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Phase 3 Study With Ciprofloxacin Dispersion for Inhalation in Non-CF Bronchiectasis (ORBIT-3)

A

Aradigm

Status and phase

Completed
Phase 3

Conditions

Non Cystic Fibrosis Bronchiectasis

Treatments

Drug: Ciprofloxacin dispersion for inhalation
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT01515007
ARD-3150-1201

Details and patient eligibility

About

This study (ARD-3150-1201, ORBIT-3) will evaluate the safety and efficacy of inhaled Pulmaquin (ciprofloxacin dispersion for inhalation) compared to inhaled placebo in subjects who have a confirmed diagnosis of non-cystic fibrosis (non-CF) bronchiectasis with a history of pulmonary exacerbations and chronic P. aeruginosa infections.

Enrollment

278 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Verified bronchiectasis diagnosis
  • Pseudomonas aeruginosa lung infection

Exclusion criteria

  • Cystic Fibrosis

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

278 participants in 2 patient groups, including a placebo group

Ciprofloxacin dispersion for inhalation
Experimental group
Description:
Liquid mixture of liposomally encapsulated and unencapsulated ciprofloxacin
Treatment:
Drug: Ciprofloxacin dispersion for inhalation
Placebo
Placebo Comparator group
Description:
Liquid formulation of empty liposomes
Treatment:
Drug: Placebo

Trial contacts and locations

109

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Data sourced from clinicaltrials.gov

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