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

NCT02658916 · ClinicalTrials.gov registry record · Phase 1

Extension Study of BIIB092 in Participants With Progressive Supranuclear Palsy (PSP) Who Participated in CN002003

A Phase 1 study, sponsored by Biogen.

Terminated
Registry status
Phase 1
Development phase
47
Enrollment target

NCT02658916 is a Phase 1 study that was terminated before completion, run by Biogen. The registered enrollment target is 47 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02658916, a Phase 1 study, was terminated before completion, sponsored by Biogen.

TERMINATED
Registry status
Phase 1
Development phase
47 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the long-term safety and tolerability of multiple intravenous (IV) infusions of BIIB092 in participants with Progressive Supranuclear Palsy (PSP). The study will also assess the pharmacodynamic (PD) effects of BIIB092 on cerebrospinal fluid (CSF) N-terminal tau, pharmacokinetics (PK), and immunogenicity of BIIB092 in participants with PSP.

Interventions

  • DRUG BIIB092

Trial Details

FieldValue
Enrollment Target 47 participants
Start Date 2016-02-22
Est. Completion 2020-03-31
Phase Phase 1

Sponsor

Biogen

334 total trials

What the Registry Record Tells You About NCT02658916

The ClinicalTrials.gov registry entry for NCT02658916 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 47 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Biogen, which has 334 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which BIIB092 is the first listed.

NCT02658916 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02658916 about?

NCT02658916 is a clinical study titled "Extension Study of BIIB092 in Participants With Progressive Supranuclear Palsy (PSP) Who Participated in CN002003". The purpose of this study is to evaluate the long-term safety and tolerability of multiple intravenous (IV) infusions of BIIB092 in participants with Progressive Supranuclear Palsy (PSP). The study will also assess the pharmacodynamic (PD) effects of BIIB092 on cerebrospinal fluid (CSF) N-terminal t...

What is the current status of trial NCT02658916?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 47 participants. The study started on 2016-02-22. Estimated completion is 2020-03-31.

What interventions are being tested in trial NCT02658916?

The interventions under investigation include: BIIB092 (DRUG).

Who is sponsoring clinical trial NCT02658916?

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

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.