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FAT LOSSNON-PEPTIDEPhase IIIGLP-1/GIP DUAL AGONISTOBESITYPHASE 3

VK2735

Also known as: VK-2735

86 views/week 0 citations 0 edits Updated 8/23/2026

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.

STRUCTURE

Molecular Composition

FORMULA
Not publicly disclosed
MOL. WEIGHT
Not publicly disclosed
TARGETS
GLP-1R · GIP-R
HALF-LIFE
~170–250 hrs (unconfirmed)
ROUTE
Subcutaneous · Oral (trial)
STATUS
Phase 3 (SC) · Phase 2 (oral)
AMINO ACID CHAIN VISUALIZATION
GLP1
GLP-1 receptor-binding domain
GLP-1R activation
NH-CO
GIP
GIP receptor-binding domain
GIP-R activation
NH-CO
FA
Fatty-acid conjugate
albumin binding, half-life extension
NH-CO
Bb
Stabilized peptide backbone
proteolytic resistance
SEQUENCEGLP1-GIP-FA-Bb
MECHANISMS

How It Works

🎯
Dual GLP-1/GIP Receptor Agonism
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 is undisclosed.
Fatty-Acid Half-Life Extension
Conjugated to a fatty acid for albumin binding, extending circulating half-life enough to support once-weekly subcutaneous dosing — the same general design approach used by semaglutide and tirzepatide.
OVERVIEW

Research Overview

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.

Mechanism of Action

// DUAL GLP-1/GIP RECEPTOR AGONISM

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.

// HALF-LIFE EXTENSION

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.

DOSAGE

Dosage & Administration

INJECTABLE (SUBCUTANEOUS) — PHASE 2 TRIAL DOSE
DOSE
Up to 15 mg
FREQUENCY
Once weekly
NOTES
Investigational trial dosing from the Phase 2 VENTURE study — not an approved or established regimen. VK2735 is not yet FDA-approved.
ORAL — PHASE 2 TRIAL DOSE
DOSE
15–120 mg (dose-escalation)
FREQUENCY
Once daily
NOTES
Investigational trial dosing from the Phase 2 VENTURE-Oral study. The oral formulation is roughly one phase behind the subcutaneous formulation, which has completed Phase 3 enrollment.

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.

CYCLING

Cycle Duration Guide

ON CYCLE
Investigational — intended for chronic use if approved, consistent with the GLP-1/GIP drug class
OFF CYCLE
Not established — VK2735 has not completed Phase 3 or received approval

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.

NOTES

Research Notes

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.

Quick Reference
FORMULA
MOL. WEIGHT0 Da
LENGTH0 amino acids
ORIGINViking Therapeutics
STATUSPhase III
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TAGS
GLP-1/GIP dual agonistobesityPhase 3fatty-acid conjugated peptideinvestigational