Evidence map›Paper›PMID 39425271›Full record

ReviewPharmacology research & perspectives2024

Obicetrapib exhibits favorable physiochemical and pharmacokinetic properties compared to previous cholesteryl ester transfer protein inhibitors: An integrated summary of results from non-human primate studies and clinical trials.

Stephen J Nicholls, Adam J Nelson, John J P Kastelein, Marc Ditmarsch, Andrew Hsieh, Judith Johnson, Danielle Curcio, Douglas Kling, Carol F Kirkpatrick, Michael H Davidson

Abstract readReview
In one paragraph

Review in Pharmacology research & perspectives, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Obicetrapib safety analysis: Pooled phase 3 clinical trial experience.American journal of preventive cardiology · 2026
    Article
  2. Review
  3. Article
  4. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Stephen J NichollsVictorian Heart Institute, Monash University, Melbourne, Victoria, Australia.
Adam J NelsonVictorian Heart Institute, Monash University, Melbourne, Victoria, Australia.
John J P KasteleinNewAmsterdam Pharma B.V, Naarden, The Netherlands.
Marc DitmarschNewAmsterdam Pharma B.V, Naarden, The Netherlands.ORCID 0000-0002-2970-1893
Andrew HsiehNewAmsterdam Pharma B.V, Naarden, The Netherlands.
Judith JohnsonNewAmsterdam Pharma B.V, Naarden, The Netherlands.
Danielle CurcioNewAmsterdam Pharma B.V, Naarden, The Netherlands.
Douglas KlingNewAmsterdam Pharma B.V, Naarden, The Netherlands.
Carol F KirkpatrickMidwest Biomedical Research, Addison, Illinois, USA.
Michael H DavidsonNewAmsterdam Pharma B.V, Naarden, The Netherlands.

Funding

NewAmsterdam Pharma, Naarden, the Netherlands
6 · The paper itself

Abstract

Anacetrapib, a cholesteryl ester transfer protein (CETP) inhibitor previously under development, exhibited an usually extended terminal half-life and large food effect and accumulated in adipose tissue. Other CETP inhibitors have not shown such effects. Obicetrapib, a potent selective CETP inhibitor, is undergoing Phase III clinical development. Dedicated assessments were conducted in pre-clinical and Phase I and II clinical studies of obicetrapib to examine the pharmacokinetic issues observed with anacetrapib. After 9 months of dosing up to 50 mg/kg/day in cynomolgus monkeys, obicetrapib was completely eliminated from systemic circulation and not detected in adipose tissue after a 13-week recovery period. In healthy humans receiving 1-25 mg of obicetrapib, the mean terminal half-life of obicetrapib was 148, 131, and 121 h at 5, 10, and 25 mg, respectively, and food increased plasma levels by ~1.6-fold with a 10 mg dose. At the end of treatment in Phase II trials, mean plasma levels of obicetrapib ranged from 194.5 ng/mL with 2.5 mg to 506.3 ng/mL with 10 mg. Plasma levels of obicetrapib decreased by 92.2% and 98.5% at four and 15 weeks post-treatment, respectively. Obicetrapib shows no clinically relevant accumulation, is minimally affected by food, and has a mean terminal half-life of 131 h for the 10 mg dose. These data support once daily, chronic dosing of obicetrapib in Phase III trials for dyslipidemia management.

Indexed as

Anticholesteremic AgentsCholesterol Ester Transfer ProteinsMacaca fascicularisOxazolidinonesAnimalsEstersFood-Drug InteractionsHalf-LifeHumansanacetrapibAnticholesteremic AgentsCholesterol Ester Transfer ProteinsEstersOxazolidinonesaccumulationanacetrapibcholesteryl ester transfer proteineliminationobicetrapibpharmacokineticstoxicokinetic

Identifiers

PMID39425271
PMCPMC11489133

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.