Tuhura Biosciences, Inc.

Ce que Tuhura Biosciences, Inc. a publié le 13 novembre 2026

Le trimestre clos le 31 mars 2026, face au même trimestre un an plus tôt.

Ce sont des trimestres isolés, pas une année glissante — les chiffres ailleurs sur ce site couvrent douze mois et seront bien plus grands. Une activité saisonnière oscille beaucoup entre les deux : ServiceNow dégage 2,0 Md$ de flux de trésorerie disponible au trimestre de décembre et 0,5 Md$ à celui de juin.

Comparé au même trimestre un an plus tôt, et non à une prévision d’analystes. Un « beat » ou un « miss » suppose un consensus, une donnée sous licence que nous n’avons pas — et se tromper est pire que de s’abstenir.

Ce qu’a dit la direction

“We continue to make significant progress across each of our programs. In October, we shared our first look at data from our open-label front line study of IFx-2.0 with Keytruda® in patients with deep-seated metastatic Merkel cell carcinoma, which showed durable, major objective anti-tumor responses in the first three patients with all responses ongoing for more than six months,”

Cité mot pour mot du communiqué, et affiché uniquement lorsque le document l’attribue à une personne nommée.

Ce que fait Tuhura Biosciences, Inc.

TuHURA Biosciences, Inc. (NASDAQ: HURA) is a Phase 3 immuno-oncology company developing novel technologies to overcome primary and acquired resistance to cancer immunotherapy, two of the most common reasons cancer immunotherapies fail to work or stop working in the majority of patients with cancer. TuHURA's lead innate immune agonist, IFx-2.0, is designed to overcome primary resistance to checkpoint inhibitors. TuHURA has initiated a single randomized placebo-controlled Phase 3 registration trial of IFx-2.0 administered as an adjunctive therapy to Keytruda® (pembrolizumab) compared to Keytruda® plus placebo in first-line treatment for advanced or metastatic Merkel Cell Carcinoma. In addition to its innate immune agonist product candidates, TuHURA is developing TBS-2025, its VISTA-inhibiting mAb in a Phase 1b clinical trial in patients with mut NPM1 r/r AML, a molecularly defined subgroup that represents approximately 35% of patients with AML. TuHURA is also leveraging its Delta Opioid Receptor technology to develop first-in-class, bi-specific, bi-functional antibody drug conjugates (ADCs) targeting Myeloid-Derived Suppressor Cells to inhibit their immune-suppressing effects on the tumor microenvironment to prevent T cell exhaustion and acquired resistance to checkpoint inhibitors and cellular therapies.