Key Insights

Highlights

Success Rate

94% trial completion (above average)

Published Results

11 trials with published results (21%)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 40/100

Termination Rate

3.8%

2 terminated out of 52 trials

Success Rate

93.8%

+7.2% vs benchmark

Late-Stage Pipeline

12%

6 trials in Phase 3/4

Results Transparency

37%

11 of 30 completed with results

Key Signals

11 with results94% success

Data Visualizations

Phase Distribution

33Total
Not Applicable (7)
P 1 (2)
P 2 (18)
P 3 (5)
P 4 (1)

Trial Status

Completed30
Recruiting7
Unknown5
Active Not Recruiting4
Terminated2
Enrolling By Invitation2

Trial Success Rate

93.8%

Benchmark: 86.5%

Based on 30 completed trials

Clinical Trials (52)

Showing 20 of 20 trials
NCT05460169Not ApplicableActive Not Recruiting

Renal Denervation in ADPKD- RDN-ADPKD Study

NCT05193981Active Not RecruitingPrimary

A Study to Evaluate Homocysteine Metabolism and Endothelial Function in ADPKD

NCT04939935Phase 3RecruitingPrimary

Implementation of Metformin theraPy to Ease Decline of Kidney Function in Polycystic Kidney Disease (IMPEDE-PKD)

NCT07228364Phase 1RecruitingPrimary

Safety, Tolerability and Pharmacokinetics of AZD1613 in Adults With Autosomal Dominant Polycystic Kidney Disease

NCT06902558Phase 2RecruitingPrimary

A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of ABBV-CLS-628 in Adult Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

NCT05190744Phase 2CompletedPrimary

Probenecid (PB) to Treat Hereditary Nephrogenic Diabetes Insipidus (NDI), ADPKD Treated With Tolvaptan, and Severely Polyuric Patients With Previous Lithium Administration

NCT03901521Enrolling By InvitationPrimary

Autosomal Dominant Polycystic Kidney Disease Somatic Mutation Biorepository

NCT05288998Active Not RecruitingPrimary

Intrarenal Microvasculature in ADPKD

NCT04344769RecruitingPrimary

Characterization of the Nrf2 Response in Patients With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

NCT04630613RecruitingPrimary

NOX4 and Related Biomarkers in ADPKD

NCT07217158Active Not RecruitingPrimary

Role of ROS and cAMP-PKA Biomarkers in ADPKD

NCT06435858Phase 2RecruitingPrimary

Short-term Effects of an SGLT2 Inhibitor on Divalent Ions in Autosomal Dominant Polycystic Kidney Disease

NCT04284657Phase 2CompletedPrimary

Pravastatin and Alkali Therapy in Patients With Autosomal Dominant Polycystic Kidney Disease

NCT05521191Phase 1CompletedPrimary

A Study of RGLS8429 in Patients With Autosomal Dominant Polycystic Kidney Disease

NCT04578548Phase 2TerminatedPrimary

A Study to Evaluate the Effects of GLPG2737 in Participants With Autosomal Dominant Polycystic Kidney Disease (ADPKD)

NCT03493802CompletedPrimary

Assessment of Longitudinal Changes in Endothelial Function and Oxidative Stress in Normotensive Patients With ADPKD

NCT06065852Recruiting

National Registry of Rare Kidney Diseases

NCT05870007Phase 2Enrolling By InvitationPrimary

Atorvastatin and Alkali Therapy in Patients With Autosomal Dominant Polycystic Kidney Disease

NCT03487913Phase 2CompletedPrimary

The ELiSA Study - Evaluation of Lixivaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease

NCT03541447Phase 2CompletedPrimary

Tolvaptan-Octreotide LAR Combination in ADPKD

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