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: Epithalon — disposition

The disposition of every submission and the amendments that resulted.

Document identifier
CEI-CP-048/3
Series
Public comment period
Version
1.0
Published
16 Feb 2026
Last reviewed
16 Feb 2026
Next review
16 Feb 2027
Identifier
10.71829/cei.cp.48
Certainty
Not rated
Cycle
2026 Q1
Window
06 Jan 2026 – 03 Feb 2026
Status
Closed
Submissions
5

§3Disposition and amendments

§3.1Disposition table

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

ReferenceRespondentPoint raisedDisposition
DRAFT-EPITHALON-MO/001Ms Rhiannon Okoye-VandergraafThe document is unreadable without specialist trainingAccepted in part
DRAFT-EPITHALON-MO/002Dr Emiliana OllerenshawThe monograph should not describe how the compound is supplied outside a regulated routeNoted, no amendment
DRAFT-EPITHALON-MO/003Dr Hyacinth Drakeford-AmadiDoses are expressed in units that differ between sectionsAccepted
DRAFT-EPITHALON-MO/004Dr Henrike JastrzębskaThe preclinical section is extensive and the clinical section is notAccepted in part
DRAFT-EPITHALON-MO/005Dr Lorcan TrelawneyAdverse event frequencies are given without the denominator or the exposure periodAccepted
5 submissions in total.

§3.2Summary by disposition

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

DispositionCountMeaning
Accepted2The 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 part2Part 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 amendment1The 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. The document is unreadable without specialist training — arising from DRAFT-EPITHALON-MO/001. Every document now opens with a plain-language summary of not more than 150 words, placed above the technical abstract and carrying the same certainty language, so that the two cannot diverge.
  2. Doses are expressed in units that differ between sections — arising from DRAFT-EPITHALON-MO/003. 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.
  3. The preclinical section is extensive and the clinical section is not — arising from DRAFT-EPITHALON-MO/004. The preclinical section is reduced in length, placed after the clinical assessment rather than before it, and opens with a standing statement that an effect observed in an animal model is not a clinical outcome and does not support a certainty rating.
  4. Adverse event frequencies are given without the denominator or the exposure period — arising from DRAFT-EPITHALON-MO/005. Every reported frequency now carries the number of participants, the number of events and the exposure period, and comparator-arm figures are reported alongside rather than in a separate table.

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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