CVL-751
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: J.P. Morgan Securities LLC
Deal Size: $350.0 million Upfront Cash: Undisclosed
Deal Type: Public Offering July 01, 2021
Details:
The Non-Dilutive Financing will fund the full Phase 3 development program for tavapadon in Parkinson’s disease, also known as the TEMPO trials.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: CVL-751
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: NovaQuest
Deal Size: $125.0 million Upfront Cash: Undisclosed
Deal Type: Financing April 13, 2021
Details:
Tavapadon is an orally-bioavailable, once-daily partial agonist that selectively targets dopamine D1/D5 receptor subtypes. The Phase 3 program will evaluate the efficacy, safety and tolerability of fixed doses (TEMPO-1) and flexible doses (TEMPO-2) of tavapadon.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: PF-06649751
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable October 30, 2020
Details:
Studies to enroll approximately 1,200 patients to determine effectiveness of tavapadon across the full spectrum of early- and late-stage parkinson’s.
Lead Product(s): Tavapadon
Therapeutic Area: Neurology Product Name: Undisclosed
Highest Development Status: Phase III Product Type: Small molecule
Partner/Sponsor/Collaborator: Not Applicable
Deal Size: Not Applicable Upfront Cash: Not Applicable
Deal Type: Not Applicable January 14, 2020