A 12-Week Study in Adult Subjects With Asthma

Phase 2

Completed

• Conditions: Asthma
• Interventions: Drug: Fluticasone Propionate (FP)

• Registration Number: NCT01516086
• Lead Sponsor: Dey

Brief Summary

This will be a multi-center, randomized, placebo controlled parallel-group study to Replicate Efficacy of Nebulized Fluticasone Propionate (FP) in Adult Subjects with Partly Controlled and Uncontrolled Asthma. Individual participation will be approximately 16 weeks, including 12 weeks of double-blind treatment.

Detailed Description

The primary outcome measure is FEV1 (Forced Expiry Volume in 1 second) and the secondary outcome measure is Peak Expiratory Flow Rate (PEFR), Asthma Control Questionnaire (ACQ), Nighttime awakenings and rescue medication usage.

Study Timeline

• Study First Submitted: 2012-01-13
• Study First Submitted QC: 2012-01-19
• Study First Posted: 2012-01-24
• Study Start: 2012-03
• Primary Completion: 2013-11
• Study Completion: 2013-11
• Status Verified: 2014-11
• Disposition First Submitted: 2014-11-24
• Disposition First Submitted QC: 2014-11-24
• Last Update Submitted: 2014-11-24
• Disposition First Posted: 2014-12-11
• Last Update Posted: 2014-12-11

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 498

Inclusion Criteria

1. A signed and dated written informed consent form prior to the conduct of any study procedures
2. Males and females between ≥ 18 and ≤ 60 years old.
3. Non-smoker for at least 1 year prior to Visit 1, with a smoking history of no more than 10 pack-years (e.g., 1 pack [20 cigarettes] per day for 10 years).

6.Ability to understand and comply with the protocol requirements (including completion of daily PEFR, PFT and ACQ), instructions and protocol-stated restrictions.

7.Women of child-bearing potential (WOCBP) must have a negative pregnancy test at the screening visit. WOCBP include: any female who has experienced menarche and is not post-menopausal (defined as amenorrhea for at least 12 consecutive months), or has not undergone surgical sterilization (hysterectomy, bilateral oophorectomy, or bilateral tubal ligation). Women who are using acceptable contraceptive medications or devices to prevent pregnancy or practicing abstinence or where partner is sterile (e.g., vasectomy) will be considered WOCBP.

WOCBP must agree to avoid becoming pregnant for the duration of the study by using adequate contraception at study entry and throughout the trial. Examples of adequate contraception include the following:

• Norplant

• Medroxyprogesterone acetate injection

• Oral contraception

• Double-barrier method (e.g., condom and spermicide)

• Abstinence, with one of the above WOCBP will be advised to notify the Investigator of any changes in their pregnancy status or any change in contraceptive use.

  8.Agreement by subject to abide by the study protocol and its restrictions.

Exclusion Criteria

1. Past or present disease, excluding asthma, which as judged by the investigator, may place the subject at increased risk of complications, interfere with study participation, or confound any of the study objectives These diseases include, but are not limited to cardiovascular disease, malignancy, gastrointestinal disease, hepatic disease, diabetes type I or uncontrolled diabetes, type II, renal disease, haematological disease, neurological disease, endocrine disease or pulmonary disease (including, but not confined to chronic bronchitis, emphysema, bronchiectasis, COPD, eosinophilic bronchitis or pulmonary fibrosis).
2. An upper or lower respiratory tract infection within 4 weeks of Visit 1 and prior to Visit 2
3. A history of hypersensitivity to the study drug or its components, including albuterol as rescue medication.
4. History of illegal drug or alcohol abuse within the past 5 years.
5. Pregnant or lactating women.
6. Use of > 8 inhalations per day of SABA on any two consecutive days from screening to randomization (Visits 1 and 2).
7. Use of an investigational drug or device within 30 days prior to screening

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Fluticasone Propionate (FP) - Arm 5	Fluticasone Propionate (FP)	FP BID
Placebo - Arm 6	Fluticasone Propionate (FP)	Placebo inhalation solution
Fluticasone Propionate (FP) - arm 1	Fluticasone Propionate (FP)	FP BID (twice daily)
Fluticasone Propionate (FP) - arm 3	Fluticasone Propionate (FP)	FP BID
FLuticasone Propionate (FP) - Arm 4	Fluticasone Propionate (FP)	FP BID
Fluticasone propionate (FP) - arm 2	Fluticasone Propionate (FP)	FP BID

Primary Outcome Measures

Name	Time	Method
FEV1 (Forced Expiry Volume in 1 second)	FEV1 at Week 12

Secondary Outcome Measures

Name	Time	Method
Peak Expiratory Flow Rate (PEFR)	PEFR at Week 12

Trial Locations

Locations (1)

CU Pharmaceutical Research; 🇺🇸 Rock Hill, South Carolina, United States