Study to Assess the Efficacy, Safety, and Tolerability of NOC-110 in Adults with Refractory or Unexplained Chronic Cough
Refractory or Unexplained Chronic CoughThis is a phase 2b, randomized, double-blind, placebo-controlled study investigating the efficacy, safety, and tolerability of Taplucainium Inhalation Powder (NOC-110) once daily in adults with refractory or unexplained chronic cough.
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Participation Requirements
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Sex:
ALL -
Eligible Ages:
18 to 80
Participation Criteria
Inclusion Criteria:
* Refractory or unexplained chronic cough for ≥ 12 months.
* Women of childbearing potential agree to follow the protocol specified contraceptive - guidance during the study.
* Males who are not vasectomized must agree to use the contraceptive methods defined in the protocol.
* Able to provide Informed Consent.
Exclusion Criteria:
* Previous exposure to taplucainium (formerly NTX-1175) or known allergy or hypersensitivity to taplucainium, its excipients/metabolites, or related compounds.
* Participants who are currently participating in another drug or device clinical study
* Participants who have participated in an Acute or Chronic Cough investigational study within 60 days before the start of the Screening.
* Current diagnosis of chronic obstructive pulmonary disease, bronchiectasis, unexplained pulmonary fibrosis, hemoptysis, bronchial asthma, or other pulmonary disease.
* Respiratory tract infection within 4 weeks of Screening or during screening period.
* Any female who is pregnant or lactating or wishing to become pregnant.
* Donation of \> 1 Unit (450 milliliter or more) of blood within 90 days prior to the first dosing.
* Alcohol or drug use disorder within the past 2 years.
* Current smoker/vaper or individuals who have given up smoking within the past 6 months, and/or those with \>20 pack-year smoking history.
* Current opiate/opioid use or medical history of opiate/opioid use disorder. History of concurrent malignancy or recurrence of malignancy in the last 2 years.
* Body Mass Index of ≥40 kg/m2.
* Positive results for human immunodeficiency virus, hepatitis B, or hepatitis C virus.
* Unable to refrain from the use of medications and treatments that can impact cough during the study.
* Have clinically significant history or evidence of poorly controlled cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, neurological, immunological, or psychiatric disorder(s).
Study Location
Recherche GCP Research
Recherche GCP ResearchMontréal, Quebec
Canada
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Inspiration Research Limited
Inspiration Research LimitedToronto, Ontario
Canada
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DIEX Recherche Victoriaville Inc.
DIEX Recherche Victoriaville Inc.Victoriaville, Quebec
Canada
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Clinique de pneumologie et du sommeil de Lanaudière
Clinique de pneumologie et du sommeil de LanaudièreSaint-Charles-Borromee, Quebec
Canada
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Dynamic Drug Advancement
Dynamic Drug AdvancementAjex, Ontario
Canada
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DIEX Recherche Sherbrooke Inc.
DIEX Recherche Sherbrooke Inc.Sherbrooke, Quebec
Canada
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Clinique Specialisee en Allergie de la Capitale
Clinique Specialisee en Allergie de la CapitaleQuébec, Quebec
Canada
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McMaster University
McMaster UniversityHamilton, Ontario
Canada
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- Study Sponsored By
- Nocion Therapeutics
- Participants Required
- More Information
- Study ID:
NCT06504446