Emylif 50 mg orodispersible film
Each orodispersible film contains 50 mg of riluzole
Excipient with known effect: Each orodispersible film contains 2 mg fructose.
This medicine also contains Sunset yellow FCF (E110).
For the full list of excipients, see section 6.1.
Orange, rectangular-shaped, orally dissolving thin film (32 mm x 22 mm) with “R50” printed in white on one side.
Emylif is indicated for the treatment of amyotrophic lateral sclerosis (ALS) in adults (see section 5.1).
Emylif has not been shown to be effective in the late stages of ALS.
Treatment with riluzole should only be initiated by specialist physicians with experience in the management of motor neurone diseases.
The recommended daily dose in adults or older people is 100 mg (50 mg every 12 hours). No significant increased benefit can be expected from higher daily doses.
Impaired renal function
Riluzole is not recommended for use in patients with impaired renal function, as studies at repeated doses have not been conducted in this population (see section 4.4).
Based on pharmacokinetic data, there are no special instructions for the use of riluzole in this population.
Impaired hepatic function
See sections 4.3, 4.4 and 5.2
The safety and efficacy of Emylif for the treatment of ALS in the pediatric population have not been established. No data are available.
Method of administration
Emylif is for oral administration.
• Hands should be clean and dry before handling Emylif so the orodispersible film does not stick to the fingers.
• Fold foil sachet along solid line at top.
• While keeping top of sachet folded over at solid line, tear down at the slit along the arrow on the side of the sachet to open.
• Remove Emylif orodispersible film from foil sachet. Each sachet contains one dose of Emylif.
• Emylif film should not be folded.
• Place Emylif film on top of the tongue, film will stick to the tongue and begin to dissolve.
• Once mouth is closed, saliva will normally be swallowed as Emylif dissolves.
• Emylif should not be taken with liquids, chewed or spitted.
• Patient should not talk while Emylif dissolves.
• After the administration of Emylif, hands should be washed.
• After the administration of Emylif, it is recommended to use caution if taking food (see section 4.4).
Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.
Hepatic disease or baseline transaminases greater than 3 times the upper limit of normal.
Patients who are pregnant or breast-feeding.
Riluzole should be prescribed with care in patients with a history of abnormal liver function, or in patients with slightly elevated serum transaminases (ALT/SGPT; AST/SGOT up to 3 times the upper limit of the normal range (ULN)), bilirubin and/or gamma-glutamyl transferase (GGT) levels. Baseline elevations of several liver function tests (especially elevated bilirubin) should preclude the use of riluzole (see section 4.8).
Because of the risk of hepatitis, serum transaminases, including ALT, should be measured before and during therapy with riluzole. ALT should be measured every month during the first 3 months of treatment, every 3 months during the remainder of the first year, and periodically thereafter. ALT levels should be measured more frequently in patients who develop elevated ALT levels.
Riluzole should be discontinued if the ALT levels increase to 5 times the ULN. There is no experience with dose reduction or rechallenge in patients who have developed an increase of ALT to 5 times ULN. Readministration of riluzole to patients in this situation cannot be recommended.
Patients should be warned to report any febrile illness to their physicians. The report of a febrile illness should prompt physicians to check white blood cell counts and to discontinue riluzole in case of neutropenia (see section 4.8).
Interstitial lung disease
Cases of interstitial lung disease have been reported in patients treated with riluzole, some of them were severe (see section 4.8). If respiratory symptoms develop such as dry cough and/or dyspnoea, chest radiography should be performed, and in case of findings suggestive of interstitial lung disease (e.g. bilateral diffuse lung opacities), riluzole should be discontinued immediately. In the majority of the reported cases, symptoms resolved after medicinal product discontinuation and symptomatic treatment.
Studies at repeated doses have not been conducted in patients with impaired renal function (see section 4.2).
In a single dose study in healthy subjects mild transient oral hypoesthesia has been reported. Median time to onset was 1 minute from the administration and median duration 40 minutes. In case oral hypoesthesia occurs, it is recommended to use caution if taking food until the symptom improves (see section 4.2).
The swallowing safety of Emylif has not been evaluated in patients with severe sialorrhea or dysphagia. Caution should be exercised when administering Emylif to these patients.
Each orodispersible film contains 2 mg. Fructose may damage teeth.
This medicinal product contains Sunset yellow FCF (E110), which may cause allergic reactions.
There have been no clinical studies to evaluate the interactions of riluzole with other medicinal products.
In vitro studies using human liver microsomal preparations suggest that CYP 1A2 is the principal isozyme involved in the initial oxidative metabolism of riluzole. Inhibitors of CYP 1A2 (e.g. caffeine, diclofenac, diazepam, nicergoline, clomipramine, imipramine, fluvoxamine, phenacetin, theophylline, amitriptyline and quinolones) could potentially decrease the rate of riluzole elimination, while inducers of CYP 1A2 (e.g. cigarette smoke, charcoal-broiled food, rifampicin and omeprazole) could increase the rate of riluzole elimination.
