The present invention relates to a modified-release composition of mazindol and its use in the treatment of attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alertness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) in particular in children, adolescents and adults. ADHD is a behavioural disorder that constitutes one of the most frequently encountered patterns in child and adolescent psychopathology. It is also present in adults. Although a recent longitudinal study raises possibility that adults presenting with the ADHD symptom picture may not have a childhood-onset neurodevelopmental disorder (Moffitt 2015), the majority of available data and scientific consensus suggest that ADHD is the same disease in both adults and paediatrics (Kooji 2010) In fact, the criteria for ADHD was changed in DSM-V (American Psychiatric Association, 2013) to more accurately characterize ADHD as a neurodevelopmental disorder, which begins in childhood but continues through adulthood for some people. In recent studies the prevalence of ADHD is estimated to be 7 to 8% of school-age children (Barbaresi 2002) and 4 to 5% of adults (Kessler 2006). Clinically, this disorder combines inattention, impulsivity and motor hyperactivity leading to impairment in academic/work, social and interpersonal functioning. Without treatment, children and adults are unable to stay on task leading to decreased academic or work performance. In addition, impulsivity may lead to decreased quality of work and dysfunctional social functioning.

The stimulents used, and commonly accepted in the pharmacological treatment of ADHD, belong to several pharmacological classes: psychostimulants (amphetamine, methylphenidate), eugregorics (armodafinil, modafinil, adrafinil), and inhibitors of monoamine oxydase B (selegiline). The improvement of inattention, impulsivity, and hyperactivity by such dopaminergic psychostimulants is often very significant, but nevertheless insufficient in many subjects. Stimulants (e.g., methylphenidate or amphetamines salts) have short half-lives and require controlled release delivery in the majority of patients. Even with controlled delivery, it is difficult to maintain adequate efficacy during school (and/or work) hours and yet achieve concentrations that will allow the patient to fall asleep and remain asleep at night. Stimulants are associated with the appearance of "on-off effects, where the coming-off effect is accompanied by a "symptom rebound" effect with a worsening of the symptoms in the early evening (e.g., a time when homework needs to be completed).

While stimulant medication is an effective treatment for many of the symptoms associated with ADHD, there are concerns about diversion of these medications for misuse and abuse, and some rare but serious cardiovascular side-effects can occur with the use of stimulant medication. Non-stimulants such as atomoxetine, clonidine and guanfacine have also been found to be efficacious in treating ADHD but the efficacy of these agents may not be comparable to that seen with stimulants (Faraone 2009). Even with stimulant treatment, optimal functioning occurs in only roughly one in four children with ADHD (Greenhill 1996). Despite considerable advances in our understanding and treatment of ADHD, the disorder remains difficult to manage and further treatment options need to be developed (Antshel 201 1)

In addition, some of the medications administered in the treatment of ADHD are not suited for administration to children, especially because of excessive size of the tablets or the administration of the medications several times a day.

Use of mazindol in treatment of attention deficit/hyperactivity disorder (ADHD), according to DSM-IV (or DSM-V) criteria, comprising administering an effective amount of mazindol to a patient in need of such treatment has been described in US 8,293,779.

Mazindol has the following chemical formula:

5-(4-chlorophenyl)-2,5-dihydro-3 H-imadazo[2,l-a]isoindol-5-ol

Mazindol is considered, in current medication classifications, as a psycho analeptic and anorexigenic medication, but also as giving rise to wakefulness, currently not authorised in France, or only authorised by TAU (Temporary Authorisation for Use) in obesity and narcolepsy. It is currently authorized in Argentina, Mexico/Central America, and Japan for use in the treatment of obesity. It is an advantageous chemical compound for dealing with malfunctioning of wakefulness mechanisms.

The essential pharmacological action of mazindol, in all species studied, in healthy animals and in humans, is hypothalamic, on the appetite-regulating dopaminergic centres (Hadler, 1972). It is metabolized extensively and the metabolites are then mostly excreted in the urine.

Mazindol is a non-amphetamine compound because of its tricyclic chemical structure. It offers a pharmacological profile very close to that of amphetamines with less abuse liability. Indeed, mazindol is not metabolised to an amphetamine -like compound, but it acts by blocking the dopamine and norepinephrine reuptake similarly to amphetamine.

