3,5,3′-triiodothyronine sulfate as thyromimetic agent and pharmaceutical formulations thereof

Abstract

The invention regards the use of triiodothyronine sulfate, commonly named T.sub.3S, as a medicament having thyromimetic activity for the treatment of pathologies due to organic deficiency of triiodothyronine (T.sub.3), as such or in association with thyroxine (T.sub.4), and pharmaceutical formulations for oral administration thereof.

Claims

1. A stable daily dosage thyroid hormone composition comprising triiodothyronine sulfate (T.sub.3S) as the active principle, in a quantity ranging, from 1 to 1000 g; a diluent consisting of: microcrystalline cellulose of the alpha type and calcium carbonate; a glidant consisting of: glycerol dibehenate; a lubricant consisting of: magnesium stearate and hydrate colloidal silica; and a disintegrant consisting of: croscarmellose or salts thereof.

2. The daily dosage of claim 1 wherein T.sub.3S is in a quantity from 2.5 to 500 g.

3. The, daily dosage of claim 2 comprising T.sub.3S in a range from 5-250 g.

4. The daily dosage of claim 2 further comprising from 5-800 g T.sub.4 (thyroxine).

5. The daily dosage of claim 1 in the form of a tablet.

6. The daily dosage of claim 5 wherein the tablet is a 80-150 mg tablet.

7. The daily dosage according to claim 5, wherein the disintegrant is present in a quantity of from 1-10 mg/tablet.

8. The daily dosage according to claim 7, wherein the disintegrant is present in a quantity of from 2-6 mg/tablet.

9. A therapeutic or prophylactic treatment method for a hypothyroid condition due to total thyroid hormone depletion before .sup.131I radiotherapy comprising administering the daily dosage according to claim 1 to a thyroidectomised patient up to 5 days before radioactive isotope administration.

10. The therapeutic treatment method of claim 9 wherein said hypothyroid condition is selected from the group consisting of: asthenia, fatigue, skin dryness, somnolence, speech fluency impairment, cold intolerance, weight gain and memory deficit.

11. A therapeutic treatment method for a hypothyroid condition comprising administering the daily dosage according to claim 1.

12. The therapeutic treatment method of claim 11 wherein said hypothyroid condition is selected form the group consisting of: asthenia, fatigue, skin dryness, somnolence, speech fluency impairment, cold intolerance, weight gain and memory deficit.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1. Panel a) T.sub.3S calibration curve by competitive ELISA; Panel b) DELFIA calibration curve. T.sub.3S was assayed at 33.6, 56, 93.3, 155.5, 259, 432, 720, 1200, 2000 pg/mL.

(2) FIG. 2. Schematic of DTPA-T.sub.3S monoamide synthesis.

(3) FIG. 3. Mean serum concentrations of T.sub.3S (ng/dl) levels in the four doses groups (native values).

(4) FIG. 4: Mean serum concentration curves of T.sub.3S and Total T.sub.3 after administration at a dose of 160 g.

SUMMARY OF THE INVENTION

(5) It has now unexpectedly been found, and this is one of the aspects of the present invention, that T.sub.3S (triiodothyronine or 3,5-diiodo-O-[3-iodo-4-(sulphoxy)phenyl]-L-thyronine), as the only active principle in a suitable composition or in association with other thyroid hormones or pro-hormones, preferably T.sub.4 (Tyroxine, or 3,5,3,5-tetraiodothyronine) and properly formulated according to the desired application for oral administration is particularly useful as a medicament to be used in all those pathologies caused by insufficient production by the body of the needed quantities of active thyroid hormones, in particular T.sub.3.

(6) Another aspect of the present invention is a non-radioactive immunoassay for T.sub.3S quantitation, preferably based on chemiluminescence and the reagents developed therein.

(7) A further object of the present invention is a method for the therapeutic treatment of a hypothyroid condition, which comprises the oral administration of T.sub.3S or the combination T.sub.3S and T.sub.4 as a thyroid hormone replacement therapy to a subject in need thereof.

(8) According to a preferred embodiment oral administration is accomplished by solid compositions, preferably in the tablet form, comprising T.sub.3S alone or in combination with a second active principle, tyroxine (T.sub.4), in a dose comprised for T.sub.3S of from 1 to 1000 g, preferably 2.5-500 g and T.sub.4 of from 1 to 800 g.

(9) Preferred active principle quantities in the formulation comprising two active principles, are the following: T.sub.3S 5-250 g and T.sub.4 5-400 g, T.sub.3S 10-100 g and T.sub.4 10-200 g.

(10) In any case, the preferred ratio between active principles (T.sub.4:T.sub.3S) is comprised to from 10:1 to 0.1:1, with a more preferred range comprised from 5:1 to 1:1. Even more preferred is the range comprised from 3:1 to 2:1 (T.sub.4:T.sub.3S).

(11) Said compositions include diluents, glidants or lubricants and disintegrants and in a preferred embodiment consist essentially of: calcium carbonate, glycerol dibehenate, croscarmellose sodium salt, hydrate colloidal silica, magnesium stearate and microcrystalline cellulose, in an even more preferred embodiment these components are present in the amounts described below for a 80-150 mg tablet:

(12) TABLE-US-00001 Calcium 20-40 mg, preferably 25-35 mg, carbonate more preferably 30 mg Glycerol 2-15 mg, preferably 4-8 mg, dibehenate more preferably 5 mg Croscarmellose 1-10 mg, preferably 2-6 mg, sodium salt more preferably 3.5 mg Hydrate 0.1-5 mg, preferably 0.5-4, colloidal more preferably 2 mg silica Magnesium 0.01-2 mg, preferably 0.1-1 mg, stearate more preferably 0.5 mg Microcrystalline Up to 110 mg cellulose

(13) This composition is endowed with optimal dissolution rates and stability of the active principle(s) for at least 24 months.

DETAILED DESCRIPTION OF THE INVENTION

(14) It has been now been surprisingly found that T.sub.3S or salts thereof is not only a physiologic T.sub.3 catabolite, but that it may be also provided as a drug and administered in hypothyroid conditions. Accordingly, this represents the main aspect of the invention.

(15) Furthermore, it has been found that T.sub.3S, once administered is converted to T.sub.3 and allows maintenance of steady levels of T.sub.3 in the body for long times (from 12 to at least 18 hrs, more preferably at least 48 hrs). This is not only particularly useful when a supplement thyroid hormone in its most active form is needed, but, once more, is completely unexpected given the rapid metabolism synthetic T.sub.3 undergoes once administered. In this case in fact a peak level is detected in serum at about 2-3 hours and after that rapidly and completely cleared from blood within 12-24 hrs.

