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
Consultation record

Submissions accepted in part — page 2

Part 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.

Submissions

390 documents · page 2 of 13

Table 1. Submissions with this disposition, on this page.

ReferenceConsultationRespondentPoint raised
DRAFT-WEIGHT-REGAI/012Draft synthesis: weight change after discontinuation of an incretin…Dr Matthias Wintringham industryA sponsor trial meeting the eligibility criteria was excluded
DRAFT-NETWORK-TRAN/002Draft methodological review: transitivity in the incretin networkDr Vasilisa ImmelmannRegulatory assessment documents were not searched
DRAFT-NETWORK-TRAN/003Draft methodological review: transitivity in the incretin networkDr Yaa KettlewellStatistical heterogeneity is treated as though it measured clinical heterogeneity
DRAFT-NETWORK-TRAN/004Draft methodological review: transitivity in the incretin networkEamon Sandringham-AduThe review protocol is described but its registration record is not linked
DRAFT-CONFLICTS-PO/007Draft conflicts-of-interest policyGeorgiana ZimmerthalThe materiality threshold for a declarable holding is set too high
DRAFT-CONFLICTS-PO/008Draft conflicts-of-interest policyIgnatius ErlingssonA four-week window is too short for a respondent without institutional support
DRAFT-CONFLICTS-PO/009Draft conflicts-of-interest policyDr Rurik Haverkamp-DialloFunding should not be accepted from any party the Institute assesses
DRAFT-FUNDING-POLI/005Draft funding and sponsorship policyIvo MountstephenReferences should carry a persistent identifier for every cited source
DRAFT-FUNDING-POLI/007Draft funding and sponsorship policyIgnatius ErlingssonA four-week window is too short for a respondent without institutional support
DRAFT-CITATION-POL/008Draft citation policyDr Vasilisa Sandringham-AduThe materiality threshold for a declarable holding is set too high
DRAFT-PROGRAMME-RE/002Draft policy: labelling of Institute-constructed programme recordsMs Rhiannon Okoye-VandergraafThe document is unreadable without specialist training
DRAFT-PROGRAMME-RE/006Draft policy: labelling of Institute-constructed programme recordsKamila UbertiniA four-week window is too short for a respondent without institutional support
DRAFT-PROGRAMME-RE/009Draft policy: labelling of Institute-constructed programme recordsDr Wojciech Kaltenbach-MensahThe secretariat answers submissions and is not itself named
DRAFT-PROGRAMME-RE/011Draft policy: labelling of Institute-constructed programme recordsDr Vasilisa ImmelmannA party criticised in an assessment should have a right of reply
DRAFT-PROGRAMME-RE/012Draft policy: labelling of Institute-constructed programme recordsDr Emiliana OllerenshawFunding should not be accepted from any party the Institute assesses
DRAFT-ENDOTOXIN-ST/002Draft standard: bacterial endotoxin testing of peptide presentationsDr Quentin ZimmerthalNothing in the standard addresses transfer of the method between laboratories
DRAFT-ENDOTOXIN-ST/006Draft standard: bacterial endotoxin testing of peptide presentationsBertrand Ollerenshaw industryThe additional determinations required would materially increase release testing cost
DRAFT-ENDOTOXIN-ST/007Draft standard: bacterial endotoxin testing of peptide presentationsThaddeus Isaksen-BalogunPoint estimates are given without an interval
DRAFT-ENDOTOXIN-ST/008Draft standard: bacterial endotoxin testing of peptide presentationsDr Jolanta UttridgeNothing addresses the container the material was held in
DRAFT-ENDOTOXIN-ST/012Draft standard: bacterial endotoxin testing of peptide presentationsDr Hortensia HollingworthNothing requires a laboratory to demonstrate ongoing performance
DRAFT-ANALYTICAL-S/003Draft scope of the analytical and methodological standards seriesEamon Sandringham-AduReferences should carry a persistent identifier for every cited source
DRAFT-ANALYTICAL-S/004Draft scope of the analytical and methodological standards seriesAmara VandergraafDefined terms are defined in a glossary the reader has to know exists
DRAFT-ANALYTICAL-S/009Draft scope of the analytical and methodological standards seriesDr Marisol Dunmore-EkpoAn index organised by certainty invites comparison between ratings that are not comparable
DRAFT-GLP1-OBESITY/002Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Dr Yaa KettlewellThe axis of the forest plot exaggerates a small difference
DRAFT-GLP1-OBESITY/005Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Ms Rhiannon Okoye-VandergraafThe document is unreadable without specialist training
DRAFT-GLP1-OBESITY/007Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Professor Bartolomeu Nkosi-LindegaardRegulatory assessment documents were not searched
DRAFT-GLP1-OBESITY/008Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Dr Liesbeth Nordhagen industryA sponsor trial meeting the eligibility criteria was excluded
DRAFT-GLP1-OBESITY/009Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Quentin Whitmarsh-ObiThe review protocol is described but its registration record is not linked
DRAFT-GLP1-OBESITY/013Draft synthesis: glucagon-like peptide-1 receptor agonists for weight…Dr Oisín RautavaaraThe choice of effect measure is not justified and changes the appearance of the result
DRAFT-LEAN-MASS-SC/001Draft scoping review: change in lean mass during pharmacologically…Ms Rhiannon Okoye-VandergraafPatient-reported outcomes are collected by the trials and not reported by the review

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