A Study to Assess Drug-drug Interaction of ZX008 in Healthy Male and Female Study Participants

NCT ID: NCT06679413

Last Updated: 2025-07-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 22 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-12-04
• Study Completion Date: 2025-06-12

Brief Summary

The purpose of the study is to assess the single-dose pharmacokinetics (PK) of 3 probe drugs (midazolam, bupropion, and metformin) before and after repeat doses of ZX008

Conditions

Healthy Study Participants

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Treatment Arm

Study participants will receive a single dose of the cocktail of probe drugs at pre-specified timepoints followed by a wash out period. The same study participants will then receive repeated oral doses of fenfluramine HCl (ZX008) and a single dose of the cocktail of probe drugs at pre-specified time points during this Treatment Period.

Group Type: EXPERIMENTAL

midazolam

Intervention Type: DRUG

Study participants will receive a pre specified single oral dose of probe drug midazolam on Day 1 and Day 22 of the study

metformin

Intervention Type: DRUG

Study participants will receive a pre-specified single oral dose of probe drug metformin on Day 1 and Day 22 of the study

bupropion

Intervention Type: DRUG

Study participants will receive a pre-specified single oral dose of probe drug bupropion on Day 1 and Day 22 of the study

fenfluramine HCl

Intervention Type: DRUG

Study participants will receive pre-specified repeated oral doses of fenfluramine HCl (ZX008) from Day 6 to 26 during the study

Interventions

midazolam

Study participants will receive a pre specified single oral dose of probe drug midazolam on Day 1 and Day 22 of the study

Intervention Type: DRUG

metformin

Study participants will receive a pre-specified single oral dose of probe drug metformin on Day 1 and Day 22 of the study

Intervention Type: DRUG

bupropion

Study participants will receive a pre-specified single oral dose of probe drug bupropion on Day 1 and Day 22 of the study

Intervention Type: DRUG

fenfluramine HCl

Study participants will receive pre-specified repeated oral doses of fenfluramine HCl (ZX008) from Day 6 to 26 during the study

Intervention Type: DRUG

Other Intervention Names

Fintepla; ZX0008

Eligibility Criteria

Inclusion Criteria

• Participant must be 18 to 55 years of age inclusive at the time of signing the informed consent form (ICF)
• Body weight of at least 50 kg and body mass index within the range 18 to 32 kg/m^2 (inclusive)
• Male or female
• Capable of giving signed informed consent as described in Appendix 1 which includes compliance with the requirements and restrictions listed in the ICF and in this protocol.

Exclusion Criteria

• Alanine aminotransferase (ALT), aspartate aminotransferase (AST), or alkaline phosphatase (ALP) above 1.1x upper limit of normal (ULN)
• Bilirubin >ULN (isolated bilirubin <1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%)
• Participant has clinically significant current or past history of cardiovascular or cerebrovascular disease, such as valvular heart disease, and/or pulmonary hypertension. Participants with any history of stroke or myocardial infarction are excluded.
• Clinically significant history or presence of electrocardiogram (ECG) or echocardiogram (ECHO) findings as judged by the investigator or designee at the Screening Visit and Check-in, including each criterion listed below:
• Abnormal sinus rhythm (heart rate outside of 40bpm and 100bpm)
• QTcF (QT interval corrected using Fridericia's formula) interval >450 msec for male participants or >470 msec for female participants (QTcF is the QT interval corrected for heart rate according to Fridericia's formula, it can be either machine read or manually overread)
• QRS interval >120 msec, confirmed by manual over read
• PR interval >220 msec
• Greater than trace aortic valve regurgitation
• Greater than trace mitral valve regurgitation
• Possible signs of pulmonary arterial hypertension (PAH) with abnormal pulmonary artery systolic pressure (PASP) or PASP >35 mmHg
• Evidence of left ventricular dysfunction (systolic or diastolic)
• Clinically significant structural cardiac abnormality, including, but not limited to, mitral valve prolapse, atrial or ventricular septal defects, and patent ductus arteriosus with reversal of shunt (right to left shunt). Note: Patent foramen ovale or a bicuspid aortic valve is not considered exclusionary
• Clinically significant abnormal blood pressure (as determined by the investigator)
• Participant has a current or past history of glaucoma
• Participant has used hepatic enzyme-inducing drugs (eg, glucocorticoids, phenobarbital, isoniazid, phenytoin, rifampicin) within 30 days before the first administration of the cocktail of 3 probe drugs (metformin, midazolam, bupropion) and through the day of discharge from the site
• Participant has used other prescription drugs, including vaccinations, over-the-counter medications, herbal/traditional medicines, or dietary supplements within 14 days before the first administration of the cocktail of probe drugs (excluding medicines for external use), with the exception of acetaminophen (up to 2 g/day)
• Consent to genotyping is required for participation in the study. Poor metabolizers of CYP (cytochrome P450) 3A4 or CYP2B6 based on genotyping and as categorized by the testing laboratory will be excluded from the study
• Positive test for alcohol and/or prohibited concomitant drugs (including cotinine) at Screening Visit and on Day -1
• Participant has donated blood or plasma or has experienced blood loss ≥500 mL within 90 days, ≥200 mL within 30 days, or has donated any blood or plasma within 14 days before first administration of study treatments
• Any consumption of food products with a known Drug-drug interaction (DDI) impact (eg, grapefruit, grapefruit juice, Seville oranges, or products containing them) for at least 1 week before Day 1 and through day of discharge from the site
• Consumption of more than 600 mg of caffeine/day (1 cup of coffee contains approximately 100 mg of caffeine, 1 cup of tea approximately 30 mg, and 1 glass of cola approximately 20 mg) within 30 days before Day 1 and through day of discharge from the site
• Participant is a current smoker or has used nicotine-containing products (eg, tobacco, patches, gum, vapes, or e-cigarettes) within 35 days before Day 1 and through day of discharge from the site

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

UCB BIOSCIENCES, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

UCB Cares

Role: STUDY_DIRECTOR

001 844 599 2273 (UCB)

Locations

Up0132 1001

Baltimore, Maryland, United States

Countries

United States

Other Identifiers

UP0132

Identifier Type: -

Identifier Source: org_study_id