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Atacicept in Multiple Sclerosis, Phase II
This study is currently recruiting participants.
Verified by EMD Serono, April 2009
First Received: March 21, 2008   Last Updated: April 10, 2009   History of Changes
Sponsors and Collaborators: EMD Serono
ZymoGenetics
Information provided by: EMD Serono
ClinicalTrials.gov Identifier: NCT00642902
  Purpose

To evaluate the safety and tolerability of atacicept and to explore if atacicept reduces Central Nervous System inflammation in subjects with RMS as assessed by frequent MRI. This study is randomised. Study medication is administered via subcutaneous (under the skin) injections.


Condition Intervention Phase
Relapsing Multiple Sclerosis
Drug: atacicept
Drug: Placebo
Phase II

MedlinePlus related topics: Multiple Sclerosis
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment
Official Title: A Randomised, Double-Blind, Placebo-Controlled, Multicentre Phase II Study to Evaluate the Safety, Tolerability and Efficacy as Assessed by Frequent MRI Measures of Three Doses of Atacicept Monotherapy in Subjects With Relapsing Multiple Sclerosis (RMS)

Further study details as provided by EMD Serono:

Primary Outcome Measures:
  • Mean number of T1 gadolinium (Gd)-enhancing lesions per subject per scan. [ Time Frame: up to 48 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Number of new T1 hypointense lesions, Proportion of subjects free from relapses during the 36-week treatment period, Nature, severity, and incidence of adverse events and infections [ Time Frame: weeks 12, 24, 36 ] [ Designated as safety issue: No ]

Estimated Enrollment: 292
Study Start Date: March 2008
Estimated Study Completion Date: April 2010
Estimated Primary Completion Date: March 2010 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
High-dose treatment with Atacicept
Drug: atacicept
Atacicept high, mid and low-dose, respectively
2: Experimental
Mid-dose treatment with Atacicept
Drug: atacicept
Atacicept high, mid and low-dose, respectively
3: Experimental
Low dose treatment with Atacicept
Drug: atacicept
Atacicept high, mid and low-dose, respectively
4: Placebo Comparator
Placebo
Drug: Placebo
Placebo will be supplied in a transparent, sterile solution for injection in pre-filled syringes matching the Atacicept pre-filled syringes, each containing 1mL. The placebo formulation to be used in this study contains trehalose and 10 mmol sodium acetate buffer (pH 5)."

  Eligibility

Ages Eligible for Study:   18 Years to 60 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of Relapsing Multiple Sclerosis (per McDonald criteria, 2005);

Exclusion Criteria:

  • Have primary progressive MS.
  • Have secondary progressive MS without superimposed relapses.
  • Relevant cardiac, hepatic and renal diseases
  • Pre treatment with immunosuppressants and immunomodulating drugs
  • Clinical significant abnormalities in blood cell counts and Ig levels
  • Clinical significant acute or chronic infections.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00642902

Contacts
Contact: Lynne Macgregor +41 22 414 4752 Lynne.Macgregor@merckserono.net

  Show 49 Study Locations
Sponsors and Collaborators
EMD Serono
ZymoGenetics
Investigators
Study Director: Dan Mikol, MD, PhD EMD Serono
  More Information

Additional Information:
No publications provided

Responsible Party: Merck Serono S.A. - Geneva an Affiliate of Merck KGaA Darmstadt, Germany ( Lynne Macgregor )
Study ID Numbers: 28063
Study First Received: March 21, 2008
Last Updated: April 10, 2009
ClinicalTrials.gov Identifier: NCT00642902     History of Changes
Health Authority: United States: Food and Drug Administration

Study placed in the following topic categories:
Morphine
Autoimmune Diseases
Multiple Sclerosis
Demyelinating Diseases
Demyelinating Autoimmune Diseases, CNS
Sclerosis
Autoimmune Diseases of the Nervous System

Additional relevant MeSH terms:
Pathologic Processes
Autoimmune Diseases
Multiple Sclerosis
Immune System Diseases
Demyelinating Diseases
Nervous System Diseases
Demyelinating Autoimmune Diseases, CNS
Sclerosis
Autoimmune Diseases of the Nervous System

ClinicalTrials.gov processed this record on May 07, 2009