Trial of Growth Hormone Therapy in Pediatric Crohn's Disease

Cincinnati Children's Hospital Medical Center

Status and phase

Completed

Phase 2

Conditions

Crohn's Disease

Treatments

Drug: cortecosteroid

Drug: growth hormone

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00109473

CCHMC IRB #: 04-12-06

IND # 71,344 (Other Identifier)

Details and patient eligibility

About

The purpose of this study is to determine whether taking a growth hormone (GH) drug called somatropin causes the intestine of a person with Crohn's Disease (CD) to heal faster when compared to a person with Crohn's Disease that does not receive growth hormone drug.

Full description

The optimal treatment goals in childhood CD include: 1) clinical remission in conjunction with mucosal healing and 2) restoration of normal growth and development. Current therapy in most cases includes induction of remission with corticosteroids followed by maintenance of remission with 6-mercaptopurine (6-MP) or mesalamine. With this approach, the goals of achieving mucosal healing with normalization of growth are not achieved in a significant number of children. GH therapy is now used in several chronic childhood diseases which are complicated by growth failure despite adequate GH secretion. These include chronic renal failure (CRF), juvenile rheumatoid arthritis (JRA), and Turner's syndrome. However, despite a comparable frequency and magnitude of permanent growth failure, the efficacy of GH therapy in this respect has not yet been determined in a controlled trial for CD. Moreover, whether GH therapy may also directly reduce disease activity and promote intestinal healing is not known. This represents a significant clinically unmet need in this patient population. Therefore, new therapeutic approaches are needed to both improve final adult height and enhance intestinal mucosal healing in children with CD.

The primary objective of this study is to determine the effect of growth hormone (GH) therapy upon colon mucosal healing in a 12 week randomized trial in children with Crohn's Disease (CD). Children with active CD will be randomized to GH + prednisone (GP) or prednisone alone (P) for a 12 week period. This study also involves a 52 week extension phase where all participants that meet eligibility will be given the opportunity to take or continue taking growth hormone for 52 weeks.

Enrollment

22 patients

Sex

All

Ages

5+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Ability to provide written informed consent
Age ≥ 5 years.
Diagnosis of Crohn's disease (CD) with ileo-colonic involvement as determined by standard clinical, radiological, and pathological criteria.
Moderate to severely active CD as defined by a PCDAI (Pediatric Crohn's Disease Activity Index) ≥ 30.
Currently taking Prednisone or Budesonide at starting dose (not tapering)
May continue stable doses of AZA/6-MP, methotrexate, and/or mesalamine at entry.
For the 52 week extension, baseline bone age ≤ 12 years for girls and ≤ 13 years for boys.
For the 52 week extension phase, remission or mild Crohn's disease as determined by a PCDAI < 30.

Exclusion criteria

Acute critical illness
Active neoplasia
Diabetes mellitus
History of intracranial lesion and/or neoplasia
Severe disease requiring hospitalization for treatment
Current therapy with infliximab as this may independently rapidly reduce clinical disease activity and promote mucosal healing
Use of prednisone or budesonide and in tapering phase
Family history of colorectal cancer before age 50
Personal or familial history of familial polyposis syndrome
Pregnancy (positive pregnancy test) prior to randomization
Any other condition that the investigator believes would pose a significant hazard to the subject if the investigational therapy were initiated
Participation in another simultaneous medical investigation or trial other than the Pediatric IBD (Inflammatory Bowel Disease) registry