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LYR-220 Design 2 for Chronic Sinusitis
Study Summary
This trial will study two different designs of the drug LYR-220 in people with CRS who have had sinus surgery. They will look at how safe and tolerated the drug is, how it is absorbed and metabolized, and how effective it is.
- Chronic Sinusitis
Timeline
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Who is running the clinical trial?
Frequently Asked Questions
What is the scope of enrolment for this experiment?
"Indeed, clinicaltrials.gov highlights that this trial is actively searching for participants. The study was initially listed on November 23rd 2021 and has been updated on October 25th 2022. 70 individuals need to be recruited from 21 separate sites."
What purpose does this experiment endeavor to accomplish?
"During the 28 week duration of this trial, Plasma MF concentrations will act as the primary measured outcome. Supplementary outcomes that are to be monitored include: Intraocular Pressure (IOP), Adverse Events and their severity, and Laboratory Values (hematology and chemistry)."
Is there any potential for harm with LYR-220 Design 2?
"LYR-220 Design 2's safety has been largely supported by data from Phase 2 trials, thus receiving a score of 2 on the scale. As such, efficacy is yet to be assessed."
In which locations is the team overseeing this medical experiment operating?
"Presently, the trial is being conducted in 21 different medical centres across America. These sites are based in Baltimore, Carlsbad and Spokane as well as 18 other places of residence. In order to reduce travelling costs for participants, it may be prudent to select a centre closest to your home address."
Is this medical experiment in need of more participants right now?
"Indeed, according to information posted on clinicaltrials.gov, this study is actively enrolling participants. The initial posting date was November 23rd 2021 with the most recent amendment made on October 25th 2022."
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