Colobreathe - Product Information
|Manufacture:||Forest Laboratories, Inc.|
|Condition:||Gram Negative Infection|
Name of the Medicinal Product
Colobreathe 1,662,500 IU inhalation powder, hard capsules
Qualitative and Quantitative Composition
Each capsule contains 1,662,500 IU, which is approximately equal to 125 mg of colistimethate sodium.
For the list of excipients, see section List of Excipients.
Inhalation powder, hard capsule (inhalation powder)
Hard transparent gelatin capsules containing a fine white powder.
Colobreathe is indicated for the management of chronic pulmonary infections due to Pseudomonas aeruginosa in patients with cystic fibrosis (CF) aged 6 years and older (see section Pharmacodynamic Properties).
Consideration should be given to official guidance on the appropriate use of antibacterial agents.
Posology and Method of Administration
To ensure proper administration of the drug, the patient should be shown how to use the inhaler by a physician or other health professional, with the first dose being given under medical supervision.
The efficacy of Colobreathe has been demonstrated in a study of 24-weeks duration. Treatment may be continued for as long as the physician considers that the patient is obtaining clinical benefit.
One capsule to be inhaled twice daily.
The dose interval should be as close as possible to 12 hours.
Children of 6 years of age and older
The same dose recommendations as for adults apply to children of 6 years of age and older.
Children below 6 years of age
The safety and efficacy of Colobreathe in children under 6 years of age has not been established. No data are available.
No dose adjustment is considered to be necessary (see section Pharmacokinetic Properties).
No dose adjustment is considered to be necessary (See section Pharmacokinetic Properties).
Method of Administration
For inhalation use only.
Colobreathe capsules are to be used only with the Turbospin powder inhaler.
If other treatments are being taken, they should be taken in the following order:
Other inhaled medicinal products
Hypersensitivity to the active substance, colistin sulphate or polymyxin B.
Special Warnings and Precautions for Use
Bronchospasm and Coughing
Bronchospasm or coughing may occur on inhalation. These reactions usually disappear or significantly diminish with continued use and may be ameliorated by appropriate treatment with beta2-agonists prior to or following dry powder colistimethate inhalation. If bronchospasm or coughing remain problematic, withdrawal of treatment should be considered.
Haemoptysis is a complication in cystic fibrosis and is more frequent in adults. The use of Colobreathe in patients with clinically significant haemoptysis should be undertaken or continued only if the benefits of treatment are considered to outweigh the risks of inducing further haemorrhage.
Acute Respiratory Wxacerbation
If acute respiratory exacerbations develop additional intravenous or oral antibacterial agent therapy should be considered.
Oral Fungal Super-Infection
After each inhalation of Colobreathe, the mouth should be rinsed with water. The rinse should not be swallowed. Rinsing may reduce the risk of developing oral fungal super-infection during treatment and may also reduce the unpleasant taste associated with colistimethate sodium.
There is very low transpulmonary absorption of colistimethate after inhalation of Colobreathe (see section Pharmacokinetic Properties). Care should still be taken in administering Colobreathe to patients who are known to have a propensity for nephrotoxic or neurotoxic events.
Caution should be taken with concomitant use of Colobreathe and parenteral or nebulised colistimethate sodium.
Caution should be taken with concomitant use of colistimethate sodium and potential nephrotoxic or neurotoxic agents, including non-depolarising muscle relaxants (see section Interaction with Other Medicinal Products and Other Forms of Interaction).
Colobreathe should be used with extreme caution in patients with myasthenia gravis because of potential for drug induced neuromuscular blockade.
Colistimethate sodium should be used with extreme caution in patients with porphyria.
Safety and efficacy have been assessed in controlled studies for up to 24 weeks. Colobreathe has only been evaluated in patients with FEV1 (% predicted) values between 25% and 75% and with no evidence of an acute exacerbation on study entry. (see section Pharmacodynamic Properties).
Interaction with Other Medicinal Products and Other Forms of Interaction
There is no experience of using Colobreathe concurrently with other inhaled antibacterial agents.
