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/ CompletedNot ApplicableIIT A Randomised, Double-blind,Single-dose,Placebo and Single-blind Active Controlled Cross-over Study in Healthy Volunteers to Access in Effects of Intranasal Chitin Micro-particles on the Release of Cytokines From Nasal Mucosa
The purpose of the study is:
To investigate whether chitin can effect healthy adults, the nasal mucosa in a direction that will enhance the immune response to infection
To investigate whether chitin influence of the nasal mucosa is well tolerated, and that there is no inflammation, as it seen with exposure to endotoxin.
/ Not yet recruitingPhase 2 A Study of Chitin Microparticles (CMP) in Subjects with Seasonal Allergic Rhinitis to Evaluate Safety and Efficacy.
First Into Man Administration of Chitin Microparticles: a Randomised,Double Blind,Placebo Controlled Parallel Group Upward Titration Evaluation of 3 Dose Levels Given Intr-Nasally Over 24 Hours,Followed by a Placebo Controlled,Randomised Parallel Group Evaluation of Safety and Biological Activity Over 7 Days in Subjects Suffering From Allergic Rhinitis
Chitin microparticles (CMP) has been demonstrated in animal studies that have modelled allergic rhinitis to be effective against a wide range of common respiratory allergens. It is an immuneenhancer.
The primary purpose of the study is to demonstrate safety in a first into man study on 24 human volunteers. The secondary objective is to demonstrate efficacy by chosing subjects that demonstrate a response to a nasal allergen challenge using grass pollen.
The subjects are being given increasing doses of CMP, supplied as a nasal spray, for 7 days followed by a nasal allergen challenge with Timothy Grass Pollen extract. Over this period nasal symptom scores, eosinophil counts and cytokine measurements will be performed.
100 Clinical Results associated with CMP Therapeutics Ltd.
0 Patents (Medical) associated with CMP Therapeutics Ltd.
100 Deals associated with CMP Therapeutics Ltd.
100 Translational Medicine associated with CMP Therapeutics Ltd.