Safety, Tolerability, and Pharmacodynamic Effect Study of PUR118

NCT ID: NCT01333904

Last Updated: 2012-09-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-02-28
• Study Completion Date: 2012-06-30

Brief Summary

The purpose of this study is to establish single and multiple dose safety in healthy subjects and subjects with mild chronic pulmonary obstructive disease (COPD). In addition, the study will evaluate preliminary proof of concept endpoints in COPD subjects such as biomarkers in sputum and mucociliary clearance.

Detailed Description

The proposed initial trial in healthy subjects and subjects with mild COPD will establish the tolerability of PUR118 in these subjects over single and short multi-day dosing periods. The study will also provide preliminary data regarding PUR118's potential impact on biomarkers in COPD. Finally, this trial will assess PUR118's effect on mucociliary clearance. This is a four part study enrolling healthy volunteers in a single ascending dose design (SAD; Part I), followed by multiple ascending dose design (MAD; Part II). Contingent on demonstration of safety in a healthy subject population, the study will enroll mild COPD subjects for a short multi-dose design (Part III) incorporating safety and pharmacodynamic endpoints. Lastly Part IV of the trial will assess the effect of PUR118 on mucociliary clearance in mild COPD subjects.

Conditions

Chronic Obstructive Pulmonary Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

PUR118

Group Type: EXPERIMENTAL

PUR118

Intervention Type: DRUG

inhaled

Interventions

PUR118

inhaled

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Healthy males or non pregnant, non lactating healthy females;
• Age 18-65 years of age;
• Must be willing and able to communicate in English and participate in the whole study;
• Must provide written informed consent.

• Males or non pregnant, non lactating females;
• Age 45-70 years;
• Current (Part III only) or ex-smokers who at least a 15 pack-year smoking history. For Part IV, subjects must be non-smokers for at least 3 months;
• Medically stable, with no evidence of uncontrolled co-existing conditions at screening;
• Must not be taking any inhaled or oral corticosteroids;
• FEV1/FVC ratio <70% and FEV1 60 - 80% (or >/= 60% for Part IV only) of predicted following administration of a bronchodilator;
• Patients must have a medical history of COPD confirmed by their General Practitioner (GP) or treating hospital physician or must have a chest x-ray (CXR) which is normal or consistent with mild COPD and excludes other clinically significant respiratory abnormalities;
• Must be willing and able to communicate in English and participate in the whole study;
• Must provide written informed consent.

Exclusion Criteria

• Current smokers and those who have smoked within the last 12 months;
• Females of child bearing age not willing to use an acceptable form of contraception;
• Presence or history of allergy requiring treatment;
• Serious adverse reaction or hypersensitivity to any drug;

• Must agree to use an adequate method of contraception;
• Upper respiratory tract infection within 30 days of the first study day, or lower respiratory tract infection within the last 60 days;
• Patients taking medication that may affect the respiratory tract within 14 days of the first study day other than their usual COPD medication;
• No active exacerbations requiring antibiotics or steroids within 60 days of dosing.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Quotient Bioresearch

INDUSTRY

Sponsor Role: collaborator

Pulmatrix Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Stuart Mair, MD

Role: PRINCIPAL_INVESTIGATOR

Quotient Bioresearch

Locations

Quotient Bioresearch

Nottingham, United Kingdom, United Kingdom

Countries

United Kingdom

Other Identifiers

601-0004

Identifier Type: -

Identifier Source: org_study_id