You are here

FDA Approves Zyprexa for Use in Combination Therapy To Treat Bipolar Disorder

INDIANAPOLIS, IN -- July 16, 2003 -- Eli Lilly and Company announced today that the U.S. Food and Drug Administration (FDA) has approved Zyprexa® (olanzapine) for use in combination with lithium or valproate (Depakote®, Abbott) for the treatment of acute manic episodes associated with bipolar I disorder. Zyprexa is the first agent to be approved for use in combination with other mood stabilizers to treat acute bipolar mania. Zyprexa was approved by the FDA in 2000 as a monotherapy for the short-term treatment of acute manic episodes associated with bipolar disorder and is the only atypical antipsychotic approved by the FDA to treat this patient population.

Since bipolar mania is often challenging to treat and many patients do not respond rapidly or completely to a single agent, they are frequently treated with a combination of therapies,"

The FDA approval is based on data from two double-blind, randomized, placebo-controlled trials which showed that bipolar patients in manic or mixed episodes, treated with Zyprexa in combination therapy, demonstrated improved manic and depressive symptoms when compared to patients treated only with lithium or valproate alone.1

Patients in manic episodes often have simultaneous depressive symptoms which can be very difficult to treat," said Keck. "Clinicians should welcome an FDA-approved combination therapy that helps them help these patients," he added.

"This new Zyprexa indication strengthens the substantial body of evidence showing that Zyprexa is a solid foundation for clinicians to use in their treatment of patients with acute bipolar mania," said Mauricio Tohen, M.D., Ph.D, Lilly Clinical Research Fellow, Lilly Research Laboratories. "At Lilly, we are committed to the continued study of Zyprexa to help provide answers that matter to clinicians in the treatment of this devastating condition."

In addition to its approval more than three years ago for short-term treatment of acute bipolar mania, Zyprexa is currently under FDA review for long-term maintenance of response in the treatment of bipolar disorder. Additionally, SymbyaxTM, an agent that combines Zyprexa with Prozac® (fluoxetine), is under FDA review for the treatment of bipolar depression. There is currently no FDA-approved treatment for bipolar depression.

About Bipolar Disorder
Bipolar disorder, also known as manic-depressive illness, affects an individual's mood, behavior, and thinking. Unlike many illnesses, symptoms may be quite different at different phases of the illness. Treatment is more challenging because some treatments that are effective in one phase of the illness may be counterproductive to another, such as the observation that antidepressant treatments can precipitate manic episodes. Symptoms vary as moods swing from the manic phase of the illness (characterized by feelings of elation/euphoria, extreme optimism, inflated self-esteem, difficulty sleeping, engaging in risky activities) to the depressive phase (feelings of extreme guilt, sadness, anxiety, and at times, suicidal thoughts). Patients also experience maintenance phases, periods of normal mood. More than 2.5 million Americans live with a diagnosis of bipolar disorder but recent research indicates the real number may be as high as 10 million. The results of untreated bipolar disorder can be catastrophic. According to the National Institute of Mental Health, nearly one in every five people with the illness ends their life by suicide. The World Health Organization estimates that bipolar disorder is the sixth leading cause of disability in the world.

Zyprexa Background
In addition to the newly approved indication, Zyprexa is indicated in the United States for the treatment of schizophrenia, the short-term treatment of acute manic episodes associated with bipolar disorder and for the long-term therapy and maintenance of treatment response of schizophrenia. Zyprexa was the first atypical antipsychotic to prove its long-term effectiveness in patients with schizophrenia. Since Zyprexa was introduced in 1996, it has been prescribed to 12 million people worldwide.

The most common treatment-emergent adverse event associated with Zyprexa in placebo-controlled, short-term schizophrenia and bipolar mania trials was somnolence. Other common events were dizziness, weight gain, personality disorder (COSTART term for non-aggressive objectionable behavior), constipation, akathisia, postural hypotension, dry mouth, asthenia, dyspepsia, increased appetite and tremor. A small number of patients experienced asymptomatic elevations of hepatic transaminase; none of these patients experienced jaundice.

Prescribing should be consistent with the need to minimize the risk of neuroleptic malignant syndrome, tardive dyskinesia, seizures and orthostatic hypotension.

In short-term (six-week) acute bipolar mania trials in combination with lithium or valproate, the most common treatment emergent adverse event associated with Zyprexa and lithium or valproate was dry mouth. Other common events were weight gain, increased appetite, dizziness, back pain, constipation, speech disorder, increased salivation, amnesia and paresthesia.

Full prescribing information is available at www.zyprexa.com.

Source: Eli Lilly and Company

Recent Headlines

U.S., Australia, and Canada Approve Endometrial Cancer Regimen
Single daily pill combines hypertension, cholesterol drugs
Drug With Androgen Deprivation Therapy Cut Risk of Death by 33% Compared With Placebo + ADT
A Diabetes Drug For People Without Diabetes
Roche Drug Outperformed Standard of Care in Phase 2 Study
One in Five Kids’ Office Visits Results in an Off-Label Rx
Related Settlement Would End Many but Not All Lawsuits
Chronic Kidney Patients With Hyperphosphatemia May Be Another Market for the Drug
Nitrosamine Impurity Also Affects Other Ranitidine Drugs