In addition, in animal toxicology studies, the toxic potential of mazindol has proved to be very low In particular, no carcinogenic effect, no mutagenic effect, no toxicology effect in reproduction were observed.

In US 8,293,779, it is disclosed that, after single or repeated oral administration, mazindol is absorbed with a t _max of 2-4 hours.. The half-life of mazindol after an immediate release formulation is 9.1±1.7h in healthy volunteers (Kim 2009); therefore, steady-state concentrations are reached after approximately 30-55 hours. The pharmacokinetics is linear (independent of the dose) for doses of between 1 mg/day and 4 mg/day. This result however relates to current immediate -release formulations of mazindol. Immediate-release pharmaceutical compositions of mazindol, such as Diminex®, Sanorex® and Teronac®, ensure the release of the active ingredient over a period of <1 h in vitro. Indeed, immediate -release pharmaceutical compositions of mazindol have been reported to undergo hydrolysis at moderate temperatures in neutral and alkaline aqueous solutions, including in human plasma. Due to the mild alkaline nature of plasma, improved mazindol stability in human plasma could be achieved by adding acidic buffer.

Such immediate release compositions thus require twice daily administration, which limits compliance in the special case of children of school age, as the second administration is often requested to be done at midday, i.e. during school time.

Even given the fact that the immediate release tablet undergoes complete in vitro dissolution within 1 hour, the time to maximum concentrations (Tmax) occurs at 3-4 hr after drug administration in healthy volunteers (Kim 2009). Rapid initial absorption will allow the earlier achievement of adequate systemic exposure to achieve desired efficacy (e.g., administer early and have onset of efficacy 1-2 hours later, when patient is at school or work)

But, to achieve once daily dosing regimen (a very desirable regimen), a controlled release portion would also be needed to assure that adequate plasma concentrations are achieved throughout the day and evening, while allowing the subject to fall asleep and remain asleep during the night. Thus, a combination product consisting of an immediate release portion (IR) and a sustained release portion (SR) would be an ideal dose form.

There is therefore a need for a pharmaceutical composition comprising mazindol with an improved release profile of active substance combining an immediate and a sustained release, an improved compliance for patients and reduced fluctuation in steady-state mazindol plasma concentrations during a dosing interval.

SUMMARY

According to a first aspect, the present invention thus relates to a mazindol oral pharmaceutical unit dosage form in the form of a multilayer matrix-type tablet comprising:

at least one immediate -release (IR) layer comprising mazindol and at least one diluent, at least one sustained-release (SR) layer comprising mazindol and at least one sustained-release, pH-independent and water-insoluble polymer,

for a total amount of mazindol comprised between 1 and 5 mg and a ratio in weight between the IR layers and the SR layers comprised between 40:60 and 80:20 preferably between 50:50 and 70:30, more preferably of 50:50.

The oral pharmaceutical unit dosage form in the form of a multilayer matrix-type tablet of the invention provides a rapid release of drug to achieve a rapid therapeutic blood level and a sustained release portion to provide a continual release of mazindol available for absorption into the patients' blood stream to achieve a prolonged therapeutic effect. This combination thus achieves a once daily regimen for the product. This oral pharmaceutical unit dosage form has the following advantages:

-Ease of swallowing

-Ease of manufacture

-The ability to control the release rate of the drug by modifying the components of each separate layer

-Superior stability compared to other dose forms, such as capsules, liquids

-Prevents patient tampering with the dose form.

- Reduced fluctuation in steady-state mazindol plasma concentrations during a dosing interval.

According to another aspect, the invention relates to a process for preparing the unit dosage form according to the invention, comprising the following steps:

(a) preparing the blend of the excipients of the IR layers,

(a') preparing the blend of the excipients of the SR layers,

(b) adding the IR blend of step (a) and the SR blend of step (a') into a multilayer, preferably a bilayer, tablets' press.

According to a further aspect, the invention relates to the unit dosage form according to the invention, for its use as medicinal product administered in repeat once-a-day form via oral route. According to a further aspect, the invention relates to the unit dosage form according to the invention, for use for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alerteness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) in particular in children, adolescents and adults.

According to a further aspect, the invention relates to a method for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alerteness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) comprising the administration, preferably in repeat once-a-day via oral route, of the unit dosage form according to the invention to a patient in need thereof, in particular in children, adolescents and adults.

