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A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia
NCT04812925 · View on ClinicalTrials.gov ↗
Study Summary
A Phase 3 study to evaluate the safety and efficacy of efgartigimod PH20 subcutaneous in adult patients with primary immune thrombocytopenia
Conditions Studied
Interventions
- BIOLOGICAL efgartigimod PH20 SC
Study Locations (20)
Other
- Investigator Site 0540001 — Buenos Aires
- Investigator site 540004 — Buenos Aires
- Investigator Site 0610012 — Garran
- Investigator Site 0610003 — West Perth
- Investigator site 610005 — Westmead
- Investigator Site 3590017 — Plovdiv
- Investigator site 0560003 — Reñaca
- Investigator site 560002 — Santiago
- Investigator site 0560004 — Temuco
- Investigator site 860013 — Beijing
- Investigator Site 0860008 — Bengbu
- Investigator site 860055 — Huizhou
- Investigator Site 0860015 — Shenzhen
- Investigator Site 0860001 — Tianjin
- Investigator Site 0860010 — Wuhan
Arkansas
- Investigator Site 0010116 — Bentonville
District of Columbia
- Investigator site 0010045 — Washington D.C.
Indiana
- Investigator Site 0010062 — Fort Wayne
Iowa
- Investigator site US0010042 — Iowa City
Oklahoma
- Investigator Site 0010095 — Oklahoma City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 173 participants |
| Start Date | 2021-11-17 |
| Est. Completion | 2026-10-01 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04812925
The ClinicalTrials.gov registry entry for NCT04812925 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 173 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is argenx, which has 96 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Primary Immune Thrombocytopenia appearing as the primary indexed condition, and to 1 intervention — of which efgartigimod PH20 SC is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04812925 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Other, Arkansas, District of Columbia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04812925 about?
NCT04812925 is a clinical study titled "A Phase 3 Study to Evaluate the Safety and Efficacy of Efgartigimod PH20 Subcutaneous in Adult Patients With Primary Immune Thrombocytopenia". A Phase 3 study to evaluate the safety and efficacy of efgartigimod PH20 subcutaneous in adult patients with primary immune thrombocytopenia
What is the current status of trial NCT04812925?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 173 participants. The study started on 2021-11-17. Estimated completion is 2026-10-01.
What conditions does trial NCT04812925 study?
This clinical trial studies the following conditions: Primary Immune Thrombocytopenia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04812925?
The interventions under investigation include: efgartigimod PH20 SC (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04812925?
This trial is sponsored by argenx, which has 96 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04812925 being conducted?
This trial has 20 study locations across Arkansas, District of Columbia, Indiana, Iowa, Oklahoma. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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