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
Public comment period · §3

Draft monograph: GHRP-2 — disposition

The disposition of every submission and the amendments that resulted.

Document identifier
CEI-CP-051/3
Series
Public comment period
Version
1.0
Published
30 Mar 2025
Last reviewed
30 Mar 2025
Next review
30 Mar 2026
Identifier
10.71829/cei.cp.51
Certainty
Not rated
Cycle
2025 Q1
Window
10 Jan 2025 – 21 Feb 2025
Status
Closed
Submissions
7

§3Disposition and amendments

§3.1Disposition table

Table 1. Every submission with its disposition. Each row links to the submission in full.

ReferenceRespondentPoint raisedDisposition
DRAFT-GHRP-2-MONOG/002Gaspard KettlewellDeclared interests should appear on the document rather than on a separate pageNoted, no amendment
DRAFT-GHRP-2-MONOG/003Dr Hyacinth Drakeford-AmadiRegistered trials that never reported are absent from the monographAccepted
DRAFT-GHRP-2-MONOG/007Adaeze Underhill-OkaforThe analytical section is longer than the clinical assessment it accompaniesAccepted in part
DRAFT-GHRP-2-MONOG/006Dr Nikolai Yeovil-BakareThe certainty rating for the principal assessed outcome cannot be traced to the contributing trialsAccepted
DRAFT-GHRP-2-MONOG/005Dr Evander Whitmarsh-ObiDoses are expressed in units that differ between sectionsAccepted
DRAFT-GHRP-2-MONOG/001Valentin TollemacheA sortable table implies a comparison the underlying data do not supportNoted, no amendment
DRAFT-GHRP-2-MONOG/004Professor Bartolomeu Nkosi-LindegaardThe monograph should not describe how the compound is supplied outside a regulated routeNoted, no amendment
7 submissions in total.

§3.2Summary by disposition

Table 2. Counts by disposition, with the meaning of each.

DispositionCountMeaning
Accepted3The submission is accepted and the draft is amended as proposed. The amendment is recorded in the amendment log of the document it changed and is traceable to the numbered submission.
Accepted in part1Part of the submission is accepted and part is not. The secretariat response states which part is which and on what ground the remainder was declined.
Noted, no amendment3The submission raises a point the Institute accepts but that does not require a change to the draft, most often because the draft already states it elsewhere. The location is given in the response.
Not accepted0The submission is not accepted. The secretariat response gives the reason. A submission that is not accepted remains published in full; the Institute does not remove a submission because it disagrees with it.

§3.3Resulting amendments

  1. Registered trials that never reported are absent from the monograph — arising from DRAFT-GHRP-2-MONOG/003. The trial list now includes every registered trial the Institute identified, with its reporting status stated, and the monograph reports the proportion of registered trials for which no result has been posted or published.
  2. The analytical section is longer than the clinical assessment it accompanies — arising from DRAFT-GHRP-2-MONOG/007. The analytical section is reduced to compound-specific content and cross-references the relevant standards for the general procedure, which shortens it substantially without removing what is not available elsewhere.
  3. The certainty rating for the principal assessed outcome cannot be traced to the contributing trials — arising from DRAFT-GHRP-2-MONOG/006. Each assessed outcome now carries its downgrade domains in the summary-of-findings row, with a short statement of the judgement made in each, so that the rating can be checked domain by domain against the contributing trials.
  4. Doses are expressed in units that differ between sections — arising from DRAFT-GHRP-2-MONOG/005. A single dose unit is now used throughout each monograph, with the source unit retained in parentheses wherever a conversion was applied, and every conversion is stated rather than performed silently.

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. International Organization for Standardization. ISO/IEC 17025:2017 General Requirements for the Competence of Testing and Calibration Laboratories. ISO/IEC Standard 2017;3rd edition. identifier not held by the Institute

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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