A Research Study in Chinese Children With a Low Level of Hormone to Grow. Treatment is Somapacitan Once a Week Compared to Norditropin® Once a Day.

  • STATUS
    Recruiting
  • End date
    Dec 31, 2023
  • participants needed
    108
  • sponsor
    Novo Nordisk A/S
Updated on 8 January 2022

Summary

The study compares 2 medicines for children who do not have enough hormone to grow: somapacitan given once a week (a new medicine) and Norditropin® given once a day (the medicine doctors can already prescribe). Researchers will test to see how well somapacitan works.

The study will also test if somapacitan is safe. Participants will either get somapacitan or Norditropin® - which treatment participants get, is decided by chance.

The study includes a 52 week treatment period and a minimum of 30 days follow up period.

Details
Condition Growth Hormone Deficiency in Children
Treatment Somapacitan, Norditropin®
Clinical Study IdentifierNCT04970654
SponsorNovo Nordisk A/S
Last Modified on8 January 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Informed consent of parent or legally acceptable representative of participant and child assent, as age-appropriate must be obtained before any trial related activities
The parent or legally acceptable representative of the child must sign and date the Informed consent form (according to local requirements)
The child must sign and date child assent form or provide oral assent (if required according to local requirements)
Prepubertal children: a) Boys: Age more than or equal to 2 years and 26 weeks and less than or equal to 11.0 years at the time of signing informed consent
Testis volume less than 4 ml. b) Girls: Age more than or equal to 2 years and 26 weeks and less than or equal to 10.0 years at the time of signing informed consent. Tanner stage 1 for breast development (no palpable glandular breast tissue)
Confirmed diagnosis of growth hormone deficiency determined by two different growth hormone stimulation tests performed within 12 months prior to randomisation, defined as a peak growth hormone level of less than or equal to 10.0 ng/ml using the WHO International Somatropin 98/574 standard
If only one growth hormone stimulation test is available before screening, then confirmation of growth hormone deficiency by second and different growth hormone stimulation test must be done
For children with at least 2 additional pituitary hormone deficiencies (other than growth hormone deficiency) only one growth hormone stimulation test is needed
Impaired height defined as at least 2.0 standard deviations below the mean height for chronological age and gender according to Chinese general population standards at screening
Impaired height velocity defined as annualised height velocity at screening less than 7cm/year for subjects between 2.5 and 3 years old and less than 5 cm/year for subjects from 3 years and above calculated over a time span of minimum 3 months and maximum 18 months prior to screening according to Chinese guideline and expert consensus on children with short stature and GH therapy
No prior exposure to growth hormone therapy or IGF-I treatment
Bone age less than chronological age at screening
Body Mass Index more than 5th and less than 95th percentile, Body Mass Index-for-age growth charts according to Chinese general population standards
IGF-I < -1.0 SDS at screening, compared to age and gender normalized range measured at central laboratory
No intracranial tumour confirmed by magnetic resonance imaging or computer tomography scan. An image or scan taken within 9 months prior to screening can be used as screening data if the medical evaluation and conclusion is available

Exclusion Criteria

Known or suspected hypersensitivity to trial product(s) or related products
Previous participation in this trial. Participation is defined as randomisation
Receipt of any investigational medicinal product within 3 months before screening or participation in another clinical trial before randomisation
Any known or suspected clinically significant abnormality likely to affect growth or the ability to evaluate growth with standing height measurements
Turner Syndrome (including mosaicisms)
Chromosomal aneuploidy and significant gene mutations causing medical "syndromes" with short stature, including but not limited to Laron syndrome, Noonan syndrome, Prader-Willi Syndrome, abnormal SHOX-1 gene analysis or absence of GH receptors
Significant spinal abnormalities including but not limited to scoliosis, kyphosis and spina bifida variants
Congenital abnormalities (causing skeletal abnormalities), including but not limited to Russell-Silver Syndrome or skeletal dysplasias
Family history of skeletal dysplasia
Children born small for gestational age (birth weight 10th percentile of the recommended gender-specific birth weight for gestational age according to national standards in China5
Children diagnosed with diabetes mellitus or screening values from central laboratory of
fasting plasma glucose more than or equal to 126 mg/dl (7.0 mmol/L) or
HbA1c more than or equal to 6.5 %
Current inflammatory diseases requiring systemic corticosteroid treatment for longer
than 2 consecutive weeks within the last 3 months prior to screening
Children requiring inhaled glucocorticoid therapy at a dose greater than 400 µg/day of inhaled budesonide or equivalents for longer than 4 consecutive weeks within the last 12 months prior to screening
Concomitant administration of other treatments that may have an effect on growth, e.g. but not limited to methylphenidate for treatment of attention deficit hyperactivity disorder (ADHD)
Diagnosis of attention deficit hyperactivity disorder
Prior history or presence of malignancy including intracranial tumours
Prior history or known presence of active Hepatitis B or Hepatitis C (exceptions to this exclusion criterion is the presence of antibodies due to vaccination against Hepatitis B)
Any clinically significant abnormal laboratory screening tests, as judged by the study doctor
Any disorder which, in the opinion of the study doctor, might jeopardise Participant's safety or compliance with the protocol
The participant or the parent/legally acceptable representative is likely to be non-compliant in respect to trial conduct, as judged by the study doctor
Children with hypothyroidism and/or adrenal insufficiency not on adequate and stable replacement therapy for at least 90 days prior to randomisation
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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