Viking Therapeutics to Highlight Clinical Data from VK2735 Obesity Program in Presentations at ObesityWeek® 2025
Rhea-AI Summary
Viking Therapeutics (NASDAQ: VKTX) will present clinical data and study designs for its obesity program VK2735 at ObesityWeek® 2025 (Nov 4–7, 2025) and at AHA Scientific Sessions 2025 (Nov 7–10, 2025).
ObesityWeek highlights: an exploratory analysis from the Phase 2 VENTURE study reporting 13-week effects of weekly subcutaneous VK2735 on weight, prediabetes prevalence, and metabolic syndrome, plus the Phase 3 VANQUISH-1 study design for subcutaneous VK2735 in adults with overweight or obesity.
AHA highlights: the Phase 3 VANQUISH-2 study design in Type 2 diabetes with obesity and an analysis of cardiometabolic condition prevalence across BMI categories. Presentation dates/times and presenting authors are listed for each poster.
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News Market Reaction 63 Alerts
On the day this news was published, VKTX gained 0.83%, reflecting a mild positive market reaction. Argus tracked a peak move of +8.5% during that session. Our momentum scanner triggered 63 alerts that day, indicating high trading interest and price volatility. This price movement added approximately $37M to the company's valuation, bringing the market cap to $4.47B at that time.
Data tracked by StockTitan Argus on the day of publication.
Poster Presentation on VENTURE Study Results Evaluating Impact of VK2735 on Prediabetes and Cardiometabolic Status
Additional Poster Presentations Scheduled for American Heart Association Scientific Sessions 2025
One ObesityWeek presentation will report results of an exploratory analysis from the company's Phase 2 VENTURE clinical trial, which evaluated 13 weeks of weekly treatment with a subcutaneous formulation of VK2735 in obese subjects. The exploratory analysis evaluated the impact of VK2735 treatment on the prevalence of prediabetes and metabolic syndrome over the 13-week study. A second presentation will highlight the design of the company's ongoing Phase 3 VANQUISH-1 study of subcutaneous VK2735 in patients with obesity or who are overweight with at least one weight-related co-morbid condition.
Viking will also make two presentations at the upcoming American Heart Association (AHA) Scientific Sessions 2025, which is being held November 7-10, 2025, in
Details of the ObesityWeek and AHA presentations are as follows:
ObesityWeek 2025
Poster Presentation:
Title: VANQUISH-1 Study Design: Phase 3 Trial of Subcutaneous VK2735 in Adults with Overweight or Obesity
Presenting Author: Karen Modesto, M.D., Vice President, Clinical Development, Viking Therapeutics
Date/Time: Wednesday, November 5, 2025, 2:30 – 3:30 p.m. Eastern Time
Poster Presentation:
Title: Impact of Subcutaneous VK2735 on Weight, Prediabetes, and Cardiometabolic Status: The VENTURE Study
Presenting Author: Harold Bays, MD, MFOMA, FTOS, FACC, FNLA, FASPC, DABOM, Louisville Metabolic and Atherosclerosis Research Center
Date/Time: Thursday, November 6, 2025, 2:30 – 3:30 p.m. Eastern Time
AHA Scientific Sessions 2025
Presentation ID: Sa2063
Title: VANQUISH-2: Phase 3, Randomized, Double-blind, Placebo-controlled, Trial of weekly subcutaneous administration of VK2735 in Obese or Overweight Adults with Type 2 Diabetes
Presenting Author: Karen Modesto, M.D., Vice President, Clinical Development, Viking Therapeutics
Date/Time: Saturday, November 8, 2025, 10:30 – 11:30 a.m. Central Time
Presentation ID: Sa2052
Title: Prevalence of Cardiometabolic Conditions Across Body Mass Index Categories: The Distinct Burden of Severe (class III) Obesity
Presenting Author: Saif Rathore, M.D., Ph.D., Sandbar Life Sciences
Date/Time: Saturday, November 8, 2025, 2:30 – 3:30 p.m. Central Time
About GLP-1 and Dual GLP-1/GIP Agonists
Activation of the glucagon-like peptide 1 (GLP-1) receptor has been shown to decrease glucose, reduce appetite, lower body weight, and improve insulin sensitivity in patients with type 2 diabetes, obesity, or both. Semaglutide is a GLP-1 receptor agonist that has been approved by the
About Viking Therapeutics, Inc.
Viking Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the development of novel first-in-class or best-in-class therapies for the treatment of metabolic and endocrine disorders, with three compounds currently in clinical trials. Viking's research and development activities leverage its expertise in metabolism to develop innovative therapeutics designed to improve patients' lives. Viking's clinical programs include VK2735, a novel dual agonist of the glucagon-like peptide 1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP) receptors for the potential treatment of various metabolic disorders. Data from a Phase 1 and a Phase 2 trial evaluating VK2735 (dosed subcutaneously) for metabolic disorders demonstrated an encouraging safety and tolerability profile as well as positive signs of clinical benefit. Concurrently, the company is evaluating an oral formulation of VK2735 in a Phase 1 trial. Viking is also developing VK2809, a novel, orally available, small molecule selective thyroid hormone receptor beta agonist for the treatment of lipid and metabolic disorders. The compound successfully achieved both the primary and secondary endpoints in a recently completed Phase 2b study for the treatment of biopsy-confirmed non-alcoholic steatohepatitis (NASH) and fibrosis. In a Phase 2a trial for the treatment of non-alcoholic fatty liver disease (NAFLD) and elevated LDL-C, patients who received VK2809 demonstrated statistically significant reductions in LDL-C and liver fat content compared with patients who received placebo. The company's newest program is evaluating a series of internally developed dual amylin and calcitonin receptor agonists (or DACRAs) for the treatment of obesity and other metabolic disorders. In the rare disease space, Viking is developing VK0214, a novel, orally available, small molecule selective thyroid hormone receptor beta agonist for the potential treatment of X-linked adrenoleukodystrophy (X-ALD). In a Phase 1b clinical trial in patients with the adrenomyeloneuropathy (AMN) form of X-ALD, VK0214 was shown to be safe and well-tolerated, while driving significant reductions in plasma levels of very long-chain fatty acids (VLCFAs) and other lipids, as compared to placebo.
For more information about Viking Therapeutics, please visit www.vikingtherapeutics.com.
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SOURCE Viking Therapeutics, Inc.