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NCT02784106 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of M2951 in Participants With Rheumatoid Arthritis

A Phase 2 study, sponsored by EMD Serono Research & Development Institute.

Completed
Registry status
Phase 2
Development phase
65
Enrollment target

NCT02784106: Completed Phase 2 study, sponsored by EMD Serono Research & Development Institute.

NCT02784106 is a Phase 2 study that has completed, run by EMD Serono Research & Development Institute. The registered enrollment target is 65 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02784106, a Phase 2 study, has completed, sponsored by EMD Serono Research & Development Institute.

COMPLETED
Registry status
Phase 2
Development phase
65 participants
Enrollment target

Study Summary

M2951 is an investigational drug under evaluation for treatment of autoimmune and inflammatory disorders. The purpose of the study is to assess the efficacy of M2951 in participants with rheumatoid arthritis (RA) currently treated with stable dose of methotrexate (MTX).

Primary Outcome

ACR 20 response: greater than or equal to (\>=) 20 percent (%) improvement in both tender joint counts (based on a total of 68 joints) and swollen joint counts (based on a total of 66 joints) together with \>=20% improvement in at least 3 of the following: 1) participant's assessment of pain; 2) participant's global assessment of disease activity; 3) physician's global assessment of disease activity; 4) participant's assessment of physical function measured by Health Assessment Questionnaire-Dis

Interventions

  • DRUG Placebo
  • DRUG M2951

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2016-07-31
Est. Completion 2017-11-14
Phase Phase 2

What the finished NCT02784106 record still lists

NCT02784106 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower).

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

NCT02784106 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02784106 about?

NCT02784106 is a clinical study titled "Safety and Efficacy Study of M2951 in Participants With Rheumatoid Arthritis". M2951 is an investigational drug under evaluation for treatment of autoimmune and inflammatory disorders. The purpose of the study is to assess the efficacy of M2951 in participants with rheumatoid arthritis (RA) currently treated with stable dose of methotrexate (MTX).

What is the current status of trial NCT02784106?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 65 participants. The study started on 2016-07-31. Estimated completion is 2017-11-14.

What interventions are being tested in trial NCT02784106?

The interventions under investigation include: Placebo (DRUG), M2951 (DRUG).

Who is sponsoring clinical trial NCT02784106?

This trial is sponsored by EMD Serono Research & Development Institute, which has 81 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02784106's enrollment target sits among peer trials

65 987th of 2000 higher than 1,005 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT02784106, the US trial registry maintained by the National Library of Medicine. NCT02784106 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.