Phoenix Children’s Hospital Research
Institute (PCRI) Website Clinical Trial Listing
** Please complete and return to Shy Walker at
swalker@phoenixchildrens.com
Study Title: Safety and Efficacy Study of Ursodeoxycholic Acid Therapy in Pediatric Primary Sclerosing
Cholangitis
Study Purpose:
Primary sclerosing cholangitis (PSC), although uncommon, is a devastating and insidiously progressive liver
disease, resulting from advancing inflammation, fibrosis and obliteration of the bile ducts in the liver,
leading to cirrhosis and end-stage liver disease. Although prognosis in children may be somewhat better
than that of adults, approximately one third of pediatric patients require transplantation by adulthood.
Other than transplantation, there is to date no therapy conclusively proven to improve the long-term
outcome. Ursodeoxycholic acid (UDCA) improves biochemical markers of liver disease, although in high
doses does not clearly improve the long-term outcome in adults, and in a recent study may have actually
worsened outcome. Childhood PSC is different from that of adult PSC in many ways, and children may
derive more short-term, as well as long-term, benefit than adults. This unique multicenter study will
carefully monitor the effects of withdrawal and restarting UDCA on liver injury and inflammation in children
with PSC. The preliminary data will help in the design of a more definitive larger study to determine if UDCA
has a beneficial role in the treatment of PSC in children.
Study Summary:
Primary sclerosing cholangitis (PSC), a devastating and insidiously progressive cholestatic liver disease,
results from advancing inflammation, fibrosis and obliteration of the intra- and extrahepatic bile ducts,
leading to cirrhosis and end-stage liver disease. PSC is an uncommon disorder (prevalence in the US of 814/100,000 with even lower prevalence in children). Although prognosis in children may be somewhat
better, approximately one third of pediatric patients require transplantation by adulthood. Other than
transplantation, there is to date no therapy conclusively proven to improve the long-term outcome.
Ursodeoxycholic acid (UDCA) improves biochemical markers of liver disease, although in high doses does
not clearly improve the long-term outcome in adults. Furthermore, a recent large adult trial of high-dose
UDCA therapy suggested a higher incidence of serious adverse events and poor outcomes with UDCA
treatment, leading many centers to discontinue UDCA therapy in adult patients. Childhood PSC is different
from the adult disease including a stronger association with both autoimmune markers and histologic
features and a trend to higher transaminases at diagnosis. Furthermore, in response to intermediate-dose
UDCA therapy, there is a more striking and prompt improvement in biochemistries as compared to adults.
In light of the prompt normalization of liver enzymes and the fact that UDCA is well tolerated in children,
pediatric hepatologists are reluctant to generalize the adult UDCA study results to children and to stop
UDCA therapy. This presents a significant dilemma: Should UDCA therapy be stopped in pediatric PSC
patients to avoid a possible adverse influence on long-term prognosis at the risk of losing a possible
beneficial effect on disease progression in children? Additional factors in children with PSC/autoimmune
hepatitis (AIH) overlap are the long-term adverse effects of corticosteroids and azathioprine use. If UDCA
therapy is effective as monotherapy, these complications may be avoided. Therefore, we propose a
preliminary UDCA withdrawal and reinstitution trial in pediatric PSC patients to collect data to support the
design of a larger, longer-term randomized, placebo-controlled trial of UDCA therapy in childhood PSC. This
pilot study, which will utilize the infrastructure and participating centers of the STOPSC (Studies of Primary
Sclerosing Cholangitis) consortium, will test the following hypotheses: 1) UDCA therapy yields a rapid
biochemical response in children with PSC, thus withdrawal would lead to increased biochemical evidence
of disease. 2) UDCA therapy suppresses liver and biliary inflammation in children with PSC, thus withdrawal
of therapy would result in a burst of inflammatory activity and an increase in serum cytokine biomarkers, 3)
Biochemical control of childhood PSC with histologic features of AIH is dependent upon treatment with
immunosuppression in addition to UDCA, therefore childhood PSC without histologic features of AIH will
worsen significantly with UDCA withdrawal compared to PSC with histological features of AIH.
Basic Eligibility Criteria:
Ages Eligible for Study:
5 Years to 21 Years
Inclusion Criteria:
1. Male or female < 21 years of age, no racial or ethnic restrictions
2. Pediatric PSC diagnosed as per the criteria developed by STOPSC (2 of 3 required):
o
Serum GGT increased more than 50% above the upper limit of normal for age
o
Endoscopic retrograde cholangiopancreatography (ERCP), percutaneous transhepatic
cholangiography (PTC) or magnetic resonance cholangiopancreatography (MRCP) findings of
intrahepatic and/or extrahepatic bile duct irregularities consistent with PSC
o
Liver biopsy abnormalities consistent with chronic biliary injury Note that these criteria will include
patients with small duct PSC who have normal biliary imaging with the required biochemical and
histologic criteria.
3. Patients with PSC/AIH overlap will also be included who meet the criteria for PSC plus have liver
histologic features of AIH.
4. Biochemically quiescent liver disease defined by an ALT and GGT < 2.0 X upper limit of normal (ULN)
measured on two separate occasions > 2 weeks apart
5. Prior and on-going UDCA therapy at a dose of at least 13 mg/kg/day or 600 mg/day for more than 6
months
6. Ability to swallow pills
7. Quiescent inflammatory bowel disease (IBD) as reflected by a modified Pediatric Ulcerative Colitis
Activity Index score of less than 6 or a modified Pediatric Crohn's Disease Activity Index score of less
than 15.
8. Not excluded by the STOPSC pediatric PSC exclusion criteria (see Appendix) that are designed to
minimize misdiagnosis due to other primary liver diseases, previous biliary injury/surgery,
therapies, or systemic disorders that may secondarily affect the liver and/or biliary tract.
9. Subjects will remain on all current medications, including those for IBD and immunosuppressive
therapy.
10. Female subjects of childbearing age will be required to have a pregnancy test, and if sexually active,
will be required to use an accepted method of birth control during the course of the study.
11. Parent or legal guardian must be willing to provide signed and dated informed consent
documentation. Assent from the child or adolescent will be obtained as appropriate.
Exclusion Criteria:
1. Evidence of decompensated cirrhosis:
o
Cirrhosis as defined by biopsy findings or evidence of portal hypertension with no other known
cause and:

Platelet count < 100,000 or,

Spleen palpable more than 2 cm below the left costal margin or,

Ascites or,

Varices or other GI manifestation of portal hypertension
o
Decompensated liver disease defined by:

Serum total bilirubin (TB) > 5 mg/dl and direct bilirubin (DB) > 1 mg/dl or,

Prothrombin time (PT) prolonged by more than 3 seconds after parenteral vitamin K administration
or,

Ascites requiring diuretic therapy or,

Serum albumin < 3 g/dl
2. Evidence of acute liver failure:
o
No prior history of liver disease and
o
PT > 20 seconds or INR > 2.0 unresponsive to parenteral vitamin K administration or,
o
PT > 15 seconds or international normalized ratio (INR) > 1.5 with change in mental status
ascribable to hepatic encephalopathy
3. History of cholangitis or bile duct strictures requiring intervention
4. Liver transplantation
Study Location(s):
University of Tennessee, Icahn School of Medicine at Mount Sinai, Ann & Robert H Lurie Children's Hospital
of Chicago, University of Colorado, Denver, University of California, San Francisco, University of Pittsburgh,
Phoenix Children's Hospital, Children's Hospital of Philadelphia, Children's Healthcare of Atlanta,
Children's Hospital Los Angeles
Study Contact(s):
Ozelm Bulut Pinar, MD