FDA Approves Aripiprazole for Maintaining Efficacy in Bipolar I Disorder
Mar 14, 2005 - 8:49:38 AM
Bristol-Myers Squibb Company and Otsuka Pharmaceutical Co., Ltd. announced that the U.S. Food and Drug Administration (FDA) approved ABILIFY® (aripiprazole) Tablets and Oral Solution for maintaining efficacy in patients with Bipolar I Disorder with a recent manic or mixed episode who had been stabilized and then maintained for at least six weeks.
The FDA approved aripiprazole for the treatment of acute bipolar mania, including manic and mixed episodes associated with bipolar disorder, on September 29, 2004.
Clinical data demonstrated that patients who had been stabilized on aripiprazole for at least six weeks experienced a significant delay in time to relapse, the primary outcome measure for this study, as compared with those randomized to placebo .
The majority of these relapses were due to manic rather than depressive symptoms. There is insufficient data to know whether aripiprazole is effective in delaying the time to occurrence of depression in patients with Bipolar I Disorder. Physicians who elect to use aripiprazole for extended periods, that is, longer than six weeks, should periodically re- evaluate the long-term usefulness of the drug for the individual patient.
"This approval of aripiprazole is important news for patients who suffer from Bipolar I Disorder with manic and mixed episodes, as relapse is unfortunately, very common," said John Zajecka, M.D., Director, Treatment Research Center, and Associate Professor of Psychiatry, Rush University Medical Center. "As a physician, it is very encouraging to know that patients can benefit from aripiprazole throughout the different phases of their treatment."
The latest FDA approval is based on the positive results of a randomized, double-blind, multicenter, placebo-controlled trial designed to compare the maintenance of efficacy of aripiprazole versus placebo, measured by time to relapse. In this study, patients who had recently experienced a manic or mixed episode were first stabilized with aripiprazole for at least six consecutive weeks.
After meeting the stabilization criteria [Young Mania Rating Scale Total Score (Y-MRS) less than or equal to 10 and Montgomery-Asberg Depression Rating Scale (MADRS) less than or equal to 13 during four consecutive visits over a minimum of six weeks], 161 patients were given aripiprazole or placebo in the double-blind, randomization phase .
The primary endpoint was time to relapse of manic and depressive symptoms. Of those patients who experienced a relapse, patients treated with aripiprazole relapsed significantly later than placebo-treated patients (p-value equals 0.020) .
In addition, the total number of relapses was significantly fewer in patients treated with aripiprazole than with placebo (25 percent versus 43 percent, respectively; p-value equals 0.013) . The majority of these relapses were due to manic rather than depressive symptoms.
There is insufficient data to know whether aripiprazole is effective in delaying the time to occurrence of depression in patients with Bipolar I Disorder. The adverse events reported during this trial were generally consistent with those reported in other long-term placebo-controlled trials of aripiprazole.
"Bristol-Myers Squibb is pleased that aripiprazole received this important new treatment indication, now providing one medication that can help physicians and patients manage the illness," said Anthony Hooper, president, U.S. Pharmaceuticals, Bristol-Myers Squibb. "Our company is committed to providing important new treatment options for the millions of people suffering from mental illness and addressing the needs of their healthcare providers and families."
"We are extremely pleased that aripiprazole, the first and only available dopamine partial agonist, has reached another important milestone in the treatment of mental illness," said Tatsuo Higuchi, president and representative director, Otsuka Pharmaceutical Co., Ltd. "With this new indication, patients who have had success with aripiprazole during a manic or mixed phase can safely and effectively address their continuing therapy needs."
Aripiprazole is indicated for the treatment of schizophrenia, acute manic and mixed episodes associated with bipolar disorder, and now for maintaining efficacy in patients with Bipolar I Disorder with a recent manic or mixed episode who had been stabilized and then maintained for at least six weeks. Since its initial approval in 2002, over 3.7 million prescriptions have been written in the United States .
Aripiprazole is available by prescription only. In addition to administration as a once-daily oral tablet, aripiprazole was recently FDA-approved in an oral solution formulation. Now available in U.S. pharmacies, aripiprazole Oral Solution is an important new treatment option for adult patients who are unable to or have difficulty swallowing tablets, and provides flexibility in addressing individual patient needs. Patients should talk to their healthcare provider for more information. To learn more about aripiprazole and for full product information, please visit the related link.
