Phase
Condition
Collagen Vascular Diseases
Idiopathic Inflammatory Myopathies
Lupus
Treatment
PF-06823859 low
Placebo Arm
PF-06823859 high
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria for Patients with Skin Predominant Activity:
Must have CDASI Activity score of greater than or equal to 14, and have failed at least 1 standard of care systemic treatment, (eg, corticosteroids).
Confirmation of DM by the investigator and two of the following:
Gottron's papules;
Gottron's sign;
Heliotrope eruption;
Nailfold changes, (dilated capillary loops, capillary dropout, cuticular hypertrophy and/or rugged cuticles;
Photodistributed violaceous erythema, (skin that is exposed to sunlight and appears purplish/reddish, and patchy in appearance;
Positive DM serology -
Post DM diagnosis; standard of care workup for DM must have been completed prior to entry into this research study.
Willing to provide 8 biopsies during the course of the research study
Inclusion Criteria for Patients with Muscle Predominant Activity:
MMT-8 ≤136/150 and PhGA, VAS ≥3 cm (0-10 cm) by visual analog scale (VAS)
Sum of PhGA, VAS, PtGA, and extramuscular global assessment VAS scores is ≥10 cm (0-10 cm) VAS for each.
Participant has failed at least two or more adequate courses of an immunosuppressive agent or immunomodulatory agent, including IVIG, at a dose known to be effective for rheumatologic diseases.
Exclusion Criteria for Patients with Skin Predominant Activity:
Investigator site staff or members of their family.
Acute and Chronic present medical conditions
Intake of greater than 15 mg of prednisone or equivalent per day
Pregnant or breastfeeding females. Fertile men and women who will not comply with the use of 2 effective birth control methods as per the research protocol
Have required management of acute or chronic infections
Have pre existing demyelinating disorder such as multiple sclerosis, or other severe neurological deficits.
Clinically significant lab abnormalities
Any health condition that may be worsened by immunosuppression
Exclusion Criteria for Patients with Muscle Predominant Activity:
Similar to patients with skin predominant activity; Intake of >20 mg oral prednisone/day, or equivalent
Study Design
Connect with a study center
Emeritus Research
Camberwell, Victoria 3124
AustraliaSite Not Available
Sinclair Dermatology
East Melbourne, Victoria 3002
AustraliaSite Not Available
Cabrini Health Limited
Malvern, Victoria 3144
AustraliaSite Not Available
Universitaetsklinikum Erlangen Hautklinik Studienambulanz
Erlangen, 91054
GermanySite Not Available
Universitaetsklinikum Muenster (UKM)
Muenster, 48149
GermanySite Not Available
Universitaetsklinikum Tuebingen
Tuebingen, 72076
GermanySite Not Available
Pécsi Tudományegyetem Klinikai Központ / University of Pécs, Clinical Center
Pécs, Baranya 7362
HungarySite Not Available
University of Debrecen
Debrecen, Hajdú-bihar H-4032
HungarySite Not Available
University of Szeged
Szeged, 6720
HungarySite Not Available
Ospedale Policlinico San Martino
Genova, GE 16132
ItalySite Not Available
IRCCS Istituto Clinico Humanitas
Rozzano, Milan 20089
ItalySite Not Available
Nova Reuma spolka partnerska
Bialystok, 15-707
PolandSite Not Available
ReumaClinic Gabinet Reumatologiczny, Dr Izabela Domysławska
Białystok, 15-166
PolandSite Not Available
Centrum Medyczne Plejady
Krakow, 30-363
PolandSite Not Available
Kliniczny Szpital Wojewodzki nr 1 im. Fryderyka Chopina w Rzeszowie
Rzeszow, 35-055
PolandSite Not Available
Hospital Universitari Vall d'Hebron
Barcelona, 08035
SpainSite Not Available
Hospital Universitario 12 de Octubre
Madrid, 28041
SpainSite Not Available
Hospital Quiron Infanta Luisa
Sevilla, 41010
SpainSite Not Available
The University of Alabama at Birmingham
Birmingham, Alabama 35249
United StatesSite Not Available
University of Alabama at Birmingham
Birmingham, Alabama 35233
United StatesSite Not Available
Mayo Clinic Arizona Research Pharmacy
Phoenix, Arizona 85054
United StatesSite Not Available
Mayo Clinic
Scottsdale, Arizona 85259
United StatesSite Not Available
Attune Health Research Inc.
