Phase
Condition
N/ATreatment
Tolvaptan (OPC-41061)
Clinical Study ID
Ages 28-12 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female subjects between 28 days and < 12 weeks of age, inclusive at the timeof enrollment.
- Must have clinical and imaging features that are consistent with a diagnosis of ARPKDwith all the following characteristics:
- Nephromegaly (> 2 standard deviations from age appropriate standard viaultrasound)
- Multiple renal cysts
- History of oligohydramnios or anhydramnios
- Ability for parent or guardian to provide written, informed consent prior toinitiation of any trial-related procedures, and ability, in the opinion of theprincipal investigator, to comply with all the requirements of the trial.
Exclusion
Exclusion Criteria:
- Premature birth (≤ 32 weeks gestational age)
- Anuria or RRT, defined as intermittent or continuous hemodialysis, peritonealdialysis, hemofiltration, hemodiafiltration or history of kidney transplantation
- Evidence of syndromic conditions associated with renal cysts (other than ARPKD)
- Abnormal liver function tests including ALT and AST, > 1.2 × ULN
- Parents with renal cystic disease
- Need for chronic diuretic use
- Cannot be monitored for fluid balance
- Has or at risk of having sodium and potassium electrolyte imbalances
- Has or at risk of having significant hypovolemia as determined by investigator
- Clinically significant anemia, as determined by investigator
- Severe systolic dysfunction defined as ejection fraction < 14%
- Serum sodium levels < 130 mmol/L or >145 mmol/L
- Taking any other experimental medications
- Require ventilator support
- Taking medications known to induce CYP3A4
- Having an infection including viral that would require therapy disruptive to IMPdosing
- Platelet count <50,000 µL
- Significant Portal Hypertension
- Bladder dysfunction or difficulty voiding
- Taking vasopressin agonist
- Having concomitant illness or taking medications that are likely to confound endpointassessments.
- History of cholangitis
- Received or scheduled to receive a liver transplant
Study Design
Study Description
Connect with a study center
Universitair Ziekenhuis Gent
Gent, Oost-Vlaanderen B-9000
BelgiumActive - Recruiting
UZ Leuven
Leuven, 3000
BelgiumActive - Recruiting
University Hospital of Cologne
Cologne, Nordrhein-Westfalen 50937
GermanySite Not Available
IRCCS Giannina Gaslini
Genova, Liguria 16147
ItalySite Not Available
Uniwersytecki Dzieciecy Szpital Kliniczny im. L. Zamenhofa
Białystok, 15-274
PolandSite Not Available
Instytut "Pomnik - Centrum Zdrowia Dziecka"
Warszawa, 04-730
PolandSite Not Available
Hospital Universitari Vall D Hebron
Barcelona, 08035
SpainActive - Recruiting
Universitat de Barcelona - Hospital Sant Joan de Deu Barcelona (HSJDB)
Barcelona, 08950
SpainActive - Recruiting
Hospital Universitario Virgen del Rocio
Sevilla, 41013
SpainActive - Recruiting
Great Ormond Street
London, WC1N 3JH
United KingdomSite Not Available
Royal Manchester Children's Hospital
Manchester, M13 9WL
United KingdomSite Not Available
Children's National Medical Center
Washington, District of Columbia 20010
United StatesActive - Recruiting
Emory University
Atlanta, Georgia 30322
United StatesSite Not Available
Northwestern University Feinberg School of Medicine - Ann & Robert H. Lurie Children's Hospital of Chicago - Neonatology
Chicago, Illinois 60611
United StatesSite Not Available
Johns Hopkins Pediatric Specialty Clinic
Baltimore, Maryland 21287-0001
United StatesSite Not Available
C.S. Mott Children's Hospital
Ann Arbor, Michigan 48109-5283
United StatesActive - Recruiting
Mayo Clinic
Rochester, Minnesota 55905
United StatesSite Not Available
Cincinnati Children's Hospital
Cincinnati, Ohio 45229
United StatesActive - Recruiting
Cleveland Clinic
Cleveland, Ohio 44195
United StatesSite Not Available
Primary Children's Hospital
Salt Lake City, Utah 84113-1103
United StatesSite Not Available
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