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Trial · Interventional

CompletedPhase 3Results postedRegistry data

Saizen in Intra-uterine Growth Retardation

Overview

Status
Completed
Phase
Phase 3
Enrollment
91 participants (actual)
Sponsor
Merck KGaA, Darmstadt, Germany · Industry
Design
Randomized · Open label (no masking)
Countries
Not stated
Start
Nov 1998
Primary completion
Feb 2010
Completion
Feb 2010
First posted
22 Jul 2011 (estimated)
Last update posted
18 Sept 2013 (estimated)
Conditions
Children Born With Serious Intra-uterine Growth Retardation

Timeline

1 trial · 1 completed · 1 with posted results

  • Completed
  • Ongoing
  • Not yet recruiting
  • Stopped
  • Estimated dates (est.)
  • Results posted
200020052010
  1. Ph 3

    Saizen in Intra-uterine Growth Retardation

    NCT01400698

    Nov 1998 to Feb 2010

Registry summary

Text and fields below are the sponsor's entries at ClinicalTrials.gov, shown as posted.

Study of safety of Saizen® in children born with serious intra-uterine growth retardation (IUGR) treated to final height. An open, phase III study involving 17 centers in France. The study enrolled children who have completed 3 or 2 years of treatment and at least one year of post treatment observation in the Sponsor Studies GF 4001 (Safety and Efficacy of Saizen in the Treatment of Young Children Born with Severe IUGR) or GF 6283 (Effect of Intermittent versus Continuous Saizen Therapy in Young Children Born with Severe IUGR), respectively. Detailed description: Serious IUGR is a syndrome characterized by low birth length and weight for gestational age (less than 10 percentile). The secretion of growth hormone in response to provocative stimuli (e.g. arginine, insulin) is normal in these children. Apart from low birth weight, children born with IUGR may have minor or major malformations. A catch-up period with a supraphysiological growth velocity generally occurs during the first 6 to 24 months of life in 80 to 90 percent (%) of these children. This generally allows them to reach normal height. That means that conversely, approximately 10 to 20% of children do maintain a statural handicap. Puberty occurs at a normal age and the retardation in bone maturation present during the first years of life disappears very quickly. This leads to short adult stature in subjects who have not shown spontaneous catch-up during the first years of life. A safe and effective means of promoting growth without accelerating the timing or tempo of puberty would therefore be desirable.

Interventions

  • Saizen® ADrug
  • Saizen® BDrug
  • Observation onlyOther

Arms3

  • Experimental

    Saizen® (Continuous or intermittent treatment)

  • Experimental

    Saizen® (Observed and then continuous or no treatment)

  • Other

    Observation only

Primary outcomes2

Outcomes the sponsor listed as primary.

  1. Final Height

    Time frame · One year after final height was attained up to 10.6 years

    Registry description

    Final height was defined as the height reached 1 year after height velocity (HV) was less than 2 centimeter/year (cm/year). Height velocity was the change in height since the previous year's measurement. Height was measured with a wall-mounted stadiometer (or in supine position if the participant's age was less than 3 years) and the measurement was repeated thrice by the same observer. The mean of the values obtained in the repeated measurements was taken for the analysis.

  2. Height Standard Deviation Score (HSDS)

    Time frame · One year after final height was attained up to 10.6 years

    Registry description

    HSDS was calculated as height minus reference mean height divided by SD of the reference mean height, both given by the reference growth table (Sempe) for the corresponding chronological age at the height measurement. Greater HSDS indicate greater height. (Sempe M et al., 1979)

Secondary outcomes(1)
  1. Parental Adjusted Height Standard Deviation Score (PAHSDS)

    Time frame · One year after final height was attained up to 10.6 years

    Registry description

    PAHSDS is the distance between the participant's current and target heights, expressed in units of SD of the height distribution of the reference population. Target height is a measure of the height which the participant could hypothetically reach based only on his parents' heights. Target height standard deviation score (THSDS) was calculated as target height minus mean adult height of the reference population divided by SD of the mean adult height of the reference population.

Posted results

Values are shown as posted at ClinicalTrials.gov, with their units. PepBank has not converted, pooled or compared them.

Primary outcome results

Primary outcomeMean· One year after final height was attained up to 10.6 years

Final Height

GroupValue (cm)Spread
Non-Final Height: Not Treated145.9016.08
Non-Final Height: Treated150.0612.89
Final Height: Not Treated153.278.71
Final Height: Treated155.598.38
Primary outcomeMean· One year after final height was attained up to 10.6 years

Height Standard Deviation Score (HSDS)

GroupValue (standard deviation score)Spread
Non-Final Height: Not Treated-1.450.76
Non-Final Height: Treated-1.901.73
Final Height: Not Treated-2.331.01
Final Height: Treated-1.990.88
Secondary and other outcome results(3)
Secondary outcomeMean· One year after final height was attained up to 10.6 years

Parental Adjusted Height Standard Deviation Score (PAHSDS)

GroupValue (standard deviation score)Spread
Non-Final Height: Not Treated-0.820.59
Non-Final Height: Treated-1.521.92
Final Height: Not Treated-1.641.61
Final Height: Treated-1.241.39
Post hoc outcomeMean· Up to 10.6 years

Duration of Treatment

GroupValue (years)Spread
Non-Final Height: Treated4.092.92
Final Height: Treated4.512.20
Post hoc outcomeMean· Up to 10.6 years

Duration of Participation in the Study

GroupValue (years)Spread
Non-Final Height: Not Treated2.082.27
Non-Final Height: Treated5.292.89
Final Height: Not Treated4.102.87
Final Height: Treated7.022.06

Adverse events, as posted

Adverse events as posted: participants affected out of participants at risk, by group
GroupDeathsSerious eventsOther events
Not TreatedIncluded all participants who did not receive r-hGH 0.067 mg/kg/day sc either continuously or intermittently.–1 / 3216 / 32
TreatedIncluded all participants who received r-hGH 0.067 mg/kg/day sc either continuously or intermittently.–13 / 5952 / 59

Each cell reads participants affected / participants at risk, as the registry posted them.

Registry data comes from ClinicalTrials.gov. Study results come from studies, not from the registry. How PepBank works

Studies2

Studies that cite this trial.

More studies

2 studies on this page

Indexing hint: Randomized controlled trial · 2006

Intermittent recombinant growth hormone treatment in short children born small for gestational age: four-year results of a randomized trial of two different treatment regimens.

Simon et al. 2006Hormone researchcited by 7

PMID 16772718DOI 10.1159/000093832PUB-16772718

Full text at the publisher
Publisher page

Indexing hint: Randomized controlled trial · 1998

Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardation.

Fjellestad-Paulsen et al. 1998Acta paediatrica (Oslo, Norway : 1992)cited by 17

PMID 9641731DOI 10.1080/08035259850158209PUB-09641731

Full text at the publisher
Publisher page

Eligibility

Who could join, as posted.

Sex
All
Age
Not stated
Healthy volunteers
Not accepted
Inclusion and exclusion criteria, as posted
Inclusion Criteria: * Previous inclusion, good compliance and normal completion of GF4001 or GF6283 in the treatment of growth failure in children born with serious IUGR (3-year continuous r-hGH treatment in GF4001 or 2-year continuous or intermittent r-hGH treatment in GF6283). * Increase in height greater than 0.5 standard deviation (SD) during the first 2 years of r-hGH treatment in GF4001 or after 2 years of continuous or intermittent r-hGH treatment in GF6283. * A written Informed Consent at the beginning of the pre-study visit must be obtained from the parent(s)/legal guardian(s), with the understanding that consent may be withdrawn by the subject or parents at any time without prejudice to their future medical care. Children able to understand the trial should personally sign and date the written informed consent, too. * Other protocol-defined inclusion criteria may apply. Exclusion Criteria: * Known multiple malformation syndrome with severe psychomotor retardation and/or body hemihypertrophy. * Severe psychomotor retardation. * Severe congenital malformations. * Other protocol-defined exclusion criteria may apply.

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