Elvanse 20mg, 40mg and 60mg Capsules - Product Information
|Condition:||ADHD (Attention Deficit Hyperactivity Disorder), Binge Eating Disorder|
|Ingredients:||lisdexamfetamine dimesylate, microcrystalline cellulose, croscarmellose sodium, magnesium stearate, gelatin, black ink (shellac and black iron oxide E172)|
Name of the Medicinal Product
Elvanse 20 mg capsules, hard.
Elvanse 40 mg capsules, hard.
Elvanse 60 mg capsules, hard.
Qualitative and Quantitative Composition
20 mg Capsules: Each capsule contains 20 mg lisdexamfetamine dimesylate, equivalent to 5.9 mg of dexamfetamine.
40 mg Capsules: Each capsule contains 40 mg lisdexamfetamine dimesylate, equivalent to 11.9 mg of dexamfetamine.
60 mg Capsules: Each capsule contains 60 mg lisdexamfetamine dimesylate, equivalent to 17.8 mg of dexamfetamine.
For the full list of excipients, see section List of Excipients.
Elvanse 20 mg capsule: ivory opaque body and ivory opaque cap, printed 'S489' and '20 mg' in black ink.
Elvanse 40 mg capsule: white opaque body and blue/green opaque cap, printed 'S489' and '40 mg' in black ink.
Elvanse 60 mg capsule: aqua blue opaque body and aqua blue opaque cap, printed 'S489' and '60 mg' in black ink.
Each capsule measures approximately 16 mm long and 6 mm wide.
Elvanse is indicated as part of a comprehensive treatment programme for attention deficit/hyperactivity disorder (ADHD) in children aged 6 years and over when response to previous methylphenidate treatment is considered clinically inadequate.
Treatment must be under the supervision of a specialist in childhood and/or adolescent behavioural disorders. Diagnosis should be made according to DSMIV criteria or the guidelines in ICD10 and should be based on a complete history and evaluation of the patient. Diagnosis cannot be made solely on the presence of one or more symptom.
The specific aetiology of this syndrome is unknown, and there is no single diagnostic test. Adequate diagnosis requires the use of medical and specialised psychological, educational, and social resources.
A comprehensive treatment programme typically includes psychological, educational and social measures as well as pharmacotherapy and is aimed at stabilising children with a behavioural syndrome characterised by symptoms which may include chronic history of short attention span, distractibility, emotional lability, impulsivity, moderate to severe hyperactivity, minor neurological signs and abnormal EEG. Learning may or may not be impaired.
Elvanse is not indicated in all children with ADHD and the decision to use the drug must be based on a very thorough assessment of the severity and chronicity of the child's symptoms in relation to the child's age and potential for abuse, misuse or diversion.
Appropriate educational placement is essential, and psychosocial intervention is generally necessary. The use of Elvanse should always be used in this way according to the licensed indication.
Posology and Method of Administration
Treatment must be initiated under the supervision of an appropriate specialist in childhood and/or adolescent behavioural disorders.
Dosage should be individualised according to the therapeutic needs and response of the patient. Careful dose titration is necessary at the start of treatment with Elvanse.
The starting dose is 30 mg taken once daily in the morning. When in the judgment of the clinician a lower initial dose is appropriate, patients may begin treatment with 20 mg once daily in the morning.
The dose may be increased by 10 or 20 mg increments, at approximately weekly intervals. Elvanse should be administered orally at the lowest effective dosage.
The maximum recommended dose is 70 mg/day; higher doses have not been studied.
In patients with severe renal insufficiency (GFR 15 to <30 mL/min/1.73 m2 or CrCl <30 mL/min) the maximum dose should not exceed 50 mg/day. Further dosage reduction should be considered in patients undergoing dialysis (see section Pharmacokinetic Properties.
Treatment must be stopped if the symptoms do not improve after appropriate dosage adjustment over a 1month period. If paradoxical aggravation of symptoms or other intolerable adverse events occur, the dosage should be reduced or discontinued.
Method of administration
Elvanse may be taken with or without food.
Elvanse may be swallowed whole, or the capsule opened and the entire contents emptied and mixed with a soft food such as yogurt or in a glass of water or orange juice. If the contents include any compacted powder, a spoon may be used to break apart the powder in the soft food or liquid. The contents should be stirred until completely dispersed. The patient should consume the entire mixture of soft food or liquid immediately; it should not be stored. The active ingredient dissolves completely once dispersed; however, a film containing the inactive ingredients may remain in the glass or container once the mixture is consumed.
The patient should not take anything less than one capsule per day and a single capsule should not be divided.
In the event of a missed dose, Elvanse dosing can resume the next day. Afternoon doses should be avoided because of the potential for insomnia.
Prior to prescribing, it is necessary to conduct a baseline evaluation of a patient's cardiovascular status including blood pressure and heart rate. A comprehensive history should document concomitant medications, past and present co morbid medical and psychiatric disorders or symptoms, family history of sudden cardiac/unexplained death, and accurate recording of pretreatment height and weight on a growth chart (see section Contraindications and section Special Warnings and Precautions For Use).
