Safety and efficacy of daclizumab in relapsing-remitting multiple sclerosis: 3-year results from the SELECTED open-label extension study.

Abstract

BACKGROUND:

Daclizumab is a humanized monoclonal antibody against CD25 that modulates interleukin 2 signaling. The SELECT TRILOGY of clinical studies (SELECT/SELECTION/SELECTED) evaluated the safety and efficacy of daclizumab in patients with relapsing-remitting multiple sclerosis (RRMS). We report the long-term safety and efficacy of daclizumab 150 mg subcutaneous every 4 weeks in patients with RRMS in the SELECTED open-label extension study.

METHODS:

An interim intent-to-treat analysis of all enrolled patients was performed in January 2014 for this ongoing study.

RESULTS:

The SELECTED study enrolled 90% of patients who completed SELECTION. In the safety and efficacy analysis (N = 410), median treatment time in SELECTED was 25 months (range, <1-45). Adverse events (AEs) were reported in 76% of patients, serious AEs (SAEs) excluding MS relapse in 16%, and treatment discontinuation due to AEs including multiple sclerosis (MS) relapse in 12%. AEs were primarily of mild to moderate severity, and common AEs (≥10%), excluding MS relapse, were nasopharyngitis (12%) and upper respiratory tract infection (12%). Most commonly reported SAEs (in ≥3 patients), excluding MS relapses, were increased serum hepatic enzymes, pneumonia, ulcerative colitis, and urinary tract infection (<1% each). Incidences of AE groups of interest include cutaneous events (28%), cutaneous SAEs (2%), gastrointestinal SAEs (2%), hepatic SAEs, (1%) and malignancies (1%). The incidence of AEs, SAEs, and treatment-related study discontinuations did not increase over time and no deaths were reported. The adjusted annualized relapse rate (95% confidence interval (CI)) analyzed at 6-month intervals was 0.15 (0.10-0.22) for weeks 97-120 and 0.15 (0.10-0.21) for weeks 121-144. In year 3, the adjusted mean (95% CI) number of new/newly enlarging T2 hyperintense lesions was 1.26 (0.93-1.72) and the mean (median) annualized change in brain volume was -0.32% (-0.34%).

CONCLUSIONS:

The AE incidence did not increase with extension of therapy into year 3 in SELECTED; the safety profile was similar to that previously observed. The clinical efficacy of daclizumab was sustained over the 3 years comprising the SELECT TRILOGY, although potential selection bias cannot be excluded.

TRIAL REGISTRATION:

Clinicaltrials.gov NCT01051349; first registered January 15, 2010.

• Authors: Ralf Gold, Ernst-Wilhelm Radue, Gavin Giovannoni, Krzysztof Selmaj, Eva Havrdova, Dusan Stefoski, Till Sprenger, Xavier Montalban, Stanley Cohan, Kimberly Umans, Steven J Greenberg, Gulden Ozen, Jacob Elkins
• Journal: BMC neurology (BMC Neurol) Vol. 16 Pg. 117 (Jul 26 2016) ISSN: 1471-2377 [Electronic] England
• PMID: 27461166 (Publication Type: Clinical Trial, Comparative Study, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't)

Chemical References

• Antibodies, Monoclonal, Humanized
• Immunoglobulin G
• Immunosuppressive Agents
• Interleukin-2 Receptor alpha Subunit
• Daclizumab
• Aspartate Aminotransferases
• Alanine Transaminase

Topics

• Adult
• Alanine Transaminase (drug effects)
• Antibodies, Monoclonal, Humanized (administration & dosage, adverse effects, therapeutic use)
• Aspartate Aminotransferases (drug effects)
• Brain (drug effects)
• Cohort Studies
• Colitis, Ulcerative (chemically induced)
• Daclizumab
• Drug Eruptions (etiology)
• Female
• Follow-Up Studies
• Humans
• Immunoglobulin G (administration & dosage, adverse effects, therapeutic use)
• Immunosuppressive Agents (administration & dosage, adverse effects, therapeutic use)
• Injections, Subcutaneous
• Intention to Treat Analysis
• Interleukin-2 Receptor alpha Subunit (administration & dosage, therapeutic use)
• Longitudinal Studies
• Male
• Middle Aged
• Multiple Sclerosis, Relapsing-Remitting (drug therapy)
• Nasopharyngitis (chemically induced)
• Pneumonia (chemically induced)
• Recurrence
• Respiratory Tract Infections (chemically induced)
• Safety
• Treatment Outcome
• Urinary Tract Infections (chemically induced)