Pyxis Oncology, Inc. ((PYXS)) announced an update on their ongoing clinical study.
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Pyxis Oncology, Inc. is conducting a clinical study titled ‘A Phase 1/2, Open-label, Global, Multicenter, Dose-Escalation and Dose-Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of PYX-201 in Combination With Pembrolizumab in Participants With Advanced Solid Tumors.’ The study aims to identify the recommended Phase 2 doses and maximum tolerated dose of PYX-201 when used with pembrolizumab, targeting advanced solid tumors. This research is significant as it could lead to new treatment options for these challenging conditions.
The study is testing two drugs: PYX-201 and pembrolizumab. Both are administered through intravenous infusions. PYX-201 is an experimental drug, while pembrolizumab is a well-known immunotherapy treatment.
This interventional study is non-randomized and follows a sequential intervention model. It is open-label, meaning no masking is involved, and its primary purpose is treatment-focused.
The study began on January 22, 2025, with the latest update submitted on September 25, 2025. These dates are crucial as they indicate the study’s progress and current status in the recruiting phase.
The update from this study could influence Pyxis Oncology’s stock performance positively if the results show promise, as it would enhance their portfolio in oncology treatments. Collaborations with industry giant Merck Sharp & Dohme LLC further strengthen the study’s potential impact. Investors should watch for developments, as successful outcomes could shift market dynamics, especially in the competitive oncology sector.
The study is ongoing, and further details can be accessed on the ClinicalTrials portal.