Last updated: 11/07/2018 19:17:27
A 12-month, open-label trial to assess the long-term safety of salmeterol 50 mg bid via the DISKUS in adolescent and adult patients with asthma.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A 12-month, open-label trial to assess the long-term safety of salmeterol 50 mg bid via the DISKUS in adolescent and adult patients with asthma.
Trial description: A 12-month, open-label trial to assess the long-term safety of salmeterol 50 mg bid via the DISKUS in adolescent and adult patients with asthma.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Mitchell DQ, Montealegre F, Lawrence M, Manning M, Scott C, Wang Y, et al. Adherence with twice-daily peak expiratory flow (PEF) monitoring via Airwatch and treatment with Serevent Diskus in mild-to-moderate persistent asthma for 1 year. AM. J. RESPIR. CRIT. CARE MED. 1998; 157(3):A636.
Noveck RJ, Dvorin D, Kernerman S, Flescher J, Scott C, Wang Y, et al. Response to nebulized ventolin in asthmatic patients treated with Serevent diskus twice-daily for 1 year. AM. J. RESPIR. CRIT. CARE MED. 1998; 157(3):A400.
White M, Given J, Grady J, Manning M, Montealegre F, Scott C, Wang Y, Stahl E. Socioeconomic status and ethnicity as factors in asthma in adolescents and adults. J Allergy Clin Immunol.1998: A18371.
Medical condition
Asthma
Product
salmeterol
Collaborators
Not applicable
Study date(s)
May 1995 to October 1996
Type
Not applicable
Phase
3
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1996-31-10
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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