Success Metrics

Clinical Success Rate
83.3%

Based on 15 completed trials

Completion Rate
83%(15/18)
Active Trials
0(0%)
Results Posted
80%(12 trials)
Terminated
3(15%)

Phase Distribution

Ph phase_3
2
10%
Ph phase_2
1
5%
Ph phase_4
9
45%
Ph phase_1
3
15%
Ph not_applicable
1
5%

Phase Distribution

3

Early Stage

1

Mid Stage

11

Late Stage

Phase Distribution16 total trials
Phase 1Safety & dosage
3(18.8%)
Phase 2Efficacy & side effects
1(6.3%)
Phase 3Large-scale testing
2(12.5%)
Phase 4Post-market surveillance
9(56.3%)
N/ANon-phased studies
1(6.3%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

78.9%

15 of 19 finished

Non-Completion Rate

21.1%

4 ended early

Currently Active

0

trials recruiting

Total Trials

20

all time

Status Distribution
Completed(15)
Terminated(4)
Other(1)

Detailed Status

Completed15
Terminated3
Withdrawn1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
20
Active
0
Success Rate
83.3%
Most Advanced
Phase 4

Trials by Phase

Phase 13 (18.8%)
Phase 21 (6.3%)
Phase 32 (12.5%)
Phase 49 (56.3%)
N/A1 (6.3%)

Trials by Status

completed1575%
withdrawn15%
terminated315%
unknown15%

Recent Activity

Clinical Trials (20)

Showing 20 of 20 trials
NCT02949908

MEasuring Satisfaction of Treatment With REbif After Initial Treatment of Multiple Sclerosis (MS)

Terminated
NCT02064816Phase 4

A Study of Rebif® in Subjects With Relapsing Multiple Sclerosis

Completed
NCT00078338Phase 4

Rebif® Versus Copaxone® in the Treatment of Relapsing Remitting Multiple Sclerosis

Completed
NCT02254304Phase 4

Effectiveness of Rebif® in Clinically Isolated Syndrome and Relapsing Multiple Sclerosis Using RebiSmart™

Completed
NCT02823951

Patient Real-world Clinical, Neurological, Tolerability, and Safety Outcomes for Tecfidera® and Rebif®

Completed
NCT01085318Phase 4

Rebif Advanced Magnetic Resonance Imaging (MRI) and Immunology Pilot Trial

Completed
NCT01198132Phase 2

A Multicentre Study of the Efficacy and Safety of Supplementary Treatment With Cholecalciferol in Patients With Relapsing Multiple Sclerosis Treated With Subcutaneous Interferon Beta-1a 44 µg 3 Times Weekly

Completed
NCT01791244Phase 4

A Phase 4 Study to Assess the Impact of Patient Support Program on Health Related Quality of Life and Adherence in Subjects With Relapsing-Remitting Multiple Sclerosis Administered Rebif® With the RebiSmart™ Device

Completed
NCT02359877Phase 1

Open Label Study of Tolerability, Pharmacokinetics and Pharmacodynamics of BCD-054 (Pegylated Interferon Beta-1a), IM and SC, Compared to Rebif® and Avonex® in Healthy Volunteers

Completed
NCT02117050Phase 4

RESOunD: REbif Satisfaction On Discontinuing Oral Dimethyl Fumarate

Terminated
NCT02364986Phase 1

Immune- and miRNA-response to Recombinant Interferon Beta in Healthy Volunteers and Patients With Relapsing Remitting Multiple Sclerosis

Unknown
NCT01601119

Impact of Disease Modifying Therapies (DMTs) and Associated Support Services in Relapsing Multiple Sclerosis (RMS) Patients

Completed
NCT01207648

Retrospective Cohort Study of Rebif® Use in Pediatric Multiple Sclerosis (MS) Subjects (REPLAY)

Completed
NCT02269930Phase 1

Study to Evaluate the Pharmacokinetic Profiles of BIIB017 (Peginterferon Beta-1a) and Rebif® (Interferon Beta-1a) in Healthy Volunteers

Completed
NCT00287079Phase 3

A Prospective Study Looking at the Use of Rebif® in Subjects With Clinically Isolated Syndrome

Completed
NCT00317941Phase 4

Safety Study in Relapsing-remitting Multiple Sclerosis (RRMS) Patients Receiving Betaferon or Rebif

Completed
NCT00101959Phase 4

Implementation Study of Treatment Optimization Recommendations on Relapsing-Remitting Multiple Sclerosis (RR MS) Subjects

Withdrawn
NCT00292266Phase 3

A Study of Rebif® Compared With Avonex® in the Treatment of Relapsing-remitting Multiple Sclerosis (MS)

Completed
NCT00202995Phase 4

Randomized Study Designed to Look at Disease Progression Using 2 Currently FDA Approved Drugs for the Treatment of RRMS

Terminated
NCT00137176Not Applicable

EARLY IFNb-1a and Atorvastatin Combination Therapy of Isolated Clinical Syndrome Suggestive of Multiple Sclerosis

Completed

All 20 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
20