A Study of AB-106 in Chinese Healthy Adult Men Evaluated the Effects of Itraconazole and Rifampicin on AB-106 PK

NCT05357820 | Completed Phase 1

• 1 other identifier: AB-106-C110
• Study Type: interventional
• Target: 56
• Locations: 1 country
• Sites: 1

Brief Summary

AB-106-C110 is China-only study, for investigating the drug interaction between AB-106 and CYP3A4 inhibitor (Itraconazole)/CYP3A4 inducer (Rifampin)（n=56）

Conditions

Solid Tumor

Outcome Measures

Primary Outcomes (2)

• AB-106 PK Exposure Parameters

  Peak Plasma Concentration (Cmax)

  29 days

• AB-106 PK Exposure Parameters

  Area under the plasma concentration versus time curve (AUC)

  29 days

Secondary Outcomes (7)

• AB-106 PK Parameters

  29 days

• AB-106 PK Parameters

  29 days

• AB-106 PK Parameters

  29 days

• AB-106 PK Parameters

  29 days

• AB-106 PK Parameters

  29 days

Study Arms (2)

Itraconazole cohort

EXPERIMENTAL

Drug: AB-106, Itraconazole

Rifampicin cohort

EXPERIMENTAL

Drug: AB-106, Rifampicin

Interventions

AB-106, Itraconazole DRUG

single dose AB-106 at Day1, Itraconazole QD at Day14\~Day28, single dose AB-106 at Day17

Itraconazole cohort

AB-106, Rifampicin DRUG

single dose AB-106 at Day1, Itraconazole QD at Day14\~Day32, single dose AB-106 at Day21

Rifampicin cohort

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• The subject is willing to give written informed consent.
• The subject is capable to communicate well with investigator and comply with comply with protocol throughout the study.
• Aged between 18 to 55 at giving written informed consent.
• Chinese male healthy subjects (No clinical abnormality by medical history query, physical examination, vital signs, 12 lead ECG and clinical laboratory test)
• Body weight greater than 50.0 kg, and body mass index between 19 and 26 kg/m2, inclusive.
• For fertile males, agree to use effective contraception methods during the study intervention period and for at least 90 days after the last dose of investigational drug, and agree not to donate sperm during this period.

You may not qualify if:

• Any presence or history of clinically significant hematology, nephrology, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, mental, neurological, or allergic diseases (including drug allergy, but not including untreated, asymptomatic seasonal allergies when administered).
• Any clinically significant laboratory abnormality (hematology, biochemistry \[fasting\], coagulation, thyroid function, urinalysis.)
• systolic blood pressure (SBP) \< 90 mmHg or ≥140 mmHg, diastolic blood pressure (DBP) \< 50 mmHg or ≥ 90 mmHg, and clinically significant abnormality based on the judgment of investigators
• Any presence or history of eye disease in whom the risk is increased by the participation to the study or treatment with investigational drug in the opinion of the investigator, such as glaucoma, retinal detachment, vitreous turbidity, and moths.
• The 12-lead ECG showed QTcF \> 450 milliseconds (msec) or QRS interval \> 120 msec. If QTcF exceeds 450 msec, or QRS exceeds 120 msec, the ECG should be repeated 2 more times, and the average of 3 QTcF or QRS values should be used to determine subject's eligibility.
• Fever within 5 days before the administration.
• Active hepatitis B virus (HBV) surface antigen, hepatitis C virus antibody (HCV Ab), human immunodeficiency virus (HIV) or treponema pallidum (TP) antibody
• Within 28 days prior to the first dose of study treatment, use of food or drugs that are known potent CYP3A4 inhibitors including (but not limited to) atazanavir, clarithromycin, indinavir, itraconazole, ketoconazole, nefazodone, nelfinavir, ritonavir, saquinavir, telithromycin, aceto-eandomycin, voriconazole, grapefruit, grapefruit juice, grapefruit, citrus fruits or grapes Pomelo mixed species; or potent CYP3A4 inducers including (but not limited to) carbamazepine, phenobarbital, phenytoin, rifabutin, and rifampin and St. John's wort; or CYP3A4 substrates with narrow therapeutic window including (but not limited to)dihydroergotamine, ergotamine, pimozide, astemizole, cisapride, and terfenadine.
• Chinese herbal medicine or tonic must be withdrawn at least 28 days prior to the first dose of study treatment; Any clinical study drug is prohibited within 3 months or 5 half-lives prior to the first dose of investigational drug; Any prescription/over-the-counter drug/dietary supplement is prohibited within 14 days or 5 half-lives prior to the first dose of investigational drug; as an exception, acetaminophen/paracetamol can be used at a dose of 1 g/day.
• Vaccinated with live or attenuated vaccine within 28 days prior to the first dose of study treatment
• Subject is unwilling to withdraw foods containing caffeine or purines (such as coffee, tea, cola, chocolate) from 48h before first dose to finishing the last PK sample collection.
• Alcohol intake is greater than 14 units/week (1 unit of alcohol is equivalent to 360 mL of beer, or 150 mL of wine, or 45 mL of baijiu), or subject is unwilling to withdraw alcohol from 48h before first dose to finishing the last PK sample collection.
• Smoking more than 5 cigarette per day, or subject is unwilling to withdraw nicotine from 48h before first dose to finishing the last PK sample collection.
• Any drug abuse, or taking any soft drug (such as marijuana) or hard drugs (heroin, cocaine, etc.) from 1 year before and during the study period.
• Any significant surgical history within 6 months prior to the first dose of study treatment.

Sponsors & Collaborators

• Nuvation Bio Inc.: lead

Study Sites (1)

Xuanwu Hospital of Capital Medical University

Beijing, China

Location

MeSH Terms

Interventions

Itraconazole; Rifampin

Intervention Hierarchy (Ancestors)

Triazoles; Azoles; Heterocyclic Compounds, 1-Ring; Heterocyclic Compounds; Piperazines; Rifamycins; Heterocyclic Compounds, 4 or More Rings; Heterocyclic Compounds, Fused-Ring; Lactams, Macrocyclic; Macrocyclic Compounds; Polycyclic Compounds

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 9, 2021
• First Posted: May 3, 2022
• Study Start: July 19, 2021
• Primary Completion: December 3, 2021
• Study Completion: December 3, 2021
• Last Updated: November 21, 2024

Record last verified: 2022-04

Locations

CN (1)