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Managing Tardive Dyskinesia: New Data from Phase 3 Study of Ingrezza

Check out new data from phase 3 study of Ingrezza for the real-world management of tardive dyskinesia.

Eiryw robertsNeurocrine biosciencesGoodideas adobestockNeurocrine bioscienceAbnormal involuntary movement scaleDrug administrationHealth psychol resPatient global impressionClinical global impressionIngrezza sprinkleHealth psychol

FDA Clears Ingrezza Sprinkle for Bipolar-Linked Tardive Dyskinesia

FDA Clears Ingrezza Sprinkle for Bipolar-Linked Tardive Dyskinesia
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United statesNew yorkNeurocrine biosciencesEiryw robertsAdam margoliusJosephf goldbergIcahn school of medicine at mount sinaiMental health americaNational alliance on mental illnessDrug administrationEveryday heathIngrezza sprinkleCleveland clinicMayo clinicIcahn schoolMount sinai

FDA Approves New Ingrezza Formulation for Patients Who Have Difficulty Swallowing

Each Ingrezza Sprinkle capsule contains oral granules consisting of valbenazine, a vesicular monoamine transporter 2 inhibitor.

Neurocrine biosciencesEiryw robertsDrug administrationIngrezza sprinkleChief medical officer

Ingrezza Sprinkle Capsules Received FDA Approval for Tardive Dyskinesia in Adults

The new formulation was approved to help patients with tardive dyskinesia who have trouble swallowing.

Eiryw robertsMitchell mathisNeurocrine biosciencesDivision of psychiatry productsDrug administrationIngrezza sprinkleChief medical officerFast trackPriority reviewBreakthrough therapyPsychiatry productsDrug evaluation

Neurocrine Biosciences Huntington s disease drug gets FDA approval

By Sruthi Narasimha Chari (Reuters) -The U.S. Food and Drug Administration (FDA) has approved the granule formulation of Neurocrine Biosciences' Ingrezza drug to treat movement disorders associated with Huntington's disease (HD), the company said on Tu.

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