Key Insights

Highlights

Success Rate

100% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Low Risk

Score: 27/100

Termination Rate

0.0%

0 terminated out of 20 trials

Success Rate

100.0%

+13.5% vs benchmark

Late-Stage Pipeline

15%

3 trials in Phase 3/4

Results Transparency

40%

6 of 15 completed with results

Key Signals

6 with results100% success

Data Visualizations

Phase Distribution

14Total
Not Applicable (2)
P 1 (5)
P 2 (4)
P 3 (1)
P 4 (2)

Trial Status

Completed15
Withdrawn2
Recruiting1
Unknown1
Not Yet Recruiting1

Trial Success Rate

100.0%

Benchmark: 86.5%

Based on 15 completed trials

Clinical Trials (20)

Showing 20 of 20 trials
NCT06481150Phase 4CompletedPrimary

A Novel Approach for Reducing Hyperoxaluria and Kidney Stone Risk.

NCT06578754Not Yet RecruitingPrimary

Validation Testing for Plasma Oxalate Levels in the Biochemical Laboratory at the Galilee Medical Center, in Collaboration With the Biochemistry Laboratory at CHARITE Hospital in Berlin, and Testing the Relationship Between Oxalate Levels and Vitamin C Levels in Plasma

NCT02780297RecruitingPrimary

Prospective Research Rare Kidney Stones (ProRKS)

NCT06138327Phase 1WithdrawnPrimary

A Study of BMN 255 in Participants With Non-Alcoholic Fatty Liver Disease And Hyperoxaluria

NCT05443932Phase 4Unknown

Dapagliflozin and Hydrochlorothiazide in Recurring Kidney Stone Patients

NCT04119765Completed

Plasma Oxalate in Patient With Short Bowel

NCT03095885Not ApplicableCompleted

A Pilot Study of Oxalate Absorption in Secondary Hyperoxaluria

NCT04756024CompletedPrimary

Reference Interval of Spot Urinary Oxalate to Creatinine Ratio in Children

NCT04571359Completed

Spot Urine Oxalate to Creatinine Ratio and 24 Hours Urinary Oxalate

NCT00588120Phase 1Completed

Enteric Oxalate Absorption Study in Unclassified Hyperoxaluria

NCT02289755Phase 2CompletedPrimary

Evaluating ALLN-177 for Reducing Urinary Oxalate Excretion in Calcium Oxalate Kidney Stone Formers With Hyperoxaluria

NCT02503345Phase 2Completed

Evaluate the Effect of ALLN-177 in Reducing Urinary Oxalate in Patients With Hyperoxaluria and Kidney Stones

NCT02038543Phase 1CompletedPrimary

Hydroxyproline Influence on Oxalate Metabolism

NCT02547805Phase 2Completed

Evaluate the Effect of ALLN-177 in Reducing Urinary Oxalate in Patients With Secondary Hyperoxaluria and Kidney Stones Over 28 Days

NCT02404701Not ApplicableCompletedPrimary

Effect of Over-the-counter Dietary Supplements on Kidney Stone Risk

NCT00280215Phase 3WithdrawnPrimary

Renal Protective Effect of ACEI and ARB in Primary Hyperoxaluria

NCT00283387Phase 2CompletedPrimary

Efficacy of Betaine for Reduction of Urine Oxalate in Patients With Type 1 Primary Hyperoxaluria

NCT01127087Phase 1CompletedPrimary

Oxazyme in Patients With Hyperoxaluria

NCT00587041Phase 1Completed

Use of Oral Probiotics to Reduce Urinary Oxalate Excretion

NCT00199459Completed

Proteomic Study of Urinary Stone Disease

Showing all 20 trials

Research Network

Activity Timeline