Consistent with other stimulants, the potential for abuse, misuse or diversion of Elvanse should be considered prior to prescribing (see section Special Warnings and Precautions For Use).
Growth, psychiatric, and cardiovascular status should be continually monitored (see also section Special Warnings and Precautions For Use).
- Blood pressure and pulse should be recorded on a centile chart at each adjustment of dose and at least every six months.
- Height, weight, and appetite should be recorded at least sixmonthly with maintenance of a growth chart.
- Development of de novo or worsening of preexisting psychiatric disorders should be monitored at every adjustment of dose and then at least every six months and at every visit.
Patients should be monitored for the risk of diversion, misuse, and abuse of Elvanse.
Pharmacological treatment of ADHD may be needed for extended periods. The physician who elects to use Elvanse for extended periods (over 12 months) should reevaluate the usefulness of Elvanse at least yearly, and consider trial periods off medication to assess the patient's functioning without pharmacotherapy, preferably during times of school holidays.
In adolescents whose symptoms persist into adulthood and who have shown clear benefit from treatment, it may be appropriate to continue treatment into adulthood (see sections Special Warnings and Precautions For Use and Pharmacodynamic Properties).
Children Under 6 years
Elvanse should not be used in children under the age of 6 years. Safety and efficacy in this age group has not been established.
Dexamfetamine clearance is reduced in the elderly so dose adjustment may be required (see sections Pharmacokinetic Properties).
Patients with renal impairment
Due to reduced clearance in patients with severe renal insufficiency (GFR 15 to <30 mL/min/1.73 m2 or CrCl <30 mL/min ) the maximum dose should not exceed 50 mg/day. Further dosage reduction should be considered in patients undergoing dialysis. Lisdexamfetamine and dexamfetamine are not dialysable.
Patients with hepatic impairment
No studies have been conducted in patients with hepatic impairment.
Hypersensitivity to sympathomimetic amines or any of the excipients listed in section List of Excipients.
Concomitant use of monoamine oxidase inhibitors (MAOI) or within 14 days after MAOI treatment (hypertensive crisis may result; see section Interaction With Other Medicinal Products and Other Forms of Interaction).
Hyperthyroidism or thyrotoxicosis.
Symptomatic cardiovascular disease.
Moderate to severe hypertension.
Special Warnings and Precautions For Use
Abuse and dependence
Stimulants including Elvanse have a potential for abuse, misuse, dependence, or diversion for nontherapeutic uses that physicians should consider when prescribing this product. Stimulants should be prescribed cautiously to patients with a history of substance abuse or dependence.
Tolerance, extreme psychological dependence, and severe social disability have occurred with the abuse of stimulants. There are reports of patients who have increased the dosage of amfetamine to levels many times higher than recommended; abrupt cessation following prolonged high dosage administration results in extreme fatigue and mental depression. Changes are also noted on the sleep EEG. Manifestations of chronic intoxication with amfetamines may include severe dermatoses, marked insomnia, irritability, hyperactivity, and personality changes. The most severe manifestation of chronic intoxication is psychosis, often clinically indistinguishable from schizophrenia.
Cardiovascular adverse events
Sudden death in patients with preexisting structural cardiac abnormalities or other serious heart problems
Children and adolescents: Sudden death has been reported in children and adolescents taking CNS stimulants, including those with structural cardiac abnormalities or other serious heart problems. Although some serious heart problems alone carry an increased risk of sudden death, stimulant products generally should not be used in children or adolescents with known serious structural cardiac abnormalities, cardiomyopathy, serious heart rhythm abnormalities, or other serious cardiac problems that may place them at increased vulnerability to the sympathomimetic effects of a stimulant drug.
Adults: Sudden deaths, stroke, and myocardial infarction have been reported in adults taking stimulant drugs at usual doses for ADHD. Although the role of stimulants in these adult cases is also unknown, adults have a greater likelihood than children of having serious structural cardiac abnormalities, cardiomyopathy, serious heart rhythm abnormalities, coronary artery disease, or other serious cardiac problems. Adults with such abnormalities should also generally not be treated with stimulant drugs.
Hypertension and other cardiovascular conditions
Stimulant medications cause a modest increase in average blood pressure (about 24 mmHg) and average heart rate (about 36 bpm), and individuals may have larger increases. While the mean changes alone would not be expected to have shortterm consequences, all patients should be monitored for larger changes in heart rate and blood pressure. Caution is indicated in treating patients whose underlying medical conditions might be compromised by increases in blood pressure or heart rate, e.g., those with preexisting hypertension, heart failure, recent myocardial infarction, or ventricular arrhythmia.
The use of Elvanse is contraindicated in patients with symptomatic cardiovascular disease and also in those patients with moderate to severe hypertension(see section Contraindications).
Cardiomyopathy has been reported with chronic amfetamine use. It has also been reported with Elvanse.
Assessing cardiovascular status in patients being treated with stimulant medications
All patients who are being considered for treatment with stimulant medications should have a careful history (including assessment for a family history of sudden death or ventricular arrhythmia) and physical exam to assess for the presence of cardiac disease, and should receive further cardiac evaluation if findings suggest such disease (e.g., electrocardiogram or echocardiogram). Patients who develop symptoms such as exertional chest pain, unexplained syncope, or other symptoms suggestive of cardiac disease during stimulant treatment should undergo a prompt cardiac evaluation.
Psychiatric adverse events
Administration of stimulants may exacerbate symptoms of behaviour disturbance and thought disorder in patients with preexisting psychotic disorders.
Particular care should be taken in using stimulants to treat ADHD patients with comorbid bipolar disorder because of concern for possible induction of mixed/manic episode in such patients. Prior to initiating treatment with a stimulant, patients with comorbid depressive symptoms should be adequately screened to determine if they are at risk for bipolar disorder; such screening should include a detailed psychiatric history, including a family history of suicide, bipolar disorder, and depression.
Emergence of new psychotic or manic symptoms
Treatment emergent psychotic or manic symptoms, e.g., hallucinations, delusional thinking, or mania in children and adolescents without prior history of psychotic illness or mania can be caused by stimulants at usual doses. If such symptoms occur, consideration should be given to a possible causal role of the stimulant, and discontinuation of treatment may be appropriate.
Aggressive behaviour or hostility is often observed in children and adolescents with ADHD, and has been reported in clinical trials and the postmarketing experience of some medications indicated for the treatment of ADHD including Elvanse. Stimulants may cause aggressive behaviour or hostility. Patients beginning treatment for ADHD should be monitored for the appearance of or worsening of aggressive behaviour or hostility.
Stimulants have been reported to exacerbate motor and phonic tics and Tourette's syndrome. Therefore, clinical evaluation for tics and Tourette's syndrome in children and their families should precede use of stimulant medications.
Longterm suppression of growth (height and weight)
Stimulants have been associated with a slowing of weight gain and a reduction in attained height. Growth should be monitored during treatment with stimulants, and patients who are not growing or gaining weight as expected may need to have their treatment interrupted. Height, weight, and appetite should be recorded at least 6monthly.
In a controlled study of patients aged 6 to 17 years the mean (SD) changes in body weight after seven weeks were 2.35 (2.084) kg for Elvanse, +0.87 (1.102) kg for placebo, and 1.36 (1.552) kg for methylphenidate hydrochloride.
There is some clinical evidence that stimulants may lower the convulsive threshold in patients with prior history of seizure, in patients with prior EEG abnormalities in absence of seizures, and very rarely, in patients without a history of seizures and no prior EEG evidence of seizures. In the presence of new onset or worsening seizures, the drug should be discontinued.
Difficulties with accommodation and blurring of vision have been reported with stimulant treatment.
Prescribing and dispensing
The least amount of Elvanse feasible should be prescribed or dispensed in order to minimise the risk of possible overdose by the patient.
Use with other sympathomimetic drugs
Elvanse should be used with caution in patients who use other sympathomimetic drugs (see section Interaction With Other Medicinal Products and Other Forms of Interaction.
Use in adults
Safety and efficacy have not been established for the routine continuation of treatment beyond 18 years of age. If treatment withdrawal has not been successful when an adolescent has reached 18 years of age continued treatment into adulthood may be necessary. The need for further treatment of these adults should be reviewed regularly and undertaken annually.
Interaction With Other Medicinal Products and Other Forms of Interaction
In vitro enzyme inhibition
In vitro experiments with human microsomes indicate minor inhibition of CYP2D6 by amfetamine and minor inhibition of CYP1A2, 2D6, and 3A4 by one or more metabolites. Although the clinical significance of this interaction is likely to be minimal, consideration should be given when medications metabolised by these pathways are administered.
Agents whose blood levels may be impacted by Elvanse
Extended release guanfacine: In a drug interaction study, administration of an extended release guanfacine in combination with Elvanse induced a 19% increase in guanfacine maximum plasma concentrations, whereas, exposure (area under the curve; AUC) was increased by 7%. These small changes are not expected to be clinically meaningful. In this study, no effect on dexamfetamine exposure was observed following coadministration of extended release guanfacine and Elvanse.
Extended release venlafaxine: In a drug interaction study, administration of 225 mg extended release venlafaxine, a CYP2D6 substrate, in combination with 70 mg Elvanse induced a 9% decrease in the Cmax and 17% decrease in the AUC for the primary active metabolite odesmethylvenlafaxine and a 10% increase in Cmax and 13% increase in AUC for venlafaxine. Dexamfetamine may be a weak inhibitor of CYP2D6. Lisdexamfetamine has no effect on the AUC and Cmax of the composite of venlafaxine and odesmethylvenlafaxine. These small changes are not expected to be clinically meaningful. In this study, no effect on dexamfetamine exposure was observed following coadministration of extended release venlafaxine and Elvanse.
