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Phenylephrine modified-release
tablets for nasal congestion: A
randomized, placebo-controlled
trial in allergic rhinitis patients
Eli O. Meltzer MD, Paul H. Ratner MD
MBA, and Thomas McGraw PhD
Background
• Ephedrine and pseudoephedrine
decongestants can be converted into
methamphetamine.
• Phenylephrine (PE) is not used in
methamphetamine manufacture.
• Pseudoephedrine medications were moved
behind the counter (BTC) which may be a
deterrent to legitimate access.
• Work began on a 12-hour 30 mg bid modified
release PE to avoid BTC and oral PE 10 mg
immediate release 4-hour dosing
inconvenience.
Background
• The study formulation was evaluated in several
bioequivalence studies comparing a single dose of
30 mg 12 Hour modified-release PE tablet to three
10 mg Immediate Release PE tablets each
consecutively dosed four hours apart.
• The systemic drug levels (AUC) were higher (ratio
about 160%), whereas peak levels (Cmax) were
similar (ratio about 98%) when modified and
immediate release dosage forms were compared
(Merck & Co, Inc., data on file).
• Therefore, it can be assumed that the efficacy of
three10 mg doses every 4-hours would be similar
to one 30 mg dose over a 12-hour period.
Major Inclusion Criteria
• Documented or self-reported history of fall
pollen allergic rhinitis.
• Documented skin test reaction to fall pollen
allergens.
• Signs and symptoms of nasal congestion.
Major Exclusion Criteria
• Significant medical condition.
• Started allergen immunotherapy within 1
month of enrollment, or anticipates
immunotherapy dose change during the trial.
• Documented evidence of acute or significant
chronic sinusitis.
• Clinically significant nasal disorders.
• Asthma except mild intermittent asthma.
• Systemic, topical (>1% hydrocortisone), or
nasal corticosteroids use in the last 30 days.
Study Design
RQLQ: Rhinoconjunctivitis Quality of Life Questionnaire;
PEH-MR: modified-release phenylephrine HCL
Primary Endpoint
• Mean change from baseline in daily reflective
congestion score over the entire treatment period.
• Subject symptom assessment recorded twice
daily:
– Reflective: severity over the preceding 12 hrs.
– Instantaneous: severity right now (secondary
endpoint).
• Subjects rated congestion on a 4-point scale of
severity (0= no symptoms, 1= mild, 2= moderate
3= severe).
Patient Disposition
PEH-MR: modified-release phenylephrine hydrochloride.
Mean change from baseline in
reflective nasal congestion score
There was no statistical difference between treatment groups.
Discussion
• Questions raised about PE efficacy
resulted in a 2007 FDA Advisory
Committee Meeting that concluded further
efficacy data is required.
• PE was not significantly different from
placebo for the relief on nasal congestion
in allergen challenge chamber trials that
concluded pseudoephedrine (Horak 2009),
or a combination of loratadine-montelukast
(Day 2009) were effective.
Discussion
• PE was not significantly different from
placebo in a dose-ranging study of 10 to
40 mg doses administered every 4 hours
for 7 days in patients with nasal
congestion caused by allergic rhinitis
(Meltzer 2015).
• The results of this study provide evidence
that an oral dose of 30 mg PE does not
relieve nasal congestion.
Selected References
• Hendeles L., Hatton R. C. Oral phenylephrine: an ineffective replacement for
pseudoephedrine? J Allergy Clin Immunol 2006; 118: 279–80.
• Eccles R. Substitution of phenylephrine for pseudoephedrine as a nasal
decongeststant. An illogical way to control methamphetamine abuse. Br J Clin
Pharmacol 2007; 63: 10–14.
• Hatton R. C., et al. Efficacy and safety of oral phenylephrine: systematic review and
meta-analysis. Ann Pharmacother 2007; 41: 381–90.
• Horak F., et al. A placebo-controlled study of the nasal decongestant effect of
phenylephrine and pseudoephedrine in the Vienna Challenge Chamber. Ann
Allergy Asthma Immunol. 2009;102:116–120.
• Day J. H., et al. Efficacy of loratadine-montelukast on nasal congestion in patients
with seasonal allergic rhinitis in an environmental exposure unit. Ann Allergy
Asthma Immunol. 2009;102:328–338.
• Meltzer E.O., Ratner P.H., McGraw T. Oral Phenylephrine HCl for Nasal Congestion
in Seasonal Allergic Rhinitis: A Randomized, Open-label, Placebo-controlled Study.
The Journal of Allergy and Clinical Immunology: In Practice 2015; 3: 702-708, ISSN
2213-2198, http://dx.doi.org/10.1016/j.jaip.2015.05.007.

