118 Participants NeededMy employer runs this trial

VX-433 for Narcolepsy

MI
Overseen ByMedical Information
Age: 18 - 65
Sex: Any
Trial Phase: Phase 1
Sponsor: Vertex Pharmaceuticals Incorporated

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial explores a new treatment, VX-433, for narcolepsy, a condition that causes excessive daytime sleepiness. Researchers aim to determine the safety and tolerability of VX-433 at various doses and its interactions with other drugs like midazolam and bupropion. Participants will receive either a single dose, multiple doses, or a placebo (inactive substance) to compare effects. This study may suit nonsmokers who have not smoked in the last three months. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the opportunity to be among the first to receive this new treatment.

Is there any evidence suggesting that VX-433 is likely to be safe for humans?

A previous study focused on the safety of VX-433 as it was tested for narcolepsy. The trial is in its early stages (Phase 1), marking the first time VX-433 is tested in humans. At this stage, the primary goal is to assess how the body tolerates the drug and to monitor for any side effects.

Since VX-433 is in Phase 1, safety data from this trial are not yet available. However, treatments in this phase undergo close monitoring. This careful observation helps quickly identify any adverse events or unwanted effects in participants.

The trial also includes a segment where VX-433 is administered alongside other drugs like midazolam and bupropion. This part aims to understand how VX-433 interacts with other medications.

While this trial phase primarily focuses on safety, it is too early to draw conclusions about how well-tolerated VX-433 is. Participants receive close monitoring to ensure any side effects are promptly addressed.12345

Why do researchers think this study treatment might be promising for narcolepsy?

Researchers are excited about VX-433 for narcolepsy because, unlike current treatments like modafinil or sodium oxybate, VX-433 may offer a novel approach by targeting the underlying mechanisms of the disorder differently. While many existing treatments primarily focus on managing symptoms, VX-433 is being explored for its potential to address the condition at its root. This innovative drug could provide more effective and long-lasting relief for those living with narcolepsy, possibly improving their quality of life significantly.

What evidence suggests that VX-433 might be an effective treatment for narcolepsy?

Research has shown that VX-433 is under investigation as a potential treatment for narcolepsy, a sleep disorder characterized by extreme daytime tiredness and sudden muscle weakness, known as cataplexy. In this trial, participants will be randomized into different treatment arms, including single ascending dose, multiple ascending dose, and drug-drug interaction studies with VX-433. Although limited human data exists on VX-433, it belongs to a new class of drugs targeting a brain chemical called orexin, which aids in wakefulness. Similar drugs focusing on orexin have demonstrated promising results, helping patients stay awake longer and reducing cataplexy episodes. These early indications suggest that VX-433 might help manage narcolepsy symptoms, but further research is necessary to confirm its effectiveness.12678

Are You a Good Fit for This Trial?

This trial is for adults with narcolepsy who are nonsmokers or have quit smoking at least 3 months ago, have a BMI between 18 and 30, and weigh over 50 kg. Participants must meet certain health standards set by the study team.

Inclusion Criteria

Body mass index (BMI) of 18.0 to 30.0 kilogram per meter square (kg/m2), inclusive
A total body weight of more than 50 kg
Nonsmoker or ex-smoker for at least 3 months before screening with current nonsmoking status confirmed by urine or blood cotinine at screening

Exclusion Criteria

I have not had a fever or acute illness in the past 14 days.
I have a condition that may affect how my body absorbs medicine.
I am a woman who is or could become pregnant, breastfeeding, or planning pregnancy soon.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Part A: Single Ascending Dose (SAD)

Participants receive a single dose of VX-433 or placebo

1 week

Part B: Multiple Ascending Dose (MAD)

Participants receive multiple doses of VX-433 or placebo

2-3 weeks

Part C: Drug Drug Interaction

Participants receive midazolam and bupropion, followed by VX-433 for 17 days, and then midazolam and bupropion again

3 weeks

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • VX-433

Trial Overview

The study is testing different doses of a new drug called VX-433 to see how safe it is and how the body processes it. It also looks at how VX-433 affects other drugs (midazolam, bupropion) compared to placebo.

How Is the Trial Designed?

5

Treatment groups

Experimental Treatment

Placebo Group

Group I: Part C: Drug Drug InteractionExperimental Treatment3 Interventions
Group II: Part B: Multiple Ascending Dose (MAD)Experimental Treatment1 Intervention
Group III: Part A: Single Ascending Dose (SAD)Experimental Treatment1 Intervention
Group IV: Part A: PlaceboPlacebo Group1 Intervention
Group V: Part B: PlaceboPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Vertex Pharmaceuticals Incorporated

Lead Sponsor

Trials
267
Recruited
36,100+
Dr. David Altshuler profile image

Dr. David Altshuler

Vertex Pharmaceuticals Incorporated

Chief Medical Officer since 2020

MD, PhD

Dr. Reshma Kewalramani profile image

Dr. Reshma Kewalramani

Vertex Pharmaceuticals Incorporated

Chief Executive Officer since 2020

MD, trained in internal medicine and nephrology

Citations

NCT07584434 | A Phase 1, First-in-human Study of VX-433

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure.

Efficacy of Once-Nightly Sodium Oxybate in Patients ... - PMC

This analysis confirms the statistically significant improvements in ability to stay awake, overall improvement, and number of cataplexy ...

VX-433 Enters Phase I Trial for Narcolepsy Type 1

The inclusion of both probes after 17 days of VX-433 dosing is consistent with regulatory expectations for new oral small molecules

XYWAV Clinical Studies for Narcolepsy

EFFICACY IN CATAPLEXY AND EXCESSIVE DAYTIME SLEEPINESS. XYWAV was demonstrated to have an impact on both cataplexy and EDS. Patients randomized to discontinue ...

Real-World Data on the Benefits of Once-Nightly Oxybate ...

Both experts noted significant improvements in patient adherence and daytime functioning compared with twice-nightly dosing, as well as reduced ...

A Comprehensive Review of Current and Emerging ... - PMC

It is indicated for excessive daytime sleepiness (EDS) in narcolepsy and obstructive sleep apnea (OSA), especially in narcolepsy type 1 with ...

Narcolepsy Pipeline Insights, Drugs Report

Narcolepsy Key Products. Samelisant; ORX750; TAK-861; VX-433. Explore comprehensive insights into Narcolepsy epidemiology trends, patient population forecasts ...

Pitolisant Safety Data Shows Positive Signs for Those With ...

Results of a recent analysis of safety data evaluating pitolisant's impact on patients with narcolepsy suggest that the therapy is both generally safe and well ...