- December 1999: the D3 project is launched, initially for another indication
- December 2002: the molecule is first synthesized
- August 2003: patent application is filed
- October-November 2004: Forest and Mitsubishi research cooperation agreements signed
- November 2004: first clinical trials launched in Europe
- November 2006: launch of a phase II clinical trial in the schizophrenia indication
- June 2007: launch of a Phase II clinical trial in the mania indication
- June 2009: launch of a Phase II clinical trial in the bipolar depression and major depression indication
- On 17 September 2015, Allergan and Richter receives approval from the US Food and Drug Administration (FDA) to market Vraylar in the United States
- March 2016: market entry with Vraylar in the US
- March 2016: the EMA accepts the registration application for cariprazine
- August 2016: Richter and Recordati sign a licensing agreement to distribute Cariprazine in Western Europe
- 17 July 2017, Richter receives a marketing authorisation from the European Commission for the marketing of Reagila in the EU
- May 28, 2019: FDA approves the extended Summary of Product Characteristics for VRAYLAR for the treatment of depressive episodes associated with bipolar I disorder
- May 2019-June 2021: various license agreements (Australia and New Zealand, Latin America, MENA region, Singapore, Thailand, South Korea, Japan, Taiwan)
- December 2022: FDA Approves cariprazine as an Adjunctive Treatment for Major Depressive Disorder
Cariprazine publications - by areas 2006-2024
Cariprazine versus risperidone monotherapy for treatment of predominant negative symptoms in patients with schizophrenia: a randomised, double-blind, controlled trial
Published: Lancet, March 2017
Quality-adjusted life year difference in patients with predominant negative symptoms of schizophrenia treated with cariprazine and risperidone
Published: Journal of Comparative Effectiveness Research, May 2017