VK2735 — EU research guide.
VK2735 (Viking Therapeutics) is a dual GLP-1 / GIP receptor agonist in clinical development for obesity, in both subcutaneous and oral formulations. It is investigational and not approved anywhere.
What is VK2735?
VK2735 is an investigational dual agonist of the GLP-1 and GIP receptors developed by Viking Therapeutics — the same dual-incretin mechanism class as tirzepatide. It is being developed in two formulations: a once-weekly subcutaneous injection and a once-daily oral tablet, with the goal of covering both the injectable and oral obesity markets with one molecule.
What does the research show?
In a Phase 2 study of the subcutaneous formulation (VENTURE), VK2735 produced mean weight loss of up to ~14.7% over 13 weeks, with the weight-loss curve still declining at the end of dosing (no plateau). The oral tablet's Phase 2 VENTURE-Oral trial (reported August 2025) met its primary and secondary endpoints, with up to ~12.2% mean weight loss from baseline at 13 weeks, though a notable dropout rate was discussed by analysts. The subcutaneous programme has advanced into Phase 3 (VANQUISH-1 and VANQUISH-2). As of mid-2026 VK2735 is not approved by any regulator.
EU legal status
Not approved in the EU. VK2735 is an investigational pharmaceutical owned by a single developer; it is not a generic research peptide and has no legitimate consumer or research-supply route. Material sold under this name on the gray market cannot be assumed to be authentic VK2735.
Molecular information
Pharmacokinetics
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