First-In-Human Study to Evaluate Safety, Tolerability, and PK of Intravenous ATB200 Alone and When Co-Administered With Oral AT2221

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

April 30, 2016

Primary Completion Date

August 22, 2024

Study Completion Date

August 22, 2024

Conditions
Pompe Disease
Interventions
DRUG

ATB200

DRUG

AT2221

Trial Locations (19)

15213

University of Pittsburgh, Pittsburgh

19104

Perelman Center for Advanced Medicine, Philadelphia

19380

Abramson Cancer Center Chester County Hospital, West Chester

22030

Lysosomal & Rare Disorders Research & Treatment Center (LDRTC), Fairfax

27710

Duke University Medical Center, Durham

30033

Emory University Division of Medical Genetics, Decatur

32610

University of Florida, Gainesville

44791

University Children's Hospital Department of Neuropediatrics and Inborn Metabolic Disorders, St. Josefs-Hospital, Bochum

49525

Infusion Associates, Grand Rapids

59405

Great Falls Clinic, LLP, Great Falls

80336

Friedrich-Baur-Institure, Dep of Neurology - University Munich, Munich

85028

Neuromuscular Research Centre, Phoenix

92868

University of California Irvine, Orange

08103

Rutgers New Jersey Medical School, Newark

05006

Womens & Childrens Hospital, Adelaide, North Adelaide

Unknown

Erasmus Medical Center, Rotterdam

01051

School of Medicine, University of Auckland, Auckland

B15 2TH

University Hospital Birmingham NHS Foundation Trust, Queen Elizabeth Medical Center, Birmingham

M6 8HD

Salford Royal NHS Foundation Trust, Salford

Sponsors
All Listed Sponsors
lead

Amicus Therapeutics

INDUSTRY

NCT02675465 - First-In-Human Study to Evaluate Safety, Tolerability, and PK of Intravenous ATB200 Alone and When Co-Administered With Oral AT2221 | Biotech Hunter | Biotech Hunter