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| | | ![]() Cipralex Approved in Europe for Treatment of Obsessive Compulsive Disorder An exciting new treatment option for patients with this chronic, disabling disorder COPENHAGEN, DENMARK -- January 18, 2007 -- H. Lundbeck A/S is pleased to announce the approval of Cipralex® (escitalopram) in Europe for the treatment of obsessive-compulsive disorder (OCD). The approval is based on two pivotal studies demonstrating that Cipralex® is effective and well-tolerated in the treatment of OCD with the added benefit of encouraging rates of remission and relapse prevention in OCD patients.1,2 OCD is a chronic, highly debilitating disorder that is characterised by recurrent, distressing thoughts and impulses (obsessions) and/or repetitive behaviours (compulsions).3 It is the 10th leading cause of disability of all medical conditions in the industrialised world and affects all aspects of quality of life.4 "The approval of Cipralex® in OCD is exciting news for patients living with this disabling condition," said Professor Joseph Zohar, Division of Psychiatry, Sheba Medical Center, Tel Aviv, Israel and President of the International College of Obsessive Compulsive Spectrum Disorders (ICOCS). "Society often underestimates the impact of OCD on daily life and it is vital for patients to have access to a treatment that is both well-tolerated and effective in reducing the symptoms and associated social disability that patients with OCD encounter on a daily basis." One pivotal study by Stein et al., demonstrated that treatment with Cipralex® provided significant symptom relief, improvement in social disability and good tolerability in what was described in the study as a very large cohort of OCD patients. The 24-week study investigated the efficacy and tolerability of Cipralex® and found that:1 • Both 10 and 20mg/daily Cipralex® were efficacious and well-tolerated in the treatment of OCD1 • Compared with placebo, Cipralex® 20mg/day was associated not only with lower symptoms scores mid-way through the study but also with earlier onset, increased response and increased remission rates1 • Cipralex® was better tolerated than paroxetine, with fewer withdrawals from the Cipralex® group due to adverse events1 Another study, by Fineberg et al., was designed to compare the efficacy of Cipralex® with that of placebo in preventing relapse over 24 weeks in outpatients with OCD who had responded to 16 weeks prior open-label treatment with Cipralex®.2 This is important because although 50-60% of patients with OCD currently respond to treatment, only a minority of those patients achieve remission.5 Results included: • Cipralex® 10 or 20 mg/day was well tolerated by patients with OCD, had an effect on OCD-symptoms during 16 weeks of open-label treatment and significantly reduced the risk of relapse in patients with OCD during continued treatment of up to 24 weeks2 • The primary efficacy analysis showed a statistically significantly superior effect of Cipralex® relative to placebo on the time to relapse of OCD, with a 52% rate of relapse in the placebo group versus a 23% rate in the Cipralex® group2 • The risk of relapsing was 2.7 times higher for the placebo group compared to patients treated with Cipralex®2 "Given the chronic nature of OCD and associated serious disability, we need to focus not only on the acute phase, but also on how to prevent relapse. As the patient needs to take the medication for extended periods of time, the tolerability of the compound is a key factor in increasing patient adherence to treatment." continued Professor Zohar. "Cipralex® is an effective and well tolerated treatment with encouraging data on remission and relapse prevention and is therefore a valuable addition to our current options for OCD therapy." Dose finding study: At week 12 – the primary efficacy endpoint – 20mg Cipralex® showed a statistically significant greater improvement in the Yale-Brown Obsessive Compulsive Scale (Y-BOCS) compared to placebo (P <.005). 10mg Cipralex® compared to placebo was (P =.052). At week 24 dosages of Cipralex® 10mg (P <.05) and 20mg (P <.005) showed a statistically significant greater improvement in the Yale-Brown Obsessive Compulsive Scale (Y-BOCS) than in the placebo group – as did paroxetine 40mg (P <.05).1 Relapse prevention study The primary endpoint was time to relapse. The result of this primary analysis showed a significant difference in favour of Cipralex® (P <.001). The number of relapses during treatment with Cipralex® (23%) was significantly lower compared to the patients in the placebo group (52%) (P <.001). The risk of relapsing was 2.7 times higher for the placebo group compared to patients treated with Cipralex®.2 About OCD • Up to 2/3 of individuals with OCD suffer from co-morbid depression at some time during their illness6
SOURCE: H. Lundbeck A/S
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