(16) Furthermore, it has also been found that T.sub.3S can be administered orally and this represents a further and particularly advantageous aspect of the invention. In fact its biological activity, measured for example by total T.sub.3 levels in the serum of thyrectomized individuals, is detected after oral administration. This result is quite unexpected because, at variance with thyroid hormones which are not very soluble in water, T.sub.3S or salts thereof is a polar molecule whose gastrointestinal absorption was expected to be rather inefficient. Therefore the present invention discloses that oral administration is possible and that by this route: a) T.sub.3S is found in the bloodstream thus demonstrating that it crosses the gastrointestinal barrier, b) is converted into the more active thyroid hormone, T.sub.3, c) maintains T.sub.3 levels in serum after administration for quite a long time (at least 48 hours).

(17) According to this finding, a further object of the present invention is represented by a method for the therapeutic treatment of a hypothyroid condition, which comprises the oral administration of T.sub.3S or the combination T.sub.3S and T.sub.4 as a thyroid hormone replacement therapy for a subject in need thereof. Clinical signs of hypothyroidism are the following: asthenia, fatigue, skin dryness, somnolence, speech fluency impairment, cold intolerance, weight gain and/or memory deficit. Accordingly, any of these conditions may be improved by the oral administration of T.sub.3S alone or in combination with T.sub.4.

(18) In general, oral administration of T.sub.3S and salts thereof in pharmaceutical compositions is proposed according to a preferred aspect of the invention for treating any hypothyiroid conditions or for any T.sub.3 replacement therapy. The therapeutic treatment comprises administering compositions comprising T.sub.3S, either alone in a dose comprised for T.sub.3S of from 1 to 1000 g, preferably from 2.5 to 500 g, more preferably from 5 to 250 g, or in combination with a second active principle, thyroxine (T.sub.4) (combination compositions) wherein T.sub.4 is present from 1 to 800 g.

(19) Preferred active principle quantities in the combination compositions are the following: T.sub.3S 5-250 g and T.sub.4 5-400 g, T.sub.3S 10-100 g and T.sub.4 10-200 g.

(20) In any case, for combination compositions a preferred ratio between active principles (T.sub.4:T.sub.3S) is comprised from 10:1 to 0.1:1, with a more preferred range comprised from 5:1 to 1:1. Even more preferred is the range comprised from 3:1 to 2:1 (T.sub.4:T.sub.3S).

(21) Preferred administration of the compositions is in a single daily dosage form.

(22) Particularly preferred in the therapy of hypothyroidism, representing a further aspect of the present invention, is the association of T.sub.3S with T.sub.4. The hormonal association which, in theory, should more accurately mime the normal thyroid secretion is represented by a combination of T.sub.4 with T.sub.3. Actually, pharmaceutical compositions comprising both of said iodothyronines, formulated in proportions similar to the ones of the normal physiologic secretion, have already been tried and marketed. Unfortunately, the oral simultaneous administration of T.sub.4 with T.sub.3 was not able to reproduce the normal thyroid hormones serum levels, because of pharmacokinetics of T.sub.3. In fact, T.sub.3 undergoes a very quick absorption and an equally quick elimination after oral administration; its elimination rate is about 20 times higher than the one of T.sub.4. For this reason administration of T.sub.3 gives raise to a dangerous peak excess in hormone concentration, if compared to the normal physiologic levels, followed by a much too fast drop to sub-physiologic levels. Thus, today most of the specialised physicians prefer using T.sub.4 alone, even if in this way production of T.sub.3 only depends on the periferic deiodination of T.sub.4, because direct secretion of T.sub.3 by thyroid does not exists or is seriously insufficient.

(23) On the contrary, the association of the invention avoids the above problems, because it has unexpectedly been found that, for example, after oral administration, T.sub.3S provides T.sub.3 serum levels that increase in a gradual way and keep steady for long periods of time, thus preventing the formation of too high peaks.

(24) Another unexpected advantage deriving from the use of T.sub.3S in the treatment of pathologies due to organic deficiency of T.sub.3 consists in its recently found systemic thyromimetic activity linked to a poor inhibition of TSH secretion. This effect is particularly useful in the case of thyroidectomized patients suffering from thyroid carcinoma, when administration of T.sub.4 must be suspended in view of carrying out radiotherapy. In such a case administration of T.sub.3S instead of T.sub.4 may alleviate a patient's symptoms or disease, such as asthenia, fatigue, skin dryness, somnolence, speech fluency impairment, cold intolerance, weight gain and/or memory deficit without interfering with radioactive iodine (usually .sup.131I) radiotherapy.

(25) According to this observation, a further aspect of the invention relates to T.sub.3S administration in thyroidectomized patients in case of .sup.131I radiotherapy when T.sub.4 administration must be suspended. In fact, T4 is usually suspended at least 40 days before radiotherapy to allow an optimal radioisotope uptake. The lack of thyroid hormones for such a long time is usually very badly tolerated by the organism which is completely depleted of thyroid hormones within a few days, thus suffering from asthenia, fatigue, skin dryness, somnolence, speech fluency impairment, cold intolerance, weight gain or memory deficit. In contrast, T.sub.3S, due to its low thyromimetic properties, can be administered, preferably by the oral route, up to at least 5 days, more to preferably up to at least 4, 3, or 2 days, before radiotherapy.

(26) Another further advantage of T.sub.3S in the therapy of hypothyroidism regards its autolimitation capability. In fact, it is actively deiodinated by type I MD, which, on its part, is stimulated by thyroid hormones. In hypothyroid subjects type I MD activity is reduced; thus T.sub.3S elimination is slowed. As a matter of fact, its effect on the body is greater. On the contrary, in case of over administration, type I MD activity is increased, thus giving more T.sub.3S elimination, i.e. limiting possible undesired collateral effects.

(27) Last but not least, a further advantage of T.sub.3S is represented by the fact that it is a metabolite normally present in the body, usually non-active, i.e. non-toxic.

(28) Accordingly, another main aspect of the present invention regards pharmaceutical formulations comprising T.sub.3S as an active principle, as such or in combination with other thyroid hormones or pro-hormones. Particularly preferred are formulations comprising T.sub.3S in association with T.sub.4.

(29) The preferred ratio of the two active principles (T.sub.4:T.sub.3S) in composition comprising both active principles ranges from 10:1 to 0.1:1, with a more preferred range comprised from 5:1 to 1:1. Even more preferred is the range comprised from 3:1 to 2:1 (T.sub.4:T.sub.3S).

(30) Said formulations differ in the dosage of the active principle or principles, or in the type of pharmaceutical form provided, depending on the administration route used with enteral administration being preferred.

(31) According to this embodiment, compositions for oral administration, either liquid or solid are both suitable. Preferred liquid compositions should take into account the generally poor solubility of thyroid hormones such as T.sub.4 and salts thereof, as well as the usually good solubility of T.sub.3 sulphate and salts thereof. Furthermore, the use of lactose, glucose and sucrose should be avoided.

