Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02125578 · ClinicalTrials.gov registry record · Phase 1

A Multiple Dose Safety Study of PEG-IFN in Healthy Volunteers

A Phase 1 study, sponsored by Biogen.

Completed
Registry status
Phase 1
Development phase
69
Enrollment target

NCT02125578: Completed Phase 1 study, sponsored by Biogen.

NCT02125578 is a Phase 1 study that has completed, run by Biogen. The registered enrollment target is 69 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02125578, a Phase 1 study, has completed, sponsored by Biogen.

COMPLETED
Registry status
Phase 1
Development phase
69 participants
Enrollment target

Study Summary

The primary objectives are to identify the highest safe and well-tolerated dose and frequency of BIIB017 (PEGylated Interferon Beta-1a) subcutaneous (SC), within the range of 63 to 188 mcg, when given every other week or every 4 weeks to healthy volunteers (HV).

Interventions

  • DRUG Placebo
  • DRUG BIIB017 (PEGylated Interferon Beta-1a)

Trial Details

FieldValue
Enrollment Target 69 participants
Start Date 2008-03
Est. Completion 2008-05
Phase Phase 1
Biogen

334 total trials

What the finished NCT02125578 record still lists

NCT02125578 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 69 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02125578 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02125578 about?

NCT02125578 is a clinical study titled "A Multiple Dose Safety Study of PEG-IFN in Healthy Volunteers". The primary objectives are to identify the highest safe and well-tolerated dose and frequency of BIIB017 (PEGylated Interferon Beta-1a) subcutaneous (SC), within the range of 63 to 188 mcg, when given every other week or every 4 weeks to healthy volunteers (HV).

What is the current status of trial NCT02125578?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 69 participants. The study started on 2008-03. Estimated completion is 2008-05.

What interventions are being tested in trial NCT02125578?

The interventions under investigation include: Placebo (DRUG), BIIB017 (PEGylated Interferon Beta-1a) (DRUG).

Who is sponsoring clinical trial NCT02125578?

This trial is sponsored by Biogen, which has 334 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02125578's enrollment target sits among peer trials

69 774th of 2000 higher than 1,225 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT04020575 · 69 participants · Phase 1

    Autologous huMNC2-CAR44 or huMNC2-CAR22 T Cells for Breast Cancer Targeting Cleaved Form of MUC1 (MUC1*)

  • NCT04163614 · 69 participants · NA

    Blood Pressure Slopes and Ultrafiltration in Hemodialysis Patients

  • NCT04164641 · 69 participants · NA

    Noraxon myoRESEARCH™ Software Gait Analysis Evaluation and Orthotic Gait Correction in Reducing Diabetic Foot Ulceration Or Subsequent Amputation in Patients With a History of a Diabetic Foot Ulceration

  • NCT04493372 · 69 participants · NA

    Deciphering Preserved Autonomic Function After Spinal Cord Injury

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02125578, the US trial registry maintained by the National Library of Medicine. NCT02125578 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.