Ph 1/2 Study Evaluating Safety and Tolerability of Inhaled AP-PA02 in Subjects With Chronic Pseudomonas Aeruginosa Lung Infections and Cystic Fibrosis

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

December 22, 2020

Primary Completion Date

December 14, 2022

Study Completion Date

December 14, 2022

Conditions
Cystic FibrosisPseudomonas AeruginosaPseudomonasLung InfectionLung Infection Pseudomonal
Interventions
BIOLOGICAL

AP-PA02

Bacteriophage administered via inhalation

OTHER

Placebo

Inactive Placebo administered via inhalation

Trial Locations (20)

10595

New York Medical College, Valhalla

19104

The Hospital of the University of Pennsylvania, Philadelphia

21205

Johns Hopkins University, Baltimore

29425

Medical University of South Carolina, Charleston

33606

University of South Florida, Tampa

37232

Vanderbilt University Medical Center, Nashville

43205

Nationwide Children's Hospital, Columbus

44106

University Hospitals Cleveland Medical Center, Cleveland

48201

Harper University Hospital, Detroit

52242

University of Iowa, Iowa City

60208

Northwestern University, Chicago

66160

The University of Kansas Medical Center, Kansas City

75390

University of Texas Southwestern, Dallas

83712

St. Luke's Cystic Fibrosis Center of Idaho, Boise

90027

Children's Hospital Los Angeles, Los Angeles

98195

University of Washington, Seattle

02114

Massachusetts General Hospital, Boston

02115

Boston Children's Hospital, Boston

08901

Rutgers Robert Wood Johnson Medical School, New Brunswick

53792-9988

University of Wisconsin, Madison

Sponsors
All Listed Sponsors
collaborator

Cystic Fibrosis Foundation

OTHER

lead

Armata Pharmaceuticals, Inc.

INDUSTRY