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NCT02792699 · ClinicalTrials.gov registry record · Phase 3

Study to Assess if ABP 798 is Safe & Effective in Treating Moderate to Severe Rheumatoid Arthritis (RA) Compared to Rituximab

A Phase 3 study, sponsored by Amgen.

Completed
Registry status
Phase 3
Development phase
311
Enrollment target

NCT02792699: Completed Phase 3 study, sponsored by Amgen.

NCT02792699 is a Phase 3 study that has completed, run by Amgen. The registered enrollment target is 311 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (60% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02792699, a Phase 3 study, has completed, sponsored by Amgen.

COMPLETED
Registry status
Phase 3
Development phase
311 participants
Enrollment target

Study Summary

This trial is designed to determine what effects the human body has on the investigational medicine, ABP 798, and what effects the body has on the investigational medicine after you have been given it, and if this is comparable to what is seen for the licensed medicine, rituximab, in patients with moderate or severe RA. This study will also assess if the investigational medicine is safe and effective in treating moderate or severe RA compared to the licensed medicine.

Primary Outcome

Area under the serum concentration-time curve from time 0 extrapolated to infinity (AUCinf) following the second infusion of the first dose (day 15). Concentrations of ABP-798 and rituximab were quantified using a validated electrochemiluminescent method. AUCinf was estimated using the linear trapezoidal rule.

Interventions

  • DRUG ABP 798
  • DRUG Rituximab (US)
  • DRUG Rituximab (EU)

Trial Details

FieldValue
Enrollment Target 311 participants
Start Date 2016-05-17
Est. Completion 2018-10-08
Phase Phase 3
Amgen

558 total trials

What the finished NCT02792699 record still lists

NCT02792699 is an interventional study that assigns participants to a tested intervention. The registered 311 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (60% lower).

The record links to 0 conditions, and to 3 interventions - of which ABP 798 is the first listed.

NCT02792699 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02792699 about?

NCT02792699 is a clinical study titled "Study to Assess if ABP 798 is Safe & Effective in Treating Moderate to Severe Rheumatoid Arthritis (RA) Compared to Rituximab". This trial is designed to determine what effects the human body has on the investigational medicine, ABP 798, and what effects the body has on the investigational medicine after you have been given it, and if this is comparable to what is seen for the licensed medicine, rituximab, in patients with m...

What is the current status of trial NCT02792699?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 311 participants. The study started on 2016-05-17. Estimated completion is 2018-10-08.

What interventions are being tested in trial NCT02792699?

The interventions under investigation include: ABP 798 (DRUG), Rituximab (US) (DRUG), Rituximab (EU) (DRUG).

Who is sponsoring clinical trial NCT02792699?

This trial is sponsored by Amgen, which has 558 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02792699's enrollment target sits among peer trials

311 1106th of 2000 higher than 894 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 NCT02792699, the US trial registry maintained by the National Library of Medicine. NCT02792699 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.