Emylif is contraindicated in pregnancy (see sections 4.3 and 5.3). Clinical experience with riluzole in pregnant women is lacking.
Emylif is contraindicated in breast-feeding women (see sections 4.3 and 5.3). It is not known whether riluzole is excreted in human milk.
Fertility studies in rats revealed slight impairment of reproductive performance and fertility at doses of 15 mg/kg/day (which is higher than the therapeutic dose), probably due to sedation and lethargy.
Patients should be warned about the potential for dizziness or vertigo, and advised not to drive or operate machinery if these symptoms occur.
No studies on the effects on the ability to drive and use machines have been performed.
Summary of safety profile
In phase III clinical studies conducted in ALS patients treated with riluzole, the most commonly reported adverse reactions were asthenia, nausea and abnormal liver function tests.
Tabulated summary of adverse reactions
Undesirable effects ranked under headings of frequency are listed below, using the following convention: 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) and very rare (<1/10,000), not known (cannot be estimated from the available data)
Blood and lymphatic system disorders
Severe neutropenia (see section 4.4)
Immune system disorders
Anaphylactoid reaction, angioedema
Nervous system disorders
Headache, dizziness, oral paresthesia, somnolence
Respiratory, thoracic and mediastinal disorders
Interstitial lung disease (see section 4.4)
Diarrhoea, abdominal pain, vomiting
Skin and subcutaneous tissue disorders
Abnormal liver function tests
General disorders and administration site conditions
Description of selected adverse reactions
Increased alanine aminotransferase usually appeared within 3 months after the start of therapy with riluzole; they were usually transient and levels returned to below twice the ULN after 2 to 6 months while treatment was continued. These increases could be associated with jaundice. In patients (n=20) from clinical studies with increases in ALT to more than 5 times the ULN, treatment was discontinued and the levels returned to less than 2 times the ULN within 2 to 4 months in most cases (see section 4.4). Study data indicate that Asian patients may be more susceptible to liver function test abnormalities - 3.2% (194/5995) of Asian patients and 1.8% (100/5641) of Caucasian patients.
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: Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Neurological and psychiatric symptoms, acute toxic encephalopathy with stupor, coma, and methaemoglobinaemia have been observed in isolated cases.
In case of overdose, treatment is symptomatic and supportive.
Pharmacotherapeutic group: other nervous system drugs, ATC code: N07XX02.
Mechanism of action
Although the pathogenesis of ALS is not completely elucidated, it is suggested that glutamate (the primary excitatory neurotransmitter in the central nervous system) plays a role for cell death in the disease.
Riluzole is proposed to act by inhibiting glutamate processes. The mode of action is unclear.
Clinical efficacy and safety
In a trial, 155 patients were randomised to riluzole 100 mg/day (50 mg twice daily) or placebo and were followed-up for 12 to 21 months. Survival, defined as patients who were alive, not intubated for mechanical ventilation and tracheotomy-free, was significantly extended for patients who received riluzole as compared to patients who received placebo. The median survival time was 17.7 months versus 14.9 months for riluzole and placebo, respectively.
In a dose-ranging trial, 959 patients with ALS were randomised to one of four treatment groups: riluzole 50, 100, 200 mg/day, or placebo and were followed-up for 18 months. In patients treated with riluzole 100 mg/day, survival was significantly higher compared to patients who received placebo. The effect of riluzole 50 mg/day was not statistically significant compared to placebo and the effect of 200 mg/day was essentially comparable to that of 100 mg/day. The median survival time approached 16.5 months versus 13.5 months for riluzole 100 mg/day and placebo, respectively.
In a parallel group study designed to assess the efficacy and safety of riluzole in patients at a late stage of the disease, survival time and motor function under riluzole did not differ significantly from that of placebo. In this study the majority of patients had a vital capacity less than 60%.
In a double-blind placebo-controlled trial designed to assess the efficacy and safety of riluzole in Japanese patients, 204 patients were randomised to riluzole 100 mg/day (50 mg twice daily) or placebo and were followed-up for 18 months. In this study, the efficacy was assessed on inability to walk alone, loss of upper limb function, tracheostomy, need for artificial ventilation, gastric tube feeding or death. Tracheostomy-free survival in patients treated with riluzole did not differ significantly from placebo. However, the power of this study to detect differences between treatment groups was low. Meta-analysis including this study and those described above showed a less striking effect on survival for riluzole as compared to placebo although the differences remained statistically significant.
The pharmacokinetics of riluzole have been evaluated in healthy male volunteers after single oral administration of 25 to 300 mg and after multiple-dose oral administration of 25 to 100 mg bid. Plasma levels increase linearly with the dose and the pharmacokinetic profile is dose-independent. With multiple dose administration (10 day-treatment at 50 mg riluzole bid), unchanged riluzole accumulates in plasma by about 2 fold and steady-state is reached in less than 5 days.
Riluzole is rapidly absorbed after oral administration with maximal plasma concentrations occurring within 60 to 90 minutes (Cmax=173 ± 72 (sd) ng/ml). About 90% of the dose is absorbed and the absolute bioavailability is 60 ± 18%.
