Kilambi News
Thursday, October 29, 2026

Viking widens loss as four VK2735 Phase 3 trials run

Life Sciences Thursday, October 29, 2026 - Updated Oct 29, 2026 07:06

Viking Therapeutics reported a third quarter net loss of $183.2 million, or $1.55 per share, on October 28, as it started the SUNRISE Phase 3 program for oral VK2735 alongside its two subcutaneous VANQUISH trials, ending the quarter with $960 million in cash and investments.

Why it matters: Viking is now funding four registration trials of the same obesity molecule in two formulations at once, a spending pace that tests whether a mid cap challenger can reach the market Lilly and Novo Nordisk already own.

Data as of Third quarter and nine months ended September 30, 2026, reported October 28, 2026. Viking has no product revenue; all figures are spending, loss and cash position from the filing.

Viking Therapeutics lost $183.2 million in the third quarter, or $1.55 per share, against a loss of $90.8 million, or $0.81 per share, a year earlier, the company reported on October 28 in results furnished to the SEC. Research and development spending was $166.8 million in the quarter, and the nine month loss reached $469.5 million, or $4.03 per share. The wider loss is the cost of running a Phase 3 obesity program at full speed, not a revenue shortfall: Viking has no marketed products.

The program expanded again in the quarter. The SUNRISE Phase 3 program for the oral tablet form of VK2735, the company’s dual GLP-1 and GIP receptor agonist, was initiated, making it the third and fourth registration trials under way. The ongoing VANQUISH program tests the weekly subcutaneous form over 78 weeks at doses of 7.5, 12.5 and 17.5 milligrams: VANQUISH-1 enrolled about 4,500 adults with obesity and VANQUISH-2 about 1,000 adults with obesity and type 2 diabetes. The earlier Phase 2 VENTURE study showed weight reductions of up to 14.7 percent after 13 weekly doses with no sign of a plateau.

Viking also reported positive results from its first VK2735 maintenance dosing study, in which patients moved from weekly induction to less frequent dosing, and started Part 2 of that study, testing daily oral, every other week and monthly subcutaneous maintenance against placebo. Its second metabolic candidate, the dual amylin and calcitonin receptor agonist VK3019, is nearing completion of a Phase 1 single ascending dose study, with a 28 day multiple ascending dose study expected to start in the first quarter of 2027.

The balance sheet is built for the burn. Concurrent offerings of common stock and convertible senior notes in the quarter raised about $575 million gross and about $550 million net, lifting cash, cash equivalents and short term investments to $960 million at September 30, from $706 million at the end of 2025. At the third quarter spending pace, that cash funds the four trials and the start of commercial build out, but Viking’s valuation still rests entirely on Phase 3 data that has not yet read out.

Sources

  1. Viking Therapeutics reports third quarter 2026 financial results and provides corporate update, Form 8-K Exhibit 99.1 (accession 0001193125-26-436145) - Viking Therapeutics, Inc., via SEC EDGAR - 2026-10-28
  2. Viking Therapeutics reports third quarter 2026 financial results and provides corporate update - Viking Therapeutics, Inc., via PR Newswire, carried by Morningstar - 2026-10-28