High-Stability Packaged Solutions of T4 Thyroid Hormone

Abstract

The invention relates to highly stable alcohol-free, water-glycerol solutions of T4 thyroid hormone, with a reduced amount of T3 impurity, packaged via specific container arrangements. The containers are multi-barrier ones, in which a number of layers of specific materials separate the solution from contact with the external environment.

Claims

1. A pharmaceutical preparation of T4 thyroid hormone, in ready-to-use packaging, consisting of a container pre-filled with an alcohol-free water-glycerol solution of hormone T4, said container being selected from: (a) a one-component LDPE plastic container, placed in a sealed sachet consisting of laminated films made of a plurality of different materials selected from the following: polyethylene, aluminium, polyethylene terephthalate, ionomer resins, paper, ethylene vinyl alcohol, copolymer resins, propylene, and fluorinated-chlorinated resins; or (b) a multi-component laminated plastic container, said container comprising multiple layers of plastic materials selected from: polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride; polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals and aluminium bonded to plastics.

2. A pharmaceutical preparation according to claim 1, wherein the T4/glycerol weight ratio in the water-glycerol solution is in the range from about 4 to about 400 ppm.

3. A pharmaceutical preparation according to claim 1, wherein the water-glycerol solution contains less than about 2.5% of T3 impurity.

4. A pharmaceutical preparation according to claim 1, wherein the water-glycerol solution contains less than about 2.0% of T3 impurity.

5. A pharmaceutical preparation according to claim 1, wherein the water-glycerol solution contains less than about 1.8% of T3 impurity.

6. A pharmaceutical preparation according to claim 1, wherein the preparation is in a single-dose form and contains about 5 μg to about 350 m T4 thyroid hormone.

7. A pharmaceutical preparation according to claim 1, wherein the preparation is in a single-dose form and contains about 5 μg to about 250 m T4 thyroid hormone.

8. A pharmaceutical preparation according to claim 1, wherein the plastic container has a thickness of between about 150 μm to about 1000 μm.

9. A pharmaceutical preparation according to claim 1, wherein the plastic container has a thickness of between about 200 μm and about 800 μm.

10. A pharmaceutical preparation according to claim 1, wherein the sachet comprises laminated films selected from the group consisting of: polyethylene, aluminium and polyethylene terephthalate; polyethylene, aluminium and paper; or the group consisting of ionomer resins, aluminium and paper.

11. A pharmaceutical preparation according to claim 1, wherein the sachet has an overall thickness of between about 40 and about 100 μm.

12. A pharmaceutical preparation according to claim 1, wherein the sachet has an overall thickness of between about 50 and about 90 μm.

13. A method of treating a disease associated with T3 and/or T4 hormone deficiency, the method comprising administering a pharmaceutical preparation according to claim 1 to a patient in need thereof.

14. A pharmaceutical preparation comprising: (a) a composition of an alcohol-free water/glycerol solution of T4 thyroid hormone; (b) a single-dose container for containing the solution; whereby less than 2.5% of the T4 thyroid hormone in the solution converts to T3 thyroid hormone after 12 months under Long Term Storage Conditions.

15. A pharmaceutical preparation according to claim 14 wherein the conversion of T4 thyroid hormone to T3 thyroid hormone is less than for a pharmaceutical preparation in a similar single-dose container comprising a water-glycerol-alcohol solution of T4 thyroid hormone after 12 months under Long-Term Storage Conditions.

16. A pharmaceutical composition comprising an alcohol-free water/glycerol solution of T4 thyroid hormone that is capable of storage in a single-dose container whereby the pharmaceutical composition demonstrates less the 2.5% conversion of T4 thyroid hormone to T3 thyroid hormone for 12 months under Long Term Storage Conditions.

17. A method of treating thyroid hormone deficiency comprising administering the composition of the alcohol-free water/glycerol solution of T4 thyroid hormone according to claim 14 to a patient in need thereof.

18. A method of treating thyroid hormone deficiency comprising administering a pharmaceutical composition according to claim 16 to a patient in need thereof.

