Research

Hormonal

The Russian semaglutide-based drug Velgia® (WRYC12301) demonstrates bioequivalence, high safety, and lack of immunogenicity compared to the reference drug Wegovy® at doses of 0.25 mg and 2.4 mg.

This study confirms that the Russian semaglutide product Velgia® is bioequivalent to the brand-name Wegovy® at both 0.25 mg and 2.4 mg doses. It has a comparable safety profile with mild side effects and no detected immunogenicity (antibody formation). For patients seeking this treatment, this generic option offers the same pharmacokinetic exposure as the reference drug.

ModerateSupportsMEDIUM confidence
In the course of the study, the bioequivalence of the study and reference drugs was confirmed. A high safety profile and absence of immunogenicity were demonstrated for the Russian drug Velgia® (WRYC12301, semaglutide, solution for a subcutaneous administration, JSC Biochemik, Russia) in comparison with the reference drug (semaglutide, solution for a subcutaneous administration, Novo Nordisk A/S, Denmark) in doses of 0.25 mg/dose (0.68 mg/mL) and 2.4 mg/dose (3.2 mg/mL).
Ametov As et al. · Pharmacy & Pharmacology · 2025

Why this rating

The study is a small, open-label, randomized bioequivalence trial (n=60) conducted in a single location, lacking long-term clinical efficacy data on weight loss.

Source

Comparative analysis of pharmacokinetic parameters, bioequivalence, safety, tolerability and immunogenicity of semaglutide-based drug for the treatment of obesity

Ametov As et al. · Pharmacy & Pharmacology · 2025

DOI 10.19163/2307-9266-2024-12-3-231-246

rct · n=60Cited 1×
Read the paper
DOI resolved against Crossref · corpus check 2026-06-10

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