A Food-Effect, Drug-Drug Interaction, and Pharmacokinetics Study of NX-5948 in Healthy Adult Subjects

A Phase 1, 2-Part, Placebo-Controlled, Double-Blinded Study to Assess the Effect of Food and Drug-Drug Interaction of Fluconazole on the Pharmacokinetics of NX-5948

This is a Phase 1, 2-part double-blinded (with respect to NX-5948/placebo), placebo-controlled study. Part 1 is a randomized, 3 period cross-over food-effect (FE) and drug-drug interaction (DDI) study. Part 2 is a single-period PK evaluation study.

Study Overview

• Status: Completed
• Conditions: Healthy Volunteers
• Intervention / Treatment: Drug: IP; Drug: Matching Placebo

Detailed Description

Part 1:

Periods 1 and 2: Subjects will be randomized to 1 of 2 treatment sequences in a 1:1 ratio. In each treatment sequence, subjects will be randomized to receive either active NX-5948 or placebo in a 7:2 ratio. Subjects will receive a single dose of NX-5948 or placebo under fasting or fed conditions as per randomization schedule to evaluate the effect of food on the single- dose pharmacokinetics (PK) of NX-5948 in healthy subjects.

Period 3: Fluconazole will be administered every day for 8 consecutive days with a single dose of NX-5948/placebo coadministered on Day 4 to evaluate the effect of fluconazole on the single dose PK of NX-5948 in healthy subjects.

Part 2:

Subjects will be randomized to receive either active NX-5948 or placebo to assess single-period PK.

Parts 1 and 2: Safety will be monitored throughout the study by repeated clinical and laboratory evaluations.

• Study Type: Interventional
• Enrollment (Actual): 32
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Nebraska
    • Lincoln, Nebraska, United States, 68502
      • Celerion

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

Subjects must fulfill all of the following inclusion criteria to be eligible for participation in the study:

• Healthy, adult, male, 18-55 years of age
• Subjects must follow protocol-specified contraception guidance as described in the protocol.
• Continuous non-smoker who has not used nicotine and tobacco containing products for at least 3 months prior to the first dosing based on subject self-reporting.
• Body mass index (BMI) ≥ 18.0 and ≤ 30.0 kg/m2 at the screening visit.
• Medically healthy with no clinically significant medical history, physical examination, clinical laboratory profiles, vital signs, and 12-lead safety ECGs, at the screening visit and/or first check-in, as deemed by the PI or designee,
• Understands the study procedures in the informed consent form (ICF) and be willing and able to comply with the protocol.

Key Exclusion Criteria:

Subjects must not be enrolled in the study if they meet any of the following criteria:

• Clinically significant history or presence of respiratory, gastrointestinal, renal, hepatic, hematological, lymphatic, neoplastic (including leukemia, lymphoma, malignant melanoma), myeloproliferative, neurological, cardiovascular, psychiatric, musculoskeletal, genitourinary, immunological, dermatological, endocrine or connective tissue diseases or disorders, or any illness that, in the opinion of the PI or designee, might confound the results of the study or pose an additional risk to the subjects by their participation in the study.
• History or presence of hypersensitivity, angioedema, or idiosyncratic reaction to the study drug(s) or related compounds.

• History or presence of:

  • Significant multiple and/or severe allergies, including anaphylactic reaction.
  • Risk factors for Torsade de Pointes (e.g., heart failure, cardiomyopathy, family history of Long QT Syndrome, or sudden unexpected cardiac death at a young age).
  • Sick sinus syndrome, second or third degree atrioventricular block, myocardial infarction, pulmonary congestion, symptomatic or significant cardiac arrhythmia, prolonged QTcF interval, or conduction abnormalities.
  • Myocardial infarction, acute coronary syndrome, cerebrovascular accident, transient ischemic attack, clinically significant ventricular or atrial tachyarrhythmia as determined by the PI or designee, documented syncope without identified and corrected cause, a pacemaker or implantable cardioverter-defibrillator, cardiac or carotid/cerebral stent placement or angioplasty, or clinically significant valvular heart disease.
  • Adrenal insufficiency.
  • Skin infection.
• Positive Coronavirus disease 2019 (COVID-19) results at first check-in.
• Positive results for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or hepatitis C virus (HCV) at the screening visit.

