Ignite Creation Date:
2025-12-25 @ 2:08 AM
Ignite Modification Date:
2025-12-26 @ 3:18 AM
Study NCT ID:
NCT00053560
Status:
UNKNOWN
Last Update Posted:
2008-01-07
First Post:
2003-01-30
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
To Assess Prevention of Bone Loss in Women With Lupus Receiving Treatment With Glucocorticoids
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D008180', 'term': 'Lupus Erythematosus, Systemic'}, {'id': 'D001851', 'term': 'Bone Diseases, Metabolic'}], 'ancestors': [{'id': 'D003240', 'term': 'Connective Tissue Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}, {'id': 'D001327', 'term': 'Autoimmune Diseases'}, {'id': 'D007154', 'term': 'Immune System Diseases'}, {'id': 'D001847', 'term': 'Bone Diseases'}, {'id': 'D009140', 'term': 'Musculoskeletal Diseases'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D003687', 'term': 'Dehydroepiandrosterone'}, {'id': 'C452866', 'term': 'GL-701'}], 'ancestors': [{'id': 'D000737', 'term': 'Androstenols'}, {'id': 'D000736', 'term': 'Androstenes'}, {'id': 'D000731', 'term': 'Androstanes'}, {'id': 'D013256', 'term': 'Steroids'}, {'id': 'D000072473', 'term': 'Fused-Ring Compounds'}, {'id': 'D011083', 'term': 'Polycyclic Compounds'}, {'id': 'D015068', 'term': '17-Ketosteroids'}, {'id': 'D007664', 'term': 'Ketosteroids'}, {'id': 'D000305', 'term': 'Adrenal Cortex Hormones'}, {'id': 'D006728', 'term': 'Hormones'}, {'id': 'D006730', 'term': 'Hormones, Hormone Substitutes, and Hormone Antagonists'}, {'id': 'D045165', 'term': 'Testosterone Congeners'}, {'id': 'D012739', 'term': 'Gonadal Steroid Hormones'}, {'id': 'D042341', 'term': 'Gonadal Hormones'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE'}, 'primaryPurpose': 'PREVENTION', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'count': 155}}, 'statusModule': {'overallStatus': 'UNKNOWN', 'lastKnownStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2002-12'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2004-11', 'completionDateStruct': {'date': '2004-08'}, 'lastUpdateSubmitDate': '2007-12-26', 'studyFirstSubmitDate': '2003-01-30', 'studyFirstSubmitQcDate': '2003-02-01', 'lastUpdatePostDateStruct': {'date': '2008-01-07', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2003-02-03', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['lupus', 'systemic lupus erythematosus', 'SLE', 'bone loss', 'DHEA'], 'conditions': ['Lupus']}, 'referencesModule': {'references': [{'pmid': '18634158', 'type': 'DERIVED', 'citation': 'Sanchez-Guerrero J, Fragoso-Loyo HE, Neuwelt CM, Wallace DJ, Ginzler EM, Sherrer YR, McIlwain HH, Freeman PG, Aranow C, Petri MA, Deodhar AA, Blanton E, Manzi S, Kavanaugh A, Lisse JR, Ramsey-Goldman R, McKay JD, Kivitz AJ, Mease PJ, Winkler AE, Kahl LE, Lee AH, Furie RA, Strand CV, Lou L, Ahmed M, Quarles B, Schwartz KE. Effects of prasterone on bone mineral density in women with active systemic lupus erythematosus receiving chronic glucocorticoid therapy. J Rheumatol. 2008 Aug;35(8):1567-75. Epub 2008 Jul 15.'}]}, 'descriptionModule': {'briefSummary': 'The purpose of this clinical trial is to study the effects of GL701 on bone mineral density in women with active systemic lupus erythematosus (SLE) who are also receiving treatment with glucocorticoids (e.g., prednisone).'}, 'eligibilityModule': {'sex': 'FEMALE', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "INCLUSION CRITERIA\n\n* Women at least 18 years of age.\n* Meet ACR criteria for diagnosis of SLE.\n* Concomitant treatment with prednisone at a dose of ≥5 mg/day over the last 30 days prior to Screening visit.\n* Cumulative history of oral glucocorticoid use for at least 6 months over the last year prior to the Screening Visit (the 6 months do not have to be consecutive).\n* Patient has lumbar spine and proximal femur anatomy suitable for measurement by DXA with at least 3 evaluable vertebrae from L1 to L4.\n* SLEDAI ≥3 at the Qualifying Visit.\n* Women of child-bearing potential must have a negative serum pregnancy test (at the Screening Visit) and agree to use a reliable form of birth control while participating in the study.\n* Patient is fully ambulatory.\n* Patient has read and signed an Informed Consent Form.