Results at 60 months of patient follow-up found that:
* Alemtuzumab-treated patients demonstrated consistently lower annualized relapse rates over the entire observation period compared to those treated with Rebif. Annualized relapse rate was 0.11 in those receiving alemtuzumab, compared with 0.35 in patients receiving Rebif.
* The mean disability (EDSS) score for patients receiving alemtuzumab improved, but worsened for patients receiving Rebif.
* Over the 60-month study period, 13 percent of patients receiving alemtuzumab experienced a sustained increase in disability compared with 38 percent of patients taking Rebif.
“These long-term patient follow-up data suggest that alemtuzumab may have a significant disease modifying effect in patients with early, active, relapsing-remitting multiple sclerosis,” said Alasdair Coles, MD, Senior Lecturer, Department of Clinical Neurosciences, University of Cambridge, a lead investigator of the Phase 2 clinical trial and author of the 5-year review abstract.
“We appreciate the tremendous dedication of the patients, physicians, and nurses participating in this important trial, who enabled us to obtain these five-year data,” said Mark Enyedy, Genzyme president for Transplant, Oncology and Multiple Sclerosis. “Their efforts have provided further insights into the potential of alemtuzumab to improve long-term outcomes for patients with multiple sclerosis.” The CAMMS223 Phase 2 trial was larger and follow-up was longer than the typical Phase 2 MS trial.
Strong Benefit Seen in Patients with Highly Active Multiple Sclerosis
A second abstract presented at ECTRIMS found that patients in the Phase 2 trial with highly active RRMS had a significantly decreased annualized relapse rate when receiving alemtuzumab compared to Rebif.
Results at 36-months of patient follow-up found that:
* Annualized relapse rate was significantly reduced for patients receiving alemtuzumab. Annualized relapse rate was 0.09 in patients receiving alemtuzumab as compared with 0.47 in those receiving Rebif, a reduction of 81 percent.
* 91 percent of alemtuzumab-treated patients were free of sustained accumulation of disability, compared to 75 percent of patients taking Rebif.
More than half of the patients enrolled in the Phase 2 trial had highly active RRMS: 56 percent of alemtuzumab treated patients, and 55 percent of Rebif treated patients. Patients with highly active disease had at least two relapses in the year prior to treatment in the trial, and had at least one gadolinium enhancing brain lesion identified through magnetic resonance imaging (MRI).
“In this Phase 2 trial, alemtuzumab was significantly more effective than Rebif at reducing relapses and the accumulation of disability in patients with highly active disease, a population at a typically higher risk for poor MS outcomes,” said Dean Wingerchuk, M.D., Department of Neurology, Mayo Clinic.
Genzyme is conducting two pivotal Phase 3 trials to evaluate alemtuzumab in the treatment of MS. CARE-MS I, a randomized trial comparing alemtuzumab to Rebif, is studying early, active RRMS patients who have received no prior therapy. CARE-MS II, which also compares alemtuzumab to Rebif, is studying RRMS patients who relapsed while on other MS therapies. Data from the Phase 3 trials are expected to be available in 2011.
Alemtuzumab is an investigational drug for the treatment of MS and must not be used in MS patients outside of a formal, regulated clinical trial setting in which appropriate patient monitoring measures are in place.
About CAMMS223 Phase 2 Study
In the Phase 2 trial, 334 patients with active RRMS were randomized to treatment with alemtuzumab at one of two dose levels, or Rebif. The majority of patients last received alemtuzumab at Month 12. Patients were strongly encouraged to continue for two additional years of follow-up beyond the original three years of the study.
Sixty-eight percent of alemtuzumab patients participated in the follow-up program, and 60 percent were evaluated at 60 months. Forty-two percent of Rebif patients participated in the follow-up program, and 35 percent were evaluated at 60 months. Rater-blinded disability scores were assessed quarterly and relapses as-needed. A sensitivity analysis adjusted for patients receiving alternative disease-modifying therapy during the follow-up period, as well as for retreatment with alemtuzumab.
The five-year data review confirmed what has been previously reported. The common adverse events in the trial included infusion-associated reactions in the alemtuzumab patients and flu-like symptoms and injection site reactions in patients using Rebif. Alemtuzumab-treated patients were more likely than Rebif patients to experience infections, particularly of the upper respiratory tract; infections were predominantly mild to moderate in severity and there were no life-threatening or fatal infections.
As described previously, immune thrombocytopenic purpura (ITP), an autoimmune disease, was identified in six alemtuzumab treated patients and one Rebif patient in the Phase 2 trial. Symptoms of ITP went unrecognized in the first alemtuzumab case and led to the onset of a fatal cerebral hemorrhage. In the other five alemtuzumab-related cases, with timely diagnosis and treatment if needed, all 5 achieved durable remission of ITP.
Approximately 30 percent of alemtuzumab-treated patients developed an autoimmune thyroid-related adverse event. Thyroid disorders either normalized spontaneously or were managed using conventional therapies. One alemtuzumab-treated patient was identified through renal monitoring at month 51 to have anti-glomerular basement membrane (anti-GBM) disease, an autoimmune kidney disease. The patient was successfully treated and is in remission. Patients who experienced an autoimmune adverse event, including ITP, experienced improved control of their MS consistent with alemtuzumab’s effect in the overall study population. Patient monitoring for thyroid disorders, ITP, and anti-GBM disease is incorporated into all Genzyme-sponsored trials of alemtuzumab for the investigational treatment of MS.
Conference Call Information
A conference call and WebEx have been scheduled for today at 12:30 p.m. ET, to review the five-year patient follow-up data from Genzyme’s completed Phase 2 multiple sclerosis (MS) trial. To participate in the call, please dial 312-470-7406 and refer to pass code “Genzyme.” Instructions for the WebEx can be found on the investor events section of www.genzyme.com. Replays of the call will be available by dialing 402-998-1620 until October 22 at 11:59 p.m. ET.
One of the world’s leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. Since 1981, the company has grown from a small start-up to a diversified enterprise with more than 12,000 employees in locations spanning the globe and 2009 revenues of $4.5 billion. In 2010, Genzyme was named to the Fortune 500.