Beverly Hills, California 90211
United StatesSite Not Available
Freidenrich Center for Translational Research at Stanford University
Palo Alto, California 94304
United StatesSite Not Available
David Fiorentino
Redwood City, California 94063
United StatesSite Not Available
Stanford Investigational Pharmacy
Stanford, California 94305
United StatesSite Not Available
Mayo Clinic Florida
Jacksonville, Florida 32224
United StatesSite Not Available
University Of Miami Hospital
Miami, Florida 33125
United StatesSite Not Available
University of Miami Hospital Clinical Translational Research Site (Infusion site)
Miami, Florida 33136
United StatesSite Not Available
KU Clinical Research Center - Clinical and Translational Science Unit (CTSU)
Fairway, Kansas 66205
United StatesSite Not Available
The University of Kansas Medical Center
Kansas City, Kansas 66160
United StatesSite Not Available
Johns Hopkins Bayview Medical Center
Baltimore, Maryland 21224-6821
United StatesSite Not Available
Brigham and Women's Hospital
Boston, Massachusetts 02115
United StatesSite Not Available
Brigham and Women's Hospital - ACC
Boston, Massachusetts 02115
United StatesSite Not Available
Brigham and Women's Hospital - CTC
Boston, Massachusetts 02115
United StatesSite Not Available
Brigham and Women's Hospital - CTH
Boston, Massachusetts 02115
United StatesSite Not Available
University of Michigan
Ann Arbor, Michigan 48109
United StatesSite Not Available
Clinical Research Unit (CRU)
Minneapolis, Minnesota 55455
United StatesSite Not Available
Department of Medicine Division of Rheumatic and Autoimmune Disease
Minneapolis, Minnesota 55455
United StatesSite Not Available
Lillehei Clinical Research Unit (LCRU)
Minneapolis, Minnesota 55455
United StatesSite Not Available
University of Minnesota Health Rheumatology Clinic
Minneapolis, Minnesota 55455
United StatesSite Not Available
University of Minnesota, Department of Dermatology
Minneapolis, Minnesota 55455
United StatesSite Not Available
Center for Outpatient Health
Saint Louis, Missouri 63108
United StatesSite Not Available
Washington University School of Medicine
Saint Louis, Missouri 63110
United StatesSite Not Available
Mount Sinai Doctors Dermatology
New York, New York 10028
United StatesSite Not Available
NYU Langone Health Clinical Research Center
New York, New York 10016
United StatesSite Not Available
New York University School of Medicine
New York, New York 10016
United StatesSite Not Available
Cleveland Clinic Foundation
Cleveland, Ohio 44195
United StatesSite Not Available
OHSU, Center for Health and Healing CHH2
Portland, Oregon 97239
United StatesSite Not Available
Oregon Clinical & Translational Research Institute
Portland, Oregon 97239
United StatesSite Not Available
Oregon Health & Science University
Portland, Oregon 97239
United StatesSite Not Available
Altoona Center for Clinical Research
Duncansville, Pennsylvania 16635
United StatesSite Not Available
University of Pennsylvania
Philadelphia, Pennsylvania 19104
United StatesSite Not Available
UPMC Montefiore Clinical and Translational Research Center
Pittsburgh, Pennsylvania 15213
United StatesSite Not Available
Austin Neuromuscular Center
Austin, Texas 78756
United StatesSite Not Available
University of Texas Southwestern Medical Center
Dallas, Texas 75390-9191
United StatesSite Not Available
University of Utah MidValley Dermatology
Murray, Utah 84107
United StatesSite Not Available
Center for Clinical & Translational Science
Salt Lake City, Utah 84108
United StatesSite Not Available

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