2014-004613-93

Open label study to evaluate effect, safety and tolerability of Betaferon standard dose of 250µg in patients of Chinese origin with multiple sclerosis

Bayer HealthCare AG·EU Clinical Trials Register
Study focus
Disease/Condition
Multiple sclerosis
Sponsor & location
Primary sponsor
Bayer HealthCare AG
Timeline & enrollment
Phase
N/A
Start date
N/A
End date
N/A
Primary outcome

Any disease other than Multiple Sclerosis (MS) that could better explain the patients signs and symptoms - HIV (human immunodeficiency virus) infections - Hepatitis A - Syphilis - immunodeficiency - rheumatic disease or Sjogren syndrome - heart disease - severe depression - pregnancy or lactation - conditions interfering with Magnetic Resonance Imaging (MRI) - Gadolinium DTPA (Gadovist, contrast agent) allergy - allergy against human proteins, paracetamol, acetaminophen and ibuprofen intolerance - participation in other trial

ICD-10 classifications
Multiple sclerosisProgressive systemic sclerosisSystemic sclerosisSystemic sclerosis, unspecifiedDiffuse sclerosis
Data source
Registry
EU Clinical Trials Register
Trial ID
2014-004613-93
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for 2014-004613-93 through Pure Global AI's free database. This phase not specified trial is sponsored by Bayer HealthCare AG and is currently status unknown. The study focuses on Multiple sclerosis.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to EU Clinical Trials Register data, helping medical device and pharmaceutical companies navigate clinical research efficiently.