Evidence map›Paper›PMID 38402332›Full record

ArticleDiabetes therapy : research, treatment and education of diabetes and related disorders2024

Effect of Food Consumption on the Pharmacokinetics, Safety, and Tolerability of Once-Daily Orally Administered Orforglipron (LY3502970), a Non-peptide GLP-1 Receptor Agonist.

Xiaosu Ma, Rong Liu, Edward J Pratt, Charles T Benson, Shobha N Bhattachar, Kyle W Sloop

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in Diabetes therapy : research, treatment and education of diabetes and related disorders, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% of its field
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.

NCT03929744 phase1completednot on this map

A Single- and Multiple-Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of LY3502970 in Healthy Subjects

TypeinterventionalSponsorEli Lilly and CompanyRan2019 to 2020Enrolled133ConditionsHealthyArmsLY3502970, Placebo, Atorvastatin, Simvastatin, Midazolam
NCT05110794 phase1completednot on this map

A Phase 1 Multiple Dose Study to Investigate the Pharmacokinetics, Safety, and Tolerability of LY3502970 in Fed and Fasted Healthy Participants

TypeinterventionalSponsorEli Lilly and CompanyRan2021 to 2022Enrolled34ConditionsHealthyArmsLY3502970
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
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  5. Oral Incretin-Based Therapies for Weight Management.Current atherosclerosis reports · 2026
    Review
  6. Therapeutic peptides and proteins: Status and developments in drug delivery.Journal of controlled release : official journal of the Controlled Release Society · 2026
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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

6 authors at 1 institution in 1 country.

Xiaosu MaEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA. ma_xiaosu@lilly.com.
Rong LiuEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA.
Edward J PrattEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA.
Charles T BensonEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA.
Shobha N BhattacharEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA.
Kyle W SloopEli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, 46240, USA.
Eli Lilly (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe assessed the effect of the prandial state on the pharmacokinetics, safety, and tolerability of single and multiple doses of orforglipron (LY3502970), an oral, non-peptide glucagon-like peptide 1 receptor agonist (GLP-1 RA), in two studies (A and B).

methodsStudy A and study B were phase 1, randomized, crossover studies in healthy adults aged 18-65 years and 21-70 years, respectively. Participants received single (3 mg, study A) or multiple (16 mg, study B) oral doses of orforglipron under fasted and fed conditions. Blood samples were collected pre- and postdose to assess area under the concentration-time curve (AUC), maximum observed drug concentration (C

resultsStudy A included 12 participants (mean age 45.0 years; male 66.7%); study B included 34 participants (mean age 42.8 years; male 88.2%). GLSM AUC and C

conclusionThe observed pharmacokinetic differences due to the prandial state are unlikely to contribute to clinically meaningful differences in the efficacy of orforglipron. The safety profile was consistent with the known profiles of other GLP-1 RAs. Given the absence of prandial restrictions, orforglipron may emerge as a convenient oral treatment option for patients with type 2 diabetes or obesity.

trial registrationClinicalTrials.gov identifiers, NCT03929744 and NCT05110794.

Indexed as

Food-effectGLP-1Glycemic controlObesityOrforglipronPrandial stateT2D

Identifiers

PMID38402332
PMCPMC10951152
OpenAlexW4392138369

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.