(32) The preparation of specific pharmaceutical formulations in response to particular needs will be described in the following.

(33) Solid Compositions.

(34) It is known that thyroid hormones and especially levothyroxine sodium are compatible with some excipients but incompatible with others. Carbohydrates, such as starch and maltodextrin, are compatible with thyroid hormones, whereas lactose, glucose and sucrose, have been determined to be incompatible. By the use of suitable compatible diluents, glidants or lubricants and disintegrants, thyroid hormones can be to formulated into tablets, capsules, or powder dosage forms.

(35) Thus, preferred compositions of the present invention are prepared in the substantial absence of lactose, glucose, sucrose, polyvinylpyrrolidone, and/or a Poloxamer. According to this embodiment, the solid composition comprises diluents or fillers, glidants and/or lubricants and disintegrants. The compositions may also further comprise excipients, stabilizers, preservatives or dissolution enhancers.

(36) Preferred diluents are cellulose derivatives, such as microcrystalline cellulose, powdered cellulose, silicified microcrystalline cellulose, cellulose acetate, ethyl- or methylcellulose or salts thereof. However, other diluents may be used, such as kaolin, starch and derivatives thereof, or sodium or other alkaline inorganic salts such as trisodium phosphate, tricalcium phosphate, calcium carbonate or magnesium carbonate.

(37) Suitable disintegrants for use in the present invention include corn starch, croscarmellose and salts thereof (i.e. croscarmellose sodium) and crospovidone or salts thereof. However other disintegrants may be used such as, polymethacrylates and maltodextrin or salts thereof, pregelatinized starch and sodium starch glycolate or sodium alginate, sometimes referred to as diluents as well.

(38) Suitable lubricants for use in the present invention comprise silicates in general, including colloidal silicon dioxide hydrate silicon dioxide, hydrate colloidal silica, talc, as well as magnesium or zinc stearate the preferred ones.

(39) Suitable glidants or lubricants are chosen among glycerol dibehenate, tribasic calcium phosphate, starch derivatives, talc, magnesium and zinc stearate, sodium stearate fumarate and sodium and magnesium lauryl sulphate. Preferred glidants or lubricants are glycerol dibehenate or tribasic calcium phosphate.

(40) The term glidant comprises agents working also as lubricants, and for those, such as talc, magnesium or zinc stearate or sodium dibehenate, accordingly, classification might be interchangeable.

(41) Flavorants and colorants may be added if desired as additional optional ingredients.

(42) Thyroid hormones, especially levothyroxine sodium and T.sub.3S are particularly stable in connection with cellulose derivatives. According to this embodiment solid dosage compositions with improved and superior, stability, content uniformity, good tableting and dissolution properties which comprise T.sub.3S or salts thereof alone or in combination with T.sub.4 or salts thereof in the quantities above disclosed further in combination with a cellulose derivative, wherein microcrystalline cellulose or silicified microcrystalline cellulose are particularly preferred.

(43) Thyroid hormones are preferably prepared by the synthetic route (e.g. as described for T.sub.3S in Mol and Visser, Endocrinology 1985, 117 N.1, 1:1-8).

(44) In the solid composition, diluents are preferably present in a predominant amount, preferably in the range of 50 to 99.99% by weight. More preferably they are present in an amount of from 60 to 80% by weight, more preferably from 65-75% by weight.

(45) According to a preferred embodiment, cellulose or derivatives thereof are present and preferably a second diluent is also present, preferably calcium carbonate, up to 35% of the total diluent w/w.

(46) Preferred glidants, are selected from the group consisting of glycerol dibehnate (most preferred), talc and silica derivatives, among which magnesium trisilicate, starch or derivatives thereof, amides, tribasic calcium phosphate, are usually present in the composition in a quantity range from 1 to 10%, most preferably 4 to 6% (w/w).

(47) Lubricants are preferably selected in the group consisting of: magnesium or zinc stearate, hydrate colloidal silica and talc, more preferably magnesium stearate and hydrate colloidal silica, in a total quantity of from 0.1 to 7% even more preferably the first one comprised from 0.1 to 2% and the second comprised from 0.5 to 5%.

(48) Disintegrants for use in the present invention include starch, croscarmellose sodium and crospovidone. Preferred is croscarmellose or sodium salts thereof in a quantity ranging from 0.5 to 10% even more preferably comprised from 1-5%, most preferably comprised from 2- to 4%.

(49) The moisture content of the solid dosage form, such as of a capsule or tablet, is also important. It is preferred that the moisture content is not higher than 15%, even more preferably not higher than 10%. A buffer system may be present as a stabilizer in the solid dosage form.

(50) A significant advantage of the preparations of the present invention is that they can be prepared as a direct compression formula, dry granulation formula, or as a wet granulation formula, with or without preblending of the drug, although preferably with preblending, and still achieve remarkable stability of the resulting solid dosage form preparation.

(51) The amount of the thyroid hormone in the preparations of the present invention can vary widely, mainly depending on the administration protocol. However, due to the to high potency exhibited by most of the thyroid hormones, and especially levothyroxine sodium, normally very low amounts of this thyroid hormone will be utilized.

(52) The solid compositions comprising T.sub.3S alone comprise T.sub.3S of from 1 to 1000 g; according to a further embodiment they comprises also T.sub.4 (tyroxine): according to this embodiment (combination compositions) T.sub.3S is present in a quantity of from 2.5-500 g and T.sub.4 of from 1 to 800 g.

(53) Even more preferred active principle quantities in the formulation comprising two active principles are the following: T.sub.3S 5-250 g and T.sub.4 5-400 g, T.sub.3S 10-100 g and T.sub.4 10-200 g.

(54) In any case, the preferred ratio between active principles (T.sub.4:T.sub.3S) is comprised from 10:1 to 0.1:1, with a more preferred range comprised from 5:1 to 1:1. Even more preferred is the range comprised from 3:1 to 2:1 (T.sub.4:T.sub.3S).

(55) In the present specification, solid composition percent values refers to weight/weight (w/w) ratios and the pharmaceutical dosage form is of about 50-200 mg.

(56) The compositions of the present invention are usually prepared by blending the thyroid hormones with microcrystalline cellulose, calcium carbonate, glycerol dibehenate, crosscarmellose salt, hydrate colloidal silica.

(57) The resulting blend can be lubricated with magnesium stearate and tableted using a tablet press.