According to a further aspect of the present invention, the invention relates to the unit dosage form according to the invention, used in combination with iron as a combination product for simultaneous, separate or sequential use, in particular for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alertness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) in particular in children, adolescents and adults.

According to a further aspect, the invention relates to a method for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alerteness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) comprising the administration, preferably in repeat once-a-day via oral route, of the unit dosage form according to the invention and the administration of iron to a patient in need thereof, in particular in children, adolescents and adults.

According to a further aspect of the present invention, the invention relates to the unit dosage form according to the invention, used in combination with a psychostimulant as a combination product for simultaneous, separate or sequential use, in particular for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alerteness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) in particular in children, adolescents and adults.

According to a further aspect, the invention relates to a method for treating attention deficit disorders (ADD) or attention deficit/hyperactivity disorder (ADHD) or related deficit of alerteness (i.e, incoercible sleepiness) or decline of vigilance (i.e., daytime somnolence) or excessive daytime sleepiness (eg, narcolepsy, idiopathic hypersomnia) comprising the administration, preferably in repeat once-a-day, via oral route of the unit dosage form according to the invention and the administration of a psychostimulant to a patient in need thereof, in particular in children, adolescents and adults.

DEFINITIONS

The term "matrix-type tablet" is used in the invention to designate a tablet whose inner structure in each layer is homogeneous and identical from the center towards the periphery of the layer. Therefore, the layers of the tablets of the present invention consist of a homogeneous mixture of active ingredient in powder or granule form and of a compression matrix.

The term "compression matrix" in the present invention is used to designate all the excipients which take part in the cohesion of the tablet. Said compression matrix is both water-insoluble and has a certain permeability (hydrophilic matrix) or porous network (inert matrix) responsible for the sustained release of the active ingredient, which does not vary in relation to the pH conditions of the medium.

The term "compression mixture" is used in the present application to designate all the constituents of the tablets (the active ingredient(s), granulated or not, and the constituents of the compression matrix) before its compression in tablet form.

As used in the present invention, the term "steady-state" refers to the concentrations in the body after 4 to 7 half-lives after repeat dosing. The concentrations at steady-state differ depending on the formulation used and the dosing frequency. At steady state, plasma concentrations of mazindol will vary between Cmax(ss) (the maximum observed concentration at steady-state) and Cmin(ss) (the minimum observed concentration at steady-state).

A study with repeat doses not only provides a measure of the usual pharmacokinetic parameters (area under the curve during a dosing interval at steady-state, AUC(O-x), Cmax(ss), the time to the Cmax or Cmax(ss), Tmax), but also demonstrates the significance of the fluctuations between the steady-state peak (Cmax(ss)) and trough (Cmin(ss)) concentrations.

Tmax is the time to reach the peak concentration. This value is dependent on the absorption rate of a pharmaceutically active material.

The pharmacokinetic parameters C _max and T _max result directly from experimental plots. Repeat dosing with a drug can involve a certain accumulation of the drug, or its metabolites, the significance of which depends on the dosage schedule used.

Given a drug M, administered orally at a dose D at a dosing time interval x. As the drug is given before the previous dose is fully eliminated, the amount administered adds to the non-eliminated amount from the previous doses (superimposition principle). After a period of 4-7 half-lives, the amount of drug absorbed that enters the body is equivalent to the amount that is eliminated from the body and steady state is achieved. Concentrations vary between a trough concentration Cmin(ss) and a peak concentration Cmax(SS). As used in the present invention, "repeat oral dosing" refers to administration of the formulation of the present invention at a dose D at a dosing time interval τ of between 20 and 24 hours.

The "fluctuation" and "swing" parameters are expressed as a % and are calculated according to the following equations:

-Fluctuation: 100*(Cmax(SS) - Cmin(SS))/Cav

wherein Cav is the " average steady-state concentration", representing the AUC(O-x) divided by the dosing interval: Cav = AUC(0-x)/x

In the meaning of the present invention, the expression « reduction of fluctuations » may designate the lowering of the difference between the Cmax(SS) and Cmin(SS) or differences between the peaks and troughs, or preferably a value for the « fluctuation » parameter of between 25 % and 75 % in one embodiment, <60% in one embodiment, <50% in one embodiment, or more preferably less than 35 %.

