AU2005239716A1

AU2005239716A1 - Controlled Release Metformin Compositions

Info

Publication number: AU2005239716A1
Application number: AU2005239716A
Authority: AU
Inventors: Chen Chih-Ming; Joseph Chou; Steve Jan; Cheng Xiu-Xiu
Original assignee: Andrx Laboratories LLC
Current assignee: Andrx Laboratories LLC
Priority date: 2000-11-03
Filing date: 2005-12-02
Publication date: 2005-12-22
Anticipated expiration: 2021-10-30
Also published as: AU2005239716B2

Description

P/00/011 28/5/91 Regulation 3.2

AUSTRALIA

Patents Act 1990

ORIGINAL

COMPLETE SPECIFICATION STANDARD PATENT Name of Applicant: Actual Inventors Address for service is: Andrx Labs, LLC Chen CHIH-MING Cheng XIU-XIU Steve JAN Joseph CHOU WRAY ASSOCIATES Level 4, The Quadrant 1 William Street Perth, WA 6000 Attorney code: WR Invention Title: Controlled Release Metformin Compositions The following statement is a full description of this invention, including the best method of performing it known to me:- SCONTROLLED RELEASE METFORMIN

COMPOSITIONS

Background of the Invention The present invention relates to controlled release unit dose formulations containing an antihyperglycemic drug. More specifically, the present invention relates to an oral dosage form comprising a biguanide such as metformin or buformin or a pharmaceutically acceptable salt thereof such as metfonnin hydrochloride or the metformin salts described in United States Patent SNos. 3,957,853 and 4,080,472 which are incorporated herein by reference.

SIn the prior art, many techniques have been used toprovide controlled and extended- 0 release pharmaceutical dosage forms in order to maintain therapeutic serum levels of medicaments and to minimize the effects of missed doses of drugs caused by a lack of patient compliance.

In the prior art are extended release tablets which have an osmotically active drug core surrounded by a semipermeable membrane. These tablets function by allowing a fluid such as gastric or intestinal fluid to permeate the coating membrane and dissolve the active ingredient so it can be released through a passageway in the coating membrane or if the active ingredient is insoluble in the penneating fluid, pushed through the passageway by an expanding agent such as a hydrogel. Some representative examples of these osmotic tablet systems can be found in United States Patent Nos. 3,845,770, 3,916,899, 4,034,758, 4,077,407 and 4,783,337. United States Patent No. 3,952,741 teaches an osmotic device wherein the active agent is released from a core surrounded by a semipermeable membrane only after sufficient pressure has developed within the membrane to burst or rupture the membrane at a weak portion of the membrane.

The basic osmotic device described in the above cited patents have been refined over time in an effort to provide greater control of the release of the active ingredient. For example United States Patent Nos. 4,777,049 and 4,851,229 describe an osmotic dosage form comprising a semipermeable wall surrounding a core. The core contains an active ingredient and a modulating agent wherein the modulating agent causes the active ingredient to be released through a passageway in the semipermeable membrane in a pulsed manner. Further refinements have included modifications to the semipermeable membrane surrounding the active core such as C'I uying the proportions of the components that form the membrane; United States Patent 3s. 5,178,867, 4,587,117 and 4,522,625 or increasing the number of coatings surrounding the Stive core; U.S. Patent Nos. 5,650,170 and 4,892,739.

Although vast amounts of research has been performed on controlled or sustained release mpositions and in particular on osmotic dosage forms, very little research has been performed the area of controlled or sustained release compositions that employ antihyperglycemic drugs.

S Metformin is an oral antihyperglycemic drug used in the management ofnon-insulink pendent diabetes mellitus (NIDDM). It is not chemically or pharmacologically related to oral L fonylureas. Metfonnin improves glucose tolerance in NIDDM patients by lowering both basal i postprandial plasma glucose. Metformin hydrochloride is currently marketed as ,UCOPHAGE® tablets by Bristol-Myers Squibb Co. Each GLUCOPHAGE® tablet contains 3, 850 or 1000 mg of metfornin hydrochloride. There is no fixed dosage regimen for the nagement of hyperglycemia in diabetes mellitus with GLUCOPHAGE®. Dosage of ,UCOPHAGE@ is individualized on the basis of both effectiveness and tolerance, while not seeding the maximum recommended dose of 2550 mg per day.

Metfonnin has been widely prescribed for lowering blood glucose in patients with 3DM. However, being a short acting drug, metfonmin requires twice-daily or threees-a-day dosing. Adverse events associated with metformin use are often trointestinal in nature anorexia, nausea, vomiting and occasionally diarrhea, etc.). These 'erse events may be partially avoided by either reducing the initial and/or maintenance dose or using an extended-release dosage fomn. Another clear advantage of an extended release dosage form is a reduction in the frequency of administration. All of these findings suggest that an extended-release dosage form of metformin may improve the quality of therapy in patients with NIDDM and the safety profile relative to a conventional dosage fonn.

The limited work on controlled or sustained release formulations that employ antihyperglycemic drugs such as metformin hydrochloride includes the combination of the antihyperglycemic drug and an expanding or gelling agent to control the release of the drug from the dosage form. This research is exemplified by the teachings of WO 96/08243 and by the o GLUCOPHAGE® metfornin HCI product.

N 753, that food decreases the extent and slightly delays the absorption of metformin delivered by the GLUCOPHAGE® dosage form. This decrease is shown by approximately a 40% lower peak ,O zoncentration, a 25% lower bioavailability and a 3 5 -minute prolongation of time to peak plasma :oncentration following administration of a single GLUCOPHAGE® tablet containing 850 mg if metfonnin HC1 with food compared to the similar tablet administered under fasting t ,onditions.

C A controlled release metformin dosage form is also described in WO 99/47128. This eference describes a controlled release delivery system for metformin which includes an inner ;olid particulate phase formed of substantially uniform granules containing metformin and one or nore hydrophilic polymers, one or more hydrophobic polymers and one or more hydrophobic naterials, and an outer continuous phase in which the above granules are embedded and lispersed throughout. The outer continuous phase includes one or more hydrophilic polymers, ,ne or more hydrophobic polymers and one or more hydrophobic materials.

Our own WO 99/47125 discloses controlled release metformin formulations providing a max from 8 to 12 hours.

Objects and Summary of the Invention It is an object of the present invention to provide a controlled or sustained release of an .ntihyperglycemic drug which provides effective control of blood glucose.levels in humans.

It is a further object of the present invention to provide a method of treating human patients with non-insulin-dependent diabetes mellitus (NIDDM) on a once-a-day basis with an antihyperglycemic drug which provides effective control of blood glucose levels in humans.

It is a further object of the present invention to provide formulations for treating human patients with non-insulin-dependent diabetes mellitus (NIDDM) which provides advantages over the state-of-the-art, and which may be administered on a once-a-day basis by itself or together with other antidiabetic agents, and methods thereof.

C It is a further object of the present invention to provide a controlled or sustained release Srmulation of an antihyperglycemic drug wherein the bioavailability of the drug is not decreased the presence of food.

It is a further object of the present invention to provide a controlled or sustained release rmulation of an antihyperglycemic drug that does not employ an expanding polymer.

It is also a further object of the present invention to provide a controlled or sustained C. ease formulation of an antihyperglycemic drug that can provide continuous and non-pulsating t r rapeutic levels of the drug to an animal or human in need of such treatment over a twelve hour O twenty-four hour period.

It is an additional object of other embodiments of the present invention to provide a rtrolled or sustained release formulation for an antihyperglycemic drug that obtains peak Lsma levels from 5.5 to 7.5 hours after administration under various conditions. Alternatively, Stinme to peak plasma levels are from 6.0 to 7.0, from 5.5 to 7.0 or from 6.0 to It is also an object of this invention to provide a controlled or sustained release armaceutical formulation having a homogeneous core wherein the core component may be .de using ordinary tablet compression techniques.

In accordance with the above-mentioned objects and others, the present invention ,vides a controlled release oral dosage form comprising an antihyperglycemic drug, preferably iguanide metformin or a pharmaceutically acceptable salt thereof) that is suitable for ,viding once-a-day adminitration of the drug, wherein the dosage form provides a mean time to maximum plasma concentration (Tm, of the drug from 5.5 to 7.5 hours after administration.

The dosage form comprises the drug and a membrane. In certain preferred embodiments, the dosage form comprises a tablet.

In preferred embodiments, the controlled release oral dosage form of the present invention is a tablet comprising: a core comprising: the antihyperglycemic drug; (ii) optionally a binding agent; and S(iii) optionally an absorption enhancer; a membrane coating surrounding the core; and at least one passageway in the membrane.

S When the drug is metfonnin or a pharmaceutically acceptable salt thereof and is administered on a once-a-day basis, the daily dose may vary, from about 500 mg to about 2500 mg. Such daily dose may be contained in one controlled-release dosage form of the invention, or may be contained in more than one such dosage form. For example, a controlledrelease metformin dosage form may be formulated to contain about 1000 mg of the drug, and two Sf said dosage form may be administered together to provide once-a-day metformin therapy. The 1 iaily dose of the drug metformin or pharmaceutically acceptable salt thereof) may range tom about 500 mg to about 2500 mg, from about 1000 mg to about 2500 mg, or from about i000 mg to about 2500 mg, depending on the clinical needs of the patient.

In certain preferred embodiments, the controlled release solid oral dosage form of the )resent invention provides a width at 50% of the height of a mean plasma concentration/time unrve of the drug of metformin) from about 4.5 to about 13 hours, more preferably from bout 5.5 to about 10 hours, more preferably from about 6 to about 8 hours.

In certain embodiments, the controlled release oral dosage form of the present invention rovides a mean maximum plasma concentration of the antihyperglycemic drug which is lore than about seven times the mean plasma level of said drug at about 24 hours after dministration. In preferred embodiments, the controlled release oral dosage fonn of the present ilvention provides a mean maximum plasma concentration of the drug which is from about 7 times to about 14 times the plasma level of the drug at about 24 hours after the administration, more preferably from about 8 times to about 12 times the plasma level of the drug at about 24 hours after administration.

In certain embodiments of the present invention, when the drug is metfonnin or a phamnaceutically acceptable salt thereof, the controlled release oral dosage fonn provides a mean maximum plasma concentration (Cmax) of the drug that is about 1500 ng/ml to about 3000 ng/ml, based on administration of a 2000 mg once-a-day dose of metformin, more preferably about 1700 Sg/ml to about 2000 ng/ml, based on administration of a 2000 mg once-a-day dose of t letformin.

In certain embodiments of the present invention, when the drug is metformin or a 0 iannaceutically acceptable salt thereof, the controlled release dosage form provides a mean UC2,,, that is about 17200 ng.hr/ml to about 33900 ng.hr/ml, based on administration of a )00 mg once-a-day dose of metformin; preferably about 17200 ng.hrhnl to about 26500 Shr/ml, based on administration of a 2000 mg once-a-day dose ofmetformin; more preferably ,outl9800 ng.hr/ml to about 33900 ng.h-/ml, based on administration of a 2000 mg once-a-day Sse of metformin.

In certain embodiments of the invention, the administration of the antihyperglycemic ug, at least one metformin dosage form provides a mean AUCo, 24 from at least -ferably at least 90% of the mean AUCO 24 provided by administration of the reference standard LUCOPHAGE) twice a day, wherein the daily dose of the reference standard is equal to the ce-a day dose of metformin administered in the controlled release oral dosage form of the ssent invention.

In certain embodiments of the present invention, the controlled release dosage form libits the following dissolution profiles of the antihyperglycemic drug metformin) when ted in a USP type 2 apparatus at 75 rpm in 900 ml of simulated intestinal gastric fluid (pH )sphate buffer) at 370 C: 0-30% of the drug released after 2 hours; 10-45% of the drug -ased after 4 hours; 30-90% of the drug released after 8 hours; not less than 50% of the drug released after 12 hours; not less than 60% of the drug released after 16 hours; and not less than of the drug released after 20 hours.

In certain preferred embodiments, the controlled release solid oral dosage form exhibits the following dissolution profiles when tested in USP type 2 apparatus at 75 rpm in 900 ml of simulated intestinal gastric fluid (pH 7.5 phosphate buffer) at 370 C: 0-25% of the drug metformin or a pharmaceutically acceptable salt thereof) released after 2 hours; 20-40% of the drug released after 4 hours; 45-90% of the drug released after 8 hours; not less than 60% of the Sdrug released after 12 hours; not less than 70% of the drug released after 16 hours; and not less O than 80% of the drug released after 20 hours.

With respect to embodiments of the present invention where the antihyperglycemic drug C is metformin, it has been found that drugs such as metfonninprovide substantially linear.

pharmacokinetics up to a level of about 2 grams per day. Therefore, it is contemplated for Spurposes of the present invention that a given plasma level Cm) of metformin per specified dose will be directly proportional to other doses ofmetformin. Such proportional doses and plasma levels are contemplated to be within the scope of the invention and to be within the Sscope of the appended claims.

0 The dosage form of the present invention can provide therapeutic levels of the antihyperglycemic drug for twelve to twenty-four hour periods and does not exhibit a decrease in )ioavailability if taken with food. In fact, a slight increase in the bioavailability of the itihyperglycemic drug is observed when the controlled release dosage form of the present nvention is administered with food. In a preferred embodiment, the dosage fonn can be idministered once-a-day, ideally with or after a meal, preferably with or after the evening meal, md provides therapeutic levels of the drug throughout the day with peak plasma levels being )btained between 5.5 to 7.5 hours after administration.

The present invention is also directed to a method of lowering blood glucose levels in numan patients needing treatment for non-insulin-dependent diabetes mellitus

(NIDDM),

omprising orally administering to human patients on a once-a-day basis a dose of a drug omprising a biguanide metformin or a pharmaceutically acceptable salt thereof), said drug being contained in at least one solid oral controlled release dosage form of the present invention.

When the drug is metfonnin, the daily dose of the drug may be from about 500 mg to about 2500 mg, from about 1000 mg to about 2500 mg, or from about 2 000 mg to about 2500 mg, depending on the clinical needs of the patient.

The controlled release dosage form of the present invention provides a delayed T, as compared to the provided by GLUCOPHAGE. The delayed occurs from 5.5 to N Durs after administration. If the drug metformin) is administered at dinner time, the T.

i ould occur during the time when gluconeogenesis is usually at its highest around 2 c, The present invention also includes a method of treating patients with NIDDM S)mprising orally administering to human patients on a once-a-day basis a dose of a drug Suprising a biguanide metformin or a pharmaceutically acceptable salt thereof), contained at least one oral controlled release dosage form of the present invention. When the drug is etformin, the daily dose of the drug may be from about 500 mg to about 2500 mg, from about 1 >00 mg to about 2500 mg, or from about 2000 mg to about 2500 mg, depending on the clinical 0 eds of the patient. In certain embodiments, the method of treatment according to the present vention involves once-per-day metfomnin monotherapy as an adjunct to diet to lower blood acose in patients with NIDDM whose hyperglycemia may not be satisfactorily managed on diet )ne. In certain other embodiments, the once-a-day metformin therapy of the present invention iy be used concomitantly with a sulfonylurea, when diet and monotherapy with a Ifonylurea alone do not result in adequate glycemic control. In certain other embodiments, the ce-a-day.metformin therapy of the present invention may be used concomitantly with a tazone, when diet and monotherapy with a glitazone alone do not result in adequate icemic control.

The present invention is further directed to a method of controlling the serum glucose acentration in human patients with NIDDM, comprising administering to patients having DDM on a once-a-day basis, preferably at dinner time, an effective dose of a biguanide metformin) contained in at least one oral controlled release dosage form of the present invention.

The present invention further includes a controlled-release dosage form of a drug comprising a biguanide metformin) suitable for once-a-day administration to human patients with NIDDM, the dosage form comprising an effective amount of the drug to control blood glucose levels for up to about 24 hours and an effective amount of a controlled-release carrier to provide controlled release of the drug with a mean time to maximum plasma concentration (Tma) of the drug from 5.5 to 7.5 hours after administration and a width at 50% of Sthe height of a mean plasma concentration/time curve of the drug from about 6 to about 13 hours.

In preferred embodiments, the administration of the controlled-release dosage form occurs at fed state, more preferably at dinner time.

N In certain preferred embodiments, the controlled-release dose of the drug metfonnin )r a pharmaceutically acceptable salt thereof) according to the present invention is provided by me or more of a controlled-release tablet comprising a core comprising: the antihyperglycemic drug metfonnin or a pharmaceutically acceptable salt thereof); (ii) optionally a binding agent; and (iii) optionally an absorption enhancer; a membrane coating surrounding the core; and at least one passageway in the membrane.

In certain preferred embodiments, the mean time to maximum plasma concentration of ae drug is reached from 6.5 to 7.5 hours after administration at dinner time.

In certain embodiments of the invention when the drug is a biguanide metfonnin or a hannaceutically acceptable salt thereof), the controlled release dosage form provides upon ingle administration, a higher mean fluctuation index in the plasma than an equivalent dose of a immediate release composition administered as two equal divided doses, one divided dose at Le start of the dosing interval and the other divided dose administered 12 hours later, preferably taintaining bioavailability from at least 80% preferably from at least 90% of the immediate release composition.

In certain embodiments of the present invention, the mean fluctuation index of the dosage form is from about 1 to about 4, preferably about 2 to about 3, more preferably about In certain embodiments of the invention which exhibit a higher mean fluctuation index in the plasma than an equivalent dose of an immediate release composition administered as two equal divided doses, the ratio of the mean fluctuation index between the dosage form and the immediate release composition is about 3:1, preferably about 2:1, more preferably 1.5:1.

C When the drug is metformin or a pharmaceutically acceptable salt thereof, the doses of Sug which exhibit the above disclosed mean fluctuation indexes can be any effective dose N iministered to a patient with NIDDM for the reduction of serum glucose levels. For example, e dose can from about 500mg to about 2500mg, from about 1000mg to about 2000 mg or from D )out 850mg to about 1700mg metfomain or pharmaceutically acceptable salt thereof.

The drugs which may used in conjunction with the present invention include those drugs 1 hich are useful for the treatment of non-insulin-dependent diabetes mellitus (NIDDM), I cluding but not limited to biguinides such as metformin or bufonnin or pharmaceutically 0 ceptable salts thereof. When the drug used in the present invention is metformin, it is prefened at the metfonnin be present in a salt form, preferably as metformin hydrochloride.

The term "metfonnin" as it is used herein means metformin base or any pharmaceutically ceptable salt metformin hydrochloride.

The term "dosage fonn" as it is used herein means at least one unit dosage form of the esent invention the daily dose of the antihyperglycemic agent can be contained in 2 unit sage forms of the present invention for single once-a-day administration).

The term "morning" as it is used herein with respect to the dosing of the controlled ease formulations of the invention means that the controlled release formulation is orally ministered early in'the day after the patient has awakened from overnight sleep, generally tween about 6 a.m. and 11 a.m. (regardless of whether breakfast is eaten at that time, unless so .cified herein).

The term "dinnertime" or "at dinner" as it is used herein with respect to the dosing of the controlled release fornulations of the invention means that the controlled release formulation is orally administered at a time when dinner is normally eaten (regardless of whether a meal is actually eaten at that time, unless so specified herein), generally between about 4 p.m. and 8 p.m.

The term "bedtime" as it is used herein with respect to the dosing of the controlled release formulations of the invention means that the controlled release formulation is orally administered before the patient goes to bed in the evening, generally between about 8 p.m. and 12 p.m.

O The tenn "therapeutically effective reduction" when used herein is meant to signify that a blood glucose levels are reduced by approximately the same amount as an immnediate release Sreference standard GLUCOPHAGE) or more, when the controlled release dosage fonn is orally administered to a human patient on a once-a-day basis.

The term "sustained release" and "controlled release" are used interchangeably in this -0 application and are defined for purposes of the present invention as the release of the drug from She dosage fonn at such a rate that when a once-a-day dose of the drug is administered in the 3 sustained release or controlled-release forn, blood plasma) concentrations (levels) of the irug are maintained within the therapeutic range but below toxic levels over a period of time C aom about 12 to about 24 hours. When the drug used in the present invention is metformin preferably metforiin hydrochloride) the controlled release solid oral dosage fonr containing ;uch drug is also referred to as "Metformin

XT."

The tenn "Cma" is the highest plasma concentration of the drug attained within the dosing nterval, about 24 hours.

The tenn is the minimum plasma concentration of the drug attained within the losing interval, i.e. about 24 hours.

The term as used herein, means the plasma concentration of the drug within the osing interval, i.e. about 24-hours, and is calculated as AUC/dosing interval.

The term "Tma" is the time period which elapses.after administration of the dosage form t which the plasma concentration of the drug attains the highest plasma concentration of drug attained within the dosing interval about 24 hours).

The term "AUC" as used herein, means area under the plasma concentration-time curve, as calculated by the trapezoidal rule over the complete 24-hour interval.

The term "steady state" means that the blood plasma concentration curve for a given drug does not substantially fluctuate after repeated doses to dose of the formulation.

The term "single dose" means that the human patient has received a single dose of the drug formulation and the drug plasma concentration has not achieved steady state.

O

C The tenn "multiple dose" means that the human patient has received at least two doses of i e drug formulation in accordance with the dosing interval for that formulation on a onceday basis). Patients who have received multiple doses of the controlled release formulations of e invention may or may not have attained steady state drug plasma levels, as the term multiple S)se is defined herein.

S The term "a patient" means that the discussion (or claim) is directed to the C larmacokinetic parameters of an individual patient and/or the mean pharmacokinetic values Itained from a population of patients, unless further specified.

SThe term "mean", when preceding a pharmacokinetic value mean represents e arithmetic mean value of the phannacokinetic value taken from a population of patients dess otherwise specified geometric mean)..

The term "Degree of Fluctuation" is expressed as (Cma -Cmin)/Cg.

Brief Description of the Drawings FIG. 1 is a graph showing the relative bioavailability of the metformin XT formulation of :ample 2 to GLUCOPHAGE® for Clinical Study 2.

FIG. 2 is a graph showing the relative bioavailability of the metfonnin XT formulation Example 1 (500 mg) to GLUCOPHAGE® for Clinical Study 3.

FIG. 3 is a graph showing the difference in plasma concentration-time profiles of :tformin in eight healthy volunteers between Day 1 and Day 14 dosing following oral administration of the metformin XT formulation of Example 1, 4 x 500 mg q.d. for 14 days for Clinical Study 4.

FIG. 4 is a graph showing the mean plasma profiles and values ofpharmacokinetic parameters of the metfonnin XT formulation of Example 3 for Clinical Study FIG. 5 is a graph showing the mean plasma glucose concentration-time profiles after 4 weeks of treatment with the metfonnin XT formulation of Example 3 and GLUCOPHAGE® for Clinical Study O FIG. 6 is a graph showing the dissolution profile of a 500 mg controlled release metformin formulation of Example 1 of the present invention.

FIG. 7 is a graph showing the dissolution profile of a 850 mg controlled release N Ietformin formulation of Example 2 of the present invention.

FIG. 8 is a graph showing the dissolution profile of a 1000 mg controlled release netformin formulation of Example 3 of the present invention.

0 Detailed Description of the Invention The term antihyperglycemic drugs as used in this specification refers to drugs that are 1 isefal in controlling or managing noninsulin-dependent diabetes mellitus (NIDDM). Preferably, he antihyperglycemic drug is a biguanide such as metfonnin or buformin or a pharmaceutically cceptable salt thereof such as metfonnin hydrochloride.

It has surprisingly been found that when biguanides such as metfonnin are administered ,rally in a controlled release dosage form suitable for once-a-day dosing in the "fed" state, referably at dinner, the bioavailability is improved as compared to the administration of the ontrolled release dosage form in the "fasted" state. This is in contrast to GLUCOPHAGE®, ihich exhibits opposite characteristics. In accordance with the methods and dosage fonns of the resent invention, it has been determined that the patients suffering from NIDDM achieve nproved results lowered blood glucose levels) than GLUCOPHAGE® administered ccording to accepted protocols, on a twice-a-day basis.

The methods and dosage fonns of the invention provide the further advantage in that when dosed at dinnertime, the controlled release fonnulations of the invention provide a T,, (fi-om 5.5 to 7.5 hours) after oral administration (which is delayed relative to the reference standard, GLUCOPHAGE®), such that the level of drug is greatest at the time when human patients are manufacturing glucose at highest levels. Gluconeogenesis is well known to those skilled in the art to be greatest at night. Thus, in accordance with the invention, the Tn, of the drug occurs for example between 11: 3 0 p.m. and 1: 3 0a.m., based on a dose administered at 6:00 p.m. Likewise, such administration of the dosage form provides lower drug levels during the day 0 the afternoon) when gluconeogenesis is lower than at night. Also, the invention preferably Sovides the added benefit of lowering insulin levels. Insulin is considered a risk factor in N IDDM, in and of itself, for cardiovascular disease.

In comparison to a twice-daily dose of the reference standard (GLUCOPHAGE@), the asma levels of metfonnin are preferably lower in the afternoon. This is an advantage rticularly in patients who are under concomitant therapy with one or more additional M tidiabetic agents, such as for example, a sulfonylurea. It is known in the art that to date proximately 60% of patients being treated with metformin are also being treated with at least Se additional antidiabetic agent (such as a sulfonylurea). Sulfonylureas can possibly cause poglycemia, whereas metfonnin cannot, so there is a benefit to having lower metfonnin levels the blood during the aftenioon due to the potential for the patient to have hypoglycemia.

Accordingly, the present invention also includes a method of treating human patients with DDM comprising administering on a once-a-day basis a therapeutically effective dose of itformin in a controlled-release oral dosage form ("Metfonnin in combination with ministering an effective amount of a sulfonylurea. In preferred embodiments, metformin is Dvided by a controlled release dosage form comprising metformin or a pharmaceutically ,eptable salt thereof, the dosage form being useful for providing a once-a-day oral ministration of the drug, wherein the dosage form provides a mean time to maximum plasma acentration of metfonnin from 5.5 to 7.5 hours after administration.

In certain embodiments, the combination therapy may be provided as follows. If patients do not respond to four weeks of the maximum dose of Metformin XT (2500 mg/day) monotherapy, a sulfonylurea may be gradually added while maintaining the maximum dose of Metformin XT, even if prior primary or secondary failure to a sulfonylurea has occun-ed.

Examples of the sulfonylurea include glyburide (glibenclamid), chloropropamide, tolbutarnide, glipizide, acetohexamide and tolazamide. Although Metformin XT is preferably administered on once-a-day basis, the sulfonylurea may be administered in a different dosage form and at a different frequency.

8 With concomitant Metformin XT and sulfonylurea therapy, the desired control of blood O glucose may be obtained by adjusting the dose of each drug.

SIn certain embodiments, the foregoing objectives are met by a controlled release dosage CN Form comprising: a core comprising: IN an antihyperglycemic drug; (ii) optionally a binding agent; and e (iii) optionally an absorption enhancer; a membrane coating surrounding the core; and at least one passageway in the membrane.

The binding agent may be any conventionally known pharmaceutically acceptable binder uch as polyvinyl pyrrolidone, hydroxypropyl cellulose, hydroxyethyl cellulose, ethylcellulose, 'olymethacrylate, waxes and the lile. Mixtures of the aforementioned binding agents may also e used. The preferred binding agents are water soluble such as polyvinyl pyrrolidone having a reight average molecular weight of 25,000 to 3,000,000. The binding agent comprises pproximately about 0 to about 40% of the total weight of the core and preferably about 3% to bout 15% of the total weight of the core.

The core may optionally comprise an absorption enhancer. The absorption enhancer can e any type of absorption enhancer conmmonly known in the art such as a fatty acid, a surfactant, chelating agent, a bile salt or mixtures thereof. Examples of some preferred absorption .ahancers are fatty acids such as capric acid, oleic acid and their monoglycerides, surfactants such as sodium lauryl sulfate, sodium taurocholate and polysorbate 80, chelating agents such as citric acid, phytic acid, ethylenediamine tetraacetic acid (EDTA) and ethylene glycol-big

(B-

aminoethyl ether -N,N,N,N-tetraacetic acid (EGTA). The core comprises approximately 0 to about 20% of the absorption enhancer based on the total weight of the core and most preferably about 2% to about 10% of the total weight of the core.

In this embodiment, the core which comprises the antihyperglycemic drug, the binder which preferably is a pharmaceutically acceptable water soluble polymer and the absorption C ahancer is preferably formed by wet granulating the core ingredients and compressing the :anules with the addition of a lubricant into a tablet on a rotary press. The core may also be SInned by dry granulating the core ingredients and compressing the granules with the addition of lubricant into tablets or by direct compression.

I Other commonly haown excipients may also be included into the core such as lubricants, gments or dyes.

eC. The homogeneous core is coated with a membrane, preferably a polymeric membrane to nn the controlled release tablet of the invention. The membrane can be a semipermeable embrane by being permeable to the passage of external fluid such as water and biological fluids d being impermeable to the passage of the antihyperglycemic drug in the core. Materials that useful in forming the membrane are cellulose esters, cellulose diesters, cellulose triesters, llulose ethers, cellulose ester-ether, cellulose acylate, cellulose diacylate, cellulose triacylate, lulose acetate, cellulose diacetate, cellulose triacetate, cellulose acetate propionate, and llulose acetate butyrate. Other suitable polymers are described in United States Patent Nos.

345,770, 3,916,899, 4,008,719, 4,036,228 and 4,11210 which are incorporated herein by 7erence. The most preferred membrane material is cellulose acetate comprising an acetyl ntent of 39.3 to 40.3%, commercially available from Eastman Fine Chemicals.

In an alternative embodiment, the membrane can be formed from the above-described lymers and a flux enhancing agent. The flux enhancing agent increases the volume of fluid bibed into the core to enable the dosage form to dispense substantially all of the antihyperglycemic drug through the passageway and/or the porous membrane. The flux enhancing agent can be a water soluble material or an enteric material. Some examples of the preferred materials that are useful as flux enhancers are sodium chloride, potassium chloride, sucrose, sorbitol, mannitol, polyethylene glycol (PEG), propylene glycol, hydroxypropyl cellulose, hydroxypropyl methycellulose, hydroxyprophy methycellulose phthalate, cellulose acetate phthalate, polyvinyl alcohols, methacrylic acid copolymers and mixtures thereof. The preferred flux enhancer is PEG 400.

O The flux enhancer may also be a drug that is water soluble such as metfonnin or its 4 )harmaceutically acceptable salts or a drug that is soluble under intestinal conditions. If the flux Snhancer is a drug, the present dosage form has the added advantage of providing an immediate Selease of the drug which is selected as the flux enhancer.

The flux enhancing agent comprises approximately 0 to about 40% of the total weight of She coating, most preferably about 2% to about 20% of the total weight of the coating. The flux r nhancing agent dissolves or leaches from the membrane to form paths in the membrane for the 1 luid to enter the core and dissolve the active ingredient.

SIn altemate embodiments, the membrane may also be formed with commonly known N xcipients such as a plasticizer. Some commonly known plasticizers include adipate, azelate, nzoate, citrate, stearate, isoebucate, sebacate, triethyl citrate, tri-n-butyl citrate, acetyl tri-n-butyl itrate, citric acid esters, and those described in the Encyclopedia of Polymer Science and 'echnology, Vol. 10 (1969), published by John Wiley Sons. The prefen-ed plasticizers are iacetin, acetylated monoglyceride, grape seed oil, olive oil, sesame oil, acetyltributylcitrate, cetyltriethylcitrate, glycerin sorbitol, diethyloxalate, diethylmalate, diethylfumarate, ibutylsuccinate, diethylhnalonate, dioctylphthalate, dibutylsebacate, triethylcitrate, ibutylcitrate, glyceroltributyrate, and the like. Depending on the particular plasticizer, amounts f from 0 to about 25%, and preferably about 2% to about 15% of the plasticizer can be used ased upon the total weight of the coating.

As used herein the term passageway includes an aperture, orifice, bore, hole, weakened area or an erodible element such as a gelatin plug that erodes to form an osmotic passageway for the release of the antihyperglycemic drug from the dosage form. A detailed description of the passageway can be found in United States Patent Nos. such as 3,845,770, 3,916,899, 4,034,758, 4,063,064, 4,077,407, 4,088,864, 4,783,337 and 5,071,607 (the disclosures of which are hereby incorporated by reference).

In certain embodiments, the passageway is formed by laser drilling. In other embodiments, the passageway is formed by making an indentation onto the core prior to the membrane coating to form a weakened area of the membrane at the point of the indentation. In eferred embodiments of the invention, the dosage form contains two passageways in order -ovide the desired pharmacokinetic parameters of the formulation.

N, Generally, the membrane coating around the core will comprise from about 1% to about Yo, preferably about 1.5% to about based on the total weight of the core and coating.

The term "membrane" means a membrane that is permeable to both aqueous solutions or dily fluids and to the active drug or pharmaceutical ingredient the formulations of Scamples Thus, the membrane is porous to drug and, in a preferred embodiment, drug is i leased through the hole or passageway and through the porous membrane in solution or in vivo.

