# Weight‐Reduction and Safety Profile of Once‐Weekly Non‐Comparable Biotherapeutic Subcutaneous Semaglutide Among People With Obesity: A Real‐World Retrospective Study

**Authors:** Md Rakibul Hasan, Kishore Kumar Shil, Md Shahed‐Morshed

PMC · DOI: 10.1002/hsr2.71745 · Health Science Reports · 2026-01-08

## TL;DR

This study shows that a cheaper version of semaglutide helps people with obesity lose weight safely in real-world settings.

## Contribution

The study evaluates the real-world effectiveness and safety of a non-comparable biotherapeutic semaglutide for weight loss.

## Key findings

- Mean weight loss was 6.9% at 12 weeks and 13.3% at 24 weeks.
- 59.4% of participants experienced side effects, while 9.9% had major adverse effects.
- NCB semaglutide showed acceptable safety and weight loss in a real-world setting.

## Abstract

Semaglutide, a once‐weekly injectable glucagon‐like peptide, showed double‐digit weight reduction with an acceptable safety profile in clinical trials and real‐world studies. The efficacy and safety of non‐comparable biotherapeutic (NCB) semaglutide are not adequately reported. Our study aimed to assess the weight reduction and adverse effects of an NCB semaglutide in a real‐world setting.

This retrospective observational study conducted at three urban private practice settings collected data from an electronic record of 87 people with obesity [age (years): 32.2 ± 11.6, BMI (kg/m2): 34.4 ± 4.3, mean ± SD, Female 73(83.9%)] between 7 February 2023 and 31 December 2024 treated with variable doses and durations of NCB semaglutide. The dose, the number of injections administered between visits, weight, side effects, the decision regarding dosing, and patient compliance were recorded at each follow‐up.

The maximum prescribed doses of NCB semaglutide were 0.5 mg per week in 65 (74.7%) of participants, followed by 1.0 mg and 1.7 mg per week in 17 (19.5%) and 5 (5.7%) participants, respectively. Considering available participants of all visits (n = 192), 28 (14.6%) participants were lost to follow‐up, NCB semaglutide was ongoing in 32 (16.7%), 23 (12.0%) patients discontinued NCB semaglutide, and one patient died. The mean weight loss was 6.9% and 13.3% at 12 and 24 weeks of follow‐up, respectively. The frequency of reported any side effects and major adverse effects was 59.4% and 9.9%, respectively.

A locally available NCB semaglutide in an uncontrolled, real‐world setting showed acceptable weight loss and safety profiles among people with obesity.

The pure form of semaglutide has shown clinically meaningful weight loss and an acceptable safety profile in clinical trials and real‐world studies.Non‐comparable biotherapeutic semaglutide is cheap, but its efficacy and tolerability are not adequately reported.This retrospective observational study demonstrated an acceptable weight loss and safety profile of a locally available NCB semaglutide in individuals with obesity in a real‐world setting.

The pure form of semaglutide has shown clinically meaningful weight loss and an acceptable safety profile in clinical trials and real‐world studies.

Non‐comparable biotherapeutic semaglutide is cheap, but its efficacy and tolerability are not adequately reported.

This retrospective observational study demonstrated an acceptable weight loss and safety profile of a locally available NCB semaglutide in individuals with obesity in a real‐world setting.

## Linked entities

- **Chemicals:** semaglutide (PubChem CID 56843331)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Diseases:** Weight (MESH:D015431), Obesity (MESH:D009765), died (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12783696/full.md

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Source: https://tomesphere.com/paper/PMC12783696