-Swing: 100*(Cmax(SS) - Cmin(SS))/Cmin(SS) =A

The half-life (t½) is the time for a concentration C of a drug in a body fluid or a tissue to reach the concentration C/2.

The area under the curve during a dosing interval at stead-state, AUC(O-x), corresponds to the integral of the plasma concentration over a given dosing interval.

The AUC(O-x) is expressed in units of mass (mg, ng) x liter (or mL) ^"1 x hour, and is dependent on the bioavailability and clearance of a drug.

In the meaning of the present invention, by a profile having « reduced fluctuation » is meant a profile having a swing Δ of less than 50 % in one embodiment or <60% in one embodiment, or <35% in one embodiment.

In the meaning of the present invention, by a profile having « reduced fluctuation » is also meant a plasma profile maintained above 40 % or preferably above 50 % of the Cmax(SS) value for at least 12 hours.

An "immediate-release (IR) layer" refers to a layer that releases greater than or equal to about 80% by weight of mazindol in less than or equal to about 1 hour.

A "sustained-release (SR) layer" means a layer in which mazindol is released at a rate slower than that of an IR layer.

FIGURES

Figures 1 - 6 depict dissolution profiles of the prototype tablets of Example 3.

Figure-1 : Overlay of All Dissolution Profiles

Figure -2: Overlay of Series 1 Formulations

Figure-3: Overlay of Series 2 Formulations

Figure -4: Overlay of Dissolution Profiles for 50/50 IR/SR Ratio Tablet Formulations

Figure-5: Overlay of Dissolution Profiles for 60/40 IR/SR Ratio Tablet Formulations

Figure-6: Overlay of Dissolution Profiles for 70/30 IR/SR Ratio Tablet Formulations Figure-7: Overlay of Dissolution Profiles from Batch 100-15021 Tablets Analyzed Using UV Probes (100-15021) and HPLC Analysis (15021LC)

Figure-8: Overlay of Dissolution Profiles from Batch 100-15022 Tablets Analyzed Using UV Probes (100-15022) and HPLC Analysis (15022LC)

DETAILED DESCRIPTION

The pharmaceutical composition according to the present invention is a mazindol oral pharmaceutical unit dosage form in the form of a multilayer matrix-type tablet comprising:

at least one immediate-release (IR) layer comprising mazindol and at least one diluent,

at least one sustained-release (SR) layer comprising mazindol and at least one sustained-release, pH-independent and water-insoluble polymer,

for a total amount of mazindol comprised between 1 and 5 mg and a ratio in weight between the IR layers and the SR layers comprised between 40:60 and 80:20 preferably between 50:50 and 70:30, more preferably of 50:50.

Preferably, the unit dosage form according to the invention is a bilayer tablet.

Preferably, the unit dosage form according to the invention has a dissolution of between 60% and 80% at 1 hour, of between 70% and 90% at 2 hours, as measured in accordance with the rotating blade method at 50 rpm according to the US Pharmacopeia Method 2, in a dissolution medium 0.01N HC1, 500 mL.

Preferably, the unit dosage form according to the invention is of between 50 and 200 mg, preferably of 100 mg.

Preferably, the unit dosage form according to the invention comprises between 2 and 5 mg of mazindol, preferably of 4 mg.

Preferably, the unit dosage form according to the invention maintains the steady-state mazindol plasma concentrations obtained in vivo with a reduced fluctuation of above 40 % of the CsSmax value, preferably above 50 % of the Css _max value for at least 12 h.

Examples of diluents include: lactose, monohydrate lactose, anhydrous lactose, spray-dried lactose, calcium carbonate, calcium sulfate, calcium sulfate dehydrate, calcium lactate trihydrate, monobasic calcium sulfate monohydrate, calcium carbonate, tribasic calcium phosphate, diabasic calcium phosphate, compressible sugars, dextrates, dextrin, dextrose, calcium phosphate, kaolin, magnesium carbonate, magnesium oxide, maltodextrin, mannitol, powdered cellulose, starch, modified starch, starch hydrolyzates, pregelatinized starch, microcrystalline cellulose, powdered cellulose, cellulose and cellulose derivatives, hydroxypropylmethylcellulose, hydroxypropylmethylcellulose and sucrose, preferably lactose, anhydrous lactose, spray-dried lactose, microcrystalline cellulose, powdered cellulose, cellulose and cellulose derivatives.

