Infant, Small for Gestational Age Clinical Trial
— SAIZEN in SGAOfficial title:
An Open, Multicenter, Randomized, Controlled Trial to Evaluate the Correlation Between Spontaneous Catch-up Growth, Clinical Response to Saizen (Recombinant Human Growth Hormone, r-hGH) and Gene Expression Profiling in Children Small for Gestational Age (SGA)
| Verified date | December 2013 |
| Source | Merck KGaA |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Italy: Ethics Committee |
| Study type | Interventional |
This open, multicentric, randomized, controlled study is planned to evaluate the correlation between gene expression, spontaneous catch-up growth and therapeutic response to Saizen in SGA children.
| Status | Terminated |
| Enrollment | 25 |
| Est. completion date | July 2009 |
| Est. primary completion date | July 2009 |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | 4 Years to 6 Years |
| Eligibility |
Inclusion Criteria: - SGA at birth (defined as a length at birth equal or below the tenth percentile according to the Italian reference table of Bertini and Fabris) - Age of 24 Months - Caucasic - Born at term (i.e. after the 37th completed week of gestation) - Height equal or below (Group A) or up (Group B) the third percentile at the age of 24 months according to the Tanner reference table - Sufficient GH secretion (more than 10 nanogram (ng)/milliliter (ml)) at least to one of the tests commonly used at that age (glucagon, Levo-dopa, arginine, clonidine, Growth Hormone Releasing Hormone (GHRH), GH integrated secretion) - Normal level of Thyroid-stimulating hormone (THS), Free Triiodothyronine (FT3), Free Thyroxine (FT4), Insulin-like growth factor 1(IGF-1), insulin and haemoglobin A1c (HbA1c) - Normal level of Immunoglobulin A (IgA) - Children parents willing to comply with the protocol for the whole duration of the study - A written Informed Consent before the baseline visit must be obtained from the parent(s) / legal guardian(s) Exclusion Criteria: - Congenital malformations (including Silver-Russel syndrome) - Known abnormal karyotype, especially in girls - Twins - Severe psychomotor retardation - Previous or ongoing treatment with anabolic steroids or r-hGH - Treatments interfering with the immune system (including bacterial lysate) - Severe chronic illnesses - Autoimmune diseases |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
| Country | Name | City | State |
|---|---|---|---|
| Italy | Merck Serono S.p.A. | Roma |
| Lead Sponsor | Collaborator |
|---|---|
| Merck KGaA | Merck Serono S.P.A., Italy |
Italy,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Correlation Between Gene Expression Profiling and Catch-up Growth in Small for Gestational Age (SGA) Children | Gene expression profiling:analysis of ribonucleic acid (RNA) extracted from body tissue or fluids using Clontech Atlas Human Array to study level of activation of genes in tissue analyzed. Analysis was performed to identify possible correlation between catch-up growth (either spontaneous or drug-induced after Week 48) and therapeutic response to rhGH. Spontaneous catch up growth:shown by SGA participants having length more than third percentile at Week 96 without any treatment;drug induced growth was by SGA participants having length more than third percentile at Week 96 with drug treatment. | Baseline and Week 48 | No |
| Secondary | Percentage of Untreated Participants Who Showed a Spontaneous Catch-up Growth | Spontaneous catch up growth was the growth shown by SGA participants having length more than third percentile at Week 96 without any study drug treatment. | Baseline through Week 96 | No |
| Secondary | Number of Participants With Adverse Events (AEs), Serious Adverse Events (SAEs) and AEs Leading to Study Drug Discontinuation | AEs: any new untoward medical occurrences/worsening of pre-existing medical condition, whether or not related to study drug , SAE: any AE that resulted in death; was life threatening; resulted in persistent/significant disability/incapacity; resulted in/prolonged an existing in-patient hospitalization; was a congenital anomaly/birth defect; or was an overdose. Participants who discontinued from the study due to AE were also recorded. | Baseline through Week 96 | Yes |
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