Key Insights

Highlights

Success Rate

89% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 30/100

Termination Rate

5.0%

1 terminated out of 20 trials

Success Rate

88.9%

+2.4% vs benchmark

Late-Stage Pipeline

40%

8 trials in Phase 3/4

Results Transparency

25%

2 of 8 completed with results

Key Signals

2 with results89% success

Data Visualizations

Phase Distribution

19Total
Not Applicable (1)
Early P 1 (1)
P 1 (1)
P 2 (8)
P 3 (6)
P 4 (2)

Trial Status

Completed8
Recruiting4
Active Not Recruiting3
Unknown2
Not Yet Recruiting2
Terminated1

Trial Success Rate

88.9%

Benchmark: 86.5%

Based on 8 completed trials

Clinical Trials (20)

Showing 20 of 20 trials
NCT04557462Phase 3Active Not RecruitingPrimary

A Rollover Extension Program (REP) to Evaluate the Long-term Safety and Tolerability of Open Label Iptacopan/LNP023 in Participants With Primary IgA Nephropathy

NCT07354932Phase 2RecruitingPrimary

A Study of SHR-2173 in Participants With Primary IgA Nephropathy

NCT07582133Phase 2Not Yet RecruitingPrimary

A Trial to Evaluate the Long-term Safety and Tolerability of HRS-5965 in Patients With Primary IgA Nephropathy

NCT07498673Early Phase 1RecruitingPrimary

A Study of YKST02 in Participants With Primary IgA Nephropathy

NCT05797610Phase 3RecruitingPrimary

A Study to Evaluate the Efficacy and Safety of Sefaxersen (RO7434656) in Participants With Primary Immunoglobulin A (IgA) Nephropathy at High Risk of Progression

NCT05799287Phase 3Active Not RecruitingPrimary

A Study of Telitacicept for IgA Nephropathy (TELIGAN)

NCT07014826Phase 3RecruitingPrimary

A Trial of HRS-5965 Capsule in Primary IgA Nephropathy

NCT06982040Phase 2Not Yet RecruitingPrimary

Evaluate the Efficacy and Safety of NTQ5082 Capsules in Patients With Primary IgA Nephropathy

NCT06137768Phase 2Active Not RecruitingPrimary

A Trial of HRS-5965 Tablets in Primary IgA Nephropathy

NCT05847920Phase 2TerminatedPrimary

Efficacy and Safety of SHR-2010 Injection in the Treatment of Primary IgA Nephropathy

NCT04541043Phase 3CompletedPrimary

Efficacy and Safety in Patients With Primary IgA Nephropathy Who Have Completed Study Nef-301 (Nefigard-OLE)

NCT04014335Phase 2CompletedPrimary

A Study to Evaluate the Effectiveness and Safety of IONIS-FB-LRx, an Antisense Inhibitor of Complement Factor B, in Adult Participants With Primary IgA Nephropathy

NCT03643965Phase 3CompletedPrimary

Efficacy and Safety of Nefecon in Patients With Primary IgA (Immunoglobulin A) Nephropathy

NCT06589752CompletedPrimary

Replication of the NefIgArd Trial of TRF-budesonide in Primary IgAN

NCT04291781Phase 2CompletedPrimary

A Study of RC18 Administered Subcutaneously to Subjects With Primary IgA(Immunoglobulin A) Nephropathy

NCT04887532Phase 1CompletedPrimary

A Trial of HR19042 Capsule in Healthy Chinese Subjects

NCT02765594Phase 4UnknownPrimary

Hydroxychloroquine Sulfate Alleviates Persistent Proteinuria in IgA Nephropathy

NCT02712697Not ApplicableUnknownPrimary

Integrative Medicine of IgA Nephropathy

NCT02351752Phase 4CompletedPrimary

Hydroxychloroquine Sulfate for Reduction of Proteinuria in Patients With IgA Nephropathy: a Self- Controlled Study

NCT01738035Phase 2CompletedPrimary

The Effect of Nefecon® in Patients With Primary IgA Nephropathy at Risk of Developing End-stage Renal Disease

Showing all 20 trials

Research Network

Activity Timeline