19. A ready-to-use pharmaceutical preparation of T4 thyroid hormone packaged in a container which is pre-filled with an alcohol-free water-glycerol solution of hormone T4, said container being selected from: (a) a one-component LDPE plastic container, placed in a sealed sachet consisting of laminated films made of a plurality of materials selected from the following: polyethylene, aluminium, polyethylene terephthalate, ionomer resins, paper, ethylene vinyl alcohol, copolymer resins, propylene, and fluorinated-chlorinated resins; or (b) a multi-component laminated plastic container comprising a plurality of layers of plastic materials selected from the group consisting of: polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals, aluminium bonded to plastics, and combinations thereof.

20. A ready-to-use package of a pharmaceutical preparation of T4 thyroid hormone, the package comprising a container which is pre-filled with an alcohol-free water-glycerol solution of hormone T4, wherein the container is selected from: (a) a one-component LDPE plastic container, placed in a sealed sachet formed from laminated films comprising a plurality of materials selected from the following: polyethylene, aluminium, polyethylene terephthalate, ionomer resins, paper, ethylene vinyl alcohol, copolymer resins, propylene, and fluorinated-chlorinated resins; or (b) a multi-component laminated plastic container comprising a plurality of layers of plastic materials selected from the group consisting of: polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals, aluminium bonded to plastics, and combinations thereof.

21. A method of treating patients who undergo bariatric surgery, patients whose gastric pH is altered and have absorption problems, or patients having absorption problems caused by intake of food, the method comprising administering the composition of the pharmaceutical preparation according to claim 14 to a patient in need thereof.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0029] For the purpose of the present invention, the term “alcohol-free solution” means that the solution does not contain low-molecular weight alcohols. The term “low molecular weight alcohol” means an alkanol with molecular weight lower than 80 Dalton: e.g. methanol, ethanol, propane, propanediol, isopropanol, and similar alcohols; the term “alcohol-free” remains thus compatible with the presence of glycerol (which has a molecular weight of 92.1 Daltons) in the solution.

[0030] In an embodiment of the invention, the packaging used is a multi-barrier one, i.e. one in which several layers of different materials separate the solution from contact with the external environment. The layers may be part of the same container and/or may belong to different containers contained in one another, wherein the T4 solution is contained in the innermost container. In particular, the packaging can be composed according to the following options:

a. a one-component LDPE plastic container, placed in a sealed sachet consisting of laminated film made of different materials selected from the following: polyethylene, aluminium, polyethylene terephthalate, ionomer resins, paper, ethylene vinyl alcohol copolymer resins, polypropylene, and fluorinated-chlorinated resins; or
b. a multi-component laminated plastic container characterized by multiple layers of plastic materials selected from polyethylene, ethylene vinyl alcohol copolymer resins, polyvinyl chloride, polyvinylidene chloride, polyvinyl acetate, fluorinated-chlorinated resins, ionomer resins, cyclic olefin copolymers, polyamide, polystyrene, polycarbonate, laminated metals, and aluminium bonded to plastics.

[0031] Preferably, the plastic container referred in (a) and/or (b) is squeezable by manual compression. Also preferably, said container referred in (a) and/or (b) has a thickness of between 150 and 1000 and more preferably between 200 and 800 e.g. 600 μm±15%. The above option (a) includes the variant in which more than one LDPE plastic container, each filled with the solution of T4, is contained within a single sachet containing all of them.

[0032] In one preferred embodiment of option (a), the sachet consists of laminated films made of different materials according to the following combinations: polyethylene, aluminium and polyethylene terephthalate, polyethylene, aluminium and paper, ionomer resins, aluminium and paper.

[0033] An important contribution to the stability of the T4 solution is given by the sum of thicknesses of all the films making up the sachet, i.e. the overall thickness of the sachet made of the specific laminated films mentioned above. The overall thickness should be preferably comprised within the range of 40 to 100 more preferably of 50 to 90 These conditions advantageously combine an effective protection from T4 degradation to T3, while avoiding using excessive packaging material. If desired, values higher than 90 μm may also be used in the present invention. Examples of the above described packaging arrangements (not in association with alcohol-free solutions of T4 hormone) are described in patent application WO2013/072304, herein incorporated by reference.