Caution should be taken with concomitant use with other formulations of colistimethate as there is little experience and there is a possibility of summative toxicity.
No in-vivo interaction studies have been performed.
Colistimethate sodium and colistin have been investigated in vitro to determine the effects on the expression of cytochrome P450 (CYP) enzymes on treating primary cultures of fresh human hepatocytes. Treatment with colistimethate sodium or colistin did not induce the activity of any enzyme tested (CYP1A2, 2B6, 2C8, 2C9, 2C19 and 3A4/5).
Concomitant use of inhaled colistimethate sodium with other medications that are potentially nephrotoxic or neurotoxic, such as aminoglycosides, or neuromuscular blocking products, such as curariform agents should be undertaken with caution.
Co-treatment with colistimethate sodium and macrolides such as azithromycin and clarithromycin, or fluoroquinolones such as norfloxacin and ciprofloxacin should be undertaken with caution in patients with myasthenia gravis (see section
Fertility, Pregnancy and Lactation
There are no adequate data from the use of inhaled colistimethate sodium in pregnant women. Studies in animals using parenteral administration have shown reproductive toxicity (see section Preclinical Safety Data). Single dose intravenous studies in human pregnancy show that colistimethate sodium crosses the placenta and consequently there is potential for fetal toxicity if administered during pregnancy. Colistimethate sodium should be used in pregnancy only if the benefit to the mother outweighs the potential risk to the fetus.
Absorbed colistimethate sodium may be secreted in breast milk. A decision on whether to continue/discontinue breastfeeding or to continue/discontinue therapy with colistimethate sodium should be made taking into account the benefit of breastfeeding to the child balanced against the benefit of colistimethate therapy to the woman.
Colistimethate sodium has no notable effects on fertility in male or female rats or mice.
Effects on Ability to Drive and Use Machines
No studies on the effects of the ability to drive or use machines have been performed. However, based on the safety profile of colistimethate sodium, neurotoxity may occur with the possibility of dizziness, confusion or visual disturbances. Patients should be warned not to drive or operate machines if this occurs.
Summary of the Safety Profile
The safety of Colobreathe has been assessed in a total of 237 subjects (225 cystic fibrosis patients and 12 healthy volunteers). Of these, 187 patients aged 6 years and above were exposed to Colobreathe one capsule twice daily in a 24-week, phase 3 comparative study. There were 32 patients aged 6-12 years, 41 patients aged 13-17 years and 114 patients aged 18 years and older. The most commonly reported adverse reactions as a percent of all Colobreathe treated patients were: unpleasant taste (62%), cough (59.4%), throat irritation (43.9%), dyspnoea (16.6%) and dysphonia (10.7%). Inhalation may induce coughing or bronchospasm which may be controlled by pre-treatment with inhaled beta2 agonists.
Sore throat or mouth has been reported with nebulised colistimethate sodium and may occur with Colobreathe. This may be related to Candida albicans infection or hypersensitivity. Skin rash may also indicate hypersensitivity and if this occurs treatment should be withdrawn.
Tabulated List of Adverse Reactions
In the 24 week clinical study, the following adverse reactions were observed across all ages.
Frequencies are defined as: very common (≥1/10), common (≥1/100 to <1/10), uncommon (≥1/1,000 to <1/100), rare ((≥1/10,000 to <1/1,000), very rare <1/10,000), not known (cannot be estimated from the available data). Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness.
|Shstem Organ Class||Very Common||Common||Uncommon|
|Immune system disorders||Drug hypersensitivity|
|Metabolism and nutrition disorders||Weight fluctuation, decreased appetite|
|Nervous system disorders||Balance disorder, headache||Convulsions, somnolence|
|Ear and labyrinth disorders||Tinnitus||Ear congestion|
|Respiratory, thoracic and mediastinal disorders||Dyspnoea, cough, dysphonia, throat irritation||Haemoptysis, bronchospasm, asthma, wheezing, chest discomfort, lower respiratory tract infection, productive cough, crackles lung||Chest pain, dyspnoea exacerbated, pharyngolaryngeal pain, epistaxis, sputum purulent, abnormal chest sound, increased upper airway secretion|
|Gastrointestinal disorders||Dysgeusia||Vomiting, nausea||Diarrhoea, toothache, salivary hypersecretion, flatulence|
|Musculoskeletal and connective tissue disorders||Arthralgia|
|Renal and urinary disorders||Proteinuria|
|General disorders and administration site conditions||Pyrexia, asthenia, fatigue||Thirst|
|Investigations||Forced expiratory volume decreased|
|Injury, poisoning and procedural complications||Medication error|
In the 24-week clinical study, where Colobreathe was administered twice daily to adults and children aged 6-17, the adverse reactions identified in the paediatric population were similar to that for the overall population. The most commonly reported adverse reactions as a percent of Colobreathe treated patients were: cough (55%), unpleasant taste (51%), throat irritation (34%), dyspnoea (10%) and dysphonia (10%).
Reporting of Suspected Adverse Reactions
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.
Currently there is no experience of overdose with the use of Colobreathe. However, overdose may possibly result in higher systemic exposure.
Overdose is unlikely by the inhaled route but has been recognised after systemic use. More common signs and symptoms of intravenous overdose include unsteadiness, paraesthesia and dizziness. It can also result in neuromuscular blockade that can lead to muscular weakness, apnoea and possible respiratory arrest. Overdose can also cause acute renal failure characterised by decreased urine output and increased serum concentrations of BUN and creatinine.
There is no specific antidote, manage by supportive treatment. Measures to increase the rate of elimination of colistimethate sodium e.g. mannitol diuresis, prolonged haemodialysis or peritoneal dialysis may be tried, but effectiveness is unknown.
Pharmacotherapeutic group: antibacterials for systemic use, other antibacterials.
ATC Code: J01XB01
Mechanism of Action
Colistimethate sodium (CMS) is a cyclic polypeptide antibacterial agent that is derived from Bacillus polymyxa var. colistinus and belongs to the polymyxin group. Polymyxins work by damaging the cell membrane and the resulting physiological effects are lethal to the bacterium. Polymyxins are selective for Gram-negative bacteria that have a hydrophobic outer membrane.
Resistant bacteria are characterised by modification of the phosphate groups of lipopolysaccharide, which become substituted with ethanolamine or aminoarabinose. Naturally resistant Gram-negative bacteria, such as Proteus mirabilis andBurkholderia cepacia, show complete substitution of their lipid phosphate by ethanolamine or aminoarabinose.
Cross resistance between colistimethate sodium and polymyxin B is expected. Since the mechanism of action of the polymyxins is different from that of other antibacterial agents, resistance to colistin and polymyxin by the above mechanism alone would not be expected to result in resistance to other drug classes.
The epidemiological cut off value for colistimethate sodium for Pseudomonas aeruginosa, distinguishing the wild type population from isolates with acquired resistance traits, is 4 mg/l.
The Phase 3 clinical study was a randomised, open-label active comparator study comparing the efficacy of colistimethate sodium 1,662,500 IU dry powder for inhalation to tobramycin nebuliser solution for inhalation, 300 mg/5 ml, in 380 subjects with documented cystic fibrosis complicated by chronic pulmonary infection with Pseudomonas aeruginosa. The subjects were aged 6 years and above and had an FEV1% predicted of 25-75%. All subjects were also required to have successfully completed a minimum of two cycles of nebulised tobramycin solution run-in prior to randomisation. Subjects were randomised to receive either one 1,662,500 IU capsule of colistimethate sodium twice daily, or 300 mg of tobramycin, twice daily. It should be noted that treatment was not interrupted when patients received concomitant parenteral antibacterial agents
Efficacy was measured by the change in FEV1 % predicted compared to baseline after a 24-week treatment period.
