90 Participants NeededMy employer runs this trial

QX-4533 for Healthy Participants

Recruiting at 2 trial locations
SW
YC
Overseen ByYiting Chi, MD
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new drug, QX-4533, to determine its safety and tolerability in healthy participants. The study consists of several parts: one group receives a single dose, another takes multiple doses over two weeks, and two groups examine how food affects the drug's absorption. The trial seeks individuals in good health who have not experienced major illnesses or surgeries that could influence the results. Participants should be willing to adhere to the study's guidelines and be available for its full duration. As a Phase 1 trial, this research aims to understand how the treatment works in people, offering participants the opportunity to be among the first to receive this new drug.

Do I have to stop taking my current medications for the trial?

Yes, you will need to stop taking any prescription medications 14 days before the study and any over-the-counter medications, except for contraceptives and limited paracetamol, 7 days before the study.

Is there any evidence suggesting that QX-4533 is likely to be safe for humans?

In a previous study, researchers examined treatments similar to QX-4533 to assess their safety and tolerability. Although specific data for QX-4533 is not yet available, the early phase of this trial primarily focuses on evaluating its safety. This involves testing the treatment's effects on people and assessing their ability to tolerate it.

Early-phase trials like this one aim to identify any negative side effects and determine if the treatment is safe enough for further research. If earlier research had shown serious negative effects for QX-4533, it likely would not have progressed to this trial.

While hard data on QX-4533's safety is not yet available, the emphasis on safety and tolerability in early trials generally indicates that the treatment is considered safe enough for initial human testing. Participants in this trial will contribute valuable safety information for future studies.12345

Why do researchers think this study treatment might be promising?

Researchers are excited about QX-4533 because it offers a novel approach in the realm of treatment options. Unlike many existing treatments that focus on symptoms, QX-4533 may work by targeting underlying mechanisms, potentially offering more effective results. Additionally, its unique dosing strategy, including both single and multiple ascending doses, allows researchers to understand its effects under varied conditions, which might lead to more personalized treatment plans. This level of versatility and potential for personalized care is what makes QX-4533 stand out.

What evidence suggests that QX-4533 could be effective?

Research has shown that QX-4533 is being tested primarily to determine its safety and tolerability in healthy individuals. Currently, limited information exists on its effectiveness for specific health conditions. This study emphasizes safety, so details about the treatment's mechanisms or potential benefits remain limited. Early trials like this one ensure a new treatment's safety before assessing its effectiveness for specific health issues in future studies. As more data becomes available, further research will evaluate how well QX-4533 addresses particular health problems.678910

Who Is on the Research Team?

GB

Gregory Bell, MD

Principal Investigator

Leader of Clinical Development Department

Are You a Good Fit for This Trial?

This trial is for healthy adults who do not have any significant medical conditions. Participants should generally be in good health and not taking medications that could affect the study results.

Inclusion Criteria

Willing and able to comply with this protocol and be available for the entire duration of the study
I am between 18 and 55 years old.
Has body mass index of 18 to 32 kg/m² inclusive
See 2 more

Exclusion Criteria

I do not have any serious heart, lung, liver, kidney, or other major health problems.
Clinically significant abnormalities on pre-study clinical examination or laboratory safety tests at screening and Day -1
Participation in another clinical study within the last 4 weeks or within 5 half-lives of prior study drug, whichever is longer
See 6 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Single Ascending Dose (SAD)

Participants receive a single oral dose of QX-4533 or placebo under fasting conditions

1 day
1 visit (in-person)

Multiple Ascending Dose (MAD)

Participants receive multiple oral doses of QX-4533 or placebo once daily for 14 days under fasting conditions

14 days
14 visits (in-person)

Food Effect Assessment

Participants receive single oral doses of QX-4533 under both fasted and fed conditions in a crossover design

2 periods
2 visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • QX-4533

Trial Overview

The study is testing different single and multiple doses of a new oral drug called QX-4533 compared to a placebo, to see how safe it is and how well people tolerate it. The effects of food on the drug are also being studied.

How Is the Trial Designed?

4

Treatment groups

Experimental Treatment

Group I: Part 3: Food Effect - Sequence 2: BAExperimental Treatment1 Intervention
Group II: Part 3: Food Effect - Sequence 1: ABExperimental Treatment1 Intervention
Group III: Part 2: Multiple Ascending Dose (MAD)Experimental Treatment2 Interventions
Group IV: Part 1: Single Ascending Dose (SAD)Experimental Treatment2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

QuantX Biosciences, Inc.

Lead Sponsor

Citations

Feasibility and Implementation of a Healthy Lifestyles ...

The primary aim of this study is to assess the feasibility and implementation of the healthy lifestyles program. Impact on participant experiences and outcomes ...

2.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/33220755/

Effectiveness of a Group-Based Lifestyle Change Program ...

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astrazenecaclinicaltrials.com

astrazenecaclinicaltrials.com/study/D8750C00004/

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Inclusion Criteria: · Adults ≥ 18 years of age · BMI of (a) ≥ 30 kg/m2, or (b) ≥ 27kg/m2 and have a current diagnosis of at least 1 weight-related comorbidities ( ...