O ie term "membrane" also generically encompasses the tema "semipermeable membrane" as retofore defined.

In an alternative embodiment, the dosage form of the present invention may also mprise an effective amount of the antihyperglycemic drug that is available for immediate ease. The effective amount of antihyperglycemic drug for immediate release may be coated to the membrane of the dosage form or it may be incorporated into the membrane.

In certain preferred embodiments of the invention where the dosage fonm is prepared in :ordance with the above, the dosage form will have the following composition: qGREDIENT Preferred Most Preferred

ORE:

rug 50-98% 75-95% Binder 0-40% 3-15% Absorption Enhancer 0-20% 2-10%

COATING:

Membrane Polymer 50-99% 75-95% Flux Enhancer 0-40% 2-20% Plasticizer 0-25% or 0-30% 2-15% The dosage forms prepared according to certain embodiments of the present invention O )referably exhibit the following dissolution profile when tested in a USP type 2 apparatus at pms in 900 ml of simulated intestinal fluid (pH 7.5 phosphate buffer) and at 37'C: Time (Hours) Preferred Most Preferred 2 0-30% 0-15% or 0-25% 4 10-45% 20-40% 8 30-90% 45-90% C1 12 NTL50% NTL 16 NTL60% NTL NTL 70% NTL NTL= Not less than In the preparation of the tablets of the invention, various conventional well known lvents may be used to prepare the granules and apply the external coating to the tablets of the ivention. In addition, various diluents, excipients, lubricants, dyes, pigments, dispersants, etc.

'hich are disclosed in Remington's Phanmaceutical Sciences, 1995 Edition may be used to ptimize the formulations of the invention.

Other controlled release technologies known to those skilled in the art can be used in order to achieve the controlled release formulations of the present invention, formulations which provide a mean of the drug and/or other pharmacokinetic parameters described herein when orally administered to human patients. Such formulations can be manufactured as a controlled oral formulation in a suitable tablet or multiparticulate formulation known to those skilled in the art. In either case, the controlled release dosage form may optionally include a controlled release carrier which is incorporated into a matrix along with the drug, or which is applied as a controlled release coating.

0 An oral dosage form according to the invention may be provided as, for example, N anules, spheroids, beads, pellets (hereinafter collectively referred to as Amultiparticulates@) d/or particles. An amount of the multiparticulates which is effective to provide the desired se of drug over time may be placed in a capsule or may be incorporated in any other suitable al form.

ND In certain preferred embodiments, the tablet core or multiparticulates containing the drug coated with a hydrophobic material selected fiom an alkylcellulose and (ii) a polymeric e col. The coating may be applied in the form of an organic or aqueous solution or dispersion.

t e coating may be applied to obtain a weight gain from about 2 to about 25% of the substrate in ler to obtain a desired sustained release profile. The sustained release coatings of the present ,ention may also include an exit means comprising at least one passageway, orifice, or the like previously disclosed.

Description of Certain Preferred Embodiments The following examples illustrate various aspects of the present invention. They are not 3e construed to limit the claims in any manner whatsoever.

Example 1 A controlled release tablet containing 500 mg ofmetformin HCI and having the following mula is prepared as follows: Core Ingredients Amount (mg/tab) Metformin HC1 500.0 Povidone 3 USP 36.0 Sodium Lauryl Sulfate 25.8 Magnesium Stearate 2.8 approximate molecular weight 1,000,000; dynamic viscosity (10%w/v solution at 300-700 m Pa s.

Granulation N The metformin HCI and sodium lauryl sulfate are delumped by passing them through a O nesh screen and collecting them in a clean, polyethylene-lined container. The povidone, s dissolved in purified water. The delumped metformin HC1 and sodium lauryl sulfate are then O idded to a top-spray fluidized bed granulator and granulated by spraying with the binding olution of povidone under the following conditions: inlet air temperature of 50-70'C; Stomization air pressure of 1-3 bars; and spray rate of 10-100 ml/min.

SOnce the binding solution is depleted, the granules are dried in the granulator until the 1 ss on drying is less than The dried granules are passed through a Comil equipped with the Squivalent of an 18 mesh screen.

Tableting The magnesium stearate is passed through a 40 mesh stainless steel screen and blended Jith the metformin HC1 granules for approximately five minutes. After blending, the ranules are compressed on a rotary press fitted with 15/32" round standard concave punches.

Seal Coating (optional) The core tablet is seal coated with an Opadry material or other suitable water-soluble laterial by first dissolving the Opadry material, preferably Opadry Clear (YS-1-7006), in urified water. The Opadry solution is then sprayed onto the core tablet using a pan coater under ie following conditions: exhaust air temperature of 38-42 C; atomization pressure of 28-40 psi; ad spray rate of 10-15 ml/min. The Opadry Clear of the coating constitutes about 11.5 ig/tablet.

II. Sustained Release Coating Ingredients medients Amount (mg/tablet) Cellulose Acetate (398-10) 2 21.5 Triacetin 1.3 PEG 400 2 acetyl content 39.3 40.3% 0 The cellulose acetate is dissolved in acetone while stirring with a homogenizer. The polyethylene glycol 400 and triacetin are added to the cellulose acetate solution and stirred until a clear solution is obtained. The tablet is coated by spraying the clear coating solution N onto the seal coated tablets in a fluidized bed coater employing the following conditions: product temperature of 16-22'C; atomization pressure of approximately three bars; and spray rate of 120-150 ml/min.

r-- S Laser Drilling The coated tablets were laser drilled two holes (one hole on each side of the tablet).

Example 2 A controlled release tablet containing 850 mg ofmetformin HCI and having the following formula is prepared as follows: I. Core Ingredients Amount (me/tab) Metforin HCl 850.0 Povidone 3 USP 61.1 Sodium Lauryl Sulfate 43.9 Magnesium Stearate 4.8 Japproximate molecular weight 1,000,000; dynamic viscosity (10%w/v solution at 20C) 300-700 m Pa s.

Granulation The metformin HC1 and sodium lauryl sulfate are delumped by passing them through a 40 mesh screen and collecting them in a clean, polyethylene-lined container. The povidone, is dissolved in purified water. The delumped metformin HC1 and sodium lauryl sulfate are then added to a top-spray fluidized bed granulator and granulated by spraying with the binding solution ofpovidone under the following conditions: inlet air temperature of atomization air pressure of 1-3 bars; and spray rate of 10-100 ml/min.

Once the binding solution is depleted, the granules are dried in the granulator until the a loss on drying is less than The dried granules are passed through a Comil equipped with O the equivalent of an 18 mesh screen.

1 Tableting The magnesium stearate is passed through a 40 mesh stainless steel screen and blended with the metformin HC1 granules for approximately five minutes. After blending, Sthe granules are compressed on a rotary press fitted with 15/32" round standard concave r n punches.

NC Seal Coating (optional) The core tablet is seal coated with an Opadry material or other suitable water-soluble material by first dissolving the Opadry material, preferably Opadry Clear (YS-1-7006), in purified water. The Opadry solution is then sprayed onto the core tablet using a pan coater under the following conditions: exhaust air temperature of 38-42'C; atomization pressure of 28-40 psi; and spray rate of 10-15 ml/min. The Opadry Clear of the coating constitutes about 11.5 mg/tablet.

II. Sustained Release Coating Ingredients s Amount (mi/tablet) Cellulose Acetate (398-10) 2 24.0 Triacetin 1.4 PEG 400 acetyl content 39.3 40.3% 2.8 The cellulose acetate is dissolved in acetone while stirring with a homogenizer. The polyethylene glycol 400 and triacetin are added to the cellulose acetate solution and stirred until a clear solution is obtained. The tablet is coated by spraying the clear coating solution onto the seal coated tablets in a fluidized bed coater employing the following conditions: product temperature of 16-22 atomization pressure of approximately three bars; and spray rate of 120-150 ml/min.

0 Laser Drilling The coated tablets were laser drilled two holes (one hole on each side of the tablet).

Example 3 A controlled release tablet containing 1000 mg of metformin HC1 and having the Sfollowing formula is prepared as follows: SI. Core N Ingredients Amount (mg/tablet) S Metformin HCI 1000.0 0C Povidone 3 USP 71.9 Sodium Lauryl Sulfate 51.7 Magnesium Stearate 5.6 approximate molecular weight 1,000,000; dynamic viscosity (10%w/v solution at 20°C) 100-700 m Pa s.

