InterLeukin-7 (CYT107) to Improve Clinical Outcomes in Lymphopenic pAtients With COVID-19 Infection UK Cohort
-
- STATUS
- Recruiting
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- participants needed
- 48
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- sponsor
- Revimmune
Summary
Comparison of the effects of CYT107 vs Placebo administered IM at 10g/kg twice a week for
two weeks on immune reconstitution of lymphopenic
Description
Approximately forty-eight (48) participants will be randomized 1:1 to receive (a)
Intramuscular (IM) administration of CYT107 at 3 g/kg followed, after 48hrs of
The aim of the study is to
Details
Condition | Lymphopenia, Covid 19 |
---|---|
Age | 25years - 80years |
Treatment | Placebos, Interleukin-7 |
Clinical Study Identifier | NCT04379076 |
Sponsor | Revimmune |
Last Modified on | 19 February 2024 |
How to participate?
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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