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Interferon beta-1b

Phase 3

HIV Infections | Small molecule | Infectious Disease |Bayer AG|Last Updated: Oct 29, 2015

Success Probability

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Trial Design

Double-BlindUNCONTROLLED
Total Trials1
Total Enrollment -

FDA Designations

No designations recorded

Clinical trial landscape

Interferon beta-1b · 3 trials · 2 indications

Phase 3 3
NCT00370071Open Label Study to Evaluate Effect, Safety and Tolerability of Betaferon Standard Dose of 250µg in Patients of Chinese Origin With Multiple SclerosisMultiple Sclerosis
COMPLETED39 Analytics
NCT00185211BENEFIT Study (Betaferon® / Betaseron® in Newly Emerging Multiple Sclerosis for Initial Treatment) and BENEFIT Follow-up StudyMultiple Sclerosis
COMPLETED468 Analytics
NCT00002238Phase III Randomized Double-Blind Placebo Controlled Study To Evaluate the Safety and Efficacy of Betaseron in AIDS and Advanced ARC Patients Receiving a Reduced-Dose AZT RegimenHIV Infections
COMPLETED- Analytics
PHASE3COMPLETED
Open Label Study to Evaluate Effect, Safety and Tolerability of Betaferon Standard Dose of 250µg in Patients of Chinese Origin With Multiple Sclerosis
Multiple SclerosisUnlock trial analytics
PHASE3COMPLETED
BENEFIT Study (Betaferon® / Betaseron® in Newly Emerging Multiple Sclerosis for Initial Treatment) and BENEFIT Follow-up Study
Multiple SclerosisUnlock trial analytics
PHASE3COMPLETED
Phase III Randomized Double-Blind Placebo Controlled Study To Evaluate the Safety and Efficacy of Betaseron in AIDS and Advanced ARC Patients Receiving a Reduced-Dose AZT Regimen
HIV InfectionsUnlock trial analytics

Study Endpoints

Primary Endpoints

Difference Between the Number of Newly Active Lesions in Magnetic Resonance Imaging (MRI) Per Three Months During the 6-month Treatment Period and the Number of Newly Active Lesions During 3-month Pre-treatment
after 6 months of treatment as compared to 3-month pre-treatment

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)

Time to Clinically Definite Multiple Sclerosis (CDMS) Represented by Kaplan-Meier Estimates of the Cumulative Percentage of Participants With CDMS at Selected Points in Time
up to 60 months after start of treatment

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)

Time to Confirmed Expanded Disability Status Scale (EDSS) Progression Represented by Kaplan-Meier Estimates of the Cumulative Percentage of Participants With Confirmed EDSS Progression at Selected Points in Time
up to 60 months after start of treatment

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.

Functional Assessment of Multiple Sclerosis (FAMS) Trial Outcome Index (TOI) at Month 60
60 months after start of treatment

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.

Secondary Endpoints

Difference Between the Number of New Gadolinium (Gd)-Enhancing Lesions Per 3 Months During the 6-month Treatment Period and the Number of New Gd-enhancing Lesions During 3-month Pre-treatment
after 6 months of treatment as compared to 3-month pre-treatment
Difference Between the Number of New or Enlarging T2 Lesions Per 3 Months During the 6-month Treatment Period and the Number of New or Enlarging T2 Lesions During 3-month Pre-treatment
after 6 months of treatment as compared to the 3-month pre-treatment
Volume of Gadolinium-enhancing Lesions at Baseline, Weeks 12 and 24
Baseline, Weeks 12 and 24
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Study Design & Arms

AllocationNON_RANDOMIZED
MaskingNONE
ModelSINGLE_GROUP
PurposeTREATMENT

Treatment Arms

ArmTypeDescription
Interferon beta-1b (Betaseron, BAY86-5046)EXPERIMENTALInterferon beta-1b 250 μg (8 MIU) subcutaneously (sc) every other day (e.o.d.)
Initial IFNB-1b (Interferon beta-1b)EXPERIMENTALInitial Betaferon/Betaseron treatment (Interferon beta-1b, IFNB-1b), 250 ug administered s.c. (subcutaneous) every other day, continued in Follow-up phase
Initial PlaceboEXPERIMENTALInitial placebo treatment; Betaferon/Betaseron, 250 ug administered s.c. (subcutaneous) every other day offered in Follow-up phase (= this trial)

Interventions

NameTypeDescription
Interferon beta-1b (Betaseron, BAY86-5046)DRUGInterferon beta-1b 250 μg (8 MIU) subcutaneously (sc) every other day (e.o.d.)
Interferon beta-1bDRUG -
ZidovudineDRUG -
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Eligibility Criteria

Age Range16 Years to 55 Years
SexALL
Healthy VolunteersNo
Study Sites3

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...

Countries:ChinaAustriaBelgiumCanadaCzechiaDenmarkFinlandFranceGermanyHungaryIsraelItalyNetherlandsNorwayPolandPortugalSloveniaSpainSwedenSwitzerlandUnited KingdomUnited States
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Frequently asked questions about Interferon beta-1b

What is Interferon beta 1b used for?

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.

What does Interferon beta 1b target?

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.

Who makes Interferon beta 1b?

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.

What phase is Interferon beta 1b in?

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.

What clinical trials is Interferon beta 1b in?

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.

Is Interferon beta 1b the same as Betaseron?

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.