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NCT02634307 · ClinicalTrials.gov registry record · Phase 3

A Study of ALKS 8700 in Adults With Relapsing Remitting Multiple Sclerosis (MS) EVOLVE-MS-1

A Phase 3 study, sponsored by Biogen.

Completed
Registry status
Phase 3
Development phase
1,057
Enrollment target

NCT02634307: Completed Phase 3 study, sponsored by Biogen.

NCT02634307 is a Phase 3 study that has completed, run by Biogen. The registered enrollment target is 1,057 participants, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (37% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02634307, a Phase 3 study, has completed, sponsored by Biogen.

COMPLETED
Registry status
Phase 3
Development phase
1,057 participants
Enrollment target

Study Summary

The primary objective of this study is to evaluate the long-term safety and tolerability of ALKS 8700 for the treatment of Relapsing Remitting Multiple Sclerosis (RRMS). The secondary objective of this study is to evaluate treatment effect over time in adult participants with RRMS treated with ALKS 8700.

Primary Outcome

An AE is any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product and that does not necessarily have a causal relationship with this treatment. An AE can therefore be any unfavorable and unintended sign (including an abnormal assessment such as an abnormal laboratory value), symptom, or disease temporally associated with the use of a medicinal (investigational) product, whether or not related to the medicinal (investigational) p

Interventions

  • DRUG ALKS 8700

Trial Details

FieldValue
Enrollment Target 1,057 participants
Start Date 2015-12-10
Est. Completion 2021-11-11
Phase Phase 3
Biogen

334 total trials

What the finished NCT02634307 record still lists

NCT02634307 is an interventional study that assigns participants to a tested intervention. Its 1,057 participants enrollment target places it among the larger protocols in the corpus, above the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (37% higher).

The record links to 0 conditions, and to 1 intervention - of which ALKS 8700 is the first listed.

NCT02634307 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02634307 about?

NCT02634307 is a clinical study titled "A Study of ALKS 8700 in Adults With Relapsing Remitting Multiple Sclerosis (MS) EVOLVE-MS-1". The primary objective of this study is to evaluate the long-term safety and tolerability of ALKS 8700 for the treatment of Relapsing Remitting Multiple Sclerosis (RRMS). The secondary objective of this study is to evaluate treatment effect over time in adult participants with RRMS treated with ALKS ...

What is the current status of trial NCT02634307?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,057 participants. The study started on 2015-12-10. Estimated completion is 2021-11-11.

What interventions are being tested in trial NCT02634307?

The interventions under investigation include: ALKS 8700 (DRUG).

Who is sponsoring clinical trial NCT02634307?

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

How this trial's enrollment target compares

Where NCT02634307's enrollment target sits among peer trials

1,057 276th of 2000 higher than 1,724 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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

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Source: ClinicalTrials.gov NCT02634307, the US trial registry maintained by the National Library of Medicine. NCT02634307 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.