(58) According to the invention, the solid composition of the invention are prepared in tablets and comprise either T.sub.3S as the only active principle or T.sub.3S in combination with a second active principle, preferably T.sub.4, in the quantities and ratios above indicated, together with the following diluents, disintegrants, glidants, lubricants or excipients. In a preferred embodiment, the composition contains 1 to 1000 g T.sub.3S, in a more preferred embodiment the compositions include 2.5 to 500 g T.sub.3S or more preferably 5-250 g T.sub.3S and the following further ingredients (in amounts described below for a 80-150 mg tablet):

(59) TABLE-US-00002 Amount per Tablet Calcium 20-40 mg, preferably 25-35 mg, carbonate more preferably 30 mg Glycerol 2-15 mg, preferably 4-8 mg, dibehenate more preferably 5 mg Croscarmellose 1-10 mg, preferably 2-6 mg, sodium salt more preferably 3.5 mg Hydrate 0.1-5 mg, preferably 0.5-4, colloidal more preferably 2 mg silica Magnesium 0.01-2 mg, preferably 0.1-1 mg, stearate more preferably 0.5 mg Microcrystalline Up to 110 mg cellulose

(60) For combination compositions T.sub.3S is preferably present in a quantity of from 2.5-500 g and T.sub.4 of from 1 to 800 g, or, even more preferably: T.sub.3S: 5-250 g and T.sub.4: 5-400 g, or T.sub.3S: 10-100 g and T.sub.4 10-200 g.

(61) It is intended that the above quantities preferably refer to about 110 mg tablets, preferably for daily single dosage administration, even though the skilled artisan may envisage adjustments due to alternative composition forms and/or therapeutic treatment protocols. Due to the conversion rates of T.sub.3S to T.sub.3 within the body a single administration every two or three days may be also envisaged.

(62) According to the embodiment above for tablets, the following composition for T.sub.3S or T.sub.4 and T.sub.3S as active principle(s) (0.01-1% w/w) represents a further object of the present invention: a diluent selected from cellulose or derivatives thereof, preferably together with a second diluent, preferably calcium carbonate, up to 35% of the total diluent (w/w); a glidant, selected from glycerol dibehnate (most preferred), talc, silica derivatives among which magnesium trisilicate, amides, tribasic calcium phosphate, are usually present in the composition in a quantity range from 1 to 10%, most preferably 4 to 6% (w/w); a disintegrant selected from starch, croscarmellose sodium and crospovidone. Preferred is croscarmellose sodium salt in a quantity ranging from 0.5 to 10% even more preferably comprised from 1-5%, most preferably comprised from 2- to 4% (w/w); a lubricant selected from magnesium stearate, hydrate colloidal silica and talc, more preferably magnesium stearate and colloidal silica, in a total quantity range comprised from 0.1 to 7% even more preferably the first one comprised from 0.1 to 2% and the second comprised from 0.5 to 5% (w/w).

(63) Different tablet weight and active principle contents or different administration protocols may be envisaged for those skilled in the art.

(64) The tablets according to the preferred embodiment show optimal dissolution rates (see table below) and an optimal stability of the active principle(s) (at least 24 months).

(65) The following properties measured in conditions according to ICH Guidelines:

(66) TABLE-US-00003 Dissolution test 75% after 45 Moisture content 10% Resistance to crushing 20N HPLC Title T3S 90-110% HPLC Title T4 90-110%

(67) Liquid compositions, for example obtainable by crushing one or more tablets and dissolving such a mixture or the blended mixture in aqueous solutions are also possible. Optionally, trace amount (i.e. below 5%) of a pharmaceutically acceptable antioxidant is also present. It is contemplated that such compounds may include, for example, ammonium chloride and/or one or more iodide donors (e.g., sodium iodide).

(68) The compositions of this invention may further comprise one or more physiologically acceptable formulation excipients, such as those described in Remington, J. P, Gennaro, A. R., Remington's Pharmaceutical Sciences, Mack Publishers, Easton, (20th Edition, 2000).

(69) The compositions of this invention are particularly suitable for oral administration.

(70) The term oral formulation means that the active ingredient(s) is formulated into a product suitable for administering to an animal via the mouth. These formulations may include apart from the solid compositions described above, for example, liquids or semi-liquids, gels, pastes, oral sprays, buccal formulations, or animal feeds containing the active ingredients. Said liquid or semi-liquid compositions are typically aqueous solution.

(71) The pharmaceutical compositions described above are prepared preferably as tablets, obtainable by direct compression of the mixture above described in powder. In some such embodiments, for example, the process further comprises combining T.sub.3S or T.sub.3S and T.sub.4 in the solid compositions described above with an aqueous composition optionally comprising a buffer for the preparation of a pharmaceutical liquid composition for oral administration.

(72) It should be kept in mind that when the association is taken into account, the formulations of the present invention will also possibly comprise individually formulated doses of T.sub.3S and T.sub.4, for sequential or combined administration. In this case, one suitable kit is provided, which permits administration of said active principles in ways that can differ from patient to patient, depending on the needed therapeutic application. In such a way, the specialized physician will have a wide choice of changing the prescription according to the actual need of the patient.

(73) Just by way of a non-limitative example, in the case of oral administration, one package containing two individual blisters, which have different shape and/or color and/or different contents and/or doses, may suit the desired scope. Other possibilities exist and are easily available to the expert of the field.

(74) The pharmaceutical compositions of the present invention are usable in the treatment of pathologies due to organic deficiency of triiodothyronine (T.sub.3), like, for example, original hypothyroidism from autoimmune thyroid affections, hormonal production defects, thyroidectomy, congenital hypothyroidism, as well as some disorders due to reduced activity of type I 5-iodothyronine monodeiodinase (type I MD) which is induced, for example, by hypothyroidism, non thyroidal systemic illnesses, fast, selenium shortage and so on.

(75) Once administered to a human patient in need thereof, preferably suffering from a hypothyroid conditions, T.sub.3S levels can be measured and adjusted accordingly by a non-radioactive method immunoassay, either based on colorimetric, fluorescent or chemiluminescent detection.

(76) Accordingly, a further embodiment of the invention is represented by a non radioactive immunoassay. Preferably the immunoassay is an Enzyme Linked Immuno Assay (ELISA), more preferably a competitive ELISA in which increasing amounts of T.sub.3S compete for the binding to a solid phase bound anti-T.sub.3S antibody, (e.g. the polyclonal disclosed in Chopra et al., J. Clin. Endocrinol. Metab., 1992, 75: 189-194) with a fixed amount of T.sub.3S conjugated with an avidin-derivative detectable moiety (i.e. biotin), preferably carried out in a multi-well plate. More preferably, the avidin-derivative is a streptavidin and the detectable moiety comprises a chemiluminescent moiety (such as Alkaline Phosphatase or Horseradish Peroxidase), preferably HRP. The use of biotin-avidin interaction, combined with the various detection luminescence as techniques for signal development, allows signal amplification and increased sensitivity, comparable to a RIA test (see i.e. Chopra et al., J. Clin. Endocrinol. Metab., 1992, 75: 189-194) but without the need for radioactivitya clear advantage over the prior art. The ELISA assay, the T.sub.3S-biotin reagent and its synthesis, and kits for T.sub.3S quantitation comprising such reagent, represent a further object of the present invention.

