CimziaTreatment for Crohn's Disease -- Acute, Rheumatoid Arthritis
Update: Cimzia Now FDA Approved - April 22, 2008
UCB Submits Biologics License Application to FDA for New Treatment in Crohn's Disease
Cimzia Submission Represents a Major Step Towards the Approval of the First Ever Subcutaneous Treatment for Crohn's Disease
BRUSSELS, Belgium and ATLANTA, March 2, 2006 -- UCB announced today the submission of a Biologics License Application (BLA) to the United States Food and Drug Administration (FDA) for the approval of Cimzia (certolizumab pegol, CDP870) for the treatment of patients with Crohn's disease. If approved, Cimzia would be the first-ever biologic utilizing subcutaneous injection for the treatment of Crohn's disease.
"Our BLA submission is an important milestone for UCB; it represents the tremendous efforts of UCB's Cimzia development team, and marks UCB's entry into the biologics market," said Roch Doliveux, CEO and Chairman of the Executive Committee for UCB. "We plan to request marketing authorization from the European Agency for the Evaluation of Medicinal Products (EMEA) in a matter of weeks. UCB is also continuing its research and development work to explore additional auto-immune diseases for this promising biologic."
The BLA includes safety and efficacy data from well-controlled clinical trials in more than 1,500 patients with Crohn's disease. The pivotal studies (PRECiSE 1 and PRECiSE 2) that support the BLA submission met their primary endpoints by demonstrating that Cimzia induced clinical response and maintained clinical response and remission in a significant percentage of patients with Crohn's disease. The Cimzia BLA package represents the largest biologic clinical trial database and broadest, in terms of patient types, submitted to the FDA for Crohn's disease treatment.
"There are significant unmet needs among Crohn's patients, so additional therapeutic agents will increase our ability to provide effective long-term relief from this debilitating disease," commented William Sandborn, M.D., Professor of Medicine at the Mayo Clinic College of Medicine and a leading investigator in the Cimzia clinical trial program. "Our experience in the PRECiSE clinical trials program has shown Cimzia to be a well-tolerated and effective treatment. In addition, subcutaneous administration is a welcomed attribute for patients and can offer greater convenience."
In addition to the completed and ongoing studies in Crohn's disease, Cimzia studies are also ongoing in the treatment of rheumatoid arthritis and psoriasis.
Cimzia is the first and only PEGylated Fab' fragment of a humanized anti-TNF alpha antibody. The engineered Fab' fragment retains the biologic potency of the original antibody. Cimzia has a high affinity for human TNF alpha, selectively neutralizing the pathophysiological effects of TNF alpha. Over the past decade, TNF has emerged as a major target of basic research and clinical investigation. This cytokine plays a key role in mediating pathological inflammation, and excess TNF production has been directly implicated in a wide variety of diseases.
About PRECiSE Program
Data from PRECiSE 2, presented in October 2005 at the United European Gastroenterology Week, demonstrated that within six weeks of initiating Cimzia, 64.1 percent of patients (428 of 668) achieved a clinical response as defined by greater than or equal to 100 point reduction in the Crohn's Disease Activity Index (CDAI) score (a composite score of eight factors used to assess a patient's wellness). Responders were randomized to Cimzia 400 mg or placebo every four weeks. At the end of 26 weeks, significantly more patients, 62.8 percent (135 of 215) on Cimzia vs. 36.2 percent (76 of 210) on placebo, maintained an overall clinical response. Additionally, at 26 weeks, significantly more of Cimzia patients were in clinical remission (CDAI less than or equal to 150 points) compared to placebo patients, 47.9 percent (103 of 215) vs. 28.6 percent (60 of 210), respectively. Cimzia was generally well tolerated with an adverse event profile similar to other anti-TNF agents. The PRECiSE clinical program is composed of four studies (PRECiSE 1, 2, 3, and 4). PRECiSE 3 and 4 are both 24-month open-label trials assessing the longer-term safety and tolerability of Cimzia and are currently ongoing.
About Crohn's Disease
Crohn's disease, a chronic and debilitating inflammatory disease of the gastrointestinal tract, affects nearly one million patients worldwide and an estimated 500,000 people in the United States. People with Crohn's disease may suffer an ongoing cycle of "flare-up" and remission. Symptoms vary among people, but include persistent diarrhea, abdominal pain, and loss of appetite/weight, fever or rectal bleeding.1
1. Source: Crohn's and Colitis Foundation of America. Disease Information page: http://www.ccfa.org/info/about/crohns Accessed January 26, 2006
Posted: March 2006
- UCB's Cimzia (certolizumab pegol) Approved by the U.S. FDA for Adult Patients Suffering From Moderate to Severe Rheumatoid Arthritis - May 13, 2009
- UCB's meeting with U.S. FDA defines path forward for Cimzia in rheumatoid arthritis - February 6, 2009
- UCB Receives Complete Response Letter from U.S. FDA for Use of Cimzia in Rheumatoid Arthritis Patients - January 5, 2009
- Cimzia Approved in the US for the Treatment of Moderate to Severe Crohn's Disease - April 22, 2008
- FDA Agrees to Review Cimzia File for the Treatment of Rheumatoid Arthritis - February 6, 2008
- UCB Provides Update on Cimzia for Crohn's Disease and Rheumatoid Arthritis in the US - March 23, 2007