Diluent concentration in the IR layers can be varied between 30 and 60%, preferably 45 to 55% by weight of the total weight of the IR layers.

Preferably, the unit dosage form according to the invention comprises a lubricant in each layer.

Lubricants and glidants can be employed in the present application to prevent, reduce or inhibit adhesion or friction of ingredients of the composition. They facilitate the compression and ejection of compressed compositions from a desired die. They are compatible with the ingredients of the pharmaceutical composition, and they do not significantly reduce the solubility, hardness, chemical stability, physical stability, or the biological activity of the pharmaceutical composition. The pharmaceutically acceptable lubricants and glidants for the present application are selected from the group including but not limited to stearic acid, metallic stearates, zinc stearate, magnesium stearate, magnesium trisilicate, calcium hydroxide, tribasic calcium phosphate, magnesium carbonate, magnesium oxide, calcium stearate, glyceryl monostearate, waxes, glycerides, glyceryl behenate, glyceryl palmitostearate, silicone oil, hydrogenated vegetable oil, hydrogenated castor oil, light mineral oil, mineral oil, polyethylene glycol, methoxypolyethylene glycol, sodium acetate, sodium oleate, sodium chloride, leucine, sodium benzoate, alkyl sulfates, sodium lauryl sulfate, sodium stearyl fumarate, talc, colloidal silica, corn starch, powdered cellulose, and/or boric acid.

The preferred range of lubricants/glidants is from 0% to 1% w/w of the layer.

The sustained-release, pH-independent and water-insoluble polymer in SR layers of the tablets according to the invention is selected in the group consisting of cellulose polymers, high-molecular-weight polymers of acrylic acid that are crosslinked with either allyl sucrose or allyl ethers of pentaerythritol (Carbopol, Carbomers), polymers from the class of methacrylic acids, polyvinylalcohol derivatives, polymers of lactic and glycolic acids (PLGA), starches, waxes, polyvinyl acetate derivatives, polyvinyl pyrrolidone derivatives and mixtures thereof, preferably is selected in the group consisting of cellulose polymers and high-molecular- weight polymers of acrylic acid that are crosslinked with either allyl sucrose or allyl ethers of pentaerythritol (Carbopol, Carbomers).

Cellulose polymers include hydroxypropyl methylcellulose (HPMC), hydroxypropyl cellulose (HPC), sodium CMC, ethyl cellulose derivatives such as cellulose acetate, cellulose acetate butyrate, cellulose acetate cellulose propionate, hydroxypropylmethylcellulose acetate succinate, micro crystalline cellulose (for example such as the one supplied under the trade mark Avicel®, and ethylcellulose (for example the one supplied under the trade mark Aqualon® ethylcellulose)

Polymers from the class of methacrylic acids include the grades Eudragit®RL 12.5, RL PO and RL 100 and RS 12.5, RS PO and RS 100.

Starches include natural starches e.g. corn starches and modified starches such as pre-gelled starch,

Waxes include white or yellow beeswax, polyvinyl acetate derivatives.

Sustained-release, pH-independent and water-insoluble polymer concentration in the SR layers can be varied between 80 and 99%, preferably 90 to 97% by weight of the total weight of the SR layers.

The unit dosage form according to the invention can include anti-agglomerant agents, anti-agglomerant agents used in the present invention include talc, silicon dioxide and its derivatives, acrylic esters, castor oil derivative, cellulose compounds, iron oxides, magnesium stearate, stearic acid and or sodium stearate fumaryl.

Layers of the tablet according to the present invention can comprise a binder.

Binders according to the invention, include hydroxypropylmethylcellulose (HPMC), hydroxypropylcellulose (HPC), maltodextrin, polyvinylpyrrolidone (PVP) and or micro crystalline cellulose.

The compression matrix can advantageously include, additionally to the excipients of the compression matrix, one or more excipients intended either to promote the proper conducting of the compression process.

The invention also relates to a process for preparing the unit dosage form according to the invention, comprising the following steps:

(a) preparing the blend of the excipients of the IR layers,

(a') preparing the blend of the excipients of the SR layers,

(b) adding the IR blend of step (a) and the SR blend of step (a') into a multilayer, preferably a bilayer, tablets' press.