(77) As an alternative embodiment, the T.sub.3S immunoassay is developed for a particular fluorescence technique, known as DELFIA (Dissociation Enhanced Lanthanide to Fluorescence ImmunoAssay) by which the required sensitivity is obtained. This assay, the synthesized reagents, and kits for T.sub.3S quantitation comprising said reagents represent a further object of the invention.

(78) Thus, accordingly, a DTPA-T.sub.3S monoamide (3,5-Diiodo-N-[[(carboxymethyl) [2-[(carboxymethyl) [2-[bis(carboxymethyl)amino]ethyl]amino]ethyl]amino]acetyl]-O-[3-iodo-4-(sulfooxy)phenyl]-L-tyrosine) of Formula I, represents a chelating compound according to a preferred embodiment:

(79) ##STR00001##

(80) Other molecules can be designed and synthesized by an expert in the field, through conjugation of T.sub.3S with a variety of chelating moieties, among those suitable for complexation of lanthanide ions, e.g., nitrilotriacetic acid (NTA), ethylenediaminetetraacetic acid (EDTA), ethylenediamine-N,N-bis(2-hydroxyphenylacetic acid) (EDDHA), ethylenediaminedisuccinic acid (EDDS), propanediaminetetraacetic acid (PDTA), diethylenetriaminetetraacetic acid (DTTA), diethylenetriaminepentaacetic acid (DTPA), and similar molecules. Conjugation between the chelating agent and T.sub.3S can be obtained by a variety of methods already known to the expert in the field, including a direct amide bond formation, as exemplified in Experimental Part, or the use of bifunctional chelating agents, that may even be commercial products, such as (S)-1-p-isothiocyanatobenzyldiethylenetriaminepentaacetic acid (DTPA isothiocyanateInvitrogen cat. I24221), or similar products.

(81) Suitable lanthanide metals to be used as chelate labels are selected in the group consisting of: samarium, terbium, dysprosium and europium.

(82) Particularly preferred is the Europium chelate 3,5-Diiodo-N-[[(carboxymethyl)[2-[(carboxymethyl) [2-[bis(carboxymethyl)amino]ethyl]amino]ethyl]amino]acetyl]-O-[3-iodo-4-(sulfooxy)phenyl]-L-tyrosine (Formula II).

(83) ##STR00002##

(84) A schematic of its synthesis is shown in FIG. 2 and can be summarized as follows: DTPA dianhydride is partially hydrolysed by adding an approximately equimolar amount of water dissolved in a suitable organic solvent, then the product, mainly composed of DTPA monoanhydride is reacted with T.sub.3S, in presence of a suitable organic or inorganic base. After solvent evaporation, the oily residue is diluted with water. The resulting precipitate is collected, washed with water and dissolved in an water/acetone mixture. This crude reaction product is purified on a column of Amberlite XAD1600, or similar resin, developing with mixtures or gradients of water/acetone. The product containing fractions are collected and evaporated to dryness, yielding the desired DTPA-T.sub.3S monoamide.

(85) Lanthanide complexation is obtained according to known procedures by adding an equimolar amount of a lanthanide salt to the monoamide water solution and adjusting the pH at 7 with a suitable base (e.g. NaOH). Optionally, the lanthanide chelated product can be desalted by adsorption on a resin column (e.g. Amberlite XAD1600) and elution with water/solvent mixtures.

(86) Also in this case, a sensitivity comparable to the RIA test (see Chopra et al., ibidem) is obtained and the use of radioactive isotopes avoided this represents a clear advantage over the prior art.

(87) According to a further embodiment, the invention comprises a kit for T.sub.3S administration and dosage in serum, wherein said kit comprises an administration/therapeutic kit with a number of T.sub.3S or T.sub.3S and T.sub.4 composition daily doses (i.e. the weekly, bi-weekly, monthly or bi-monthly need), preferably in the form of tablets as described above, and a dosage kit for T.sub.3S immunodetection by a non-radioactive assay.

(88) A further preferred embodiment of the kit comprises tablets with both active principles and a kit for T.sub.3S immunodetection in serum. In a preferred embodiment the immunodetection is an ELISA test as described above.

(89) The kit comprises a container for a non radioactive immunoassay according to the alternative embodiments described above and container for the weekly need of the solid daily dosage described above. The container for the solid daily dosage may be formulated for the weekly, bimonthly, monthly or even multiple months needs, according to the patients and therapeutic treatment need.

EXPERIMENTAL SECTION

(90) As an example, absolutely non-limiting for the skilled technician, T.sub.3S may be administered for oral use at doses ranging from 1 to 1000 g, preferably from 2.5 to 500 g, more preferably from 5 to 250 g.

(91) Analogously, when in association with T.sub.4, preferred doses range from 2.5-500 g of T.sub.3S and 1 to 800 g, T.sub.4 or, even more preferably: T.sub.3S: 5-250 g and T.sub.4: 5-400 g, or T.sub.3S: 10-100 g and T.sub.4 10-200 g.

(92) Two representative formulations for oral administration, selected among the preferred ones, are hereinafter enclosed by way of an example. Obviously, said formulations have no limiting effect on the other possible variations, which may also comprise different types of administration, different doses or different components depending on the specific pharmacological application or the particular pathology.

(93) TABLE-US-00004 Example A)-Oral formulation containing T.sub.3S T.sub.3S 50 g; Calcium phosphate dibasic anhydrous 103.5 mg; Mais starch 17.65 mg; Microcrystalline cellulose 5 mg; Sodium carboxymethylamide 5 mg; Talc 5 mg; Citric acid 2.8 mg; Magnesium stearate 1 mg Example B)-Oral formulation containing T.sub.3S and T.sub.4 T.sub.3S 50 g; T.sub.4 sodium salt 125 g; Calcium phosphate dibasic anhydrous 103.5 mg; Mais starch 17.525 mg; Microcrystalline cellulose 5 mg; Sodium carboxymethylamide 5 mg; Talc 5 mg; Citric acid 2.8 mg; Magnesium stearate 1 mg

Example C

Tablets Comprising T3S

(94) Pre Mixture

(95) In a 2-L amber glass of mixer Turbola transfer a portion Avicel PH102 and a T.sub.3S salt and mix for 515.

(96) Final Mixture

(97) In a stainless steel tank of double cone mixer, transfer the pre-mixture a second portion of Avicel PH102. Mix for 10 minutes at 10 RPM.

(98) The mix was sieved in 1-mm opening sieve and the remaining excipients: Compritol 888 ATO, Syloid 244, Acdisol, Magnesium stearate and Socal S2V DC and the last portion of Avicel PH102 were added directly in the double cone mixer, with mixing for 20 minutes at 10 rpm.

