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Exploratory Ph I Trial of the Active IMP in Healthy Volunteers in Relation to COVID-19

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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.

Sponsor:
Information provided by (Responsible Party):
MedinCell S.A

Results:

Study Type Interventional
Study Design Allocation: Randomized;   Intervention Model: Sequential Assignment;   Masking: Double (Participant, Investigator);   Primary Purpose: Other
Condition Covid19
Interventions Drug: Ivermectin
Drug: Placebo
Enrollment 24

Participant Flow 

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Recruitment Details
Pre-assignment Details
Arm/Group Title 50mcg/kg (Oral) 75mcg/kg (Oral) 100mcg/kg (Oral) Matching Placebo (Oral)
Hide Arm/Group Description Ivermectin loading dose of 200 mcg/kg followed by daily doses of 50mcg/kg from D2 to D28 Ivermectin loading dose of 200 mcg/kg followed by daily doses of 75mcg/kg from D2 to D28 Ivermectin loading dose of 200 mcg/kg followed by daily doses of 100mcg/kg from D2 to D28 Placebo tablets matching the Active Investigative Medicinal Product (IMP)
Period Title: Overall Study
Started 6 6 6 6
Completed 6 6 5 6
Not Completed 0 0 1 0

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