In the context of the present invention, the diagnosis of attention- deficit/hyperactivity disorder (ADHD) is based on the clinical characteristics defined by the international classification used by ICD- 10 (International Classification of Diseases (ICD). World Health Organization) and DSM-V (Diagnostic and Statistical Manual of Mental Disorders, 5 ^th edition).

The criteria of DSM-V includes three dimensions (inattention, impulsivity and hyperactivity), normal intellectual efficiency (IQ>80, with an age between 5 and 12 years) and having isolated iron deficiency, but not anaemic, that is to say having a normal haemoglobin level. The expression "iron deficiency" means hypoferrinaemia without significant modification to the serum concentration of soluble transferrin receptors.

"ADHD symptom" designates in particular attention disorders such as inattention, impulsivity, impatience, oppositional disorders, but also daytime or night-time motor hyperactivity, restless legs syndrome, and insomnia.

Insomnia designates:

a. onset insomnia that is characterised by difficulties in falling asleep;

b. maintenance insomnia that is characterised by night-time motor hyperactivity and waking up during the night, and

c. psychopathological insomnia, generally chronic and generally linked to anxiety, stress and depressive episodes. The criteria for evaluating the efficacy of the treatment of attention- deficit/hyperactivity disorder by of the modified-release pharmaceutical composition comprising mazindol optionally in association with iron and/or a psychostimulant in the treatment of attention-deficit/hyperactivity disorder according to the present invention are the reduction (>30%) in the rating scale severity score for attention-deficit/hyperactivity symptoms AHD-RS (after 12 weeks of treatment, and an improvement in severity scores for Conner's Parent questionnaire (CPRS), Conner's Teacher questionnaire (CTRS) and CGI (clinical global impressions). Subjective somnolence is assessed using the CASS scale (child and adolescent somnolence scale). The quality of falling asleep is assessed by means of the restless legs syndrome severity scale.

The patient according to the invention is chosen from among a newborn baby, a child, an adolescent and an adult. According to a preferred embodiment, the patient is a child or an adolescent or an adult, even more preferably a child aged approximately 5 to 12 years. The patient according to the invention advantageously suffers iron deficiency, but is not anaemic. Ferritin deficiency can be measured in the serum, but also in all other biological fluids such as the cerebrospinal fluid.

A ferritin deficiency corresponds to a serum concentration of ferritin in the adult patient of less than approximately 50 μg/litre. This deficit of iron storage" (expressed by a low ferritin level) may reach ferritin concentrations of less than approximately 40 μg/l, or even less than approximately 35 μg/l, less than 30 μg/l, less than 20 μg/l, less than 15 μg/l, or even less than approximately 10 μg/l. The techniques of determining serum ferritin are well known to persons skilled in the art. The immunoenzymatic method (IMX ferritin kit, Abbot Laboratories) can be cited.

The patient according to the invention also has a normal serum concentration of receptors soluble to transferrin. Transferrin is involved in the acquisition of iron by the cells of the organism; this acquisition is controlled by the number of transferrin receptors existing on the cell surface. The concentration of these receptors can be evaluated by techniques known to persons skilled in the art such as nephelemetry (Ruivard et al. 2000 Rev Med Interne 21 : 837-843). A normal range of concentration of receptors soluble to transferrin is 2.0-4.50 mg/1 for men and 1.80-4.70 mg/1 for women (see RsTF kit Ref 2148315 from Roche). According to another aspect of the present invention, mazindol is used in combination with iron as a combination product for simultaneous, separate or sequential use.

According to a preferred method of use, the iron is used as a supplement with the patient before the administration of mazindol.

Within the meaning of the present invention, "iron" means iron in the form of an iron atom, iron salt or organic iron, or any formulation containing iron that is pharmaceutically acceptable. By way of a non-exhaustive list, the pharmaceutically acceptable iron salt is selected from ferrous salts and ferric salts, preferably from ferric ammonium citrate, ferric pyrophosphate, ferrocholinate, ferrous abscorbate, ferrous aspartate, ferrous chloride, ferrous sulphate, ferrous tartrate, ferrous fumarate, ferrous gluconate, ferrous gluceptate, ferrous sulphate glycine, ferrous lactate, ferrous oxalate and ferrous succinate.

