CompletedPhase 2NCT02965573
A Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients With Myasthenia Gravis Who Have Generalized Muscle Weakness
Studying Adult-onset myasthenia gravis
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- argenx
- Principal Investigator
- Antonio Guglietta, MD, MDargenx
- Intervention
- ARGX-113(biological)
- Enrollment
- 24 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2016 – 2017
Study locations (19)
- Investigator Site 19, Irvine, California, United States
- Investigator Site 17, Los Angeles, California, United States
- Investigator Site 15, Tampa, Florida, United States
- Investigator Site 16, Indianapolis, Indiana, United States
- Investigator Site 14, Chapel Hill, North Carolina, United States
- Investigator Site 18, Dublin, Ohio, United States
- Investigator Site 2, Ghent, Belgium
- Investigator Site 1, Leuven, Belgium
- Investigator Site 4, Montreal, Canada
- Investigator Site 3, Toronto, Canada
- Investigator Site 7, Bergamo, Italy
- Investigator Site 6, Milan, Italy
- Investigator Site 5, Roma, Italy
- Investigator Site 8, Leiden, Netherlands
- Investigator Site 10, Gdansk, Poland
- +4 more locations on ClinicalTrials.gov
Collaborators
Quintiles, Inc.
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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