Nurix Therapeutics, Inc. ((NRIX)) announced an update on their ongoing clinical study.
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Nurix Therapeutics, Inc. is conducting a Phase 1 clinical study titled ‘A Phase 1, Open-Label Study in Healthy Volunteers to Evaluate the Relative Bioavailability of NX-5948 Tablets Compared to Capsules, and the Effect of Food and an Acid-reducing Agent on the Pharmacokinetics of NX-5948.’ The study aims to assess the relative bioavailability of NX-5948 tablets versus capsules and examine how food and an acid-reducing agent affect its pharmacokinetics. This research is significant as it could influence future drug formulations and administration guidelines.
The study tests NX-5948 in both tablet and capsule forms, with the addition of esomeprazole in some cases. The goal is to determine the most effective form and conditions for administering NX-5948, which is intended to enhance drug delivery and efficacy.
This open-label, non-randomized study involves two cohorts and follows a parallel intervention model. It includes 48 healthy volunteers who will receive the drug under different conditions to evaluate its treatment potential. The study is not blinded, meaning all participants and researchers know the interventions being administered.
The study began on December 1, 2024, with primary completion and estimated completion dates yet to be announced. The most recent update was submitted on December 13, 2024. These dates are crucial for tracking the study’s progress and anticipating results that could impact drug development timelines.
For investors, this study update could signal potential growth for Nurix Therapeutics if the results are favorable, potentially boosting the company’s stock performance. The study’s outcome may also influence competitive positioning within the pharmaceutical industry, particularly in drug formulation and delivery systems.
The study is currently recruiting, and further details are available on the ClinicalTrials portal.