\n\nEXCLUSION CRITERIA\n\n* History of breast cancer or malignancy of the reproductive tract organs.\n* History of any other cancers unless no evidence of disease for 5 years.\n* History of endometrial hyperplasia.\n* End stage renal disease or receiving hemodialysis treatment.\n* Any disease or condition that would preclude the accurate measurement of bone mineral density of the lumbar spine or proximal femur by dual X-ray absorptiometry.\n* A T-score of less than or equal to - 2.5 of the L-spine or proximal femur at Screening DXA assessment.\n* Unstable cardiac disease.\n* Conditions causing bone loss such as hyperparathyroidism, Cushing's disease, thyrotoxicosis, chronic diarrheal state or malabsorption, renal tubular acidosis, or anorexia nervosa.\n* Significant hepatic disease (i.e., cirrhosis).\n* Body mass index \\> 35 kg/m2 or weight \\>300 lbs.\n* Patients who are pregnant or breast feeding.\n* Patients who require glucocorticoids by an alternate day dosing schedule.\n* Known hypersensitivity to DHEA, or the inactive ingredients used in the GL701 formulation (cornstarch, lactose, magnesium stearate).\n* Known medical contraindication or hypersensitivity to Calcium/Vitamin D.\n* Participation in any prior DHEA or GL701 study.\n* Use of investigational agents within 30 days of the Screening Visit or 10 half-lives of the agent.\n* Any condition which in the Investigator's or Sponsor's opinion is sufficient to prevent adequate compliance with the study or likely to confuse follow-up evaluation (e.g., alcoholism, drug addiction, acute withdrawal from chemical dependency, psychiatric disease).\n* The patient is taking or has taken one of the medications listed below:\n\nANTIRESORPTIVES:\n\n* Use of calcitonin within 30 days prior to Screening Visit.\n* Fluorides \\> 1 mg/day at any time prior to the study.\n* Strontium at pharmacologic dose at any time.\n\nBISPHOSPHONATE USE as follows:\n\n* Any use within 90 days prior to the Screening Visit.\n* ≥ 2 weeks of use in the last year prior to the Screening Visit.\n* ≥ 3 months of use in the last 2 years prior to the Screening Visit.\n* ≥ 1 intravenous dose over the last 2 years prior to the Screening Visit.\n* ≥ 6 months of life-time exposure prior to the Screening Visit.\n\nESTROGENIC STEROIDS (Except for oral contraceptives):\n\n* Estrogenic steroids (HRT) within 60 days of the Screening Visit.\n* Selective estrogen receptor modulator (raloxifene) within 60 days of the Screening Visit.\n\nOTHER HORMONES:\n\n* Parathyroid hormone (PTH) within six months of the Screening Visit.\n* Use of any androgens, including prescription or nutritional supplement DHEA, within 30 days of the Screening Visit."}, 'identificationModule': {'nctId': 'NCT00053560', 'briefTitle': 'To Assess Prevention of Bone Loss in Women With Lupus Receiving Treatment With Glucocorticoids', 'organization': {'class': 'INDUSTRY', 'fullName': 'Genelabs Technologies'}, 'officialTitle': 'A Randomized, Double-Blind, Multi-Center, Placebo- Controlled Study to Assess Prevention of Bone Loss by Treatment With GL701 (Prestara) in Women With Systemic Lupus Erythematosus Receiving Treatment With Glucocorticoids', 'orgStudyIdInfo': {'id': 'GL02-01'}}, 'armsInterventionsModule': {'interventions': [{'name': 'Prasterone (GL701)', 'type': 'DRUG'}]}, 'contactsLocationsModule': {'locations': [{'zip': '85724', 'city': 'Tucson', 'state': 'Arizona', 'country': 'United States', 'facility': 'University of Arizona', 'geoPoint': {'lat': 32.22174, 'lon': -110.92648}}, {'zip': '90048', 'city': 'Los Angeles', 'state': 'California', 'country': 'United States', 'facility': 'Wallace Rheumatic Study Center', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '91607', 'city': 'North Hollywood', 'state': 'California', 'country': 'United States', 'facility': 'Peng T Fan, MD & Wonil Lee, MD Partnership', 'geoPoint': {'lat': 34.17223, 'lon': -118.37897}}, {'zip': '92270', 'city': 'Rancho Mirage', 'state': 'California', 'country': 'United States', 'facility': 'Lifestyles Health Science Center', 'geoPoint': {'lat': 33.73974, 'lon': -116.41279}}, {'zip': '92093-0943', 'city': 'San Diego', 'state': 'California', 'country': 'United States', 'facility': 'University of