Granulation The metformin HC1 and sodium lau-yl sulfate are delumped by passing them through mesh screen and collecting them in a clean, polyethylene-lined container. The povidone, 7-90-F is dissolved in purified water. The delumped metformin HC1 and sodium lauryl ulfate are then added to a fluidized bed granulator and granulated by spraying with the oinding solution of povidone under the following conditions: inlet air temperature of atomization air pressure of 1-3 bars; and spray rate of 10-100 ml/min.

Once the binding solution is depleted, the granules are dried in the granulator until the loss on drying is less than The dried granules are passed through a Comil equipped with a screen equivalent to 18 mesh.

Tableting The magnesium.stearate is passed through a 40 mesh stainless steel screen and blended with the metformin HC1 granules for approximately five minutes. After blending, the granules are compressed on a rotary press fitted with 2" round standard concave punches.

Seal Coating (optional) O The core tablet is seal coated with an Opadry material or other suitable water-soluble Smaterial by first dissolving the Opadry material, preferably Opadry Clear (YS-1-7003), in Q purified water. The Opadry solution is then sprayed onto the core tablet using a pan coater C, under the following conditions: exhaust air temperature of 38-42'C; atomization pressure of 28-40 psi; and spray rate of 10-15 ml/min. The core tablet is coated with the sealing solution C until the tablet is coated with 23.0 mg/tablet of the Opadry material.

c II. Sustained Release Coating edients Amount (me/tablet) Cellulose Acetate (398-10) 2 19.0 C 19.0 Triacetin 1.1 PEG 400 2.2 2 acetyl content 39.3 40.3% The cellulose acetate is dissolved in acetone while stirring with a homogenizer. The polyethylene glycol 400 and triacetin are added to the cellulose acetate solution and stirred until a clear solution is obtained. The tablet is coated by spraying the clear coating solution onto the seal coated tablets in a fluidized bed coater employing the following conditions: product temperature of 16-22'C; atomization pressure of approximately three bars; and spray rate of 120-150 ml/min.

Laser Drilling The coated tablets were laser drilled two holes (one hole on each side of the tablet).

Color Coating (optional) Subsequent to the sustained release coating, the laser drilled tablet is coated with a color coating using Opadry White (24 mg/tablet) and waxed with Candelilla wax powder (0.4 mg/tablet).

Clinical Studies Study 1 N In study 1, a total of twelve (12) healthy subjects (six males, six females) were randomized to receive either a single oral dose of metformin XT, 850mg, prepared in Saccordance with Example 2 or b.i.d. doses of GLUCOPHAGE in assigned study periods Swhich consisted of one of the following groups: Group A metformin XT (2 x 850 mg ablets) taken at approximately 8:00 immediately followingbreakfast, Group B netformin XT (2 x 850 mg tablets) taken at approximately 6:00 immediately following linner; and Group C GLUCOPHAGE (1 x 850 mg tablet) taken at approximately 8:00 a.m., mmediately following breakfast, and at approximately 6:00 immediately following lirmer. Each drug administration was separated by a washout period of seven days. In this ;tudy, one male subject was removed from the study prior to Period II due to non-treatmentelated mononucleosis. Thus, 11 (five males and six females) subjects completed the study.

For metformin XT, plasma samples were obtained from subjects at 0 (predose), 1, 2, 4, 5, 6, 8, 10, 12, 14, 16, and 24 hour(s) after dosing. For GLUCOPHAGE, plasma amples were obtained from subjects at 0 (predose), 1, 2, 3, 4, 5, 6, 8, 10, 11, 12, 13, 14, 6, 18, 20, 22, and 24 hour(s) after the first dose in the morning. Plasma concentrations of retformin were determined using a validated HPLC method. The lower quantitation limit of ais method is 10 ng/ml. Mean plasma concentration-time profiles are shown in Fig. 1 and m-ean values ofpharmacokinetic parameters of metformin obtained from this study are presented in Table 1.

Mleax @-SD'Di 1 vaiues of pha1rnacokinetic par-ametersofne orj Ex pe2)i 11 healthy subjects (metforn-in XT, 2 x 850 mg q.d. or GLUCOPqJAGE, I x 850 mg b. i. d.) Treatment Metfonnmin XT after breakfast Metformin

XT

after dinnier AkUc C 0 a (ng-hr/nil) (nig/111) 18156 2045 (4183) (567) Tma Tag (bhr) 6 0.18 (0.40 7 0.09 (0.30.

5 0 (0) Geometric Mean Ratio* t 1 2

AUC

4.4 1.00 1.361 18277 (2961) 1929 (0.7) (0.8) 1.02 1.32 GLUCOPLAG 18050 1457 E. (3502) (217) *Ratio Metfom-jin

XT/GLUCOPH-AGE

3.5 (0.9) As shown. in Figure 1 and Table 1, when metformin XT was administered imm-ediately after either breakfast or dinner, the relative bioavailability of naetformin

XT

formuilation to GLUCOPHAGE is approximately 100%.

The results of study 1 were used to calculate the approximate degree of fluctuation (Cm. -Cmin/Cavg) of the fonnulations.

The was directly obtained from the study (see Table The C 2 V, was obtained by dividing the AUC value by the dosing interval, i.e. 24 hours. The value for Ciniwas extrapolated from Figure 1.

27 The results are set forth in Table 2 below: Table 2 Mean n 12) values of pharmacokinetic parameters of metformin XT in 12 healthy subjects (metformin XT, 2 x 850 mg q.d. and GLUCOPHAGE, 850 mg b.i.d.)

AUC

0

O

(n g-hr/mI) Cama (ng/ml) Cmin (ng/ml) Treatment Metfonnin XT after breakfast Metformin XT after dinner

I

18156 (4183) 2045 (567) 143 Cavg (ng/ml) 756 761 4 I 18277 (2961) 1929 107 (333) Degree of Fluctuation 2..51 2.39 1.65 1.41

GLUCOPHAGE

1 18050 (3502) 1457 (217) 214 (at 24 hours) 393 (between doses) 752 752 As shown in Figure 1 and Table 2, a single administration of the metformin XT 'ormulation provides a higher mean fluctuation index in the plasma than a substantially equal lose of Glucophage administered as two equal divided doses, one divided dose at the start of the dosing interval and the other divided dose administered 12 hours later.

Study 2 The study design of Study 2 is the same as Study 1 except for the formulation and the dose (4 x 500 mg total dose 2000mg, for metformin XT prepared according to Example 1 and 2 x 500 mg total dose 2000mg, for GLUCOPHAGE in the second study). In this study, 12 healthy volunteers (five males and seven females) were randomized to receive treatments and completed the study. Mean plasma concentration-time profiles and mean values ofpharmacokinetic parameters ofmetformin obtained from this study are presented in Figure 2 and Table 3.

As shown in Figure 2 and Table 3, when the metfonnin XT formulation (500 mg) O was administered immediately after dinner, the relative bioavailability of this formulation to O GLUCOPHAGE is approximately 100%, while the mean value is about the same. The Q relative bioavailability of metformin XT, however, is approximately 80% when administered N inmmediately after breakfast. A prolonged profile, together with later and similar C of metformin following administration of metfornnin XT immediately after dinner compared to GLUCOPHAGE indicated that metfonmin was released in vivo in a sustained fashion (Figure 2).

STable 3 Mean -SD, n =12) values of pharmacokinetic parameters of metformin of Example 1 in 12 healthy subjects (metformin XT, 4 x 500 mg q.d. or GLUCOPHAGE, 2 x 500 mg Geometic ean Geometric Mean Treatment Metfomin XT after breakfast Metformin XT after dinner AUCo.- (ng-hr/ml) 17322 (4984) 20335 (4360) Ratio* Cmax (ng/ml)' 2127 (545) Tm (hr) 5 (1) 7 (2) 2053 (447) Tlag (hr) 0.

(0) 0.08 (0.29) 0 (0) (hr) 6.1 (1.8 3.9 (0.6 3.6 (0.8 AUCo., 0.80 1.15 1.15 0.96 1.12 GLUCOPHAG 21181 1815 4 E (4486) (302) (3) *Ratio Metformin XT/GLUCOPHAGE

I

The results of study 2 were used to calculate the approximate degree of fluctuation of the formulations in accordance with the calculations used in study 1 (using Figure 2 to obtain the extrapolated value for Cmij).