The rate and extent of absorption is reduced when riluzole is administered with high-fat meals (decrease in Cmax of 44%, decrease in AUC of 17%).
In a bioequivalence study the total exposure of riluzole 50 mg tablets and riluzole 50 mg orodispersible film were equivalent (Cmax Ratio: 117.05%; 90% CI: 110.43-124.06%; AUC0-t Ratio: 111.82; 90% CI: 108.25-115.50; AUC0-inf Ratio: 111.83; 90% CI: 108.19-115.59).
Riluzole is extensively distributed throughout the body and has been shown to cross the blood brain barrier. The volume of distribution of riluzole is about 245 ± 69 L (3.4 L/kg). Riluzole is about 97% protein bound and it binds mainly to serum albumin and to lipoproteins.
Unchanged riluzole is the main component in plasma and is extensively metabolised by cytochrome P450 and subsequent glucuronidation. In vitro studies using human liver preparations demonstrated that cytochrome P450 1A2 is the principal isoenzyme involved in the metabolism of riluzole. The metabolites identified in urine are three phenolic derivatives, one ureido-derivative and unchanged riluzole.
The primary metabolic pathway for riluzole is initial oxidation by cytochrome P450 1A2 producing N-hydroxy-riluzole (RPR112512), the major active metabolite of riluzole. This metabolite is rapidly glucuronoconjugated to O- and N-glucuronides.
The elimination half-life ranges from 9 to 15 hours. Riluzole is eliminated mainly in the urine.
The overall urinary excretion accounts for about 90% of the dose. Glucuronides accounted for more than 85% of the metabolites in the urine. Only 2% of a riluzole dose was recovered unchanged in the urine.
Impaired renal function
There is no significant difference in pharmacokinetic parameters between patients with moderate or severe chronic renal insufficiency (creatinine clearance between 10 and 50 ml.min-1) and healthy volunteers after a single oral dose of 50 mg riluzole.
The pharmacokinetic parameters of riluzole after multiple dose administration (4.5 days of treatment at 50 mg riluzole bid) are not affected in the older people (>70 years).
Impaired hepatic function
The AUC of riluzole after a single oral dose of 50 mg increases by about 1.7 fold in patients with mild chronic liver insufficiency and by about 3 fold in patients with moderate chronic liver insufficiency.
A clinical study conducted to evaluate the pharmacokinetics of riluzole and its metabolite
N-hydroxyriluzole following repeated oral administration twice daily for 8 days in 16 healthy Japanese and 16 Caucasian adult males showed in the Japanese group a lower exposure of riluzole (Cmax 0.85 [90% CI 0.68-1.08] and AUC inf. 0.88 [90% CI 0.69-1.13]) and similar exposure to the metabolite. The clinical significance of these results is not known.
Riluzole did not show any carcinogenicity potential in either rats or mice.
Standard tests for genotoxicity performed with riluzole were negative. Tests on the major active metabolite of riluzole gave positive results in two in vitro tests. Intensive testing in seven other standard in vitro or in vivo assays did not show any genotoxic potential of the metabolite. On the basis of these data and taking into consideration the negative studies on the carcinogenesis of riluzole in the mouse and rat, the genotoxic effect of this metabolite is not considered to be of relevance in humans.
Reductions in red blood cell parameters and/or alterations in liver parameters were noted inconsistently in subacute and chronic toxicity studies in rats and monkeys. In dogs, haemolytic anaemia was observed.
In a single toxicity study, the absence of corpora lutea was noted at a higher incidence in the ovary of treated compared to control female rats. This isolated finding was not noted in any other study or species.
All these findings were noted at doses which were 2-10 times higher than the human dose of 100 mg/day.
In the pregnant rat, the transfer of 14C-riluzole across the placenta to the foetus has been detected. In rats, riluzole decreased the pregnancy rate and the number of implantations at exposure levels at least twice the systemic exposure of humans given clinical therapy. No malformations were seen in animal reproductive studies.
In lactating rats, 14C-riluzole was detected in milk.
Polacrilex resin Pullulan (E1204) Xylitol (E967)
Glycerol mono-oleate Sucralose (E955)
Flavor honey Xhanthan gum Flavor lemon
Sunset yellow FCF (E110)
White ink: purified water, Titanium dioxide (E171), Propylene glycol (E1520), Hypromellose (E464), Isopropyl alcohol, SDA 3A alcohol (ethanol and methanol).
Presence of trace levels of the antioxidant butylated hydroxytoluene (BHT, E321).
Store below 30°C.
The primary packaging material is a sachet, which will be opened and removed before application. The sachet material is composed by two identical layers of a polyester/foil laminate foil.
Each carton box contains 14, 28, 56, 112, 140 sachets.
Not all pack sizes may be marketed.
No special requirements.
Any unused product or waste material should be disposed of in accordance with local requirements.
Via Lillo del Duca 10
20091 Bresso (MI)
Tel: +39 02 665241
Fax: +39 02 66501492
Email: [email protected]
17 April 2023
10 January 2024