Independent · non-commercial · publishes on a quarterly cycle|Current cycle 2026 Q3
Compound Evidence InstituteEvidence synthesis · established 2023Graded assessments of compounds, trials, methods and supply
Document set current to 30 July 2026
Evidence synthesis · Intervention review

Gonadorelin in growth hormone deficiency and growth-hormone secretagogue pharmacology: effect on the anchor outcome

In the population defined for growth hormone deficiency and growth-hormone secretagogue pharmacology, what is the effect of Gonadorelin compared with the comparator used in its contributing trials on the anchor outcome for this indication?

Document identifier
CEI-ES-061
Series
Evidence synthesis
Version
2.3
Published
29 Aug 2026
Last reviewed
29 Aug 2026
Next review
29 Feb 2028
Identifier
10.71829/cei.syn.61
Certainty
Moderate
Cycle
2026 Q3
Review type
Intervention review
Search executed
22 May 2026

Templated review frame. This review question was generated by crossing an indication with a compound for which contributing trials exist. Its prose frame is templated and is shared with other questions of the same shape. Its included studies, its summary of findings and its certainty rating are computed from the underlying records and are not templated. The Institute publishes these questions because the alternative is to leave a question the document set can answer unanswered, and it labels them because the alternative is to present a templated frame as an authored one.

§1Abstract

§1.1Review question

In the population defined for growth hormone deficiency and growth-hormone secretagogue pharmacology, what is the effect of Gonadorelin compared with the comparator used in its contributing trials on the anchor outcome for this indication?

§1.2PICO frame

Table 1. The registered PICO frame. Any change made after protocol registration is recorded in the amendment log at §5 and is identified there as post hoc.

ElementAs registered
PopulationInsufficient endogenous growth-hormone secretion, or the pharmacological stimulation of the growth-hormone axis, assessed here principally through provocative testing and IGF-1 response.
InterventionGonadorelin administered as intravenous or subcutaneous for the approved diagnostic use.
ComparatorThe comparator used in each contributing trial, reported per trial rather than pooled across comparator types.
OutcomesAnchor outcome for this indication: Peak stimulated growth hormone. Additional outcomes: Change in IGF-1 and IGFBP-3; Body composition by DXA; Glucose tolerance.

§1.3Method in brief

A review of the effects of an intervention on pre-specified outcomes, with a quantitative synthesis where the contributing studies are sufficiently similar. The protocol was registered with the Institute's secretariat before the search was executed. The search was run on 22 May 2026 across 8 sources and is reproduced in full at §2. Screening, extraction and certainty assessment were performed independently by two members of the secretariat with disagreement resolved by a third.[1,2]

§1.4Conclusion

Moderate certainty evidence from 2 contributing trials bears on the effect of Gonadorelin on the anchor outcome for growth hormone deficiency and growth-hormone secretagogue pharmacology. The estimate the Institute carries in the monograph is: A luteinising hormone rise after gonadorelin distinguishes pituitary from hypothalamic causes of hypogonadotropic hypogonadism. The diagnostic evidence base is established and underpins the marketing authorisations.

The conclusion rests on 2 contributing studies, listed with their extracted data at §3 and summarised outcome by outcome at §4.

§1.5Limitations

References cited on this page

References are numbered in order of first citation in this document. Each superscript in the text links to its entry below.

  1. D’Hondt M, Bracke N, Taevernier L, Gevaert B, Verbeke F, Wynendaele E, De Spiegeleer B. Related impurities in peptide medicines. Journal of Pharmaceutical and Biomedical Analysis 2014;101:2–30. doi:10.1016/j.jpba.2014.06.012 · PMID 25044089
  2. Manning MC, Chou DK, Murphy BM, Payne RW, Katayama DS. Stability of protein pharmaceuticals: an update. Pharmaceutical Research 2010;27(4):544–575. doi:10.1007/s11095-009-0045-6 · PMID 20143256

Identifiers are reproduced only where the Institute holds them. Where a digital object identifier or PubMed identifier is not shown, the Institute has recorded the journal and year and has not constructed an identifier.

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