An Exploratory Study of FP01 Lozenges in Subjects With Chronic Refractory

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

See also
Status	Clinical Trial	Phase
Recruiting	`NCT05570981` - A Comprehensive Evaluation of the Impact of ATP on Laryngeal Symptoms, Hypersensitivity and Function
Completed	`NCT02993822` - A Dose-ranging Study of Orvepitant in Patients With Chronic Refractory Cough	Phase 2
Terminated	`NCT03979638` - A Dose Escalation Study of BLU-5937 in Unexplained or Refractory Chronic Cough	Phase 2

See also

Status

Clinical Trial

Phase

Recruiting

NCT05570981 - A Comprehensive Evaluation of the Impact of ATP on Laryngeal Symptoms, Hypersensitivity and Function

Completed

NCT02993822 - A Dose-ranging Study of Orvepitant in Patients With Chronic Refractory Cough

Phase 2

Terminated

NCT03979638 - A Dose Escalation Study of BLU-5937 in Unexplained or Refractory Chronic Cough

Phase 2

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT01703923
Study type	Interventional
Source	Cerecor Inc
Contact
Status	Completed
Phase	Phase 2
Start date	November 2012
Completion date	September 2013

An Exploratory Study of FP01 Lozenges in Subjects With Chronic Refractory Cough

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms