Home » Drug Information » Recently Approved Drugs » 2001
Medical Areas: Pulmonary/Respiratory Diseases
Drug Information
The following information is obtained from various newswires, published
medical journal articles, and medical conference presentations.
Company: GlaxoSmithKline
Approval Status: Approved April 2001
Treatment Area: Asthma
Ventolin HFA has been approved for the treatment or prevention
of bronchospasm in adults and children four years of age and older
with reversible obstructive airway disease, and for the prevention
of exercise-induced bronchospasm in patients four years of age and
older. Ventolin HFA is a new version of the Ventolin metered-dose
inhaler (MDI) currently marketed by GlaxoSmithKline. However unlike
the current version, the new inhaler does not use
chlorofluorocarbons (CFCs) to propel the medication. Ventolin HFA
uses an alternative propellant called HFA or hydrofluoroalkane.
CFCs have been implicated in the depletion of the ozone layer,
and as a result, the use of CFC-aerosol products in the United
States has been sharply curtailed over the last few decades. While
CFC production and importation have been banned for all commercial
purposes in the United States since 1996, an exception is made for
medical products that are considered essential with no suitable
alternatives. While no action to remove the albuterol CFC MDIs from
the market is planned at this time, the approval of Ventolin HFA
provides an additional albuterol HFA MDI option to patients and
physicians.
A 12-week, randomized, double-blind trial compared Ventolin HFA
to CFC 11/12-propelled albuterol and an HFA-134a placebo inhaler.
The trial included adolescent and adult subjects (12-76 years of
age) with mild to moderate asthma. Serial forced expiratory volume
in one second (FEV1) measurements showed that two inhalations of
Ventolin HFA produced a significantly greater improvement in FEV1
over the pretreatment value than placebo.
A second 12-week, randomized, double-blind trial evaluated the
effectiveness of switching subjects from CFC 11/12-propelled
albuterol to Ventolin HFA. In an initial run-in phase, all subjects
received CFC 11/12-propelled albuterol. During the double-blind
treatment phase, Ventolin HFA was compared to CFC 11/12-propelled
albuterol and an HFA-134a placebo inhaler in adolescent and adult
subjects with mild to moderate asthma. Serial FEV1 measurements
showed that two inhalations of Ventolin HFA produced significantly
greater improvement in pulmonary function than placebo. The
switching from CFC 11/12-propelled albuterol inhaler to Ventolin
HFA did not reveal any clinically significant changes in the
efficacy profile.
Additionally, a two-week, randomized, double-blind trial was
conducted to compare Ventolin HFA, CFC 11/12-propelled albuterol,
and an HFA-134a placebo inhaler in 135 pediatric subjects (4-11
years old) with mild to moderate asthma. Serial pulmonary function
measurements showed that two inhalations of Ventolin HFA produced
significantly greater improvement in pulmonary function than
placebo, and that there were no significant differences between the
groups treated with Ventolin HFA and CFC 11/12-propelled
albuterol.
A controlled trial in adult subjects with asthma showed that two
inhalations of Ventolin HFA taken approximately 30 minutes prior to
exercise significantly prevented exercise-induced bronchospasm
compared to an HFA-134a placebo inhaler. In addition, Ventolin HFA
was shown to be clinically comparable to a CFC 11/12-propelled
albuterol inhaler for this indication. (from Ventolin HFA Product
Information)
Adverse events reported from clinical trials include (but are
not limited to) the following:
- Throat irritation
- Upper respiratory inflammation
- Viral respiratory infections
- Cough
- Musculoskeletal pain
Overall, the adverse events were similar between Ventolin HFA
and a CFC 11/12-propelled albuterol inhaler. Additionally,
according to the results of a two-week pediatric trial, the
pediatric adverse event profile was generally similar to that of
the adult.
In vitro studies and in vivo pharmacologic studies have
demonstrated that albuterol has a preferential effect on
beta2-adrenergic receptors compared to isoproterenol.
Activation of beta2-adrenergic receptors on airway
smooth muscle leads to the activation of adenylcyclase, and to an
increase in the intracellular concentration of
cyclic-3',5'-adenosine monophosphate (cyclic AMP). This
increase of cyclic AMP leads to the activation of protein kinase A,
which inhibits the phosphorylation of myosin and lowers
intracellular ionic calcium concentrations, resulting in
relaxation. Albuterol relaxes the smooth muscles of all airways,
from the trachea to the terminal bonchioles. Albuterol acts as a
functional antagonist to relax the airway irrespective of the
spasmogen involved, thus protecting against all bronchoconstrictor
challenges. (from Ventolin HFA Product Information)
Please visit the company web site for additional information on
GlaxoSmithKline
products.
If you would like more information on asthma and other
respiratory diseases, please visit the
American Lung
Association.