An asthma research study comparing different doses of a generic formulation of Albuterol with the current marketed product for patients with asthma.
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- STATUS
- Recruiting
Summary
This study has 7 visits and can be completed in as little as 9 days or up to 7 weeks.
Description
Visits must be done in the mornings and we are scheduling subjects Monday-Saturday.
Compensation for participation is available to those who qualify.
Please contact Monica at 314-514-8509 to learn more.
Details
| Condition | Asthma |
|---|---|
| Clinical Study Identifier | TX228576 |
| Last Modified on | 26 September 2019 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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