The results of the Intent-To-Treat (ITT) population for the primary efficacy outcome are shown below:
Change in FEV1 (% predicted) from baseline at Week 24 (ITT Population)
|Adjusted Treatment difference||95% CI|
|All patients using LOCF||-0.90 (n=183)||0.35 (n=190)||-0.97||-2.74, 0.86|
|Completed patients||0.39 (n=153)||0.78 (n=171)||-0.29||-2.21, 1.71|
The data from the primary outcome parameter, change in FEV1 % predicted, are not normally distributed. The adjusted treatment difference and 95% confidence interval have been back transformed from log transformed data. The ITT population excluded patients who had been treated but demonstrated no evidence of chronic infection.
The European Medicines Agency has deferred the obligation to submit the results of studies with Colobreathe in one or more subsets of the paediatric population in Pseudomonas aeruginosa pulmonary infection/colonisation in patients with cystic fibrosis (see section Posology and Method of Administration for information on paediatric use).
Colistimethate is not significantly absorbed from the lung after inhalation of Colobreathe. After administration of 1,662, 500IU twice daily for 7 days in adult, adolescent and paediatric cystic fibrosis mean C max values of total colistimethate of up to 455ng/ml (adult mean) were observed. Tmax for total colistimethate occurred between 0.5 and 1 hour post-dose. Although the population PK analysis showed that age is a statistically significant covariate, the AUC 0-6 and dose adjusted AUC0-6(AUC 0-6 /D) for total CMS and total free colistin were similar between children and adolescents, while higher AUC 0-6 was observed in the adult group. When AUC 0-6 was adjusted by dose and body weight, a slightly higher AUC 0-6 /D/W for total CMS and total free colistin was observed in children. High PK variability was observed in all three groups. Therefore, dose adjustment in low age groups is considered not necessary.
High concentrations of total free colistin (mean 23.5mg/L) and total colistimethate (mean 178mg/L) were observed in sputum at 1 hour post-dose on Day 8 following BID dosing for 7 days across all age groups.
Absorption of colistimethate from the gastro-intestinal tract does not occur to any appreciable extent in the normal inpidual.
Protein binding is low. Polymyxins persist in the liver, kidney, brain, heart and muscle. One study in cystic fibrosis patients gives the steady-state volume of distribution as 0.09 l/kg.
Colistimethate sodium is converted to the base in vivo. As 80% of a parenteral dose can be recovered unchanged in the urine, and there is no biliary excretion, it can be assumed that the remaining drug is inactivated in the tissues. The mechanism is unknown.
A systemic absorption study showed minimal urinary excretion with less than 3% of the dose of Colobreathe excreted in the urine as colistimethate sodium and colistin. Therefore, dose adjustment in patients with renal impairment is not considered necessary. The estimated mean terminal half-lives for total CMS and total free colistin were 3.0 and 6.4 h, respectively.
Preclinical Safety Data
Nonclinical data reveal no special hazard for humans based on conventional studies of genotoxicity.
Animal studies of safety pharmacology, repeated dose toxicity or toxicity to reproduction, employing routes assuring systemic exposure, showed no particular hazard. There were no notable effects on fertility or general reproductive performance in male or female rats or mice. In embryo-fetal development studies in mice, resorptions and reduced ossification were seen, and in rats reduced fetal weights, reduced ossification and at the high dose of 10 mg colistin base per day, reduced post-natal survival. An embryo-fetal study in rabbits reported no effects at intravenous doses up to 80 mg/kg colistimethate sodium (32 mg colistin base/kg).
List of Excipients
Special Precautions for Storage
Do not store above 25°C.
Store in the primary packaging until immediately before use in order to protect from moisture.
Nature and Contents of Container
Colobreathe is available in packs containing either 8 or 56 hard capsules.
The capsules are contained in aluminium blister strips of either 8 or 14 hard capsules in each strip. The blister pack is composed of oPA/aluminium/pvc with a peelable lidding foil composed of polyester/aluminium.
Each 56 capsule pack contains one Turbospin powder inhaler device and 7 strips of 8 capsules or one Turbospin powder inhaler device and 4 strips of 14 capsules (56 hard capsules) sufficient for 4 weeks use.
Each 8 capsule pack contains one Turbospin powder inhaler device and 1 strip of 8 hard capsules sufficient for 4 days use.