(99) The mixture was pressed in 110-mg tablets by a rotary tabletting machine equipped with 7-mm diameter, round, flat jewels, with one-sided break-mark in the middle.

(100) Tablets were shown to have chemical and physical characteristics according to ICH Guidelines.

(101) Tablets were prepared and have shown to have the following characteristics:

(102) 20 g dosage (25 C./60%)

(103) TABLE-US-00005 t.sub.0 = 104.8%; 75% t.sub.3 mesi = 103.5%; Dissolution test after 45 t.sub.6 mesi = 103% Moisture content 10% Resistence to crushing 20N HPLC Title T3S 90-110% HPLC Title T4 90-110%
100 g dosage (25 C./60%)

(104) TABLE-US-00006 t.sub.0 = 94.4%; 75% t.sub.3 mesi = 94.2%; Dissolution test after 45 t.sub.6 mesi = 94.3% Moisture content 10% Resistence to crushing 20N HPLC Title T3S 90-110% HPLC Title T4 90-110%

(105) Stability tests were carried out demonstrating that tablets are stable for at least 24 months.

Example D

Quantitation of T3S by Immunoassay with Chemiluminescence Detection

(106) Synthesis of T.sub.3S Biotin Derivative

(107) Briefly, T.sub.3S biotin derivative was synthesized as follows: N-hydroxysuccinimidyl d-biotin-15-amido-4,7,10,13-tetraoxapentadecylate A (50 mg; 0.0849 mmol) was solubilized in DMAC (2 mL), to which DIPEA (14.5 uL; 0.0866 mmol) was added, while maintaining the reaction mixture under continuous stiffing at 0 C. T.sub.3S (68.4 mg; 0.0908 mmol, prepared as described in Mol & Visser, Endocrinology 1985, 117:1-7) was then added and after a few minutes the suspension was left to heat up to room temperature to give a clear solution. It was allowed to stir for 2 h, then kept overnight at the same temperature. DMAC was evaporated under reduced pressure (10 mbar; 40 C.) to give a colourless oil. The crude so obtained was dissolved in H.sub.2O and purified by Semi-preparative HPLC. The fractions containing the product were collected, concentrated and finally lyophilized to give T.sub.3S-biotin as a white solid (59.6 mg; 0.0495 mmol). Yield 58%.

(108) A polyclonal anti-T.sub.3S antiserum was obtained in rabbits as described in Chopra et al., J. Clin. Endocrinol. Metab., 1992, 75: 189-194.

(109) The assay was based on a competitive ELISA in which increasing amounts of T.sub.3S competed for the antibody binding with a fixed amount of T.sub.3S conjugated with biotin, in a white 96 well plate. The employment of the biotin-avidin interaction, which allows signal amplification, combined with luminescence as technique for signal development allowed for a sensibility comparable to the RIA test (described in Chopra et al., J. Clin. Endocrinol. Metab., 1992, 75: 189-194).

(110) Standard solutions of T.sub.3S were prepared at the following concentrations: 1000, 200, 40, 8, 1.6 pg/mL in Diluent Buffer: PBS, 0.05% Tween, 0.3% BSA

(111) The tracer solution (T.sub.3S-Biotin, 180.6 M) was prepared in the above diluent buffer. Antibody solution: T.sub.3S rabbit antiserum was diluted 1:50000 in Diluent Buffer plus 8 mM ANS, 1.2 mg/mL Sodium Salicylate.

(112) A 96 well white plate was coated over night at 4 C. with 100 L/well of 2 g/mL anti Rabbit IgG diluted in phosphate buffer pH 7.8. At the same time, Standard solutions of biotin labelled T.sub.3S were combined with the diluted antiserum and the T.sub.3S-biotin solution as reported in Table A. The mixed samples were incubated at room temperature in the dark, overnight.

(113) The day after, the plate was washed four times with Washing Buffer (0.05% Tween 20 in PBS), then incubated in Blocking Buffer (2% BSA in Washing Buffer) for 1 h at room temperature.

(114) Afterwards, the plate was rinsed four times with Washing Buffer, 100 L/well of the mixed samples were added in triplicate and the plate was incubated 3 h at room temperature.

(115) Then, the plate was rinsed three times with Washing Buffer and incubated with Streptavidin Poly-HRP (10 ng/mL in RASA, 100 L/well) for 1 h at room temperature. After additional six washes, the plate was incubated with SuperSignal ELISA Femto Maximum Sensitivity Substrate (100 L/well) for 5 min in the dark and the emitted light was read as counts per second (CPS) with a luminescence plate reader

(116) TABLE-US-00007 TABLE A Calibration Curve Preparation T3S/1 T3S- T3S/1 Antiserum biotin (L) (L) (L) CS 5 (1000 pg/mL) 250 125 50 CS 4 (200 pg/mL) 250 125 50 CS 3 (40 pg/mL) 250 125 50 CS 2 (8 pg/mL) 250 125 50 CS 1 (1.6 pg/mL) 250 125 50 B0 125 50 NSB 50

(117) The calibration curve was prepared in buffer using five concentrations of the test item in the range 1.6-1000 pg/mL. The curve is shown in FIG. 1, panel a).

Example E

Quantitation of T3S by DELFIA

(118) Preparation of: [[3,5-Diiodo-N-[[(carboxymethyl)[2-[(carboxymethyl)[2-[bis(carboxymethyl)amino]ethyl]amino]ethyl]amino]acetyl]-O-[3-iodo-4-(sulfooxy)phenyl]-L-tyrosinate(6-)]europate(3-)]trisodium (Formula II).

(119) ##STR00003##
Synthesis of Eu-DTPA-T.sub.3S Monoamide

(120) The reaction scheme of the synthesis of 3,5-Diiodo-N-[[(carboxymethyl)[2-[(carboxymethyl) [2-[bis(carboxymethyl) amino]ethyl]amino]ethyl]amino]acetyl]-O-[3-iodo-4-(sulfooxy)phenyl]-L-tyrosine (DTPA-T.sub.3S monoamide) is shown in FIG. 2. A solution of H.sub.2O (0.282 ml; 15.64 mmol) in DMAC (43 mL) was added dropwise to a suspension of N,N-bis[2-(2,6-dioxylenol orange-4-morpholinyl)ethyl]glycine A (4.27 g; 11.94 mmol) in DMAC (85 mL) at room temperature. At the end of the addition the mixture was heated to 80 C. After 4.5 h the reaction mixture was cooled to 25 C. and a solution of T.sub.3S/1 (3 g; 3.98 mmol) and DIPEA (2.71 mL; 15.92 mmol) in DMAC (85 mL) was added dropwise over 20 min DMAC was evaporated under reduced pressure (10 mbar; 40 C.). The oily residue was diluted with H.sub.2O (200 mL), obtaining precipitation of a yellowish solid that was filtered washed with H.sub.2O and dried. The crude so obtained was dissolved in Acetone/H.sub.2O 20:80 (v/v), the solution (pH=2.97) was loaded on an Amberlite XAD-1600 resin column (200 mL; diam. 6 cm) and eluted with a Acetone/H.sub.2O gradient. The fractions containing the product having similar composition were collected and evaporated to give the ligand DTPA-T.sub.3S as a solid (1.27 g; 1.15 mmol). Yield 26%.

