Compare Captisol-Enabled (CE) Budesonide + Azelastine Nasal Solution and Rhinocort Aqua + Astelin in an Environmental Exposure Chamber (EEC) Study of Allergic Rhinitis

NCT ID: NCT00940953

Last Updated: 2012-10-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 108 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-02-29
• Study Completion Date: 2008-05-31

Brief Summary

The primary objective of this study was to compare Placebo to Captisol-Enabled Budesonide + Azelastine in a single spray and two separate sprays (Budesonide + Azelastine) in patients with Seasonal Allergic Rhinitis exposed to controlled ragweed pollen.

Conditions

Seasonal Allergic Rhinitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Captisol-Enabled Budesonide + Azelastine

Group Type: EXPERIMENTAL

Budesonide + Azelastine

Intervention Type: DRUG

nasal spray, one spray per nostril at time 0 plus one spray Placebo

Rhinocort Aqua+Astelin

Group Type: ACTIVE_COMPARATOR

Budesonide + Azelastine

Intervention Type: DRUG

nasal spray, one spray of each per nostril at time 0

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

nasal spray, one spray per nostril from each of 2 bottles at time 0

Interventions

Budesonide + Azelastine

nasal spray, one spray per nostril at time 0 plus one spray Placebo

Intervention Type: DRUG

Budesonide + Azelastine

nasal spray, one spray of each per nostril at time 0

Intervention Type: DRUG

Placebo

nasal spray, one spray per nostril from each of 2 bottles at time 0

Intervention Type: DRUG

Other Intervention Names

CDX-313; Captisol; Rhinocort Aqua; Astelin; phosphate buffered saline solution

Eligibility Criteria

Inclusion Criteria

• Patients must have a clinical history of SAR
• Adults (males and females) aged 18 to 65
• Patients must have documentation of a positive skin test within 12 months of screening to ragweed allergen defined by a positive case history and a positive skin prick and/or intradermal test for ragweed allergen.
• Non-pregnant, non-lactating females, or women who are post-menopausal or are naturally or surgically sterile
• Females of childbearing potential must have a confirmed absence of pregnancy according to a negative urine pregnancy test and must be using acceptable birth control methods
• In generally good health on the basis of medical history and physical examination.
• Willingness to attend all study visits.
• Capable of following and understanding instructions.
• Willing and able to provide written informed consent prior to initiation of any study procedures, including initiation of washout of any concomitant medications

Exclusion Criteria

• Pregnancy, nursing, or plans to become pregnant or donate gametes (ova or sperm) for in-vitro fertilization
• Have clinically significant physical findings of nasal anatomical deformities causing greater than 50% obstruction based on the clinical estimate of the investigator, including nasal polyps, septal defects or other clinically significant respiratory tract malformations, recent nasal biopsy, nasal trauma, or surgery and atrophic rhinitis or rhinitis medicamentosa
• Previous participation in a budesonide study within 1 month prior to the Screening Visit.
• Currently participating in a clinical trial or has been exposed to an investigational treatment within the 30 days prior to the Screening Visit.
• A known hypersensitivity to any corticosteroid or any of the excipients in the formulation of the investigational drug (e.g., any adverse experience with budesonide, azelastine or the Captisol-containing products Vfend IV or Geodon IM).
• History of severe respiratory infection or disorder
• History of alcohol or drug abuse
• History of a positive test for HIV, hepatitis B or hepatitis C.
• Use of any of the prohibited medications within the identified exclusion periods
• Use of antibiotic therapy for acute conditions
• Initiation of immunotherapy or dose escalation during the study period.
• Non-vaccinated exposure to or active infection with chickenpox or measles within the 21 days preceding the Screening Visit.
• Exposure to systemic corticosteroids
• Use of topical corticosteroids in concentrations in excess of 1% hydrocortisone or equivalent
• History of epilepsy or seizures
• History of coronary heart disease, uncontrolled hypertension, or other clinically significant cardiovascular disease.
• Have any of the following conditions that are judged by the investigator to be clinically significant and/or affect the patient's ability to participate in the clinical trial:

• Impaired hepatic function including alcohol related liver disease or cirrhosis
• History of ocular disturbances (e.g., glaucoma or posterior subcapsular cataracts)
• Any systemic infection
• Hematological, renal, endocrine (except for controlled diabetes mellitis or postmenopausal symptoms or hypothyroidism)
• Gastrointestinal disease
• Malignancy (excluding basal cell carcinoma)
• A current neuropsychiatric condition with or without drug therapy

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Ligand Pharmaceuticals

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Deepen Patel, MD

Role: PRINCIPAL_INVESTIGATOR

Allied Research International - Cetero Research

Locations

Allied Research International - Cetero Research

Mississauga, Ontario, Canada

Countries

Canada

Other Identifiers

P2DS07001

Identifier Type: -

Identifier Source: secondary_id

CDX313CT001

Identifier Type: -

Identifier Source: org_study_id