Also known as: VK-2735
VK2735 is a late-stage investigational peptide dual GLP-1/GIP receptor agonist from Viking Therapeutics, in Phase 3 development (subcutaneous, VANQUISH-1/2) for obesity, with an oral tablet formulation one phase behind in Phase 2 (VENTURE-Oral). Not yet FDA-approved.
VK2735 is an investigational peptide dual agonist of the GLP-1 and GIP receptors, developed by Viking Therapeutics for obesity and overweight. It uses fatty-acid conjugation for albumin binding — the same general half-life-extension strategy used by semaglutide and tirzepatide — enabling once-weekly subcutaneous dosing.
Two formulations are in parallel development. The subcutaneous injectable is further along, having completed enrollment in two Phase 3 trials (VANQUISH-1 and VANQUISH-2) as of early 2026, with topline results not yet reported at the time of this entry. An oral tablet formulation is roughly one phase behind, having completed a Phase 2 trial (VENTURE-Oral) with Phase 3 trials expected to begin later in 2026 per company statements.
In its Phase 2 subcutaneous trial (VENTURE, 13 weeks), the highest dose (15 mg weekly) produced average weight loss of 14.7%, with 66% of participants losing more than 10% of body weight. The oral formulation's Phase 2 trial (VENTURE-Oral, 13 weeks, once-daily dosing up to 120 mg) produced dose-dependent weight loss up to 12.2% at the top dose, with no plateau observed through the trial's duration.
VK2735 activates both the GLP-1 receptor (central appetite suppression, slowed gastric emptying) and the GIP receptor (complementary insulinotropic and adipocyte effects) — the same dual-receptor strategy used by tirzepatide, though VK2735's specific receptor potency ratio has not been publicly disclosed in sources reviewed.
The peptide is conjugated to a fatty acid for albumin binding, extending its circulating half-life enough to support once-weekly subcutaneous dosing — mirroring the design approach used in semaglutide and tirzepatide. Exact half-life figures reported in secondary sources (~170–250 hours) were not verified against a primary regulatory source and should be treated as approximate.
VK2735 is a Viking Therapeutics investigational peptide dual GLP-1/GIP receptor agonist for obesity — not yet FDA-approved. Full backbone sequence, molecular formula, and molecular weight are not publicly disclosed. Phase 2 subcutaneous data showed 14.7% weight loss at 13 weeks (top dose); Phase 2 oral data showed 12.2% weight loss at 13 weeks with no plateau observed. Adverse events are predominantly gastrointestinal, consistent with the incretin drug class.
As an investigational compound, no cycling protocol is established. Phase 3 trials (VANQUISH-1/2) had completed enrollment but not reported topline results as of this entry.
VENTURE (Phase 2, subcutaneous, 13 weeks): 14.7% average weight loss (14.6 kg) at the 15 mg weekly dose vs. 1.7% placebo; 66% of participants lost more than 10% of body weight.
VENTURE-Oral (Phase 2, oral tablet, 13 weeks, doses 15–120 mg with titration): dose-dependent weight loss up to 12.2% (26.6 lbs) at 120 mg vs. 1.3% placebo; up to 97% of participants at the top dose achieved at least 5% weight loss and up to 80% achieved at least 10%, versus 10%/5% for placebo. No weight-loss plateau was observed through 13 weeks.
VANQUISH-1 and VANQUISH-2 (Phase 3, subcutaneous): enrollment completed (VANQUISH-1 in late 2025, VANQUISH-2 in March 2026); topline efficacy/safety results had not been reported as of this entry's sourcing.
Safety across trials to date: predominantly gastrointestinal adverse events (nausea, vomiting, diarrhea, constipation), described by the company as mostly mild-to-moderate and more frequent early in treatment. Exact backbone sequence, full molecular formula, and molecular weight are not publicly disclosed and are therefore omitted here rather than estimated.
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