• Unable to refrain from or anticipates the use of:

  • Any drugs, including prescription and non prescription medications, herbal remedies, or vitamin supplements (including kava, ginko biloba, yohimbe, and saw palmetto) beginning 14 days prior to the first dosing.
  • Any drugs known to be moderate or strong inducers and inhibitors of CYP3A4, P gp, and/or breast cancer resistance protein, including St. John's Wort, dehydroepiandrosterone, and ginseng, beginning 28 days prior to the first dosing.
  • Any acid reducing agents beginning 7 days prior to the first dosing.
• Participation in another clinical study within 30 days or within 5 half-lives (if known), prior to the first dosing, whichever is longer. The 30 day window will be derived from the date of the last blood collection or dosing, whichever is later, in the previous study to Day 1 of Period 1 of the current study.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Crossover Assignment
• Masking: Quadruple

Number of Arms

3

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Part 1: Sequence 1 (Treatment A, B, C); Period 1: NX-5948 or placebo administered under fasted conditions Period 2: NX-5948 or placebo administered under fed conditions Period 3: Fluconazole and single dose of NX-5948/placebo coadministered on Day 4	Drug: IP; NX-5948 oral; Drug: Matching Placebo; Fluconazole
Experimental: Part 1: Sequence 2 (Treatment B, A, C); Period 1: NX-5948 or placebo administered under fed conditions Period 2: NX-5948 or placebo administered under fasted conditions Period 3: Fluconazole and single dose of NX-5948/placebo coadministered on Day 4	Drug: IP; NX-5948 oral; Drug: Matching Placebo; Fluconazole
Experimental: Part 2: NX-5948 PK; Experimental: Part 2: NX-5948 PK NX-5948 or placebo administered 2 doses given 12 hours apart under fasted conditions	Drug: IP; NX-5948 oral; Drug: Matching Placebo; Fluconazole

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Part 1 Food Effect: AUC0-t for NX-5948 administered under fed and fasted conditions	To evaluate the effect of food on the single-dose pharmacokinetics (PK) of NX-5948 in healthy subjects.	9 weeks
Part 1 Food Effect: AUC0-inf for NX-5948 administered under fed and fasted conditions	To evaluate the effect of food on the single-dose pharmacokinetics (PK) of NX-5948 in healthy subjects.	Approximately 9 weeks
Part 1 Food Effect: Cmax for NX-5948 administered under fed and fasted conditions	To evaluate the effect of fluconazole on the single dose PK of NX-5948 in healthy subjects.	9 weeks
Part 1 Drug Drug Interaction: AUC0-inf for NX-5948 administered with and without fluconazole	To evaluate the effect of fluconazole on the single dose PK of NX-5948 in healthy subjects.	9 weeks
Part 1 Drug Drug Interaction: Cmax for NX-5948 administered with and without fluconazole	To evaluate the effect of fluconazole on the single dose PK of NX-5948 in healthy subjects.	9 weeks
Part 1 Drug Drug Interaction: AUC0-t for NX-5948 administered with and without fluconazole	To evaluate the effect of fluconazole on the single dose PK of NX-5948 in healthy subjects.	Approximately 9 weeks
Part 2 PK: AUC0-inf for NX-5948 administration	To evaluate the PK of NX-5948 following 2 doses of NX-5948 given 12 hours apart in healthy subjects.	6 weeks
Part 2 PK: Cmax for NX-5948 administration	To evaluate the PK of NX-5948 following 2 doses of NX-5948 given 12 hours apart in healthy subjects.	6 weeks
Part 2 PK: AUC0-t for NX-5948 administration	To evaluate the PK of NX-5948 following 2 doses of NX-5948 given 12 hours apart in healthy subjects.	Approximately 6 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Part 1: Number of participants with treatment-related adverse events as assessed by CTCAE v5.0	To evaluate safety and tolerability of single doses of NX-5948 administered alone under fed and fasting conditions and following multiple doses of fluconazole in healthy subjects.	Approximately 9 weeks
Part 2: Number of participants with treatment-related adverse events as assessed by CTCAE v5.0	To evaluate safety and tolerability of 2 doses of NX-5948 given 12 hours apart in healthy subjects.	Approximately 6 weeks

Collaborators and Investigators

• Sponsor: Nurix Therapeutics, Inc.
• Investigators: Study Director: Sarah Injac, MD PhD, Nurix Therapeutics, Inc.

Study record dates

Study Major Dates

• Study Start (Actual): August 20, 2024
• Primary Completion (Actual): October 29, 2024
• Study Completion (Actual): November 14, 2024

Study Registration Dates

• First Submitted: September 5, 2024
• First Submitted That Met QC Criteria: September 9, 2024
• First Posted (Actual): September 19, 2024

Study Record Updates

• Last Update Posted (Actual): March 25, 2025
• Last Update Submitted That Met QC Criteria: March 11, 2025
• Last Verified: March 1, 2025

More Information

Terms related to this study

• Keywords: Pharmacokinetics; Healthy participants; Pharmacodynamics; Drug-Drug Interaction; BTK Degrader; NX-5948; Food effects
• Other Study ID Numbers: NX-5948-302

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No