Clinical trial
A Parallel-design Phase 1 Study to Assess Safety, Tolerability and Pharmacokinetics/Exposure Following Different Single Dose Levels of MOR106 (Administered Subcutaneously or Intravenously) in Healthy Male Subjects (Randomized, Open-label), and in Subjects With Moderate to Severe Atopic Dermatitis (Randomized, Placebo-controlled, Double-blind, Repeated Subcutaneous Dosing Over 12 Weeks)
NCT03689829 is registered in ClinicalTrials.gov with Lakefront Biotherapeutics NV as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Parallel-design Phase 1 Study to Assess Safety, Tolerability and Pharmacokinetics/Exposure Following Different Single Dose Levels of MOR106 (Administered Subcutaneously or Intravenously) in Healthy Male Subjects (Randomized, Open-label), and in Subjects With Moderate to Severe Atopic Dermatitis (Randomized, Placebo-controlled, Double-blind, Repeated Subcutaneous Dosing Over 12 Weeks)
- Lead sponsor
- Lakefront Biotherapeutics NV
- Phase
- Phase 1
- Overall status
- Terminated
- Start date
- August 13, 2018
- Completion date
- March 2, 2020
- Enrollment
- 44 (actual)
- Sites
- 15
Conditions
As the registry lists them; a condition with its own page is linked.
atopic dermatitis, healthy