Trial reportFrontiers in endocrinology2026
Efficacy of 12-week treatment with polyethylene glycol loxenatide in obesity or overweight patients with type 2 diabetes: a multicenter, prospective cohort study based on the flash glucose monitoring system.
Trial report in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05611684 (Nanjing First Hospital, Nanjing Medical University), which is not on this map. Not yet cited in PubMed.
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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.
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.
Nanjing First Hospital, Nanjing Medical University
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Authors and funding
10 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objectives: To investigate the factors influencing the glucose-lowering efficacy of polyethylene glycol loxenatide (PEG-Loxe) added to diet, exercise, and existing glucose-lowering therapies in patients with poorly controlled type 2 diabetes mellitus (T2DM) after 12 weeks of treatment. Methods: This multicenter prospective cohort study with a pre-post intervention design, based on the FreeStyle Libre flash glucose monitoring (FGM) system, enrolled T2DM patients with inadequate glycemic control (HbA Results: Of the 500 initially enrolled patients, 246 patients were included in the final analysis. Baseline HbA Conclusions: PEG-Loxe significantly improved glycemic control in Chinese patients with T2DM who were overweight or obese. Patients who were younger, had a shorter duration of diabetes, and presented with higher baseline glucose levels appeared to derive greater benefit from the therapy. Beyond glycemic control, PEG-Loxe might also show additional benefits across multiple cardiometabolic indices. Clinical trial registration: www.clinicaltrials.gov, identifier NCT05611684.
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