According to a preferred embodiment of the invention, the iron salt is ferrous sulphate, and preferably gastro -protected ferrous sulphate.

Alternatively, the pharmaceutical acceptable iron is in the form of dextran iron, sucrose iron, poly-maltose iron, or sorbitol iron. When the iron is in the form of pharmaceutically acceptable organic iron, it is preferably iron biglycinate, iron glycinate or iron protein succinylate.

According to a preferred embodiment, the use of mazindol possibly in association with the iron according to the invention is implemented in combination with at least one compound selected from psychostimulants, as a combination product for simultaneous, separate or sequential use.

Psychostimulant compounds designate dopamine and/or noradrenaline uptake inhibitors and agonists of catecholamines. Among these, the following can be cited non- exhaustively:

1) psychostimulant compounds: methylphenidate (speciality Ritalin®, Concerta®, Equasym®, Quasym, Medikinet Retard®), armodafinil (Nuvigil®), modafinil (Sparlon®, Modiodal®, Provigil®), atomoxetine (Strattera®), bupriopion, and amphetamines such as d-amphetamine, dexedrine, dexamphetamine and lisdexamfetamine (Vyvanse®, Elvanse®). 2) L-Dopa: Modopar, Sinemat

3) selective dopamine agonists: pramipexole (Sifrol®, Mirapex®), ropinirole (Requip®, Adartrel®), lisuride, pergolide, cabergoline, etc.

In particular, when mazindol is used in association with ferrous sulphate, the quantity of ferrous sulphate administered to the patient on a daily basis is between 0.1 mg and 10 mg, preferably between 100 mg and 2 g per day, preferably approximately 500 mg, in one or more doses.

More particularly, according to the present invention, the patients undergo iron supplementation, in particular ferrous sulphate, for 12 weeks and the treatment with mazindol for 12 weeks.

According to the present invention, the composition may also comprise iron or one of its pharmaceutically acceptable salts and/or a psychostimulant.

EXAMPLES

Example 1 : Conditions for the dissolution profiles:

Dissolution Medium: 0.0 IN HC1

Medium Volume: 500 mL

USP Apparatus 2 (Paddles)

Speed: 50 rpm

Medium Temperature: 37 °C ± 0.5 °C

Test 6 tablets (unless otherwise specified)

Timepoints: 1, 2, 4, 6, 8, and 10 hours

Sample approximately 5 mL from each vessel using a syringe or autosampler with cannulae and a 10 μπι full flow filter attached.

Example 2: Process for manufacture of mazindol bilayer tablets

A, Manufacturing process for the sustained release (SR) layer (2mg. tablet)

1. Weigh the following ingredients: concentration w/w%

a. Mazindol 2.0 b. Lactose monohydrate NF/hypromellose NF (Retalac®) 97.0

c. Carbopol 97 IP 0.5

d. Magnesium stearate 0.5

Total= 100%

2. Screen ingredients a, b, c, from step 1 into the V blender and blend for 20 minutes.

3. Pass the ingredients from Step2 through the Comil .

4. Add the ingredients from Step 3 into the V blender.

5. Screen item d from Step 1 into the blender and blend for 5 minutes,

6. Collect material from Step 5 for tablet manufacture.

B. Manufacturing process for the immediate release (IR) layer (2mg) tablet:

1. Weigh the following ingredients: concentration w/w%

a. Mazindol 2.0

b. Lactose monohydrate, NF 97.5

c. Magnesium stearate 0.5 Total= 100%

2. Screen ingredients a, b, from Step 1 into the V blender and blend for 20 minutes

3. Pass ingredients from Step 2 through the Comil

4. Add ingredients from Step 3 into the V blender.

5. Screen item c from Step 1 into the blender and blend for 5 minutes.

6. Collect material from Step 5 for tablet manufacture.

C. Tablet manufacture:

1. Set bilayer press for correct weight.

2. Add the IR blend to hopper 1.

3. Add the SR blend to hopper 2.

4. Compress tablets to a total weight of lOOmg. Example 3: Dissolution profiles of the bilayer tablets of example 2:

6 bilayer tablets have been prepared. Dissolution was performed per USP monograph for Mazindol tablets.