29 O The results are set forth in Table 4 below: 0 Table 4 Mean (SD, n 12) values of pharmacokinetic parameters of metformin XT in 12 Shealthy subjects (metformin XT, 4 x 500 mg q.d. and GLUCOPHAGE, 2 x 500 mg b.i.d.)

AUC

0 Cm= Cmin Cag Degree of Treatment (ng-hr/nl (ng/ml) (ng/ml) (ng/ml) Fluctuation SMetforminXT 17322 2127 143 721 2.9 tn after breakfast (4984) (545) SMetforin XT 20335 2053 143 847 2.25 after dinner (4360) (447) GLUCOPHAGE 21181 1815 214 882 1.8 (4486) (302) (at 24 hours) 357 882 1.65 (between doses) As shown in Figure 2 and Table 4, a single administration of the metfomnin

XT

rmulation provides a higher mean fluctuation index in the plasma than an equivalent dose f Glucophage administered as two equal divided doses, one divided dose at the start of the aosing interval and the other divided dose administered 12 hours later.

Study 3 In Study 3, a multiple-dose, open-label, one-period study was conducted to evaluate the short-term tolerability and steady-state pharmacokinetics of the 500 mg metfonnin

XT

formulation used in Study 2. In this study, eight healthy volunteers (four males and four females) were randomized to receive 2000 mg of metfonnin XT (4 x 500 mg tablets) at approximately 6:00 immediately following dinner, for 14 days.

Blood samples were obtained from each subject at 0 (predose), 1, 2, 3, 4, 5, 6, 8, 12, 14, 16 and 24 hour(s) following the first dose on Day 1 and at 0 (predose), 1, 2, 3, 4, 5, 6, 8,10, 12, 14, 16, 24, 38 and 48 hour(s) following the last dose on Day 14. Blood samples were also drawn from each subject immediately prior to dosing onDays 10-13. Urine S samples were collected from each subject at the following time intervals: six hours prior to the first dose; 0-6, 6-12 and 12-24 hours after the first dose; and 0-6, 6-12, 12-24 and 24-48 Shours after the last dose.

Mean plasma profiles and values of phaamacoldnetic parameters of metformin are O presented in Table 5 below:

\O

Table c Mean Pharmacokinetic Parameters (Example 1) N Dayl 0 -Cma' Tmax AUCO-24hr (ng hr/ml) Mean 2435 6.9 22590 SD 630 1.9 3626 Day 14 Cinx Tma AUCO-24hr (ng. hr/ml) Mean 2288 6.9 24136 SD 736 2.5 7996 Following oral administration of metfonnin XT, 4 x 500 mg for 14 days, there was little or no difference in plasma concentration-time profiles of metformin in eight healthy volunteers between Day 1 and Day 14 dosing (Figure On average, trough plasma concentrations of metformin were nearly constant, ranging from 188.8 to 205.1 ng/ml on Days 10-14, indicating that the steady state ofmetformin was attained rapidly. The mean accumulation ratio was 1.01, indicating that the once-daily dose regimen of metformin

XT

results in no accumulation.

Following oral administration of a single dose (4 x 500 mg) ofmetformin

XT,

approximately 31% of the dose was excreted in the urine within the first 24 hours. On average, the renal clearance of metformin was 366 ml/min. A slightly higher renal clearance (454 ml/min) was found after multiple-dose administration of 4 x 500 mg q.d. of metformin

XT.

Gastrointestinal symptoms (diarrhea, nausea, vomiting, abdominal bloating, flatulence N and anorexia) are the most common adverse reactions to GLUCOPHAGE. In controlled trials, GLUCOPHAGE was started at low, nontherapeutic doses and gradually titrated to N higher doses. In spite of this gradual titration, GLUCOPHAGE was discontinued due to gastrointestinal reactions in approximately 4% of patients. In contrast, in the multiple-dose study, metformin XT begun at a therapeutic initial dose of 2000 mg once daily with dinner was well tolerated by all healthy volunteers. Diarrhea and nausea were the most common rn gastrointestinal reactions probably or possibly related to metformin XT. These reactions, V however, were either mild or moderate. This suggests that it may be possible to initiate Smetformin XT treatment with effective doses rather than using the slow titration from nontherapeutic doses required for GLUCOPHAGE.

Study 4 Study 4 was a study designed to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of metformin XT compared to GLUCOPHAGE after multiple-dose treatment in patients with NIDDM. Metformin XT tablets prepared according to Example 3 were used in this study. This study had a single-center, randomized, two-way crossover iesign. A total of 24 NIDDM patients who were on a stable dose of GLUCOPHAGE, Detween 1000 and 2550 mg/day, for at least 12 weeks were selected for the study. A Pretreatment Period of at least 3 weeks preceded randomization to study treatment. At the .tart of the Pretreatment Period, all patients stopped taking any other hypoglycemic agents besides GLUCOPHAGE, and the GLUCOPHAGE dose was adjusted to 1000 mg b.i.d. (with breakfast and with dinner). Following the pretreatment period, patients began Treatment Period I, which lasted 4 weeks. During Period I, a total of 12 patients were randomized to receive two 1000-mg metformin XT tablets q.d. (immediately after dinner), at approximately 6:00 and 12 were randomized to receive one 1000-mg GLUCOPHAGE tablet b.i.d.

(immediately after breakfast and immediately after dinner). Immediately following Period I, each patient was switched to the alternate medication for 4 weeks in Period H. There was no washout between treatment periods.

Plasma metformin concentrations were determined over a 24-hour period at the end of Treatment Periods I and fl as follows: immediately prior to dosing and at 1, 2, 3, 4, 5, 6, 8, 12, 14, 15, 16, 17, 18, 19, 20, 22, and 24 hours after the evening dose. One subject withdrew from the study for personal reasons after two weeks of treatment in Treatment SPeriod I, thus phannacokinetic data were obtained from 23 patients.

O Mean plasma profiles and values of pharmacokinetic parameters of metfonnin are presented in Figure 4 and Table 6. As shown in Figure 4 and Table 6, when metformin

XT

was administered immediately after dinner, the bioavailability of metformin XT relative to GLUCOPHAGE at steady state is close to 100%. Although the dose ofmetfomin XT was C twice as large as the dose of GLUCOPHAGE at dimner, the mean value was only 32% higher.

STable 6 N Mean (4 SD) values of pharmacokinetic parameters of metformin of Example 3 in 23 NIDDM patients (metformin XT, 2 x 1000 mg q.d. with dinner or GLUCOPHAGE, 1 x 1000 mg b.i.d.) Ratio* Geometric Mean Treatment AUCO-24h Cmax Tlag AUCo- 24 h C,nax (ng*hr/ml) (ng/ml) (hr) (hr) (hr) Metformin XT 26818 2849 6 0 after dinner (7052) (797) 5.4 0.96 1.32 GLUCOPHAGE 27367 2131 14 0 (5759) (489) 4 Ratio Metformin XT/GLUCOPHAGE When the metfonnin XT was administered immediately after dinner, the bioavailability of metfonnin XT relative to GLUCOPHAGE at steady state was close to 100%. However, when metformin XT was administered immediately after breakfast, the corresponding relative bioavailability of metformin XT was approximately 80%. The safety profile of metformin XT, 2000 mg given once daily either after dinner or after breakfast was comparable to that of an equal dose of GLUCOPHAGE given b.i.d. The efficacy profile of metformin XT, 2000 mg given once daily after dinner was similar to that of an equal dose of GLUCOPHAGE given b.i.d. The efficacy of metformin XT, 200 mg given once daily after breakfast, however, appeared to be comparable to or slightly less than that of GLUCOPHAGE given b.i.d.

While certain preferred and alternative embodiments of the invention have been set forth for purposes of disclosing the invention, modifications to the disclosed embodiments may occur to those who are skilled in the art. Accordingly, the S appended claims are intended to cover all embodiments of the invention and modifications thereof which do not depart from the spirit and scope of the invention.

Throughout the specification, unless the context requires otherwise, the word "comprise" or variations such as "comprises" or "comprising", will be understood to imply the inclusion of a stated integer or group of integers but not the exclusion of any other integer or group of integers.