(121) Europium chloride hexahydrate (0.17 g, 0.46 mmol) was added in portions to a solution of the ligand DTPA-T.sub.3S (0.51 g; 0.46 mmol) in H.sub.2O (50 mL) at 20 C. (pH 2.93); after each addition the suspension was stirred until complete dissolution. Once the complexation was complete the pH was adjusted to 7 with 0.1 N NaOH and the solution was desalted by elution with water/acetone from a column of Amberlite XAD-1600 resin (100 mL; diam. 3 cm). The fractions containing the desired product and free from salts were collected and evaporated to give the compound of Formula I (0.37 g, 0.28 mmol) a yellow solid. Yield: 61%.

(122) The immunoassay method and solutions were as described in the Example D, with the following exceptions: a DELFIA Wash (Perkin Elmer) was used instead of the above Washing buffer. The Tracer stock solution contained the Europium 100 M and it was stored at +4 C., protected from light. Just before use it was diluted 1:300000 in Assay Buffer to obtain a final concentration of 440 pg/mL.

(123) The assay was performed in Delfia Yellow plates (Perkin Elmer).

(124) After the 3-h incubation with the mixed samples, the Formula II diluted compound solution was added (50 L per well) to all wells. The plates were then sealed with plastic adhesive sheets and incubated under agitation for 1 h at 37 C.

(125) After three washes, the plates were tapped dry on absorbent paper, and Delfia Enhancement Solution (Perkin Elmer) was added (200 L) After 1 h at 25 C., the plates were read in a Victor3 instrument according to the Europium manufacturer protocol. A calibration curve was prepared using nine concentrations of the test item in the range 30-2000 pg/mL. The curve is shown in FIG. 1, panel b).

Example F

Clinical Trial

(126) 1) Ethical Issues

(127) This study was conducted in Pisa, Italy under the guidelines provided in the Declaration of Helsinki, ICH E6 Guideline for Good Clinical Practice, and the requirements of the European Directive 2001/20/EC, and Law Decree Jun. 24, 2003, n. 211 implementing Directive 2001/20/CE in Italy, as well as the European Commission Directive 2005/28/EC of 8 Apr. 2005, laying down principles and detailed guidelines for good clinical practice for investigational medicinal products for human use, as well as the requirements for authorization of the manufacturing or importation of such products, and related guidance.

(128) 2) Safety

(129) The study was designed to guarantee that plasma levels of total T.sub.3 could not exceed 196.6 ng/dl, the level obtained by the administration of the consolidated standard therapy of 20 g T.sub.3.

(130) 3) Protocol

(131) About 30 human subjects with surgically excised thyroids were administered a to single dose of an oral T.sub.3S composition of the invention containing 20, 40, 80 or 160 g T.sub.3S in tablet form. Serum levels of thyroid hormone including T.sub.3S and triiodothyronine (T.sub.3) as both free T.sub.3 (FT.sub.3) and total T.sub.3 (TT.sub.3) were assessed by T.sub.3S RIA, as described in Chopra et al., J. Clin. Endocrinol. Metab., 1992, 75: 189-194.

(132) Forty eight hours prior to administration of the oral T.sub.3S composition of the invention, patients were screened for the study criteria and informed consent was requested and obtained. Twenty-four hours prior to administration of the oral T.sub.3S composition of the invention the subject was examined and all specimens for laboratory tests were collected, including thyroid function tests. On the day of the administration of the oral T.sub.3S composition of the invention, a further check of the inclusion/exclusion criteria was performed and patients were given a single dose of the oral T.sub.3S composition of the invention in tablet form according to the dose group in which they were placed.

(133) The tablet composition was as follows:

(134) TABLE-US-00008 Ingredient Amount per Tablet T.sub.3S sodium salt 20.6 g Equivalent to T.sub.3S 20 g Calcium carbonate 30 mg Glycerol dibehenate 5 mg Croscarmellose sodium salt 3.5 mg Hydrate colloidal silica 2 mg Magnesium stearate 0.5 mg Microcrystalline cellulose To 110 mg

(135) The initial part of the study was aimed at determining the optimal dose: as none of the patients treated with the 20, 40, 80 and 160 g doses of the oral T.sub.3S composition of the invention had serum levels of TT.sub.3 exceeding 196.6 ng/dl, the 160 g dose was selected for use in the second part of the study.

(136) 12 subjects received a single dose of the oral composition of the invention containing 160 g T.sub.3S. The absorption of T.sub.3S was assessed by measuring the serum levels of thyroid hormones TT.sub.3, FT.sub.3, T.sub.3S, free thyroxine (FT.sub.4) and Thyrotropin (or Thyroid Stimulating hormone, TSH).

(137) T.sub.3S in serum was detected with a peak level two hours after administration of the oral composition, as shown in FIG. 1. In patients lacking a thyroid there is no endogenous T.sub.3. Thus, all T.sub.3 present in the subjects was the result of conversion of T.sub.3S from the oral compositions to T.sub.3 in vivo. By monitoring serum T.sub.3S and TT.sub.3 levels after administration of the oral T.sub.3S compositions, it was determined that T.sub.3S was converted to the clinically active TT.sub.3 in a dose related fashion.

(138) Serum levels of TSH and FT.sub.4 were determined at 24 h and 30 minutes prior to administration, and at 24 and 48 hours15 min after the administration of T.sub.3S composition. Gastrointestinal absorption of T.sub.3S was assessed by measurement of circulating serum concentrations of TT.sub.3, T.sub.3S and FT.sub.3. Circulating serum concentrations of FT.sub.3 was measured pre and post dose to verify the in-vivo T.sub.3S-FT.sub.3 conversion in patients.

(139) Safety and tolerability were assessed by monitoring adverse events and by monitoring effects on vital signs, ECG, hematology, blood chemistry and urinalysis after administration of the oral compositions of the invention.

(140) 4) Conclusions

(141) Regardless of dose, the oral T.sub.3S compositions of the invention were found to be safe and well tolerated. The mean serum concentration of T.sub.3S (in ng/dl) for each of the four dose groups in the initial part of the study is shown in FIG. 3. For each dose group T.sub.3S was present in the serum, with a peak level two hours after oral administration. As all subjects were thyroidectomised and thus lacking endogenous T.sub.3S this data establishes that the T.sub.3S from the oral compositions of the invention crosses the gastrointestinal tract and enters the bloodstream.