Agents and conditions that alter urinary pH and impact the urinary excretion and half-life of amfetamine
Ascorbic acid and other agents and conditions ( thiazide diuretics, diets high in animal protein, diabetes, respiratory acidosis) that acidify urine increase urinary excretion and decrease the halflife of amfetamine. Sodium bicarbonate and other agents and conditions (diets high in fruits and vegetables, urinary tract infections and vomiting) that alkalinise urine decrease urinary excretion and extend the halflife of amfetamine.
Monoamine oxidase inhibitors
Amfetamine should not be administered during or within 14 days following the administration of monoamine oxidase inhibitors (MAOI) because it can increase the release of norepinephrine and other monoamines. This can cause severe headaches and other signs of hypertensive crisis. A variety of toxic neurological effects and malignant hyperpyrexia can occur, sometimes with fatal outcomes (see section Contraindications).
Agents whose effects may be reduced by amfetamines
Antihypertensives: Amfetamines may decrease the effectiveness of guanethidine or other antihypertensive medications.
Agents whose effects may be potentiated by amfetamines
Amfetamines potentiate the analgesic effect of narcotic analgesics.
Agents that may reduce the effects of amfetamines
Chlorpromazine: Chlorpromazine blocks dopamine and norepinephrine receptors, thus inhibiting the central stimulant effects of amfetamines.
Haloperidol: Haloperidol blocks dopamine receptors, thus inhibiting the central stimulant effects of amfetamines.
Lithium carbonate: The anorectic and stimulatory effects of amfetamines may be inhibited by lithium carbonate.
Use with alcohol
There are limited data on the possible interaction with alcohol.
Drug/laboratory test interactions
Amfetamines can cause a significant elevation in plasma corticosteroid levels. This increase is greatest in the evening. Amfetamine may interfere with urinary steroid determinations.
Fertility, Pregnancy and Lactation
There are no adequate and well controlled studies of Elvanse in pregnant women. Dexamfetamine, the active metabolite of lisdexamfetamine, crosses the placenta.
Lisdexamfetamine dimesylate had no effect on embryofoetal development or survival when administered orally to pregnant rats and rabbits (see section Preclinical Safety Data). Administration of lisdexamfetamine dimesylate to juvenile rats was associated with reductions in growth measurements at clinically relevant exposures.
The physician should discuss Elvanse treatment with female patients who have started menstruation. Elvanse should only be used during pregnancy if the potential benefit justifies the potential risk to the foetus.
Amfetamines are excreted in human milk. Elvanse should not be used during breastfeeding.
Amfetamine has shown no harmful effects on fertility in a rat study (see section Preclinical Safety Data). The effect of Elvanse on human fertility has not been investigated.
Effects on Ability to Drive and Use Machines
Elvanse can cause dizziness, drowsiness and visual disturbances including difficulties with accommodation, diplopia and blurred vision. These could have a moderate influence on the ability to drive and use machines. Patients should be warned of these possible effects and advised that if affected, they should avoid potentially hazardous activities such as driving or operating machinery.
Summary of the Safety Profile
Adverse reactions observed with Elvanse treatment mainly reflect side effects commonly associated with stimulant use. Very common adverse reactions include decreased appetite, insomnia, dry mouth, headache and weight decreased.
Tabulated summary of adverse reactions
The following table presents all adverse reactions based on clinical trials and spontaneous reporting.
The following definitions apply to the frequency terminology used hereafter:
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)
Frequency not known (cannot be estimated from the available data).
An asterisk (*) indicates that additional information on the respective adverse reaction is provided below the table.
|System/Organ Class||Adverse Reaction||Children|
(6 to 12 years)
(13 to 17 years)
|Immune System Disorders||Anaphylactic reaction||Frequency not known||Frequency not known||Frequency not known|
|Hypersensitivity||Uncommon||Frequency not known||Uncommon|
|Metabolism and Nutrition Disorders||Decreased appetite||Very common||Very common||Very common|
|Psychiatric Disorders||*Insomnia||Very common||Very common||Very common|
|Libido decreased||Not applicable||Not reported||Common|
|Dysphoria||Uncommon||Frequency not known||Uncommon|
|Euphoria||Frequency not known||Uncommon||Uncommon|
|Bruxism||Uncommon||Frequency not known||Common|
|Psychotic episodes||Frequency not known||Frequency not known||Frequency not known|
|Mania||Uncommon||Frequency not known||Uncommon|
|Hallucination||Uncommon||Uncommon||Frequency not known|
|Aggression||Common||Uncommon||Frequency not known|
|Nervous System Disorders||Headache||Very Common||Very Common||Very Common|
|Seizure||Frequency not known||Frequency not known||Frequency not known|
|Dyskinesia||Uncommon||Frequency not known||Uncommon|
|Eye Disorders||Vision blurred||Uncommon||Frequency not known||Uncommon|
|Mydriasis||Uncommon||Uncommon||Frequency not known|
|Cardiomyopathy||Frequency not known||Frequency not known||Frequency not known|
|Vascular disorders||Raynaud's phenomenon||Uncommon||Frequency not known||Frequency not known|
|Respiratory, Thoracic and Mediastinal Disorders||Dyspnoea||Uncommon||Common||Common|
|Gastrointestinal Disorders||Dry mouth||Common||Common||Very common|
|Upper abdominal pain||Common||Common||Common|
|Hepatobilary Disorders||*Eosinophilic Hepatitis||Frequency not known||Frequency not known||Frequency not known|
|Skin and Subcutaneous Tissue Disorders||Hyperhidrosis||Uncommon||Uncommon||Common|
|*Angioedema||Frequency not known||Frequency not known||Frequency not known|
|*Stevens-Johnson Syndrome||Frequency not known||Frequency not known||Frequency not known|
|Reproductive System and Breast Disorders||Erectile dysfunction||Not applicable||Uncommon||Common|
|General Disorders and Administration Site Conditions||Irritability||Common||Common||Common|
|Investigations||Blood pressure increased||Uncommon||Common||Common|
|*Weight decreased||Very Common||Very Common||Common|
Description of selected adverse reactions
Includes insomnia, initial insomnia, and middle insomnia.
