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Lanreotide Autogel Treatment of Patients With Congenital Hyperinsulinism of Infancy

Primary Purpose

Congenital Hyperinsulinism

Status
Unknown status
Phase
Phase 4
Locations
Israel
Study Type
Interventional
Intervention
Lanreotide autogel
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Congenital Hyperinsulinism focused on measuring Congenital hyperinsulinism, Somatostatin analog, Lanreotide autogel, Hypoglycemia

Eligibility Criteria

2 Years - 8 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 2-8 years,
  • Diagnosed with congenital hyperinsulinism,
  • Treated by Octreotide continuous infusion (pump).

Exclusion Criteria:

  • Family not interested in participating.

Sites / Locations

  • Pediatric Endocrinology Unit, Sheba Medical CenterRecruiting

Outcomes

Primary Outcome Measures

Euglycemia as recorded by Continuous Glucose Monitoring System (CGMS)

Secondary Outcome Measures

Full Information

First Posted
February 17, 2010
Last Updated
December 12, 2012
Sponsor
Sheba Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01070758
Brief Title
Lanreotide Autogel Treatment of Patients With Congenital Hyperinsulinism of Infancy
Official Title
Treatment With Lanreotide Autogel (Somatostatin Analogue) in Patients With Congenital Hyperinsulinism of Infancy Already Treated With Somatostatin Analog by Pump
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2010 (undefined)
Primary Completion Date
February 2015 (Anticipated)
Study Completion Date
February 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sheba Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of our study is to evaluate the efficacy and safety of Lanreotide Autogel in children with congenital hyperinsulinism already treated with Octreotide by pump. Congenital hyperinsulinism is a genetic disorder characterized by inappropriate insulin secretion resulting in persistent hypoglycemia (low blood sugars. Patients exposed to recurrent hypoglycemic episodes are at increased risk of developmental disorders, so identification and prompt management of patients are essential. Many patients are treated with the somatostatin analog Octreotide which is administered by continuous infusion using a pump (we use an insulin pump). This treatment may pose a huge burden and be stressful for patients and families as it demands intensive daily care. In an effort to simplify the daily care of our patients and improve their quality of life we will study the efficacy and safety of Lanreotide Autogel - a long-acting somatostatin analog that can be administered by injection once a month
Detailed Description
The purpose of our study is to evaluate the efficacy and safety of Lanreotide Autogel in children with CHI already treated with Octreotide by pump. Patients and methods. Congenital hyperinsulinism (CH) is a genetic disorder characterized by dysregulated insulin secretion resulting in persistent hypoglycemia. Identification and prompt management of patients are essential, as patients exposed to recurrent hypoglycemic episodes are at increased risk of developmental disorders. Many patients are treated with the somatostatin analog Octreotide which is administered by continuous infusion using a pump. This treatment may pose a huge burden and be stressful for patients and families as it demands intensive daily care. In an effort to simplify the daily care of our patients and improve their quality of life we will study the efficacy and safety of Lanreotide Autogel(Lan-ATG)- a long-acting somatostatin analog that can be administered by injection once a month. This trial will include children with CH, who are treated with Octreotide by pump. We believe that children older than 2 years old will benefit most from this therapy. At this age, some of the parents encounter technical problems with the pump, as the children are prone to play with the pump and take out the needles. It's also very difficult to place the children in day care, because they need continuous follow up. The dose of Lan-ATG will be calculated according to the surface area of the patient. The dose used in adults is usually 60 mg and we will adapt the patient's dose according to the body surface area and also according to the daily dose of Octreotide used with the pump. The starting dose will be 40 mg/m². The patients will be gradually weaned from the pump following the first injection of Lan-ATG (10% decrease every 3-4 days for a total of a month). Every patient will serve as his/her own control. The following examinations will be done in every child: Continuous blood glucose monitoring during 72 hours with a glucosensor, to exclude asymptomatic hypoglycemia - once in 6 months. Growth velocity every 3 months. Bone age once a year. Routine laboratory tests (biochemistry, CBC and thyroid function tests) every six months. Biliary US once in 6 months. During the follow up we will try to expand the distance between injections, based on our knowledge that most of the patients with CH are known to enter remission after the age of 4-5 years.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Hyperinsulinism
Keywords
Congenital hyperinsulinism, Somatostatin analog, Lanreotide autogel, Hypoglycemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Lanreotide autogel
Other Intervention Name(s)
Somatuline autogel
Intervention Description
The dose of Lan-ATG will be calculated according to the surface area of the patient. The dose used in adults is usually 60 mg injection once a month, and we will adapt the patient's dose according to the body surface area and also according to the daily dose of Octreotide used with the pump. The starting dose will be 40 mg/m².
Primary Outcome Measure Information:
Title
Euglycemia as recorded by Continuous Glucose Monitoring System (CGMS)
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
2 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 2-8 years, Diagnosed with congenital hyperinsulinism, Treated by Octreotide continuous infusion (pump). Exclusion Criteria: Family not interested in participating.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dalit Modan, M.D.
Phone
+972-3-5305015
Email
dmodan@sheba.health.gov.il
First Name & Middle Initial & Last Name or Official Title & Degree
Kineret Mazor, M.D.
Phone
+972-3-5305015
Email
Kineret.Mazor@sheba.health.gov.il
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dalit Modan, M.D.
Organizational Affiliation
Sheba Medical Ceter, Tel-Hashomer, Israel
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Endocrinology Unit, Sheba Medical Center
City
Tel-Hashomer, Ramat-Gan
ZIP/Postal Code
52653
Country
Israel
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dalit Modan, M.D.
Phone
+972-3-5345410
Email
dmodan@sheba.health.gov.il
First Name & Middle Initial & Last Name & Degree
Dalit Modan, M.D.

12. IPD Sharing Statement

Citations:
PubMed Identifier
21697252
Citation
Modan-Moses D, Koren I, Mazor-Aronovitch K, Pinhas-Hamiel O, Landau H. Treatment of congenital hyperinsulinism with lanreotide acetate (Somatuline Autogel). J Clin Endocrinol Metab. 2011 Aug;96(8):2312-7. doi: 10.1210/jc.2011-0605. Epub 2011 Jun 22.
Results Reference
derived

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Lanreotide Autogel Treatment of Patients With Congenital Hyperinsulinism of Infancy

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