Novo Nordisk Stops Two Ziltivekimab Heart Failure Trials After Futility Verdict

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Novo Nordisk has stopped the HERMES and ATHENA Phase III trials of ziltivekimab after an interim futility analysis, six weeks after the ZEUS trial of the same drug failed on July 31. One trial remains, ARTEMIS in post-heart-attack patients, reading out in the first half of 2027. Ziltivekimab was the company's most substantial non-obesity late-stage asset, and its loss weakens the diversification case rather than near-term earnings.

NVO has halted two Phase III trials of ziltivekimab, HERMES and ATHENA, after an interim analysis returned a futility verdict. The decision was reported on September 7 and follows the failure of ZEUS, a third ziltivekimab trial, on July 31. Three setbacks in six weeks is what makes this more than a single-trial disappointment.

Ziltivekimab is an anti-inflammatory antibody targeting interleukin-6, and it was the most substantial non-obesity asset in Novo's late-stage pipeline. The cardiovascular inflammation thesis behind it is the reason the program mattered: it was the company's attempt to build a second commercial pillar alongside GLP-1s rather than an incremental line extension.

One trial survives. ARTEMIS, which studies patients recovering from a heart attack, continues, with results expected in the first half of 2027. That is now the entire remaining readout for the program, and a narrow population relative to the heart-failure indications just abandoned.

Sell-side reaction has been to trim rather than to capitulate: Seeking Alpha moved to Hold, arguing that continued GLP-1 franchise strength offsets the pipeline damage without justifying a constructive stance. That framing is a fair statement of the tension. Novo's near-term earnings do not depend on ziltivekimab, but its diversification argument largely did. What to watch: the ARTEMIS readout in 2027, whether management redirects the freed R&D spend into acquisitions, and whether the pipeline discount now attached to the shares narrows or persists.

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