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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00202384
Other study ID # NEU - FCG - 02
Secondary ID
Status Terminated
Phase
First received September 13, 2005
Last updated April 17, 2018
Start date November 2004
Est. completion date January 2011

Study information

Verified date April 2018
Source S. Andrea Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Clinical and experimental evidences suggest that there is a variability in therapeutic response to immunomodulating therapies in Multiple Sclerosis patients.

Microarrays is a technology that permits to monitor the expression levels of thousands of genes at a time.

The specific aim of this study is to identify predictive factors of therapeutic response in MS patients treated with high-dose Interferon-Beta.


Recruitment information / eligibility

Status Terminated
Enrollment 600
Est. completion date January 2011
Est. primary completion date January 2011
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria:

- diagnosis of relapsing-remitting MS (McDonald criteria)

- age between 18-55

- EDSS less or equal to 5.5

Exclusion Criteria:

- use of any other disease modifying drugs

- use of corticosteroids during 3 months before starting protocol

- clinical relapse during 1 month before starting protocol

- serious heart, renal, hepatic or haematological dysfunction defined by laboratory exams

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Italy Azienda Ospedaliera S. Andrea, II Facoltà di Medicina e Chirurgia, Università di Roma "La Sapienza" Rome

Sponsors (1)

Lead Sponsor Collaborator
S. Andrea Hospital

Country where clinical trial is conducted

Italy, 

References & Publications (4)

Bomprezzi R, Ringnér M, Kim S, Bittner ML, Khan J, Chen Y, Elkahloun A, Yu A, Bielekova B, Meltzer PS, Martin R, McFarland HF, Trent JM. Gene expression profile in multiple sclerosis patients and healthy controls: identifying pathways relevant to disease. Hum Mol Genet. 2003 Sep 1;12(17):2191-9. Epub 2003 Jul 8. — View Citation

Stürzebecher S, Wandinger KP, Rosenwald A, Sathyamoorthy M, Tzou A, Mattar P, Frank JA, Staudt L, Martin R, McFarland HF. Expression profiling identifies responder and non-responder phenotypes to interferon-beta in multiple sclerosis. Brain. 2003 Jun;126(Pt 6):1419-29. — View Citation

Waubant E, Vukusic S, Gignoux L, Dubief FD, Achiti I, Blanc S, Renoux C, Confavreux C. Clinical characteristics of responders to interferon therapy for relapsing MS. Neurology. 2003 Jul 22;61(2):184-9. Review. — View Citation

Weinstock-Guttman B, Badgett D, Patrick K, Hartrich L, Santos R, Hall D, Baier M, Feichter J, Ramanathan M. Genomic effects of IFN-beta in multiple sclerosis patients. J Immunol. 2003 Sep 1;171(5):2694-702. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Gene Expression in MS Patients Change in Gene Expression profile in MS Patients at 12 months of IFN beta 1a treatment baseline and 12 months after IFN beta 1a treatment
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