(142) The mean serum concentration of T.sub.3S and TT.sub.3 after administration of a 160 g dose of the oral composition of the invention is shown in FIG. 4 for a patient. TT.sub.3 was detected within 4-5 hours of administration of the oral T.sub.3S. As all subjects were thyroidectomised and thus lacking endogenous T.sub.3, the only T.sub.3 source is exogenously administered T.sub.3S.

(143) This data establishes that T.sub.3S is absorbed (i.e. it crosses the Gastrointestinal Barrier) and is found in serum after oral administration, is converted to the clinically active T.sub.3 in a dose-related fashion and that T.sub.3 levels in serum are still detectable 48 hrs after single dose administration.

REFERENCES

(144) 1. Chopra I J. Nature, source and relative biological significance of circulating thyroid hormones. In: Braverman L E., Utiger R D. (eds) The Thyroid, Lippincott, Philadelphia 1991, pp. 126-143. 2. Spaulding S W., Smith T J., Hinkle P M., Davis F B., Kung M P., Roth J A. Studies on the biological activity of triiodothyronine sulfate. J. Clin. Endocrinol. Metab. 1992, 74, 1062-1067. 3. Lo Presti J S., Mizuno L., Nimalysuria A., Anderson K P., Spencer C A., Nicoloff J T. Characteristics of 3,5,3-triiodothyronine sulfate metabolism in euthyroid man. J. Clin. Endocrinol. Metab. 1991, 73, 703-709. 4. Santini F., Hurd R E., Chopra I J. A study of metabolism of deaminated and sulfoconjugated iodothyronines by rat placental iodothyronine 5-monodeiodinase. Endocrinology 1992, 131, No. 4, 1689-1694. 5. Otten M H., Mol J A., Visser T J. Sulfation proceding deiodination of iodothyronines in rat hepatocytes. Science 1983, 221, 81-83. 6. Mol J A., Visser T J. Rapid and selective inner ring deiodination of T.sub.4 sulfate by rat liver deiodinase. Endocrinology 1986, 117, 8-12. 7. Kung M P., Spaulding S W., Roth J A. Desulfation of 3,5,3-triiodothyronine sulfate by microsomes from human and rat tissues. Endocrinology 1988, 122, 1195-1200. 8. Santini F., Chopra I J., Wu S Y., Solomon D H., Chua Teco G N. Metabolism of 3,5,3-triiodothyronine sulfate by tissues of the fetal rat: a consideration of the role of desulfation of 3,5,3-triiodothyronine sulfate as a source of T.sub.3. Pediatr. Res. 1992, 31, 541-544. 9. De Herder W W., Hazenberg M P., Pennock-Schroeder A M., Hennemann G., Visser T J. Rapid bacteria-dependent in vitro hydrolysis of iodothyronine conjugates by intestinal contents of humans and rats. Med. Biol. 1986, 64, 31-35. 10. Santini F., Hurd R E., Lee B., Chopra I J. Thyromimetic effects of 3,5,3-triiodothyronine sulfate in hypothyroid rats. Endocrinology 1993, 133, No.1, 105-110. 11. Santini F., Chiovato L., Ghiri P., Lapi P., Mammoli C., Montanelli L., Scartabelli G., Ceccarini G., Coccoli L., Chopra I J., Boldrini A., Pinchera A. Serum iodothyronines in human fetus and the newborn: evidence for an important role of placenta in fetal thyroid hormone homeostasis. J. Cl. Endocrinol. Metab. 1999, 84, No.2, 493-498. 12. Santini F., Pinchera A., Ceccarini G., Castagna M., Rosellini V., Mammoli C., Montanelli L., Zucchi V., Chopra I J., Chiovato L. Evidence for the role of the type III-iodothyronine deiodinase in the regulation of 3,5,3-triiodothyronine content in the human central nervous system. Eur. J. Endocrinol. 2001, 144, 577-583. 13. Santini F., Cortellazzi D., Baggiani A M., Marconi A M., Beck-Peccoz P., Chopra I J. A study of the serum 3,5,3-triiodothyronine sulfate concentration in to normal and hypothyroid fetuses at various gestational stages. J. Cl. Endocrinol. Metab. 1993, 76, No.6, 1583-1587. 14. Chopra I J., Nguyen D. Demonstration of thyromimetic effects of 3,5,3-triiodothyronine sulfate (T.sub.3S) in Euthyroid rats. Thyroid 1996, 6, No.3, 229-232.

EMBODIMENTS OF THE INVENTION

(145) 1. Triiodothyronine sulfate for use as a medicament. 2. Triiodothyronine sulphate for use as a medicament according to embodiment 1, having thyromimetic activity. 3. Triiodothyronine sulfate according to embodiment 2, for use in the treatment of pathologies due to organic deficiency of triiodothyronine. 4. Triiodothyronine sulfate according to embodiment 3, wherein said pathologies comprise original hypothyroidism from autoimmune thyroid affections, hormonal production defects, thyroidectomy, congenital hypothyroidism. 5. Triiodothyronine sulfate according to embodiment 2, for use in the treatment of disorders due to reduced activity of type I 5-iodothyronine monodeiodinase. 6. Triiodothyronine sulfate according to embodiment 5, wherein said reduced activity of type I 5-iodothyronine monodeiodinase comprises, among its grounds, hypothyroidism, non thyroidal systemic illnesses, fast, selenium shortage. 7. Pharmaceutical compositions comprising triiodothyronine sulfate as an active principle. 8. Pharmaceutical compositions according to embodiment 7, wherein said triiodothyronine sulfate is formulated in association with thyroxine. 9. Pharmaceutical compositions according to embodiment 7 and 8, wherein said compositions further comprise additives like excipients, diluents, dissolvents, solvents, carriers, dyestuffs, flavourings, sweeteners. 10. Pharmaceutical compositions according to embodiment 7, wherein triiodothyronine sulfate is administered at doses raging from 5 to 1000 g. 11. Pharmaceutical compositions according to embodiment 10, wherein triiodothyronine sulfate is administered at doses raging from 10 to 500 g. 12. Pharmaceutical compositions according to embodiment 10, wherein triiodothyronine sulfate is administered at doses raging from 25 to 250 g. 13. Pharmaceutical compositions according to embodiment 8, wherein said association is administered at doses ranging from 10 to 500 g of triiodothyronine sulfate and from 10 to 250 g of thyroxine. 14. Pharmaceutical compositions according to embodiment 8, wherein said association is administered at doses ranging from 25 to 250 g of triiodothyronine sulfate and from 25 to 200 g of thyroxine. 15. Kit for the differential or sequential administration of the pharmaceutical compositions according to embodiments 8, 9 and 11 to 14. 16. Use of triiodothyronine sulfate for the preparation of the pharmaceutical compositions according to embodiments 7 to 15.