In a 4week controlled trial of Elvanse in children aged 6 to 12 years, mean weight loss from baseline to endpoint was 0.4, 0.9, and 1.1 kg, for patients assigned to receive 30 mg, 50 mg, and 70 mg of Elvanse respectively, compared to a 0.5 kg weight gain for patients receiving placebo. Higher doses were associated with greater weight loss with 4 weeks of treatment. Careful followup for weight in children aged 6 to 12 years who received Elvanse over 12 months suggests that continuous treatment (i.e., treatment for 7 days per week throughout the year) slows growth rate measured by body weight as demonstrated by an age and sexnormalised mean change from baseline in percentile of 13.4 over 1 year. The average percentiles at baseline (n=271) and 12 months (n=146) were 60.9 and 47.2, respectively.
In a 4week controlled trial of Elvanse in adolescents aged 13 to 17 years, mean weight loss from baseline to endpoint was 1.2, 1.9, and 2.3 kg for patients assigned to receive 30 mg, 50 mg, and 70 mg of Elvanse respectively, compared to a 0.9 kg weight gain for patients receiving placebo. Careful followup for weight in adolescents aged 13 to 17 years who received Elvanse over 12 months suggests that continuous treatment (i.e., treatment for 7 days per week throughout the year) slows growth rate measured by body weight as demonstrated by an age and sexnormalised mean change from baseline in percentile of 6.5 over 1 year. The average percentiles at baseline (n=265) and 12 months (n=156) were 66.0 and 61.5, respectively.
No cases were reported in the clinical studies.
No cases were reported in the clinical studies.
No cases were reported in the clinical studies.
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 (Website: www.mhra.gov.uk/yellowcard).
The prolonged release of dexamfetamine after administration of Elvanse should be considered when treating patients with overdose.
Manifestations of acute overdosage with amfetamines include restlessness, tremor, hyperreflexia, rapid respiration, confusion, assaultiveness, hallucinations, panic states, hyperpyrexia, and rhabdomyolysis. Fatigue and depression usually follow the central nervous system stimulation. Cardiovascular effects include arrhythmias, hypertension or hypotension, and circulatory collapse. Gastrointestinal symptoms include nausea, vomiting, diarrhoea, and abdominal cramps. Fatal poisoning is usually preceded by convulsions and coma.
Management of acute amfetamine intoxication is largely symptomatic and includes gastric lavage, administration of activated charcoal, administration of a cathartic, and sedation. Acidification of the urine increases amfetamine excretion but is believed to increase risk of acute renal failure if myoglobinuria is present. If acute severe hypertension complicates amfetamine overdosage, administration of intravenous phentolamine has been suggested. However, a gradual drop in blood pressure will usually result when sufficient sedation has been achieved.
Lisdexamfetamine and dexamfetamine are not dialysable.
Pharmacotherapeutic group: Centrally Acting Sympathomimetics, ATC code: N06 BA12.
Mechanism of Action
Elvanse is a pharmacologically inactive prodrug. After oral administration, lisdexamfetamine is rapidly absorbed from the gastrointestinal tract and hydrolysed primarily by red blood cells to dexamfetamine, which is responsible for the drug's activity.
Amfetamines are noncatecholamine sympathomimetic amines with CNS stimulant activity. The mode of therapeutic action of amfetamine in ADHD is not fully established, however it is thought to be due to its ability to block the reuptake of norepinephrine and dopamine into the presynaptic neuron and increase the release of these monoamines into the extraneuronal space. The prodrug, lisdexamfetamine, does not bind to the sites responsible for the reuptake of norepinephrine and dopamine in vitro.
Clinical efficacy and safety
The effects of Elvanse in the treatment of ADHD has been demonstrated in three controlled trials in children aged 6 to 12 years, one controlled study in adolescents aged 13 to 17 years, three controlled studies in children and adolescents (6 to 17 years), and four controlled trials in adults who met the DSMIVTR criteria for ADHD.
