238. ビタミンD抵抗性くる病/骨軟化症 Vitamin D-resistant rickets Clinical trials / Disease details


臨床試験数 : 28 薬物数 : 20 - (DrugBank : 9) / 標的遺伝子数 : 3 - 標的パスウェイ数 : 16

  
8 trials found
No.TrialIDDate_
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PhaseCountries
1NCT05357573
(ClinicalTrials.gov)
August 11, 202227/4/2022Study to Assess the Safety, Pharmacokinetics and Efficacy of KRN23 in Adult Chinese Patients With TIOAn Open-Label, Multi Center, Single-Cohort, Post-Marketing Phase 4 Study to Evaluate the Efficacy, Pharmacodynamics, and Safety of the Anti-FGF23 Antibody, KRN23, in Adult Chinese Patients With Tumor-Induced Osteomalacia (TIO)Tumor-Induced Osteomalacia (TIO)Drug: KRN23Kyowa Kirin Co., Ltd.NULLRecruiting18 YearsN/AAll10Phase 4China
2NCT03775187
(ClinicalTrials.gov)
April 5, 201911/12/2018Expanded Access to BurosumabX-linked Hypophosphatemia;Tumor-Induced OsteomalaciaBiological: BurosumabUltragenyx Pharmaceutical IncKyowa Kirin Co., Ltd.AvailableN/AN/AAllNULL
3NCT03510455
(ClinicalTrials.gov)
February 27, 201926/4/2018BGJ398 for the Treatment of Tumor-Induced OsteomalaciaBGJ398 for the Treatment of Tumor-Induced OsteomalaciaTumor-Induced Osteomalacia;Oncogenic OsteomalaciaDrug: BGJ398National Institute of Dental and Craniofacial Research (NIDCR)NULLCompleted18 Years85 YearsAll4Phase 2United States
4NCT02722798
(ClinicalTrials.gov)
April 20167/3/2016A Study of KRN23 in Subjects With Tumor-Induced Osteomalacia or Epidermal Nevus SyndromeA Phase 2 Open-Label Trial to Assess the Efficacy and Safety of KRN23 in Patients With Tumor-Induced Osteomalacia or Epidermal Nevus Syndrome and a Post-marketing Study of KRN23 Switched From the Phase 2 TrialTumor-Induced Osteomalacia or Epidermal Nevus SyndromeDrug: KRN23Kyowa Kirin Co., Ltd.NULLCompleted18 YearsN/AAll14Phase 2Japan;Korea, Republic of
5JPRN-JapicCTI-163191
23/4/201508/03/2016A Phase 2 Open-Label Trial of KRN23A Phase 2 Open-Label Trial to Assess the Efficacy and Safety of KRN23 in Patients with Tumor-Induced Osteomalacia or Epidermal Nevus Syndrome Tumor-Induced Osteomalacia or Epidermal Nevus SyndromeIntervention name : KRN23
INN of the intervention : burosumab
Dosage And administration of the intervention : repeated SC administration, intraindividual dose adjustment
Control intervention name : -
INN of the control intervention : -
Dosage And administration of the control intervention : -
Kyowa Kirin Co., Ltd.NULLcomplete18BOTH6Phase 2Japan, Asia except Japan
6NCT02304367
(ClinicalTrials.gov)
March 24, 201524/11/2014Study of Burosumab (KRN23) in Adults With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)A Phase 2 Open-Label Trial to Assess the Efficacy and Safety of KRN23, an Antibody to FGF23, in Subjects With Tumor-Induced Osteomalacia (TIO) or Epidermal Nevus Syndrome (ENS)-Associated OsteomalaciaTumor Induced Osteomalacia (TIO);Epidermal Nevus Syndrome (ENS)Biological: BurosumabUltragenyx Pharmaceutical IncNULLActive, not recruiting18 YearsN/AAll17Phase 2United States
7NCT01748812
(ClinicalTrials.gov)
November 16, 201211/12/2012Cinacalcet for Fibroblast Growth Factor 23 (FGF23)-Mediated Hypophosphatemia (Hypophosphatemic Rickets)Open-label Dose-titration Study of the Tolerability and Efficacy of Cinacalcet to Treat Fibroblast Growth Factor 23 (FGF23)-Mediated HypophosphatemiaOsteomalaciaDrug: OsteomalaciaNational Institute of Dental and Craniofacial Research (NIDCR)NULLTerminated18 Years70 YearsAll1Phase 1United States
8ChiCTR-OOC-16010095
2006-01-012016-12-07Oral Phosphate Supplements Play an Important Role in Improving the Bone Mineral Density of Hypophosphatemic Osteomalacia PatientsEffect of Phosphate on hypophosphatemia Hypophosphatemic OsteomalaciaA1:received phosphate solution doses at a frequency dependent upon measured serum phosphorus levels;A2:received phosphate solution doses only every three to four days;A3:received no phosphate solution;A:Hypophosphatemic Osteomalacia;B:Control;The Second Xiangya Hospital, Central South UniversityNULLCompletedBothA1:3;A2:5;A3:3;A:21;B:105;China