Viking advances four Phase 3 obesity trials, reports positive VK2735 maintenance data
Viking said its SUNRISE oral Phase 3 trials for VK2735 have begun alongside the ongoing VANQUISH subcutaneous studies, while a maintenance-dosing readout showed durable weight loss with less frequent dosing.
Viking Therapeutics reported third quarter 2026 financial results and a pipeline update on October 28, 2026. The company said it had initiated the SUNRISE Phase 3 program with the oral tablet formulation of VK2735, representing the third and fourth registration trials underway, designed to closely mirror the ongoing VANQUISH Phase 3 program for the subcutaneous formulation.1 The SUNRISE program includes SUNRISE-1 in adults with obesity and SUNRISE-2 in obese or overweight adults with type 2 diabetes, each a randomized, double-blind, placebo-controlled trial testing once-daily oral VK2735 for 68 weeks, targeting enrollment of 560 adults each, with doses of 27.5 mg, 35 mg, 55 mg, or placebo.1
On the subcutaneous side, both VANQUISH studies continued to advance on track during the quarter, with completion expected in 2027.1 VANQUISH extension studies are set to begin in the first quarter of 2027, allowing participants to continue treatment for up to an additional 52 weeks, with results expected in 2028.1
Viking also disclosed positive results from Part 1 of a two-part maintenance dosing study, which showed VK2735 could achieve significant weight loss during induction and maintain a high percentage of that loss long-term using lower and less frequent dosing regimens.1 Week 21 weight loss ranged from approximately 16% to 19% versus approximately 0% for placebo, with 98% of treated subjects achieving at least 5% weight loss.1 Mean weight loss retained at Week 33 ranged from 83% to 97% with every-other-week dosing and 82% to 90% with monthly dosing, compared with 61% for placebo.1 Part 2 of the maintenance study, evaluating oral and additional subcutaneous regimens, has begun, with results expected in 2027.1
Separately, the Phase 1 single ascending dose study of amylin agonist VK3019 is nearing completion, with a multiple ascending dose study planned for the first quarter of 2027.1
On financials, Viking closed concurrent upsized public offerings of common stock and convertible senior notes in September, generating approximately $575.0 million in gross proceeds, leaving the company with $960 million in cash, cash equivalents and short-term investments at quarter end.1 The company said these resources will support ongoing Phase 3 trials, earlier-stage programs, and commercial infrastructure as it prepares for a potential launch of VK2735.1
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