In clinical studies conducted in children and adults, the effects of Elvanse were ongoing at 13 hours after dosing in children and at 14 hours in adults when the product was taken once daily in the morning.
Three hundred and thirtysix patients aged 617 years were evaluated in the pivotal Phase 3 European Study SPD489 325. In this sevenweek randomised doubleblind, doseoptimised, placebo and activecontrolled study, Elvanse showed significantly greater efficacy than placebo.
The ADHD Rating Scale is a measure of the core symptoms of ADHD. The placeboadjusted mean reduction from baseline in patients treated with Elvanse on the ADHDRSIV Total Score was 18.6 (p<0.001). At every ontreatment visit and at Endpoint the percentages of subjects who met predefined response criteria (a ≥30% reduction from Baseline in ADHDRSIV Total Score and a CGII value of 1 or 2) was significantly higher (p<0.001) for Elvanse when compared to placebo. The endpoint of this study is defined in Table 1. The results were also significantly higher for Elvanse when compared to placebo when the individual components of the response criteria were evaluated. In addition, mean scores for ADHD symptoms following treatment discontinuation did not exceed baseline scores prior to treatment, indicating there was no rebound effect.
In addition to a reduction in symptoms, clinical studies have demonstrated that Elvanse significantly improves functional outcomes. Specifically, in Study SPD489325, 75.0% of subjects on Elvanse showed Improvement (defined as “very much improved” or “much improved”) on the Clinical Global ImpressionImprovement (CGII) rating scale compared to 14.2% on placebo (p<0.001).
Elvanse showed significant improvement in child achievement in academic performance, as measured by the Health Related Quality of life instrument, Parent Report Form of the Child Health and Illness ProfileChild Edition (CHIP CE:PRF) Achievement Domain. Elvanse demonstrated a significant improvement from baseline compared to placebo (Elvanse: 9.4 versus Placebo 1.1) with a mean difference between the two treatment groups of 10.5 (p<0.001).
|Change in ADHDRS IV Total Score|
|Least Square Mean||-24.3||-5.7||-18.7|
|Effect size (versus Placebo)||1.804||N/A||1.263|
|P-value (versus Placebo)||<0.001||N/A||<0.001|
|Patients Showing a response2||83.7% (87/104)||22.6% (24/106)||68.2% (73/107)|
|Difference in response from placebo||61.0||N/A||45.6|
|P-value (versus Placebo)||<0.001||N/A||<0.001|
|Patients Showing Improvement3||75.0% (78/104)||14.2% (15/106)||58.9 % (63/107)|
|Difference in improvement from placebo||60.8||N/A||44.7|
|P-value (versus Placebo)||<0.001||N/A||<0.001|
|Change in CHIPCE: PRF Achievement Domain|
|Least Square Mean||9.4||-1.1||6.4|
|Effect size (versus Placebo)||1.280||N/A||0.912|
|Pvalue (versus Placebo)||<0.001||N/A||<0.001|
1 Endpoint = the last ontreatment postBaseline visit of the dose optimisation or dose maintenance Period (Visits 17) with a valid value
2 Response is defined as percentage reduction from Baseline in the ADHDRSIV Total Score of ≥30%
3Improvement (“very much improved” or “much improved”)
Similar results for ADHDRS and CGII have been shown in two placebo controlled studies, one in children (n=297) and the other in adolescents (n=314), both conducted in the United States.
A doubleblind, randomised, activecontrolled, doseoptimisation study was conducted in children and adolescents aged 6 to 17 years (n=267) who met DSMIV criteria for ADHD. In this nineweek study, patients were randomised (1:1) to a daily morning dose of Elvanse (30, 50 or 70 mg/day), or atomoxetine (dosed as appropriate for the subject's weight up to 100 mg). During a 4week Dose Optimisation Period, patients were titrated until an optimal dose, based on treatment emergent adverse events and clinical judgement, was reached. Patients treated with Elvanse had a shorter time to first response compared to patients treated with atomoxetine (median 13.0 vs 21.0 days, respectively; p=0.003), where response was defined as having a CGII score of 1 (very much improved) or 2 (much improved) at any of the double blind treatment visits. Across all of the double blind treatment visits, the proportion of responders in the Elvanse group was consistently higher than the proportion of responders in the atomoxetine group. The difference ranged from 1624 percentage points. At the study endpoint the least square mean changes from baseline in ADHDRSIV Total Score for Elvanse and atomoxetine were 26.1 and 19.7, respectively, with a betweengroup difference of 6.4.
