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Musculoskeletal Ultrasound in Predicting Early Dose Titration With Tocilizumab (RASTS)

This study has been completed.
Sponsor:
Collaborator:
Genentech, Inc.
Information provided by (Responsible Party):
Dr. Veena Ranganath, University of California, Los Angeles
ClinicalTrials.gov Identifier:
NCT01717859
First received: October 19, 2012
Last updated: May 23, 2017
Last verified: May 2017
  Purpose
The purpose of this research study is to determine if a change in inflammation or baseline inflammation seen on the ultrasound is a good indicator of how rheumatoid arthritis patients respond to TCZ 4mg/kg and whether early prediction of dose escalation is possible by utilizing ultrasound inflammatory measures.

Condition Intervention Phase
Rheumatoid Arthritis Drug: Tocilizumab Phase 4

Study Type: Interventional
Study Design: Intervention Model: Single Group Assignment
Masking: No masking
Primary Purpose: Other
Official Title: Musculoskeletal Ultrasound in Predicting Early Dose Titration With Tocilizumab

Resource links provided by NLM:


Further study details as provided by Dr. Veena Ranganath, University of California, Los Angeles:

Primary Outcome Measures:
  • Baseline to month 3 change in total power Doppler synovitis score of 30 joints (range 0-90) [ Time Frame: Baseline, 3 Month ]
    30 joints will be evaluated.


Secondary Outcome Measures:
  • Baseline to month 3 change in total B-mode synovial hypertrophy score of 30 joints (range 0-90) [ Time Frame: Baseline, 3 Month ]
    30 joints will be evaluated.

  • Baseline to month 3 change in composite of power Doppler and synovial hypertrophy of 30 joints (range 0-180) [ Time Frame: Baseline, 3 Month ]
    30 joints will be evaluated.

  • Baseline to month 3 change in MBDA [ Time Frame: Baseline, 3 Month ]
  • Baseline to month 3 change in DAS28ESR [ Time Frame: Baseline, 3 month ]
    28 joint will be evaluated.

  • Baseline to month 3 change in CDAI [ Time Frame: Baseline, 3 month ]

Enrollment: 53
Study Start Date: September 2014
Study Completion Date: April 2017
Primary Completion Date: April 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Tocilizumab
All subjects will receive tocilizumab.
Drug: Tocilizumab
All subjects will start at 4mg/kg. After 3 months, if DAS28 > 3.2, dosage will be escalated to 8 mg/kg.
Other Name: Actemra

  Eligibility

Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria
  1. Patient must meet 1987 ACR criteria,
  2. Age > 18 years of age,
  3. Baseline DAS28/ESR>4.4,
  4. Stable concomitant DMARDs,
  5. Stable prednisone <10mg or equivalent, and
  6. Power Doppler score of >=10
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01717859

Locations
United States, California
UCLA David Geffen School of Medicine, Division of Rheumatology
Los Angeles, California, United States, 90095
Sponsors and Collaborators
University of California, Los Angeles
Genentech, Inc.
Investigators
Principal Investigator: Veena Ranganath, MD, MS UCLA David Geffen School of Medicine, Division of Rheumatology
  More Information

Responsible Party: Dr. Veena Ranganath, M.D., M.S., Assistant Clinical Professor, University of California, Los Angeles
ClinicalTrials.gov Identifier: NCT01717859     History of Changes
Other Study ID Numbers: ML28542
ML28542 ( Other Identifier: Genentech Inc. )
Study First Received: October 19, 2012
Last Updated: May 23, 2017

Keywords provided by Dr. Veena Ranganath, University of California, Los Angeles:
Rheumatoid Arthritis

Additional relevant MeSH terms:
Arthritis
Arthritis, Rheumatoid
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases
Connective Tissue Diseases
Autoimmune Diseases
Immune System Diseases

ClinicalTrials.gov processed this record on June 28, 2017