Success Metrics

Clinical Success Rate
60.0%

Based on 6 completed trials

Completion Rate
60%(6/10)
Active Trials
11(46%)
Results Posted
117%(7 trials)
Terminated
4(17%)

Phase Distribution

Ph phase_4
2
8%
Ph phase_1
1
4%
Ph phase_2
5
21%
Ph phase_3
14
58%

Phase Distribution

1

Early Stage

5

Mid Stage

16

Late Stage

Phase Distribution22 total trials
Phase 1Safety & dosage
1(4.5%)
Phase 2Efficacy & side effects
5(22.7%)
Phase 3Large-scale testing
14(63.6%)
Phase 4Post-market surveillance
2(9.1%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

60.0%

6 of 10 finished

Non-Completion Rate

40.0%

4 ended early

Currently Active

11

trials recruiting

Total Trials

24

all time

Status Distribution
Active(13)
Completed(6)
Terminated(4)
Other(1)

Detailed Status

Completed6
Recruiting6
Active, not recruiting5
Terminated4
unknown1
Enrolling by invitation1

Development Timeline

Analytics

Development Status

Total Trials
24
Active
11
Success Rate
60.0%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (4.5%)
Phase 25 (22.7%)
Phase 314 (63.6%)
Phase 42 (9.1%)

Trials by Status

active_not_recruiting521%
terminated417%
unknown14%
completed625%
enrolling_by_invitation14%
not_yet_recruiting14%
recruiting625%

Recent Activity

Clinical Trials (24)

Showing 20 of 24 trialsScroll for more
NCT07570316Phase 3

A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease

Recruiting
NCT07760818Phase 2

A Study to Assess Efficacy and Safety of Efgartigimod in Adults With Sjogren's Disease-associated Sensorimotor Polyneuropathy or Sensory Polyneuropathy (SERENITY)

Not Yet Recruiting
NCT06655155Phase 2

A Study to Assess the Efficacy and Safety of Efgartigimod PH20 SC in Adults With Systemic Sclerosis

Recruiting
NCT05979441Phase 3

A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Active Idiopathic Inflammatory Myopathy

Enrolling By Invitation
NCT07596849Phase 3

A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC PFS in Adult Participants With Graves' Disease.

Recruiting
NCT06558279Phase 3

A Study to Assess Efficacy and Safety of Efgartigimod PH20 SC in Adults With Ocular Myasthenia Gravis

Active Not Recruiting
NCT06392386Phase 2

A Study of Efgartigimod PH20 SC in Children Between 2 and Less Than 18 Years of Age With Generalized Myasthenia Gravis

Recruiting
NCT07264426

Real-World Efgartigimod Effectiveness in CIDP: A Prospective Study

Recruiting
NCT06684847Phase 3

A Study of the Efficacy and Safety of Efgartigimod in Patients With Primary Sjögren's Syndrome

Active Not Recruiting
NCT04777734

Pre-Approval Access for Efgartigimod PH20 SC in Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Unknown
NCT06307626Phase 3

A Study of Efgartigimod PH20 SC Given by Prefilled Syringe in Adults With Thyroid Eye Disease.

Terminated
NCT06307613Phase 3

A Study of Efgartigimod PH20 SC Given by Prefilled Syringe in Adults With Thyroid Eye Disease

Terminated
NCT06909214Phase 4

A Study to Evaluate the Clinical Outcomes of Efgartigimod PH20 SC in Adults With New-onset Generalized Myasthenia Gravis (gMG)

Recruiting
NCT05681481Phase 3

A Phase 3 Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid

Terminated
NCT06637072Phase 4

A Study to Assess Adults With CIDP Transitioning From IVIg to Efgartigimod PH20 SC

Active Not Recruiting
NCT04818671Phase 3

Evaluating the Long-Term Safety and Tolerability of Efgartigimod PH20 SC Administered Subcutaneously in Patients With Generalized Myasthenia Gravis

Completed
NCT04812925Phase 3

A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia

Active Not Recruiting
NCT05267600Phase 2

A Phase 2/3 Study of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid

Completed
NCT04280718Phase 2

A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Chronic Inflammatory Demyelinating Polyneuropathy (CIDP, an Autoimmune Disorder That Affects the Peripheral Nerves)

Active Not Recruiting
NCT04598477Phase 3

A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod PH20 SC in Adults With Pemphigus (Vulgaris or Foliaceus)

Terminated

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
24