Dose-ranging Study to Evaluate Efficacy of SLV339 in Pancreatic Exocrine Insufficiency Due to Chronic Pancreatitis

NCT00630279 — Phase 2, Terminated, 56 participants, Solvay Pharmaceuticals

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A Multi-center, Single-blind, Parallel-design, Randomized, Placebo-controlled, Dose-ranging Study to Evaluate Oral Recombinant Microbial Lipase Efficacy in Patients With Pancreatic Exocrine Insufficiency Due to Chronic Pancreatitis

RegistryNCT00630279
StatusTerminated - This trial discontinued March 7,2009 due to high screen failure rate.
PhasePhase 2
Study typeInterventional; randomized, parallel, masking: double, treatment
Enrollment56 (Actual)
SponsorSolvay Pharmaceuticals (Industry)
ConditionsPancreatic Exocrine Insufficiency Due to Chronic Pancreatitis
InterventionsPlacebo, Recombinant Microbial Lipase SLV339 (Drug)
Datesstart 2008-02-01, primary completion 2009-03-01, completion 2009-03-01, first posted 2008-03-06, last updated 2009-08-06
Locations50 sites in Czechia, Denmark, Hungary, Latvia, Poland, Russia, Sweden

Related Papers Related Patents Related Grants Related Experts
All trials for Pancreatic Exocrine Insufficiency Due to Chronic Pancreatitis All trials of Placebo All trials of Recombinant Microbial Lipase SLV339

-Summary

This study is to estimate the efficacy of a number of doses in patients with pancreatic insufficiency

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+Arms and interventions

ArmTypeInterventionsDescription
1Placebo comparatorDrug: Placebo
2ExperimentalDrug: Recombinant Microbial Lipase SLV339
3ExperimentalDrug: Recombinant Microbial Lipase SLV339
4ExperimentalDrug: Recombinant Microbial Lipase SLV339
  • Placebo (Drug): Placebo
  • Recombinant Microbial Lipase SLV339 (Drug): oral, 150 mg/d, 7 days treatment
  • Recombinant Microbial Lipase SLV339 (Drug): oral, 300 mg/d, 7 days treatment
  • Recombinant Microbial Lipase SLV339 (Drug): oral, 600 mg/d, 7 days treatment

+Outcome measures

Primary outcomes

  • CFA (Coefficient of Fat Absorption) [from baseline to end of 7 days treatment]

Secondary outcomes

  • CNA, stool fat, stool weight, nutritional parameters, clinical symptomatology [from baseline to end of 7 days treatment]

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Subject > 18 years;
* Pancreatic exocrine insufficiency confirmed and documented in medical history by either a pathophysiological direct or indirect pancreatic function test or clinical symptoms of steatorrhea stool fat that resolved or improved substantially upon pancreatic enzyme supplementation;
* Patients on a stable daily dose of pancreatic enzymes for 3 months;
* Subjects with CP with or without partial pancreatectomy due to CP, confirmed in medical history by either CT , ERCP, plain film with pancreatic calcifications, ultra-sonography (calcifications, duct dilatation), magnetic resonance pancreatography, endoscope ultrasound, other radiological diagnosis captured by tools such as Cambridge classification and /or histology;
* CFA < 80% at time of randomization

Exclusion Criteria:

* Evidence of major surgery (except gall bladder removal or appendectomy) or other relevant diseases as revealed by history, physical examination, and laboratory assessments which may interfere with the absorption, distribution, metabolism or elimination of the study drug or constitute a risk factor when taking the study medication;
* Investigational drug intake within 90 days prior to the pre-assessment visit;
* Ileus or acute abdomen;
* Allergic disease such as hypersensitivity pneumonitis, aspergillus mediated asthma or allergic broncho-pulmonary aspergillosis;
* Stenosis or regurgitation of the esophagus or stomach;
* Known HIV infection, acute phase of CP

+Locations (50)

FacilityCityCountryStatus
Site 4206BrnoCzechia
Site 4203Hradec KrálovéCzechia
Site 4202PragueCzechia
Site 4205PragueCzechia
Site 4201TáborCzechia
Site 4204Ústí nad OrlicíCzechia
Site 4503HerningDenmark
Site 4502HvidovreDenmark
Site 4501OdenseDenmark
Site 3612BékéscsabaHungary
Site 3607BudapestHungary
Site 3614BudapestHungary
Site 3615DebrecenHungary
Site 3602DunaújvárosHungary
Site 3610EgerHungary
Site 3604GyulaHungary
Site 3606PécsHungary
Site 3613SopronHungary
Site 3609SzegedHungary
Site 3601SzekszárdHungary
Site 3611SzentesHungary
Site 3608TatabányaHungary
Site 3603VácHungary
Site 3605ZalaegerszegHungary
Site 3702DaugavpilsLatvia
Site 3701RigaLatvia
Site 3703RigaLatvia
Site 3704RigaLatvia
Site 3705RigaLatvia
Site 4808BialystokPoland
Site 4809GdanskPoland
Site 4810GdanskPoland
Site 4805KatowicePoland
Site 4811LodzPoland
Site 4807PoznanPoland
Site 4814PoznanPoland
Site 4802SkierniewicePoland
Site 4804SopotPoland
Site 4801WarsawPoland
Site 4806WarsawPoland
Site 4812WroclawPoland
Site 4813WroclawPoland
Site 0901MoscowRussia
Site 0904MoscowRussia
Site 0908MoscowRussia
Site 0909MoscowRussia
Site 0910MoscowRussia
Site 4602GothenburgSweden
Site 4603StockholmSweden
Site 4601UmeåSweden

+Investigators

  • Global Clinical Director Solvay, Study director, Solvay Pharmaceuticals