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More info
You can access this
clinical trial
if you have
Disease, Pulmonary
and you are
over 35
years old
This is an early phase trial to determine
the dosage and safety of the new treatment.
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The purpose

Objectives of the study are to investigate the safety, tolerability and levels of ciprofloxacin in the lung after single and multiple inhalative administration to patients with mild to moderate COPD (stage I-II according to GOLD Criteria).

Provided treatments

  • Drug: Ciprofloxacin (Cipro inhale, BAYQ3939)
  • Drug: Ciprofloxacin (Cipro inhale, BAYQ3939)
  • Drug: Ciprofloxacin (Cipro inhale, BAYQ3939)
  • Drug: Placebo

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01052298. The sponsor of the trial is Bayer and it is looking for 25 volunteers for the current phase.
Official trial title:
Randomized, Single-blinded, Placebo-controlled Study to Evaluate the Safety and Tolerability, the Pulmonary Deposition and Pharmacokinetics of Ciprofloxacin in Patients With Mild to Moderate Chronic Obstructive Pulmonary Disease (GOLD I - II), Following Inhalation of Ciprofloxacin PulmoSphere Inhalation Powder.