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Clinical Trial Finder
Anti-Infective Closed to Enrollment
Study of CMTX-101 in adults with cystic fibrosis chronically infected with Pseudomonas aeruginosa (Clarametyx CMTX101-P1-CT002 Part 2)
This study will test the safety and tolerability of a single dose of CMTX-101 delivered through an IV infusion. CMTX-101 is a drug intended to help treat infections in the lung.
Part 2 of this study will be placebo controlled. This means that some participants will receive the study drug, and some participants will receive a placebo. All participants will receive one dose of either the study drug or a placebo followed by 28 days of inhaled antibiotics. Researchers will measure safety and tolerability by monitoring adverse events and changes in vital signs and by conducting physical exams. They will also track how the body processes CMTX-101 by measuring how much of the drug is in the blood, and they will measure the effect of the study drug on P. aeruginosa in sputum.
This study may require blood draws, physical exams, and sputum collection.
Eligibility
See other primary eligibility criteria for more information.
-
Age:
18 Years and Older -
Mutation(s):
No Mutation Requirement -
FEV1% Predicted:
30% or greater
For more information about the results of this study and where it was conducted, visit ClinicalTrials.gov.
Other Primary Eligibility Criteria
Potential participants must be receiving inhaled antibiotics, either cycled or continuous or continuous alternating (CAT)
Study Design
-
Study Type: ?more info
Interventional -
Randomized Study: ?more info
Yes -
Placebo Controlled: ?more info
Yes -
Length of Participation:
8 weeks -
Number of Study Visits:
8
Additional Information
-
Phase: ?more info
Phase Two -
Study Sponsor: ?more info
Clarametyx BioSciences -
Study Drugs:
Study Sites
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Closed to Enrollment
Alabama
The Children's Hospital Alabama, University of Alabama at Birmingham, Birmingham, AL 35233
-
Closed to Enrollment
California
Stanford University Medical Center, Palo Alto, CA 94304
-
Closed to Enrollment
California
University of California, San Francisco, SF, CA 94143
-
Closed to Enrollment
Colorado
National Jewish Health, Denver, CO 80206
-
Closed to Enrollment
Florida
Central Florida Pulmonary Group, Orlando, FL 32803
-
Closed to Enrollment
Idaho
Saint Luke's Cystic Fibrosis Center of Idaho, Boise, ID 83702
-
Closed to Enrollment
Kansas
University of Kansas Medical Center, Kansas City, KS 66160
-
Closed to Enrollment
Maryland
Johns Hopkins University, Baltimore, MD 21205
-
Closed to Enrollment
Michigan
University of Michigan, Michigan Medicine, Ann Arbor, MI 48109
-
Closed to Enrollment
New York
New York Medical College at Westchester Medical Center, Valhalla, NY 10595
-
Closed to Enrollment
New York
Lenox Hill Cystic Fibrosis Center, New York, NY 10028
-
Closed to Enrollment
Ohio
Rainbow Babies and Children's Hospital/University Hospitals Cleveland Medical Center, Cleveland, OH 44106
-
Closed to Enrollment
Ohio
Nationwide Children's Hospital, Columbus, OH 43205
-
Closed to Enrollment
Pennsylvania
Hershey Medical Center Pennsylvania State University, Hershey, PA 17033
-
Closed to Enrollment
Pennsylvania
University of Pennsylvania, Philadelphia, PA 19104
-
Closed to Enrollment
Pennsylvania
University of Pittsburgh Medical Center, Pittsburgh, PA 15224
-
Closed to Enrollment
South Carolina
Medical University of South Carolina, Charleston, SC 29425
-
Closed to Enrollment
Tennessee
Vanderbilt Children's Hospital, Nashville, TN 37232
-
Closed to Enrollment
Utah
Adult Cystic Fibrosis Center at the University of Utah, Salt Lake City, UT 84112
-
Closed to Enrollment
Virginia
Virginia Commonwealth University, Richmond, VA 23219
-
Closed to Enrollment
Washington
Seattle Children's Hospital, Seattle, WA 98115
Eligibility
See other primary eligibility criteria for more information.
-
Age:
18 Years and Older -
Mutation(s):
No Mutation Requirement -
FEV1% Predicted:
30% or greater -
Pseudomonas Status:
Positive Respiratory Cultures Required
For more information about the results of this study and where it was conducted, visit ClinicalTrials.gov.
Other Primary Eligibility Criteria
Potential participants must be receiving inhaled antibiotics, either cycled or continuous or continuous alternating (CAT)
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