Data was collected using Pion Rainbow UV probes on n=3 tablets per batch. % Release values are reported as the average of either two or three tablets per prototype batch.

The bilayer tablet formulations are based on two sustained release (SR) formulations and one immediate release (IR) formulation.

The IR formulation is combined at three mass/mass ratios (IR SR = 50/50, 60/40, & 70/30) with each SR formulation to create 6 bilayer tablet prototypes.

The quantitative formulations for each of the prototype tablets are given in tables 1 and 2 along with their R&D batch number designation.

Table-1 formulations include the SR formulation which utilizes HPMC and Carbopol 971P to modulate Mazindol dissolution and are categorized as Series 1 prototype formulations. Table-2 formulations include the SR formulation which incorporates two different molecular weight grades of HPMC to modulate Mazindol dissolution and are categorized as Series 2 prototype formulations.

Table-3 reports the dissolution testing results for each of the prototype formulations. Table-1 : Series 1 Prototype Tablet Formulations

Batch Number 100-15018 100-15019 100-15020

IR layer/SR layer Ratio 50/50 60/40 70/30

IR Layer Formulation

Ingredients mg/Tablet mg/Tablet mg/Tablet

Mazindol 0.5 0.6 0.7

Lactose Monohydrate 49.25 59.1 68.95

Magnesium Stearate 0.25 0.3 0.35

SR Layer Formulation

Mazindol 0.5 0.4 0.3 Lactose/HPMC K4M (Retalac ^® ) 49 39.2 29.4

Carbopol 971P 0.25 0.2 0.15

Magnesium Stearate 0.25 0.2 0.15

Table-2: Series 2 Prototype Tablet Formulations

Batch Number 100-15021 100-15022 100-15023

IR layer/SR layer Ratio 50/50 60/40 70/30

IR Layer Formulation

Ingredients mg/Tablet mg/Tablet mg/Tablet

Mazindol 0.5 0.6 0.7

Lactose Monohydrate 49.25 59.1 68.95

Magnesium Stearate 0.25 0.3 0.35

SR Layer Formulation

Mazindol 0.5 0.4 0.3

Lactose/HPMC K4M (Retalac ^® ) 36.75 29.4 22.05

H PMC K100M 12.5 10 7.5

Magnesium Stearate 0.25 0.2 0.15

Table-3: Dissolution Results for Prototype Tablet Batches (UV Probe Analysis Data)

Batch # 100-15018 100-15019 100-15020 100-15021 100-15022 100-15023

Formulation Series 1 Series 2

IR/SR Ratio 50/50 60/40 70/30 50/50 60/40 70/30

Time (Hours) % Released % Released % Released % Released % Released % Released

0.5 60.07% 63.29% 75.33% 64.81% 69.79% 71.62%

1 69.01% 76.04% 87.15% 73.78% 78.84% 80.63%

1.5 74.97% 80.03% 89.50% 80.00% 83.40% 83.91%

2 80.47% 84.20% 91.17% 84.32% 86.23% 86.29%

3 86.31% 89.64% 95.69% 91.21% 91.58% 91.63%

4 90.87% 92.71% 96.48% 94.11% 94.52% 94.44% 5 93.57% 94.78% 97.19% 96.40% 95.85% 95.21%

6 95.47% 96.13% 97.49% 98.03% 97.09% 96.81%

7 96.48% 97.27% 99.30% 98.58% 97.92% 97.72%

8 97.92% 98.80% 99.45% 99.06% 98.50% 99.39%

9 98.57% 99.61% 98.84% 99.91% 98.77% 98.94%

10 99.87% 99.44% 99.65% 99.77% 99.36% 100.00%

All prototype tablet batches were tested in two distinct dissolution runs, one n=3 run analyzed using the UV probes and one n=4 run using HPLC analysis.

Table-4 reports the results for the n=3, UV analyzed dissolution testing compared to the n=4, HPLC analyzed dissolution testing for batches 100-15021 and 100-15022.

Table-4: UV Probe Analysis vs. HPLC Analysis of Dissolution Samples

The dissolution data for the prototype tablets reveal the Series 1 formulations to have the greatest differentiation among the dissolution profiles at the early time points.

The Series 2 formulations display a slighter differentiation at these time points for the range of SPv/IR layer weight ratios. REFERENCES

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