Clinical Trial Finder

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Clinical trials are listed below.

  • Restore CFTR FunctionEnrolling Location: USA

    Phase 2 study of riociguat in adults with CF , protocol number Bayer 63-2521/17020

    This study is taking place at multiple care centers across the U.S. It will look at the safety, tolerability and effectiveness of the oral drug riociguat and will use a placebo control.

    • Age:

      18 Years and Older

    • Mutation(s):

      Two copies F508del

    • FEV1% Predicted:

      60 to 90%

    • Number of Visits:

      9

    • Length of Participation:

      28 days

    Contact us about this clinical Trial >
  • Nutritional-GIEnrolling Location: USA

    ASSURE: Study of Relizorb in people with CF who receive enteral tube feeding , protocol number Alcresta 0000498

    This open label study is taking place at multiple care centres across the US. It will look at the safety, tolerability and effectiveness of Relizorb, a new digestive enzyme cartridge for people using enteral tube feedings.

    • Age:

      4 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      Less than 100%

    • Number of Visits:

      5

    • Length of Participation:

      4 months

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  • Nutritional-GIClosed to enrollment Location: USA

    SOLUTION: Study of Liprotamase in people with CF , protocol number Anthera AN-EP13331

    This study is taking place at multiple care centres across the US. It will look at the safety and effectiveness of the drug Liprotamase in people with CF who are currently taking digestive enzymes.

    • Age:

      7 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      30% or greater

    • Number of Visits:

      10

    • Length of Participation:

      28 weeks

    Contact us about this clinical Trial >
  • Nutritional-GIEnrolling Location: USA

    SIMPLICITY: Phase 3 study of liprotamase in people with CF-related pancreatic insufficiency , protocol number Anthera AN-EP13332

    This two-part study is taking place at multiple care centres across the US. It will look at the safety and effectiveness of a new, water-soluble formulation of liprotamase.

    • Age:

      28 Days to 17 Years

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      No FEV1 Limit

    • Number of Visits:

      7

    • Length of Participation:

      24 weeks

    Contact us about this clinical Trial >
  • Anti-InflammatoryCompleted with results Location: USA

    AquADEKs-2: Effects of an antioxidant-enriched multivitamin on inflammation and oxidative stress in people with CF , protocol number AquADECKs-IP-12

    This study took place at multiple care centres across the US. It looked at the effects on an anti-oxidant enriched multivitamin supplement on inflammation and oxidative stress in people with CF.

    • Age:

      10 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      40 to 100%

    • Number of Visits:

      4

    • Length of Participation:

      20 weeks

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  • ObservationalCompleted with results Location: USA

    BONUS: Baby Observational and Nutritional Study , protocol number BONUS-IP-11, BONUS10K0

    This study took place at multiple care centres across the US. It aimed to gain a better understanding of the factors that interfere with good growth in infants with CF.

    • Age:

      Less than 15 weeks

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      No FEV1 Limit

    • Number of Visits:

      9

    • Length of Participation:

      12 months

    Contact us about this clinical Trial >
  • Anti-InfectiveCompleted with results Location: USA

    Tobramycin Inhalation Powder (TIP) in People with Cystic Fibrosis , protocol number Novartis CTBM100C2401

    This open-label study assessed the long term safety of tobramycin inhalation powder (TIP) in people with cystic fibrosis and chronic Pseudomonas aeruginosa lung infection.

    • Age:

      6 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      25 to 75%

    • Number of Visits:

      9

    • Length of Participation:

      52 weeks

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  • Anti-InfectiveClosed to enrollment Location: USA

    Tobramycin Inhalation Powder (TIP) in People with Cystic Fibrosis Extension Study , protocol number Novartis CTBM100C2401E1

    The purpose of this extension study is to collect additional safety data from patients taking TIP who have completed the core study "Tobramycin Inhalation Powder (TIP) in People with Cystic Fibrosis".

    • Age:

      6 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      25 to 75%

    • Number of Visits:

      8

    • Length of Participation:

      48 weeks

    Contact us about this clinical Trial >
  • ObservationalEnrolling Location: USA

    Phase 4 TOBI Podhaler observational study , protocol number Novartis CTBM100C2407

    This study is taking place at multiple care centres across the US. It will look at the effectiveness and long term safety of the TOBI Podhaler and other FDA-approved inhaled antipseudomonal drugs.

    • Age:

      6 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      25 to 80%

    • Number of Visits:

      22

    • Length of Participation:

      60 months

    Contact us about this clinical Trial >
  • ObservationalClosed to enrollment Location: USA

    TOBI Podhaler Usability Study , protocol number Novartis CTBM100C2412

    This study took place at multiple care centres across the US. It looked at how well people are able to understand and follow the TOBI Podhaler instructions for use.

    • Age:

      6 Years and Older

    • Mutation(s):

      No Mutation Requirement

    • FEV1% Predicted:

      25% or greater

    • Number of Visits:

      2

    • Length of Participation:

      1 month

    Contact us about this clinical Trial >
  • Displaying results 71-80 (of 130)
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