Phase 2 Cystic Fibrosis Trial, Completed NCT00930982 Sponsor: Bayer Condition: Cystic Fibrosis
Back to Cystic Fibrosis

Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial enrolled 124 people in total — 60 received an inhaled form of the antibiotic ciprofloxacin (called Ciprofloxacin Inhale or BAYQ3939) and 64 received a placebo (an inactive inhaled treatment). The trial was primarily measuring how much the amount of bacteria in participants' sputum (mucus coughed up from the lungs) changed after 29 days of treatment. It also tracked a range of secondary measures, including lung function, how long it took before participants needed antibiotic treatment for a flare-up of their condition, and self-reported quality of life. The reported data shows that, for the primary outcome — change in bacterial load in sputum — the ciprofloxacin inhale group had an average reduction of 2.94 units (measured on a logarithmic scale, which is a way of expressing very large or small numbers more simply) compared to a reduction of 0.32 units in the placebo group. For the secondary lung function measures (how much air participants could breathe out), the reported changes from baseline were small in both groups across multiple time points, with figures generally close to zero in both directions. The time-to-flare-up data was reported as "not available" in the submitted results. For self-reported quality of life, the reported scores on both questionnaires were broadly similar between the two groups across the measurement time points, with no large numerical differences noted in the data. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 2 Cystic Fibrosis Trial, Completed

NCT00930982
Completed Phase 2 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have been officially diagnosed with bronchiectasis (a lung condition where the airways are permanently widened) that is either of unknown cause or happened after a lung infection, and is not related to cystic fibrosis.
  • Your lung condition has been stable and your treatment routine has not changed for at least the past 30 days.

Who may not be able to join:

  • Your lung function test results (specifically a breathing test called FEV1) show that your lungs are either severely limited (below 35% of expected) or only mildly affected (above 80% of expected) (confirm with trial site).
  • You have a condition called allergic bronchopulmonary aspergillosis, which is a lung allergy reaction to a specific type of fungus.
  • You have an immune system condition that requires you to receive regular immunoglobulin (antibody) replacement treatment.
  • You have an inflammatory bowel disease, such as Crohn's disease or ulcerative colitis.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 9 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Bayer Study Director, Bayer

Australian sites

, Concord, New South Wales
, South Brisbane, Queensland
, Woollongabba, Queensland
, Adelaide, South Australia
, Adelaide, South Australia
, Heidelberg, Victoria
, Prahran, Victoria
, Nedlands, Western Australia

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Completed
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
1 June 2009
Est. completion
1 September 2010

Where this trial is recruiting

🇦🇺 Australia 🇩🇪 Germany 🇪🇸 Spain 🇸🇪 Sweden 🇬🇧 United Kingdom 🇺🇸 United States

8 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Change From Baseline in Total Bacterial Load in the Sputum at End of Treatment (Day 29).

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 9 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov