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Investigational drug for COVID-19
Study Summary
This trial tests the safety, how well tolerated it is, and how it moves through the body of a new inhalable drug for COVID-19.
- COVID-19
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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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Frequently Asked Questions
Does this study accept participants above the age of sixty?
"This medical trial is accepting participants from the age of majority to 55 years old."
To what extent can experimental drug treatments be hazardous to patients?
"Due to the limited clinical data available, Investigational drug is given a safety rating of 1 on our internal scale. As this is only Phase 1 trials, further research needs to be conducted in order ascertain its efficacy and overall level of safety."
Is this research venture open for enrollment?
"Affirmative, clinicaltrials.gov reveals that this research project is currently recruiting members. Initially posted on November 7th 2022 and last updated on January 10th 2023, the trial requires 44 individuals from one medical centre to join in their investigation."
Could you provide an estimate of the number of participants currently approved for this clinical trial?
"Correct, the information on clinicaltrials.gov reveals that this trial is actively enrolling patients. It was first published on November 7th 2022 and most recently updated on January 10th 2023, with 44 participants needed from a single site."
What kind of individuals is this investigation targeting?
"This investigation is searching for 44 adults aged 18-55 suffering from SARS-CoV2 infection. To be eligible, patients must agree to use two medically accepted methods of contraception if they are of childbearing potential, have normal laboratory results and ECG readings at screening, not smoke within the last 3 months, test negative for COVID-19 antigens during screening and qRT-PCR on Day -1, maintain a BMI between 18.0 - 32.0 kg/m2 (inclusive), possess no serious or chronic underlying disease which would impede study conduct or data interpretation per investigators judgement; women should also pass"
Who else is applying?
What state do they live in?
What site did they apply to?
What portion of applicants met pre-screening criteria?
How many prior treatments have patients received?
Why did patients apply to this trial?
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