In addition, maintenance of effect was demonstrated in a doubleblind, placebocontrolled, randomised withdrawal study conducted in children and adolescents ages 6 to 17 (n=157) who met the diagnosis of ADHD (DSMIV criteria). Patients were optimised to openlabel Elvanse for an extended period (at least 26 weeks) prior to entry into the 6week randomised withdrawal period. Eligible patients were randomised to continue receiving their optimised dose of Elvanse or to switch to placebo. Patients were observed for relapse (treatment failure) during the 6week doubleblind phase. Treatment failure was defined as a ≥50% increase (worsening) in the ADHDRS Total Score and a ≥2point increase in the CGIS score compared to scores at entry into the doubleblind randomised withdrawal phase. Treatment failure was significantly lower (p<0.001) for the Elvanse subjects (15.8%) compared to placebo (67.5%). For the majority of subjects (70.3%) who were treatment failures regardless of treatment, ADHD symptoms worsened at or before the week 2 visit following randomisation.
The effectiveness of Elvanse in the treatment of ADHD was established in a doubleblind, randomised, placebo controlled, parallelgroup study conducted in 420 adult patients aged 18 to 55 years who met DSMIV criteria for ADHD. Significant improvements in ADHD symptoms, based upon investigator ratings on the ADHDRS with adult prompts total score, were observed for all Elvanse doses compared to placebo. Treatment with Elvanse significantly reduced the degree of functional impairment as measured by improvement on the CGII rating scale compared to placebo.
In addition, maintenance of effect was demonstrated in a doubleblind, placebocontrolled, randomised withdrawal design study that enrolled adults (n=123) who met DSMIV criteria for ADHD and who, at study entry, had been treated with Elvanse for a minimum of 6 months. A significantly lower proportion of patients treated with Elvanse met relapse criteria (8.9%) compared to patients receiving placebo (75.0%) in the doubleblind randomised withdrawal phase. Relapse was defined as a ≥50% increase from randomisation in ADHDRSIV Total Score and a ≥ 2 point increase in CGIS score relative to the CGIS score at randomisation.
Abuse liability studies
In a human abuse liability study, when equivalent oral doses of 100 mg lisdexamfetamine dimesylate and 40 mg immediaterelease dexamfetamine sulphate were administered to individuals with a history of drug abuse, lisdexamfetamine dimesylate 100 mg produced subjective responses on a scale of “Drug Liking Effects” (primary endpoint) that were significantly less than dexamfetamine immediaterelease 40 mg. However, oral administration of 150 mg lisdexamfetamine dimesylate produced increases in positive subjective responses on this scale that were comparable to the positive subjective responses produced by 40 mg of oral immediaterelease dexamfetamine and 200 mg of diethylpropion.
Intravenous administration of 50 mg lisdexamfetamine dimesylate to individuals with a history of drug abuse produced positive subjective responses on scales measuring “Drug Liking”, “Euphoria”, “Amfetamine Effects”, and "Benzedrine Effects" that were greater than placebo but less than those produced by an equivalent dose (20 mg) of intravenous dexamfetamine.
After oral administration, lisdexamfetamine dimesylate is rapidly absorbed from the gastrointestinal tract of healthy adults and children (6 to 12 years) with ADHD, thought to be mediated by the high capacity PEPT1 transporter.
Food does not affect the observed AUC and Cmax of dexamfetamine in healthy adults after singledose oral administration of Elvanse 70 mg capsules but prolongs Tmax by approximately 1 hour (from 3.8 hours at fasted state to 4.7 hours after a high fat meal). After an 8hour fast, the AUCs for dexamfetamine following oral administration of lisdexamfetamine dimesylate in solution and as intact capsules were equivalent.
In 18 children (6 to 12 years) with ADHD, the Tmax of dexamfetamine was approximately 3.5 hours following singledose oral administration of lisdexamfetamine dimesylate either 30 mg, 50 mg, or 70 mg administered after an 8hour overnight fast. The Tmax of lisdexamfetamine dimesylate was approximately 1 hour. Linear pharmacokinetics of dexamfetamine after singledose oral administration of lisdexamfetamine dimesylate was established over the dose range of 30 mg to 70 mg in children aged 6 to 12 years.
Weight/dose normalised AUC and Cmax were 22% and 12% lower, respectively, in adult females than in males on day 7 following a 70 mg/day dose of lisdexamfetamine for 7 days. Weight/dose normalised AUC and Cmax values were the same in girls and boys following single doses of 3070 mg.
There is no accumulation of dexamfetamine at steady state in healthy adults and no accumulation of lisdexamfetamine dimesylate after oncedaily dosing for 7 consecutive days.
Lisdexamfetamine dimesylate is converted to dexamfetamine and llysine, which occurs by metabolism in blood primarily due to the hydrolytic activity of red blood cells. Red blood cells have a high capacity for metabolism of lisdexamfetamine as in vitro data demonstrated substantial hydrolysis occurs even at low hematocrit levels. Lisdexamfetamine is not metabolised by cytochrome P450 enzymes.
Amfetamine is oxidised at the 4 position of the benzene ring to form 4hydroxyamfetamine, or on the side chain α or β carbons to form alphahydroxyamfetamine or norephedrine, respectively. Norephedrine and 4hydroxyamfetamine are both active and each is subsequently oxidised to form 4hydroxynorephedrine. Alphahydroxyamfetamine undergoes deamination to form phenylacetone, which ultimately forms benzoic acid and its glucuronide and the glycine conjugate hippuric acid. Although the enzymes involved in amfetamine metabolism have not been clearly defined, CYP2D6 is known to be involved with formation of 4hydroxyamfetamine.
