Overview

Careers

We have a pipeline of novel, first-in-class or best-in-class therapies for the treatment of metabolic and endocrine disorders

Viking’s research and development activities leverage its expertise in metabolism to develop innovative therapeutics designed to improve patients’ lives. The company’s clinical programs include VK2809, a novel, orally available, small molecule selective thyroid hormone receptor beta agonist for the treatment of lipid and metabolic disorders, which is currently being evaluated in a 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 is also developing 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 obesity demonstrated an encouraging safety and tolerability profile as well as positive signs of clinical benefit. The company is also evaluating an oral formulation of VK2735 in a Phase 1 trial. In the rare disease space, the company 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). VK0214 is currently being evaluated in a Phase 1b clinical trial in patients with the adrenomyeloneuropathy (AMN) form of X-ALD.

Development Programs Indication Preclinical Phase 1 Phase 2 Phase 3 Status
VK2735 (Dual GLP-1/GIP agonist) Obesity
73%
Phase 2 VENTURE study recently completed
VK2735 Oral (Dual GLP-1/GIP agonist) Obesity
46%
Phase 1 ongoing;
Phase 2 planned
VK2809 (TRβ Agonist) NASH
73%
Phase 2b VOYAGE trial recently completed
VK0214 (TRβ Agonist) X-ALD
40%
Phase 1b study recently completed