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PE modified-release tablets for nasal congestion

  • 1. Phenylephrine modified-release tablets for nasal congestion: A randomized, placebo-controlled trial in allergic rhinitis patients Eli O. Meltzer MD, Paul H. Ratner MD MBA, and Thomas McGraw PhD
  • 2. Background • Ephedrine and pseudoephedrine decongestants can be converted into methamphetamine. • Phenylephrine (PE) is not used in methamphetamine manufacture. • Pseudoephedrine medications were moved behind the counter (BTC) which may be a deterrent to legitimate access. • Work began on a 12-hour 30 mg bid modified release PE to avoid BTC and oral PE 10 mg immediate release 4-hour dosing inconvenience.
  • 3. Background • The study formulation was evaluated in several bioequivalence studies comparing a single dose of 30 mg 12 Hour modified-release PE tablet to three 10 mg Immediate Release PE tablets each consecutively dosed four hours apart. • The systemic drug levels (AUC) were higher (ratio about 160%), whereas peak levels (Cmax) were similar (ratio about 98%) when modified and immediate release dosage forms were compared (Merck & Co, Inc., data on file). • Therefore, it can be assumed that the efficacy of three10 mg doses every 4-hours would be similar to one 30 mg dose over a 12-hour period.
  • 4. Major Inclusion Criteria • Documented or self-reported history of fall pollen allergic rhinitis. • Documented skin test reaction to fall pollen allergens. • Signs and symptoms of nasal congestion.
  • 5. Major Exclusion Criteria • Significant medical condition. • Started allergen immunotherapy within 1 month of enrollment, or anticipates immunotherapy dose change during the trial. • Documented evidence of acute or significant chronic sinusitis. • Clinically significant nasal disorders. • Asthma except mild intermittent asthma. • Systemic, topical (>1% hydrocortisone), or nasal corticosteroids use in the last 30 days.
  • 6. Study Design RQLQ: Rhinoconjunctivitis Quality of Life Questionnaire; PEH-MR: modified-release phenylephrine HCL
  • 7. Primary Endpoint • Mean change from baseline in daily reflective congestion score over the entire treatment period. • Subject symptom assessment recorded twice daily: – Reflective: severity over the preceding 12 hrs. – Instantaneous: severity right now (secondary endpoint). • Subjects rated congestion on a 4-point scale of severity (0= no symptoms, 1= mild, 2= moderate 3= severe).
  • 8. Patient Disposition PEH-MR: modified-release phenylephrine hydrochloride.
  • 9. Mean change from baseline in reflective nasal congestion score There was no statistical difference between treatment groups.
  • 10. Discussion • Questions raised about PE efficacy resulted in a 2007 FDA Advisory Committee Meeting that concluded further efficacy data is required. • PE was not significantly different from placebo for the relief on nasal congestion in allergen challenge chamber trials that concluded pseudoephedrine (Horak 2009), or a combination of loratadine-montelukast (Day 2009) were effective.
  • 11. Discussion • PE was not significantly different from placebo in a dose-ranging study of 10 to 40 mg doses administered every 4 hours for 7 days in patients with nasal congestion caused by allergic rhinitis (Meltzer 2015). • The results of this study provide evidence that an oral dose of 30 mg PE does not relieve nasal congestion.
  • 12. Selected References • Hendeles L., Hatton R. C. Oral phenylephrine: an ineffective replacement for pseudoephedrine? J Allergy Clin Immunol 2006; 118: 279–80. • Eccles R. Substitution of phenylephrine for pseudoephedrine as a nasal decongeststant. An illogical way to control methamphetamine abuse. Br J Clin Pharmacol 2007; 63: 10–14. • Hatton R. C., et al. Efficacy and safety of oral phenylephrine: systematic review and meta-analysis. Ann Pharmacother 2007; 41: 381–90. • Horak F., et al. A placebo-controlled study of the nasal decongestant effect of phenylephrine and pseudoephedrine in the Vienna Challenge Chamber. Ann Allergy Asthma Immunol. 2009;102:116–120. • Day J. H., et al. Efficacy of loratadine-montelukast on nasal congestion in patients with seasonal allergic rhinitis in an environmental exposure unit. Ann Allergy Asthma Immunol. 2009;102:328–338. • Meltzer E.O., Ratner P.H., McGraw T. Oral Phenylephrine HCl for Nasal Congestion in Seasonal Allergic Rhinitis: A Randomized, Open-label, Placebo-controlled Study. The Journal of Allergy and Clinical Immunology: In Practice 2015; 3: 702-708, ISSN 2213-2198, http://dx.doi.org/10.1016/j.jaip.2015.05.007.