Claims

1. A controlled release oral dosage form for the reduction of serum glucose levels in human patients with NIDDM, comprising an effective dose of at least N one suitable antihyperglycemic drug or a pharmaceutically acceptable salt thereof and a controlled-release carrier, said dosage form being suitable for Sproviding once-a-day oral administration of the drug or pharmaceutically I acceptable salt thereof, wherein the dosage form provides a mean time to S maximum plasma concentration (Tmax) of the drug from 5.5 to 7.5 hours after CN administration following dinner.

2. The controlled release dosage form of claim 1, wherein said at least one antihyperglycemic drug is a biguanide.

3. The controlled release dosage form of claim 2, wherein said biguanide is metformin or pharmaceutically acceptable salt thereof.

4. The controlled release oral dosage form of claim 1 or 3, which provides a mean time to maximum plasma concentration (Tmax) of the drug from 6.0 to hours after the administration of the dose. The controlled release oral dosage form of claim 1 or 3, which provides a mean time to maximum plasma concentration (Tmax) of the drug from

5.5 to hours after the administration of the dose.

6. The controlled release oral dosage form of claim 1 or 3, which provides a mean time to maximum plasma concentration (Tmax) of the drug from about to 7.5 hours after the administration of the dose.

7. The controlled release oral dosage form of claim 1 or 3, which exhibits the following dissolution profiles when tested in a USP type 2 apparatus at 75 rpm in 900 ml of simulated intestinal fluid (pH 7.5 phosphate buffer) and at 37 C: O 0-30% of the drug is released after 2 hours;

10-45% of the drug is released after 4 hours;

30-90% of drug is released after 8 hours; not less than 50% of the drug is released after 12 hours; not less than 60% of the drug is released after 16 hours; and not less than 70% of the drug is released after 20 hours. 8. The controlled release oral dosage form of claim 1 or 3, which exhibits the following dissolution profiles when tested in a USP type 2 apparatus at 75 rpm in 900 ml of simulated intestinal fluid (pH 7.5 phosphate buffer) and at 37 C: 0-25% of the drug is released after 2 hours; 20-40% of the drug is released after 4 hours;

45-90% of the drug is released after 8 hours; not less than 60% of the drug is released after 12 hours; not less than 70% of the drug is released after 16 hours; and not less than 80% of the drug is released after 20 hours. 9. The controlled release oral dosage form of claim 1 or 3, which provides a width at 50% of the height of a mean plasma concentration/time curve of the drug from about 4.5 to about 13 hours. 10. The controlled release oral dosage form of claim 1 or 3, which provides a width at 50% of the height of a mean plasma concentration/time curve of the drug from about 5.5 to about 10 hours. 11. The controlled release oral dosage form of claim 3, which provides a mean maximum plasma concentration of metformin which is more than about N 7 times the mean plasma level of said metformin at about 24 hours after the S administration. O 12. The controlled release oral dosage form of claim 3, which provides a mean maximum plasma concentration (Cmax) of metformin which is from about 7 IN times to about 14 times the plasma level of said metformin at about 24 hours after administration. 13. The controlled release oral dosage form of claim 3, which provides a mean S maximum plasma concentration (Cma) of metformin which is from about 8 times to about 12 times the plasma level of said metformin at about 24 hours after administration. 14. The controlled release oral dosage form of claim 3, which provides a mean maximum plasma concentration (Cmax) of metformin from about 1500 ng/ml to about 3000 ng/ml, based on administration of a 2000 mg once-a-day dose of metformin. The controlled release oral dosage form of claim 3, which provides a mean maximum plasma concentration of metformin from about 1700 ng/ml to about 2000 ng/ml, based on administration of a 2000 mg once-a-day dose of metformin. 16. The controlled release oral dosage form of claim 3, which provides a mean AUCo-2 4 hr of at least 80% of the mean AUCO- 2 4 provided by administration of an immediate release reference standard twice a day, wherein the daily dose of the reference standard is substantially equal to the once-a-day dose of metformin administered in the controlled release oral dosage form. 17. The controlled release oral dosage form of claim 3, which provides a meimmediate release reference standard twice a day, wherein the daily dose c of the reference standard is substantially equal to the once-a-day dose of _J metformin administered in the controlled release oral dosage form. (N O 18. The controlled release oral dosage form of claim 3, which provides a mean AUCD- 2 4 hr from about 17200 ng.hr/ml to about 33900 ng.hr/ml, based on administration of a 2000 mg once-a-day dose of metformin. I 19. The controlled release oral dosage form of claim 3, which provides a mean AUCO-24hr from about 17200 ng.hr/ml to about 26500 ng.hr/ml, based on N administration of a 2000 mg once-a-day dose of metformin. The controlled release oral dosage form of claim 3, which provides a mean AUCO- 2 4 hr from about 19800 ng.hr/ml to about 33900 ng.hr/ml, based on administration of a 2000 mg once-a-day dose of metformin. 21. The controlled release oral dosage form of claim 3, which provides a mean plasma concentration-time profile of metformin substantially as set forth in FIG. 1, based on administration of a 1700 mg once-a-day dose of metformin. 22. The controlled release oral dosage form of claim 3, which provides a mean plasma concentration-time profile of metformin substantially as set forth in FIG. 2, based on administration of a 2000 mg once-a-day dose of metformin. 23. The controlled release oral dosage form of claim 3, which provides a mean plasma concentration-time profile of metformin substantially as set forth in FIG. 4, based on administration of a 2000 mg once-a-day dose of metformin at dinner. 24. The controlled release oral dosage form of claim 21 which provides a mean t 1 12 from 2.8 to 4.4. 38 c- 25. The controlled release oral dosage form of claim 3, which provides a mean plasma glucose concentration-time profile substantially as set forth in FIG. based on administration of a 2000 mg once-a-day dose of metformin at dinner. 26. The controlled release oral dosage form of claim 9, which provides a mean time to maximum plasma concentration of metformin from 6.0 to Chours after the administration. C 27. The controlled release oral dosage form of claim 9, which provides a mean time to maximum plasma concentration of metformin from 5.5 to hours after administration at dinner time. 28. The controlled release oral dosage form of claim 9, which provides a mean time to maximum plasma concentration of metformin from 6.0 to hours after administration. 29. The controlled release dosage form of claim 3, wherein the metformin is g: a core comprising: the metformin or a pharmaceutically acceptable salt; (ii) optionally a binding agent; and (iii) optionally an absorption enhancer; a membrane coating surrounding the core; and at least one passageway in the membrane. The controlled release oral dosage form of claim 29, wherein said membrane is a semipermeable membrane. 31. A controlled release oral dosage form for the reduction of serum glucose I a single administration of said dosage form provides a higher mean fluctuation index in the plasma than a substantially equal dose of an immediate release S composition administered as two equal divided doses, one divided dose at the start of the dosing interval and the other divided dose administered 12 hours later. 32. The controlled release oral dosage form of claim 31 wherein the mean I-- 33. The controlled release oral dosage form of claim 32 wherein the mean S fluctuation index of the dosage form is from about 2 to about 3. C 34. The controlled release oral dosage form of claim 33 wherein the mean fluctuation index of the dosage form is about The controlled release oral dosage form of claim 31 wherein the ratio of the mean fluctuation index between the dosage form and the immediate release composition is about 3:1. 36. The controlled release oral dosage form of claim 35 wherein the ratio of the mean fluctuation index between the dosage form and the immediate release composition is about 2:1. 37. The controlled release oral dosage form of claim 36 wherein the ratio of the mean fluctuation index between the dosage form and the immediate release composition is about 1.5:1. 38. The controlled release oral dosage form of claim 31 wherein said dosage form comprises metformin or a pharmaceutically acceptable salt thereof. 39. The controlled release oral dosage form of claim 31 wherein said dosage form maintains bioavailability from at least about 80% of the immediate release composition. The controlled release oral dosage form of claim 31 wherein the substantially Sequal dose of the dosage form and the immediate release composition comprises from about 500 mg to about 2500 mg metformin or pharmaceutically acceptable salt thereof. 41. The controlled release oral dosage form of claim 40 wherein the substantially Sequal dose of the dosage form and the immediate release composition N comprises from about 1000 mg to about 2000 mg metformin or Spharmaceutically acceptable salt thereof. (N 42. The controlled release oral dosage form of claim 40 wherein the substantially equal dose of the dosage form and the immediate release composition comprises from about 850 mg to about 1700 mg metformin or pharmaceutically acceptable salt thereof. Dated this SECOND day of DECEMBER

2005. Andrx Labs. LLC Applicant Wray Associates Perth, Western Australia Patent Attorneys for the Applicant