Assessment of Macrophage Activation syndromE in STill's Disease
NCT06405152 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 75
Last updated 2024-10-21
Summary
Assessment of Macrophage activation syndrome in STill's disease: retrospective chart analysis of patient History, Symptom resolution and Treatment characteristics
Conditions
- Macrophage Activation Syndrome
- Still's Disease, Adult-Onset
- Stills Disease, Juvenile-Onset
Interventions
- OTHER
-
Chart review
Retrospective Chart Review
Sponsors & Collaborators
-
Swedish Orphan Biovitrum
lead INDUSTRY
Principal Investigators
-
Uwe Ullman, MD · Swedish Orphan Biovitrum AG Riehenring 182, 4058 Basel, Switzerland
Eligibility
- Min Age
- 6 Months
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-09-27
- Primary Completion
- 2024-09-26
- Completion
- 2024-09-26
Countries
- United States
- Canada
- France
- Germany
- Italy
- Netherlands
- Spain
Study Locations
More Related Trials
-
Facioscapulohumeral Dystrophy in Children
NCT02625662 ·Status: COMPLETED
-
"The MaP Study": Mapping the Patient Journey in MMA and PA
NCT03484767 ·Status: COMPLETED
-
German Observational Multicenter Study of Patients With Fabry Disease Under Chaperone Therapy With Migalastat-HCl.
NCT03135197 ·Status: COMPLETED
-
Study of Infigratinib in Children With Achondroplasia
NCT04265651 ·Status: COMPLETED ·Phase: PHASE2
-
Observational Study of Patients With Mucopolysaccharidosis (MPS) VI Who Previously Participated in ASB-00-02
NCT01387854 ·Status: COMPLETED
-
An Observational Study in Children and Adults With Stargardt Disease
NCT06591806 ·Status: RECRUITING
-
Faslodex in McCune-Albright Syndrome
NCT00278915 ·Status: COMPLETED ·Phase: PHASE2
-
Studies in Patients With Tuberous Sclerosis Complex
NCT03276195 ·Status: COMPLETED
-
Natural History Study of Infantile and Juvenile GM1 Gangliosidosis (GM1) Patients
NCT04041102 ·Status: COMPLETED
-
Open-Label Extension Study of the Long-Term Effects of Migalastat HCL in Patients With Fabry Disease
NCT02194985 ·Status: COMPLETED ·Phase: PHASE3
-
A Prospective Natural History Study of Mucopolysaccharidosis Type IIIB (MPS IIIB)
NCT03227042 ·Status: ACTIVE_NOT_RECRUITING
-
A Prospective Natural History and Outcome Measure Discovery Study of Charcot-Marie-Tooth Disease, Type 4J
NCT06151600 ·Status: RECRUITING
-
Screening Trial for Pain Relief in Schwannomatosis (STARFISH)
NCT05684692 ·Status: RECRUITING ·Phase: PHASE2
-
Screening for Fabry Disease in a Pediatric Population at Risk
NCT02152189 ·Status: COMPLETED
-
Ten Year Follow-up in FSHD: the FOCUS 3 Study
NCT06911190 ·Status: RECRUITING
-
The Natural History of Infantile Globoid Cell Leukodystrophy
NCT00983879 ·Status: COMPLETED
-
Miglustat in Niemann-Pick Type C Disease
NCT00517153 ·Status: COMPLETED ·Phase: PHASE2
-
Copper Histidinate Treatment for Menkes Disease
NCT04074512 ·Status: APPROVED_FOR_MARKETING
-
Angelman Syndrome Natural History Study-FAST UK
NCT05100810 ·Status: RECRUITING
-
Longitudinal Study of Bone Disease in Children with Mucopolysaccharidoses (MPS) I, II, and VI
NCT01521429 ·Status: COMPLETED
-
Screening for the Transthyretin-Related Familial Amyloidotic Polyneuropathy (TTR FAP)
NCT01705626 ·Status: COMPLETED
-
Gene Therapy for Fanconi Anemia, Complementation Group A
NCT04248439 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
Phase I/IIa Trial of scAAV1.tMCK.NTF3 for Treatment of CMT1A
NCT03520751 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1/PHASE2
-
Evaluate Safety and Biological Activity of ATYR1940 in Participants With Early Onset Facioscapulohumeral Muscular Dystrophy
NCT02603562 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Clinical Study of Aldurazyme in Patients With Mucopolysaccharidosis (MPS) I
NCT00912925 ·Status: COMPLETED ·Phase: PHASE3