Not all pack sizes may be marketed.
The Turbospin is an inspiratory flow driven dry powder inhaler made of polypropylene and stainless steel.
Special Precautions for Disposal and Other Handling
For capsules there are no special requirements for disposal. The Turbospin device should be discarded after completion of the treatment pack.
Colobreathe capsules should only be administered using the Turbospin inhaler device.
Taking Colobreathe using the Turbospin inhaler
Preparing the Turbospin
- Remove the cap. It comes away with a gentle pull.
- Unscrew the mouthpiece, exposing the chamber of the Turbospin inhaler.
- Remove a single capsule from the blister pack. Once you have removed the capsule it must be used immediately.
- Gently insert the capsule into the chamber with the widest end first. No force is required.
- Now replace the mouthpiece by screwing it back into place.
- To pierce the capsule:
- Hold the inhaler with the mouthpiece upright, gently push the piston upwards until the visible line is reached – you will feel resistance at this point and this will lock the capsule in place ready for piercing. Hold that position before continuing to follow through with the piercing.
- Now, with the capsule locked in place, continue pushing the piston as far as it will go and then release.
- The capsule is now pierced and the contents can be inhaled.
- Do not pierce the capsule more than once. You may see a small amount of powder released from the capsule chamber after the capsule is pierced, this is normal.
- Breathe out slowly. Place the mouthpiece between your lips and teeth. Ensure there is a seal between your lips and the mouthpiece. Take care not to cover the air slits with your fingers or mouth during inhalation.
- Then, breathe in slowly and deeply through your mouth at a rate sufficient for you to hear or feel the capsule spinning.
- Remove the Turbospin inhaler from your mouth and hold your breath for about 10 seconds or for as long as is comfortable, then breathe out slowly.
- If you do not hear the capsule spinning, the capsule may be stuck in the compartment. If this occurs, you can loosen the capsule by gently tapping the chamber of the inhaler. Do not try to loosen the capsule by repeatedly pressing the piston. If the capsule cannot be loosened and the powder cannot be inhaled, dispose of the broken capsule and any powder remaining in it and use another.
- Inhale the medicine again by repeating Steps 7 and 8 to ensure you have emptied the capsule.
- You can check whether the capsule is empty by unscrewing the mouthpiece and checking the capsule. If it is not empty, repeat steps 7, 8 and 9 until you have inhaled all of the contents.
- Once all the contents have been inhaled, rinse your mouth out well with water and spit out.
- When the capsule is empty, unscrew the mouthpiece, then remove and discard the empty capsule.
Piercing the capsule and inhaling the Medicine
Removing the Empty Capsule from the Turbospin
As you breathe in slowly, you suck air through the body of the Turbospin inhaler into the capsule chamber. The tiny particles of medication in the capsule are picked up by the airflow and carried down your airway into your lungs.
Occasionally, very small pieces of the capsule shell can get into your mouth or airways.
- If this happens, you may be able to feel these pieces on your tongue or in your airways.
- The capsule shell is made of gelatin, which is harmless to humans if swallowed or inhaled.
- The chances of the capsule breaking into pieces are increased if the capsule is pierced more than once during Step 6.
Marketing Authorisation Holder
Forest Laboratories UK Ltd
Marketing Authorisation Number(s)
EU/1/11/747/001 56 hard capsules (4 strips of 14 capsules)
EU/1/11/747/002 8 hard capsules (1 strip of 8 capsules)
EU/1/11/747/003 56 hard capsules (7 strips of 8 capsules)
Date of First Authorisation/Renewal of the Authorisation
Date of Revision of the Text
Detailed information on this medicinal product is available on the website of the European Medicines Agency http:/www.ema.europa.eu.
Company Contact Details
Forest Laboratories UK Limited (a subsidiary of Actavis PLC)
Whiddon Valley, Barnstaple, Devon, EX32 8NS, UK
+44 (0)1271 346106
Medical Information e-mail
+44 (0)1271 311 200
Medical Information Direct Line
+44(0)1271 385 257