Pentosan polysulfate ( DrugBank: Pentosan polysulfate )


3 diseases
IDDisease name (Link within this page)Number of trials
19Lysosomal storage disease1
26HTLV-1-associated myelopathy1
226Interstitial cystitis with Hunners ulcer1

19. Lysosomal storage disease


Clinical trials : 899 Drugs : 684 - (DrugBank : 99) / Drug target genes : 51 - Drug target pathways : 182
No.TrialIDDate_
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1EUCTR2014-000350-11-DE
(EUCTR)
28/05/201410/03/2014Treatment of patients, who have Mucopolysaccharidosis Type I, receiving pentosan polysulfate subcutaneous injections weeklyAn open label, randomized study to investigate the safety of weekly pentosan polysulfate injections in adult patients with Mucopolysaccharidosis Type I receiving enzyme replacement therapy. Mucopolysaccharidosis type I (alpha-L-Iduronidase deficiency)
MedDRA version: 17.0;Level: LLT;Classification code 10056888;Term: Mucopolysaccharidosis IS;System Organ Class: 100000004850
MedDRA version: 17.0;Classification code 10056887;Term: Mucopolysaccharidosis IH/S;Classification code 10028094;Term: Mucopolysaccharidosis IH;System Organ Class: 100000004850;Therapeutic area: Diseases [C] - Nutritional and Metabolic Diseases [C18]
Trade Name: Pentosan Polysulfat SP 54® injection solution
Product Name: Pentosan Polysulphate SP54®
INN or Proposed INN: PENTOSAN POLYSULFATE SODIUM
Other descriptive name: Pentosan Polysulphate SP54
Multiplex Pharma Holdings LLCNULLNot RecruitingFemale: yes
Male: yes
6Germany

26. HTLV-1-associated myelopathy


Clinical trials : 29 Drugs : 47 - (DrugBank : 29) / Drug target genes : 34 - Drug target pathways : 119
No.TrialIDDate_
enrollment
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1JPRN-UMIN000015587
2014/11/0403/11/2014Clinical trial with NaPPS for HTLV-1-associated myelopathy (HAM) patientsClinical trial with NaPPS for HTLV-1-associated myelopathy (HAM) patients - Clinical trial with NaPPS for HAM patients HTLV-1-associated myelopathy (HAM)period of intervention: 12 weeks
0-4 weeks: Normal saline solution by subcutaneous injection
4-12 weeks: NaPPS(Pentosan Polysulfate sodium) 50 mg by subcutaneous injection
period of intervention: 12 weeks
0-4 weeks: Normal saline solution by subcutaneous injection
4-12 weeks: NaPPS(Pentosan Polysulfate sodium) 100 mg by subcutaneous injection
period of intervention: 12 weeks
0-4 weeks: NaPPS 100mg/week by subcutaneous injection
4-12 weeks: NaPPS(Pentosan Polysulfate sodium) 50 mg by subcutaneous injection
period of intervention: 12 weeks
0-4 weeks: NaPPS 100mg/week by subcutaneous injection
4-12 weeks: NaPPS(Pentosan Polysulfate sodium) 100
100 mg by subcutaneous injection
ReqMed Company, LtdNULLComplete: follow-up complete20years-oldNot applicableMale and Female12Phase 2Japan

226. Interstitial cystitis with Hunners ulcer


Clinical trials : 145 Drugs : 156 - (DrugBank : 51) / Drug target genes : 64 - Drug target pathways : 146
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
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agemin
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PhaseCountries
1NCT00086684
(ClinicalTrials.gov)
September 20037/7/2004Effectiveness and Safety Study of Pentosan Polysulfate Sodium for the Treatment of Interstitial CystitisRandomized, Double-Blind, Placebo-Controlled, Parallel Group Evaluation of the Efficacy and Tolerability of Two Different Doses of ELMIRON for the Treatment of Interstitial CystitisInterstitial CystitisDrug: Pentosan polysulfate sodium 100 mg;Drug: PlaceboJohnson & Johnson Pharmaceutical Research & Development, L.L.C.NULLTerminated18 YearsN/AAll369Phase 4United States;Canada