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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 Oct 18, 2026, 4:55 AM 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 9, 2016 (Actual)
Primary completion
Jul 2, 2018 (Actual)
Completion
Jul 2, 2018 (Actual)
Last update posted
Jun 12, 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 12, 2020 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02833350 live on ClinicalTrials.gov.

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