As with all antipsychotic medications, including aripiprazole, a rare condition referred to as neuroleptic malignant syndrome (NMS) has been reported. As with all antipsychotic medications, prescribing should be consistent with the need to minimize the risk of tardive dyskinesia (TD).
Cerebrovascular adverse events (e.g., stroke, transient ischemic attack), including fatalities, have been reported at an increased incidence in clinical trials of elderly patients with dementia-related psychosis treated with aripiprazole, including a significant dose response relationship in a fixed dose trial.
Aripiprazole is not approved for the treatment of patients with dementia-related psychosis.
Hyperglycemia, including some serious cases ranging from ketoacidosis, hyperosmolar coma, or death, has been reported in patients treated with atypical antipsychotics. Aripiprazole was not included in epidemiologic studies suggesting this risk; therefore the risk of hyperglycemia with aripiprazole is not known. However, there have been few reports of hyperglycemia in patients treated with aripiprazole. Patients should be appropriately tested before and monitored during treatment.
Aripiprazole may be associated with orthostatic hypotension and should be used with caution in patients with known cardiovascular disease, cerebrovascular disease, or conditions which would predispose them to hypotension.
As with other antipsychotic drugs, aripiprazole should be used with caution in patients with a history of seizures or with conditions that lower the seizure threshold. Seizures occurred in 0.3% of bipolar patients treated with aripiprazole in placebo-controlled trials.
Like other antipsychotics, aripiprazole may have the potential to impair judgment, thinking or motor skills. Patients should not drive or operate hazardous machinery until they are certain aripiprazole does not affect them adversely.
Disruption of the body's ability to reduce core body temperature has been attributed to antipsychotics. Appropriate care is advised for patients who may exercise strenuously, be exposed to extreme heat, receive concomitant medications with anticholinergic activity, or be subject to dehydration.
As antipsychotics have been associated with esophageal dysmotility and aspiration, aripiprazole should be used cautiously in patients at risk for aspiration pneumonia.
As the possibility of a suicide attempt is inherent in psychotic illness and bipolar disorder, close supervision of high-risk patients should accompany drug therapy.
Physicians should determine if a patient is pregnant or intends to become pregnant while taking aripiprazole. Patients should be advised not to drink alcohol, or breast-feed while taking aripiprazole.
Both CYP3A4 and CYP2D6 are responsible for aripiprazole metabolism. Agents that induce CYP3A4 (e.g., carbamazepine) could cause an increase in aripiprazole clearance and lower blood levels. Inhibitors of CYP3A4 (e.g., ketoconazole) or CYP2D6 (e.g., quinidine, fluoxetine, or paroxetine) can inhibit aripiprazole elimination and cause increased blood levels.
Commonly observed adverse events reported with aripiprazole in 3-week bipolar mania trials at a greater than or equal to 5% incidence for aripiprazole and at a rate at least twice the rate of placebo include, respectively, akathisia (15% vs 4%), constipation (13% vs 6%), and accidental injury (6% vs 3%).
Treatment-emergent adverse events reported with aripiprazole in short-term trials at an incidence greater than or equal to 10% and greater than placebo, respectively, include:
-headache (31% vs 26%)
-agitation (25% vs 24%)
-anxiety (20% vs 17%)
-insomnia (20% vs 15%)
-nausea (16% vs 12%)
-dyspepsia (15% vs 13%)
-somnolence (12% vs 8%)
-akathisia (12% vs 5%)
-lightheadedness (11% vs 8%)
-vomiting (11% vs 6%) and
-constipation (11% vs 7%).
The adverse events reported in a 26-week, double-blind schizophrenia trial comparing aripiprazole and placebo were generally consistent with those reported in the short-term, placebo-controlled schizophrenia trials, except for a higher incidence of tremor: 9% for aripiprazole vs 1% for placebo. In addition, in a long-term (52-week), active-controlled study, the incidence of tremor for aripiprazole was 4%.
Aripiprazole is taken once daily with or without food.
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