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Find Clinical Drug Pipeline Developments & Deals for Pimavanserin
Pimavanserin tablet is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, which is used treatment for Parkinson's disease.
Nuplazid (pimavanserin) is an atypical antipsychotic 5-HT2A receptor inverse agonist, which is being evaluated for the treatment of patients with schizophrenia.
Nuplazid (pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, which is used treatment for Parkinson’s disease-related hallucinations and delusions who also have dementia.
NUPLAZID (Pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors and prevents psychosis symptoms associated with Parkinson's Disease Psychosis.
Nuplazid (pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, demonstrated no appreciable binding affinity for dopamine (including D2), histamine, muscarinic, or adrenergic receptors.
Nuplazid (pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, which is used Treatment of Hallucinations and Delusions Associated with Alzheimer’s Disease Psychosis.
Nuplazid (pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, which is used Treatment of Alzheimer’s Disease Psychosis.
ACP-103 (pimavanserin) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors, demonstrated no appreciable binding affinity for dopamine, histamine, muscarinic, or adrenergic receptors in vitro.
ACP-103 (pimavanserin tartrate) is a selective serotonin inverse agonist and antagonist preferentially targeting 5-HT2A receptors for the treatment of hallucinations and delusions associated with Alzheimer’s disease psychosis.
Resubmission for Nuplazid (pimavanserin) provides additional analyses from two previously conducted clinical studies, HARMONY1 and Study -0192, to support a proposed indication for treatment of ADP and is intended to address issues raised in FDA’s CRL.
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