MerLion Pharmaceuticals GmbH
8
0
0
7
Key Highlights
Risk & Performance
Pipeline Risk Assessment
Pipeline Risk Assessment
Based on historical performance
Moderate Risk
Score: 45/100
12.5%
1 terminated/withdrawn out of 8 trials
87.5%
+1.0% vs industry average
0%
0 trials in Phase 3/4
14%
1 of 7 completed trials have results
Key Signals
Enrollment Performance
Analytics
Activity Timeline
Global Presence
Clinical Trials (8)
Effect of Age and Gender on the PK and Tolerability of Finafloxacin
Role: lead
Finafloxacin for the Treatment of cUTI and/or Acute Pyelonephritis
Role: lead
Pharmacokinetic Profile in Plasma and Epithelial Lining Fluid of Finafloxacin
Role: lead
Safety and Tolerability of Single and Multiple Intravenous Doses of Finafloxacin in Healthy Subjects
Role: lead
Efficacy and Safety Study of Finafloxacin Used in Helicobacter Pylori Infected Patients
Role: lead
Finafloxacin 300 mg Twice a Day (b.i.d.) Versus Ciprofloxacin 250 mg Twice a Day (b.i.d) in Patients With Lower Uncomplicated UTI (uUTI)
Role: lead
First Time in Man Study of Finafloxacin Hydrochloride
Role: lead
First Time in Man Trial for Friulimicin B
Role: lead
All 8 trials loaded