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Completed Phase 2 Interventional Results available

Safety and Efficacy Study of GDC-0853 Compared With Placebo and Adalimumab in Participants With Rheumatoid Arthritis (RA)

ClinicalTrials.gov ID: NCT02833350

Public ClinicalTrials.gov record NCT02833350. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 4:10 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Two-Cohort Randomized Phase II, Double-Blind, Parallel Group Study in Patients With Active Rheumatoid Arthritis Evaluating the Efficacy and Safety of GDC-0853 Compared With Placebo and Adalimumab in Patients With an Inadequate Response to Previous Methotrexate Therapy (Cohort 1) and Compared With Placebo in Patients With an Inadequate Response or Intolerance to Previous TNF Therapy (Cohort 2)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter, Phase II, randomized, double-blind, placebo-controlled, active comparator (Cohort 1 only), parallel-group, dose-ranging study to evaluate the efficacy and safety of GDC-0853 in participants with moderate to severe active RA and an inadequate response to previous methotrexate (MTX) therapy (Cohort 1) or MTX and tumor necrosis factor (TNF) therapy who may have also had exposure to no more than one non-TNF inhibitor biologic (Cohort 2).

Study identification

NCT ID
NCT02833350
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genentech, Inc.
Industry
Enrollment
578 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 8, 2016
Primary completion
Jul 1, 2018
Completion
Jul 1, 2018
Last update posted
Jun 11, 2020

2016 – 2018

United States locations

U.S. sites
23
U.S. states
10
U.S. cities
21
Facility City State ZIP Site status
Pinnacle Research Group; Llc, Central Anniston Alabama 36207
Arizona Arthritis & Rheumatology Associates, P.C. Glendale Arizona 85306
Medvin Clinical Research Covina California 91723
TriWest Research Associates, LLC El Cajon California 92020
Saint Jude Heritage Medical Grp Fullerton California 92835
Stanford University School of Medicine Stanford California 94305-5151
RASF-Clinical Research Center Boca Raton Florida 33486
ZASA Clinical Research Boynton Beach Florida 33472
Clinical Research of West Florida Clearwater Florida 33765
InVentiv Health Miami Florida 33136
Omega Research Consultants Orlando Florida 32810
McIlwain Medical Group Tampa Florida 33613
Institute of Arthritis Research Idaho Falls Idaho 83404
Advanced Clinical Research Meridian Idaho 83642
Medication Management Greensboro North Carolina 27408
Oregon Health and Science University Portland Oregon 97239
Clinical Research Center of Reading Wyomissing Pennsylvania 19610
Metroplex Clinical Research Dallas Texas 75231
Baylor Research Inst. Dallas Texas 75246
Accurate Clinical Management - VO Houston Texas 77004
Accurate Clinical Research Houston Texas 77089
Crossroads Clinical Research, LLC Victoria Texas 77901
Danville Orthopedic Clinic, Inc.; Research Department Danville Virginia 24541

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 127 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02833350, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 11, 2020 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02833350 live on ClinicalTrials.gov.

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