California San Diego', 'geoPoint': {'lat': 32.71571, 'lon': -117.16472}}, {'zip': '94578', 'city': 'San Leandro', 'state': 'California', 'country': 'United States', 'facility': 'East Bay Rheumatology Group', 'geoPoint': {'lat': 37.72493, 'lon': -122.15608}}, {'zip': '33334', 'city': 'Fort Lauderdale', 'state': 'Florida', 'country': 'United States', 'facility': 'Center for Rheumatology, Immunology and Arthritis', 'geoPoint': {'lat': 26.12231, 'lon': -80.14338}}, {'zip': '32806-6264', 'city': 'Orlando', 'state': 'Florida', 'country': 'United States', 'facility': 'Rheumatology Associates of Central Florida', 'geoPoint': {'lat': 28.53834, 'lon': -81.37924}}, {'zip': '33614', 'city': 'Tampa', 'state': 'Florida', 'country': 'United States', 'facility': 'Tampa Medical Group, P.A.', 'geoPoint': {'lat': 27.94752, 'lon': -82.45843}}, {'zip': '60611', 'city': 'Chicago', 'state': 'Illinois', 'country': 'United States', 'facility': 'Northwestern University', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '70121', 'city': 'New Orleans', 'state': 'Louisiana', 'country': 'United States', 'facility': 'Ochsner Clinic Foundation', 'geoPoint': {'lat': 29.95465, 'lon': -90.07507}}, {'zip': '21205', 'city': 'Baltimore', 'state': 'Maryland', 'country': 'United States', 'facility': 'Johns Hopkins University', 'geoPoint': {'lat': 39.29038, 'lon': -76.61219}}, {'zip': '65804', 'city': 'Springfield', 'state': 'Missouri', 'country': 'United States', 'facility': "St. John's Medical Research Group", 'geoPoint': {'lat': 37.21533, 'lon': -93.29824}}, {'zip': '63110', 'city': 'St Louis', 'state': 'Missouri', 'country': 'United States', 'facility': 'Washington University School of Medicine', 'geoPoint': {'lat': 38.62727, 'lon': -90.19789}}, {'zip': '11203', 'city': 'Brooklyn', 'state': 'New York', 'country': 'United States', 'facility': 'SUNY Downstate Medical Center', 'geoPoint': {'lat': 40.6501, 'lon': -73.94958}}, {'zip': '11030', 'city': 'Manhasset', 'state': 'New York', 'country': 'United States', 'facility': 'North Shore University Hospital, Division of Rheumatology', 'geoPoint': {'lat': 40.79788, 'lon': -73.69957}}, {'zip': '10461', 'city': 'The Bronx', 'state': 'New York', 'country': 'United States', 'facility': 'Albert Einstein Medical School', 'geoPoint': {'lat': 40.84985, 'lon': -73.86641}}, {'zip': '74114', 'city': 'Tulsa', 'state': 'Oklahoma', 'country': 'United States', 'facility': 'Oklahoma Center for Arthritis Therapy', 'geoPoint': {'lat': 36.15398, 'lon': -95.99277}}, {'zip': '97201', 'city': 'Portland', 'state': 'Oregon', 'country': 'United States', 'facility': 'Oregon Health & Science University', 'geoPoint': {'lat': 45.52345, 'lon': -122.67621}}, {'zip': '16635', 'city': 'Duncansville', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'Altoona Center for Clinical Research', 'geoPoint': {'lat': 40.42341, 'lon': -78.4339}}, {'zip': '15261', 'city': 'Pittsburgh', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'University of Pittsburgh', 'geoPoint': {'lat': 40.44062, 'lon': -79.99589}}, {'zip': '37232', 'city': 'Nashville', 'state': 'Tennessee', 'country': 'United States', 'facility': 'Vanderbilt University', 'geoPoint': {'lat': 36.16589, 'lon': -86.78444}}, {'zip': '77555', 'city': 'Galveston', 'state': 'Texas', 'country': 'United States', 'facility': 'University of Texas, Medical Branch', 'geoPoint': {'lat': 29.30135, 'lon': -94.7977}}, {'zip': '23462', 'city': 'Virginia Beach', 'state': 'Virginia', 'country': 'United States', 'facility': 'Sentara Medical Group DBA', 'geoPoint': {'lat': 36.85293, 'lon': -75.97799}}, {'zip': '98104', 'city': 'Seattle', 'state': 'Washington', 'country': 'United States', 'facility': 'Seattle Rheumatology Associates', 'geoPoint': {'lat': 47.60621, 'lon': -122.33207}}, {'zip': '14000', 'city': 'Mexico City', 'country': 'Mexico', 'facility': 'Immunology/Rheumatology Instituto Nacional de Ciencias Medicas y Nutricion, S.Z.', 'geoPoint': {'lat': 19.42847, 'lon': -99.12766}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Genelabs Technologies', 'class': 'INDUSTRY'}, 'responsibleParty': {'oldNameTitle': 'Kenneth E. Schwartz, MD/Vice President, Medical Affairs', 'oldOrganization': 'Genelabs Technologies, Inc.'}}}}