Search for content, post, videos

Positive EU opinion for Lundbeck

lundbeck-research

Lundbeck and Otsuka Pharmaceutical announce that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) has issued a positive opinion on Rxulti (brexpiprazole) for the treatment of schizophrenia in adults.

A final decision from the European Commission is expected within 67 days.

Brexpiprazole

Brexpiprazole is a once-daily second generation (atypical) oral antipsychotic; it provides a combination of partial agonist activity at serotonin 5-HT1A and dopamine D2 receptors, and antagonist activity at serotonin 5-HT2A receptors. Brexpiprazole exhibits high affinity for these receptors as well as for noradrenaline alpha1B/2C receptors.

The submission to the EMA included efficacy and safety data of brexpiprazole in schizophrenia from six placebo-controlled clinical trials. The safety data were further included from a large cohort of patients evaluated in four long-term, open-label trials which included patients rolled over from the short-term trials as well as patients with no prior exposure to brexpiprazole.

The Phase III efficacy trials comprise three short-term, phase III, fixed-dose trials; one phase III, short-term, flexible-dose trial with quetiapine as active reference; and one phase III, long-term maintenance (relapse-prevention) trial. In the three fixed‑dose, short‑term trials (trials 1, 2 and 3, subjects were randomized to brexpiprazole 0.25 mg once daily, 1 mg once daily, 2 mg once daily, 4 mg once daily or placebo. Trial 4 assessed the efficacy, safety, and tolerability of brexpiprazole in a flexible dose range of 2 to 4 mg/day and 400 to 800 mg quetiapine XR for assay sensitivity.6 In the short‑term trials, the primary efficacy endpoint was defined as the mean change from baseline to week 6 in Positive and Negative Syndrome Scale (PANSS) total scores.

Co-development with Otsuka

In the long‑term trial designed to assess the maintenance of effect of brexpiprazole by assessing the delay in time to impending relapse of schizophrenia, brexpiprazole demonstrated a significantly longer time to relapse compared with patients on placebo (p < 0.0001).7

Together, the trials demonstrated that brexpiprazole is an effective and well-tolerated treatment for schizophrenia.

Brexpiprazole was discovered by Otsuka and is being co-developed by Otsuka and Lundbeck. Following the European Commission’s final decision, Otsuka and Lundbeck will work with local pricing and reimbursement bodies in countries throughout Europe to help ensure that eligible patients are able to access this medicine.