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- Klinische proef NCT07678463
A Single and Multiple Ascending Dose Escalation and Food Effect Study of QX-4533 in Healthy Participants
A Three-part, Phase 1, Single and Multiple Ascending Dose Escalation and Food Effect Study in Healthy Participants to Assess the Safety, Tolerability, and Pharmacokinetics of QX-4533
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This study will consist of 3 parts: Part 1: A randomized, double-blind, placebo-controlled single ascending dose (SAD) evaluation, including an open-label crossover food effect (FE) assessment in 1 cohort.
Part 2: A 14-day randomized, double-blind, placebo-controlled multiple ascending dose (MAD) evaluation.
Part 3: An open-label, 2-period crossover FE assessment.
Studietype
Inschrijving (Geschat)
Fase
- Fase 1
Contacten en locaties
Studiecontact
- Naam: Shu Wang, MD
- Telefoonnummer: +86 18036618586
- E-mail: shu.wang@quantxbio.com
Studie Contact Back-up
- Naam: Yiting Chi, MD
- Telefoonnummer: +86 13482779422
- E-mail: Yiting.Chi@quantxbio.com
Studie Locaties
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Queensland
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Brisbane, Queensland, Australië
- Werving
- Nucleus Network Brisbane (Q-pharm)
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Contact:
- Anthony Johnson
- Telefoonnummer: 07 3707 2787
- E-mail: a.johnson@nucleusnetwork.com.au
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:
- Male or female between 18 and 55 years of age (inclusive) at screening.
- Understands the study procedures and is capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
- Willing and able to comply with this protocol and be available for the entire duration of the study.
- In good general health, determined by no clinically significant findings in the opinion of the Investigator from medical history, physical examination, 12-lead electrocardiogram (ECG), clinical laboratory findings, and vital signs at screening and Day -1.
- Has body mass index of 18 to 32 kilograms per meter square (kg/m^2) inclusive.
Exclusion Criteria:
- History or presence of significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, or neurologic disease according to the Investigator.
- History of any Gastrointestinal (GI) procedures (e.g., bariatric surgery) that could impair gastrointestinal absorption.
- History of any illness that, in the opinion of the Investigator, might confound the results of the study or pose additional risk to the participant.
- Clinically significant abnormalities on pre-study clinical examination or laboratory safety tests. Laboratory safety assessments (e.g., serum chemistry, hematology, coagulation) will be performed at screening and on Day -1 (if screening is prior to Day -1) to confirm eligibility.
- Treatment with a live (attenuated) vaccine within 8 weeks before the screening visit.
- Positive hepatitis B surface antigen, human immunodeficiency virus antibody, or hepatitis C antibody at the screening visit.
- Use of any prescription within 14 days prior to study treatment administration or use of any over-the-counter medications including food supplements and herbal medications (e.g., St. John's wort), except for contraceptive medications and as needed (pro re nata) paracetamol (not exceeding 2 g/day) within 7 days prior to study treatment administration.
- Participant has participated in another clinical study within the last 4 weeks or within 5 half-lives of the prior study drug, whichever is longer.
- Participants that currently use (including "recreational use") any illicit drugs or have a history of drug abuse in the last 2 years.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Fundamentele wetenschap
- Toewijzing: Gerandomiseerd
- Interventioneel model: Sequentiële toewijzing
- Masker: Dubbele
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Part 1: Single Ascending Dose (SAD)
Participants will receive a single oral dose of QX-4533 or placebo on Day 1, under fasting conditions.
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QX-4533 tablets
QX-4533 matched-placebo tablets
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Experimenteel: Part 2: Multiple Ascending Dose (MAD)
Participants will receive multiple oral doses of QX-4533 or placebo, once daily for 14 days under fasting conditions.
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QX-4533 tablets
QX-4533 matched-placebo tablets
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Experimenteel: Part 3: Food Effect - Sequence 1: AB
Participants will receive single oral dose of QX-4533 on Day 1 of Period 1 under fasted condition (A) followed by single oral dose of QX-4533 on Day 1 of Period 2 under fed (high fat meal) condition (B).
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QX-4533 tablets
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Experimenteel: Part 3: Food Effect - Sequence 2: BA
Participants will receive a single oral dose of QX-4533 on Day 1 of Period 1 under fed (high fat meal) condition (B) followed by single oral dose of QX-4533 on Day 1 of Period 2 under fasted condition (A).
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QX-4533 tablets
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Number of Participants with Treatment-emergent Adverse Events (TEAEs)
Tijdsspanne: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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Number of Participants with Clinically Significant Change from Baseline in Clinical Laboratory Parameters
Tijdsspanne: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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Secundaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
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Maximum Observed Plasma Concentration (Cmax)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Time of the Maximum Measured Concentration (Tmax)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Area Under the Concentration-Time Curve from Time Zero to the Last Quantifiable concentration-time point (AUClast)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Area Under the Concentration-Time Curve from Time Zero Extrapolated to Infinity (AUCinf)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Apparent Volume of Distribution at Steady State (Vz/F)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Apparent Clearance (CL/F)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Terminal Elimination Half-Life (t½el)
Tijdsspanne: Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Day 1 (Part 1); Day 1, Day 7, and Day 14 (Part 2)
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Number of Participants with Clinically Significant Changes in Electrocardiogram (ECG) Findings
Tijdsspanne: From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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From enrollment through the safety follow-up visit (up to Day 9 [Part 1] and Day 23 [Part 2])
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Studie stoel: Gregory Bell, MD, Leader of Clinical Development Department
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- QX4533-001
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
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product vervaardigd in en geëxporteerd uit de V.S.
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