Following the oral administration of a 70 mg dose of radiolabelled lisdexamfetamine dimesylate to 6 healthy subjects, approximately 96% of the oral dose radioactivity was recovered in the urine and only 0.3% recovered in the faeces over a period of 120 hours. Of the radioactivity recovered in the urine 42% of the dose was related to amfetamine, 25% to hippuric acid, and 2% intact lisdexamfetamine. Plasma concentrations of unconverted lisdexamfetamine are low and transient, generally becoming nonquantifiable by 8 hours after administration. The plasma elimination halflife of lisdexamfetamine typically averaged less than one hour in studies of lisdexamfetamine dimesylate in volunteers. The halflife of dexamfetamine is 11 hours.
The pharmacokinetics of dexamfetamine is similar in children (aged 6 to 12) and adolescents (aged 13 to 17) ADHD patients, and healthy adult volunteers. Any differences in kinetics seen after oral administration are a result of differences in mg/kg dosing.
Systemic exposure to dexamfetamine is similar for men and women given the same mg/kg dose.
Formal pharmacokinetic studies for race have not been conducted. There is no evidence of any impact of ethnicity on the pharmacokinetics of Elvanse.
In a pharmacokinetic study of 40 subjects (8 subjects in each of five renal functional groups: normal, mild impairment, moderate impairment, severe impairment, and end stage renal disease) dexamfetamine clearance was reduced from 0.7
L/hr/kg in normal subjects to 0.4 L/hr/kg in subjects with severe renal impairment (GFR 15 to < 30 mL/min1.73m2 or CrCl <30 mL/min).
In a study of 47 subjects aged 55 years of age or older amfetamine clearance was approximately 0.7 L/hr/kg for subjects 55 to 74 years of age and 0.55 L/hr/kg for subjects ≥75 years of age. This is slightly reduced compared to younger adults (approximately 1 L/hr/kg for subjects 18 to 45 years of age).
Preclinical Safety Data
In repeat dose toxicity studies the major findings were changes in behaviour, such as increased activity typical of stimulant administration, with associated reductions in body weight gain, growth measurements and food intake, considered to be a consequence of an exaggerated pharmacological response.
Lisdexamfetamine dimesylate was not genotoxic when tested in vitro in the Ames test and the mouse lymphoma assay or in vivo in the mouse bone marrow micronucleus test. Carcinogenicity studies of lisdexamfetamine dimesylate have not been performed. No evidence of carcinogenicity was found in studies in which d, lamfetamine (enantiomer ratio of 1:1) was administered to mice and rats in the diet for 2 years at doses of up to 30 mg/kg/day in male mice, 19 mg/kg/day in female mice, and 5 mg/kg/day in male and female rats.
Lisdexamfetamine dimesylate had no effect on embryofoetal development or survival when administered orally to pregnant rats at doses up to 40 mg/kg/day, and rabbits at doses up to 120 mg/kg/day.
No adverse effects on nervous system development or reproductive function were observed following repeat dose administration of lisdexamfetamine dimesylate to juvenile rats and dogs.
Amfetamine (d to lenantiomer ratio of 3:1) did not adversely affect fertility or early embryonic development in the rat at doses of up to 20 mg/kg/day.
A number of studies in rodents indicate that prenatal or early postnatal exposure to amfetamine (d or d,l) at doses similar to those used clinically can result in longterm neurochemical and behavioural alterations. Reported behavioural effects include learning and memory deficits, altered locomotor activity, and changes in sexual function. Similar studies have not been conducted for Elvanse.
List of Excipients
Black ink (shellac and black iron oxide E172).
Capsule shell colourants
20 mg: titanium dioxide (E171) and yellow iron oxide (E172).
40 mg: titanium dioxide (E171), brilliant blue FCF (E133), black iron oxide (E172) and yellow iron oxide (E172).
60 mg: titanium dioxide (E171) and brilliant blue FCF (E133).
Special Precautions For Storage
Do not store above 25°C.
Nature and Contents of Container
High density polyethylene bottle and a polypropylene child resistant cap with a foil inner seal.
Pack sizes: 28 or 30.
Not all pack sizes may be marketed.
Special Precautions For Disposal and Other Handling
Any unused medicinal product or waste material should be disposed of in accordance with local requirements.
Marketing Authorisation Holder
Shire Pharmaceutical Contracts Limited
Hampshire International Business Park
Marketing Authorisation Number(s)
PL 08081/0062 – 064
Company Contact Details
Shire Pharmaceuticals Limited
Hampshire International Business Park, Chineham, Basingstoke, Hampshire , RG24 8EP
Medical Information Direct Line
0800 055 6614
Customer Care direct line
+44 (0)1256 894 107
+44 (0)1256 894 000
Medical Information email