Approval Probability
TA Base Rate
Adjusted LOA
ML Risk
Interferon beta-1b · 3 trials · 2 indications
The primary efficacy variable was calculated by subtracting the number of newly active lesions during the 3-month pre-treatment period from the cumulative number of newly active lesions during the 6-month treatment period divided by 2 (number of newly active lesions per three months, new lesion frequency per 3 months)
CDMS could be reached due to a qualifying relapse or sustained progression of 1.5 points on the expanded disability status scale (EDSS) as compared to the lowest EDSS obtained during screening or Day 1. The validity of CDMS diagnoses was confirmed by a central committee. The EDSS scale quantifies disability in MS in 8 functional systems, values vary between 0="normal neurological examination" and 10="death due to MS" measured in half-points on an ordinal scale. Time to CDMS = date of CDMS - date of Day 1 + 1 or time to CDMS = date of last clinical visit - date of Day 1 + 1 (right-censored)
EDSS progression was defined as an increase in the expanded disability status scale (EDSS) of 1.0 point compared to the lowest EDSS score obtained during the screening or baseline visit, if this score was \<= 5.5. A confirmed EDSS progression status was defined as an EDSS progression observed at two consecutive scheduled visits at least 140 days apart from each other. The EDSS scale is a method of quantifying disability in multiple sclerosis in eight functional systems and values vary between 0="normal neurological examination" and 10="death due to MS" measured in half-points on a scale.
As an index of health related quality of life in people diagnosed with MS, the FAMS Trial Outcome Index covers overall physical health (sum of sub-scale scores Mobility, Symptoms, Thinking/Fatigue, Additional Concerns) with a score range from 0 to 148. A higher score reflects a higher overall physical health as reported by patients.
| Arm | Type | Description |
|---|---|---|
| Interferon beta-1b (Betaseron, BAY86-5046) | EXPERIMENTAL | Interferon beta-1b 250 μg (8 MIU) subcutaneously (sc) every other day (e.o.d.) |
| Initial IFNB-1b (Interferon beta-1b) | EXPERIMENTAL | Initial Betaferon/Betaseron treatment (Interferon beta-1b, IFNB-1b), 250 ug administered s.c. (subcutaneous) every other day, continued in Follow-up phase |
| Initial Placebo | EXPERIMENTAL | Initial placebo treatment; Betaferon/Betaseron, 250 ug administered s.c. (subcutaneous) every other day offered in Follow-up phase (= this trial) |
| Name | Type | Description |
|---|---|---|
| Interferon beta-1b (Betaseron, BAY86-5046) | DRUG | Interferon beta-1b 250 μg (8 MIU) subcutaneously (sc) every other day (e.o.d.) |
| Interferon beta-1b | DRUG | - |
| Zidovudine | DRUG | - |
Inclusion Criteria: * Chinese origin * diagnosis of Relapsing remitting multiple sclerosis or secondary progressive multiple sclerosis Exclusion Criteria: * Any disease other than Multiple Sclerosis (MS) that could better explain the patients signs and symptoms * HIV (human immunodeficiency virus...
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Interferon beta 1b is used for the treatment of multiple sclerosis, including relapsing-remitting multiple sclerosis, and is also being studied for HIV infections. It is developed by Bayer AG (ticker: BAYRY) and is currently in Phase 3 clinical development for these indications.
Interferon beta 1b is a small molecule that works by modulating the immune system to reduce inflammation and prevent nerve damage in multiple sclerosis. It is a type of interferon beta, which has antiviral and immunomodulatory properties, helping to decrease the frequency and severity of relapses in patients with relapsing-remitting multiple sclerosis.
Interferon beta 1b is developed by Bayer AG, a multinational pharmaceutical company headquartered in Germany. Bayer AG is publicly traded under the ticker symbol BAYRY on the OTC market. The drug is being investigated for multiple sclerosis and HIV infections.
Interferon beta 1b is currently in Phase 3 clinical development for multiple sclerosis and HIV infections. It has completed several Phase 3 trials, including the BENEFIT study and the BEYOND follow-up study, which evaluated its efficacy and safety in patients with multiple sclerosis.
Interferon beta 1b has been studied in several clinical trials, including NCT00185211 (BENEFIT study), NCT00235989 (extension study), NCT00370071 (study in Chinese patients), and NCT00459667 (BEYOND follow-up). These trials have been completed and involved patients with multiple sclerosis, including relapsing-remitting forms.
Yes, Interferon beta 1b is also known as Betaseron or Betaferon. These are brand names for the same drug, which is used to treat multiple sclerosis. In clinical trials, it has been referred to as Betaferon or Betaseron, and it is being developed by Bayer AG.