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. 2015 Jul 24;10:1427–1442. doi: 10.2147/COPD.S83758

Table 1.

New pharmacotherapies in COPD management

Agency approval Indication GOLD grade Efficacy
Safety and adverse effects General remarks
FEV1 improvement Exercise Exacerbations Health status and symptoms
New LAMA monotherapy
Aclidinium US, EU GOLD B, C, D ++ ++ ++ ++ Bronchospasm, nasopharingitis (6%), headache (5%), dry mouth (<2%) Faster onset of action to tiotropium, better nighttime FEV1, BID dosing
Glycopyrronium EU GOLD B, C, D +++ ++ ++ ++ Antimuscarinic and cardiac side effects similar to placebo Rapid onset, very good safety profile
Umeclidinium US, EU GOLD B, C, D ++ ++, ++, ++, Minimal antimuscarinic side effects Combined with vilanterol
New LABA monotherapy
Indacaterol US, EU GOLD B, C, D +++ ++ ++ ++ Cough (6.5%), headache (5.1%), nausea (2.4%) Improved cardiovascular safety profile and lung function compared to salmeterol
Vilanterol US, EU GOLD B, C, D ++ ++, ++, ++ Nasopharingitis (10%), headache (9%), dry mouth (< 10%)
Olodaterol US GOLD B, C, D ++ ++ ++ Nasopharyngitis (11%), dizziness (>2%), rash (>2%), arthralgia (>2%)
Abediterol +++ Better lung function impact in comparison to indacaterol
New LAMA-LABA combination therapy
Umeclidinium and vilanterol US, EU GOLD C, D +++ ++ ++ No increase in adverse events compared to placebo First LAMA-LABA approved by the US FDA for maintenance treatment
Glycopyrronium and indacaterol EU GOLD C, D +++ +++ +++ No increase in adverse events compared to tiotropium or glycopyrronium alone Significantly better FEV1 and SGRQ compared to tiotropium and glycopyrronium alone
Tiotropium and olodaterol GOLD C, D +++ + +++ No significant difference in adverse events compared to monocomponents Significant improvement in SGRQ score was only seen in the 5/5 μg dosing
Aclidinium and formoterol EU GOLD C, D +++ −/++ Nasopharingitis (7.8%), headache (7.5%) Significant improvement in FEV1 1-hour postdosing compared to monocomponents
Glycopyrrolate and formoterol GOLD C, D +++ Improvement in FEV1 from 0 hours to 12 hours versus monotherapy with glycopyrrolate, formoterol, or tiotropium
New LABA-ICS combination therapies
Vilanterol and fluticasone US, EU GOLD C, D + +++ Compared to vilanterol alone, FDC leads to an increased risk of pneumonia Once-daily FDC of LABA-ICS
Indacaterol and mometasone GOLD C, D ++
Formoterol and ciclesonide GOLD C, D ++ ++ Oral candidiasis was the most common adverse event Noninferiority comparison to combined fluticasone propionate/salmeterol in asthma
Formoterol and fluticasone EU, Japan GOLD C, D +++ Approved for asthma, but in Phase III clinical trials for moderate to severe COPD More rapid bronchodilator effect than fluticasone propionate/salmeterol
Triple LABA-LAMA-ICS therapy GOLD C, D ++ ++ No significant difference in adverse events compared to dual or monocomponents A 40% reduction in mortality compared with ICS/LABA in a retrospective analysis
Dual muscarinic antagonist-β2-agonists ++a Transient hypokalemic effect in 3/41 patients receiving additional high-dose salbutamol GSK961081 has demonstrated effective bronchoprotection in early trials
Oral medications
Roflumilast US, EU GOLD C, D ++a ++ Weight loss, nausea, diarrhea, and psychiatric symptoms Recommended use only in advanced COPD as an add-on therapy
Azithromycin US, EU GOLD C, D ++ QT interval prolongation, ototoxicity, and drug-drug interactions Careful risk-benefit assessment given the side-effect profile
Moxifloxacin US, EU GOLD C, D ++ −/++ Significant Gl side effects compared to the placebo group Intermittent pulsed therapy with 5 days of moxifloxacin every 8 weeks for six courses
Simvastatin US, EU GOLD C, D No significant difference in fatal or nonfatal adverse events No significant difference in exacerbations in one randomized, placebo-controlled trial

Notes: No improvement in the published literature; +nonsignificant improvement; ++significantly improved compared to placebo; +++significantly improved to other drugs of the same class;

in combination therapy;

a

improved FEV1 from baseline.

Abbreviations: GOLD, Global Initiative for Chronic Obstructive Lung Disease; LAMA, long-acting muscarinic antagonist; US, United States; EU, European Union; BID, twice daily; LABA, long-acting β-2 sympathomimetic agonist; FDA, Food and Drug Administration; FEV1, forced expiratory volume in I second; SGRQ, St George’s Respiratory Questionnaire; ICS, inhaled corticosteroid; FDC, fixed-dose combination; Gl, gastrointestinal.