Success Metrics

Clinical Success Rate
45.5%

Based on 5 completed trials

Completion Rate
45%(5/11)
Active Trials
3(21%)
Results Posted
160%(8 trials)
Terminated
6(43%)

Phase Distribution

Ph phase_3
2
14%
Ph phase_1
4
29%
Ph phase_2
8
57%

Phase Distribution

4

Early Stage

8

Mid Stage

2

Late Stage

Phase Distribution14 total trials
Phase 1Safety & dosage
4(28.6%)
Phase 2Efficacy & side effects
8(57.1%)
Phase 3Large-scale testing
2(14.3%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

45.5%

5 of 11 finished

Non-Completion Rate

54.5%

6 ended early

Currently Active

3

trials recruiting

Total Trials

14

all time

Status Distribution
Active(3)
Completed(5)
Terminated(6)

Detailed Status

Terminated6
Completed5
Active, not recruiting3

Development Timeline

Analytics

Development Status

Total Trials
14
Active
3
Success Rate
45.5%
Most Advanced
Phase 3

Trials by Phase

Phase 14 (28.6%)
Phase 28 (57.1%)
Phase 32 (14.3%)

Trials by Status

completed536%
terminated643%
active_not_recruiting321%

Recent Activity

Clinical Trials (14)

Showing 14 of 14 trials
NCT04903197Phase 1

Study of VAY736 as Single Agent and in Combination With Select Antineoplastic Agents in Patients With Non-Hodgkin Lymphoma

Terminated
NCT05350072Phase 3

Two-arm Study to Assess Efficacy and Safety of Ianalumab (VAY736) in Patients With Active Sjogren's Syndrome

Active Not Recruiting
NCT05349214Phase 3

Three-arm Study to Assess Efficacy and Safety of Ianalumab (VAY736) in Patients With Active Sjogren's Syndrome

Active Not Recruiting
NCT03217422Phase 2

ADCC Mediated B-Cell dEpletion and BAFF-R Blockade

Completed
NCT03827798Phase 2

Study of Efficacy and Safety of Investigational Treatments in Patients With Moderate to Severe Hidradenitis Suppurativa

Active Not Recruiting
NCT03656562Phase 2

Study the Efficacy and Safety of VAY736 and CFZ533 in SLE Patients

Completed
NCT03400176Phase 1

VAY736 in Combination With Ibrutinib in Patients With CLL on Ibrutinib

Terminated
NCT02962895Phase 2

Safety and Efficacy of VAY736 in Patients With Primary Sjogren's Syndrome (pSS)

Completed
NCT03287414Phase 2

Study of Pharmacodynamics, Pharmacokinetics, Safety and Tolerability of VAY736 in Patients With Idiopathic Pulmonary Fibrosis

Terminated
NCT01930175Phase 2

Study of Efficacy and Safety of VAY736 in Patients With Pemphigus Vulgaris

Terminated
NCT02149420Phase 2

PD of VAY736 in Patients With Primary Sjögren's Syndrome

Completed
NCT02038049Phase 2

A Study to Assess the Effect of a Single Infusion of VAY736 on Disease Activity in Patients With Relapsing-remitting Multiple Sclerosis

Terminated
NCT02675803Phase 1

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of VAY736 in Rheumatoid Arthritis Patients

Completed
NCT02137889Phase 1

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VAY736 in Relapsed or Refractory CLL Patients

Terminated

All 14 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
14