[0034] The water-glycerol solution used in the present invention can typically contain a T4:glycerol weight ratio comprised between 0.004:1000 and 0.4:1000 (i.e. 4 to 400 ppm). If the solution is formulated as a dose unit form, the suitable dose unit will typically contain from 5 to 350 μg (or preferably 5 to 250 m) of T4 in 1 g of glycerol.

[0035] All ratios and amounts of glycerol are herein calculated based on glycerol as a pure substance. In practice however, glycerol is handled as a concentrated solution in water, typically at 85% w/w. It is thus understood that the water component of the present solutions may be derived, at least in part, from the water content of commercial glycerol. The water content of 85% glycerol is normally sufficient to obtain the solutions according to the invention. The addition of further amounts of water remains in any case possible within the scope of the invention.

[0036] The present T4 solutions contain a reduced amount of T3 impurity, where “reduced” means that T3 may be present at a maximum concentration of 2.5%, preferably 2.0%, more preferably 1.8%. Said values of T3 impurity are calculated herein as follows: (T3 m/mL being present in the sample/T4 μg/mL being present in the sample)*100. The reduced amount of T3 impurity is a consequence of the high level of storage stability reached (in terms of limited T4 to T3 conversion), as supported in the experimental section. In particular, at the end of the stability period (25° C.±2° C./60±5% R.H.), the pharmaceutical preparation according to the invention showed a T4 content of not less than 95% of the initial concentration, and total impurities were within the standard acceptability criteria.

[0037] Moreover, the pharmaceutical preparation according to the invention has minimal or no microbiological contamination, with TAMC (total aerobic microbial count) values≤100 CFU/g, TYMC (total yeast and mould count) values≤10 CFU/g, and absence of E. coli, thus being practical to use and not susceptible to accidental contamination.

[0038] The pharmaceutical preparation according to the invention is conveniently used to treat disorders associated with thyroid hormone T3 and/or T4 deficiency. It is preferably administered orally, i.e. it is suitable for oral administration. It is noted that, although the present T4 solutions do not contain T3 (or contain it in extremely low amounts), their use extends to treat T3 deficiency since T4 is physiologically converted into T3 by the organism after administration.

[0039] A further aspect of the invention therefore relates to the use of a water-glycerol solution of thyroid hormone T4 in a packaging as described above, to prepare a medicament for the treatment of disorders associated with thyroid hormone T3 and/or T4 deficiency. The medicament is preferably suitable for oral administration.

[0040] A further aspect of the invention relates to a pharmaceutical preparation of a water-glycerol solution of thyroid hormone T4 in a packaging as described above, for use in the treatment of disorders associated with thyroid hormone T3 and/or T4 deficiency. The preparation is preferably suitable for oral administration.

[0041] A further aspect of the invention relates to a method of treating disorders associated with thyroid hormone T3 and/or T4 deficiency comprising administering a water-glycerol solution of thyroid hormone T4 packaged as described above, to a patient in need thereof. The solution is preferably suitable for oral administration.

[0042] A further aspect of the invention relates to a method of treating bariatric patients (that is, patients who undergo bariatric surgery), using the inventive package. A further aspect of the invention relates to a method of treating patients whose gastric pH is altered and thus have absorption problems or whose absorption problems may be caused by intake of food. The inventive package can be administered to such bariatric patients or such patients having altered gastric pH or altered absorption related to food intake for treatment of their respective conditions.

[0043] The present invention thus provides new packaged solutions of T4, being advantageously more stable to an unwanted premature conversion of T4 in T3 than prior solutions of T4. The increased stability ensures a more reproducible and constant amount of administered hormone, avoiding possible overdosing due to excessive administration of T3 impurities. The non-use of volatile alcohols like ethanol brings a further advantage in that the formulation does not suffer from accidental reduction of alcohol content, which reflects in an unwanted variation of hormone solubility/stability of the solution. Furthermore, the absence of such alcohols in the present water-glycerol solutions did not substantially change the overall stability of the solution in terms of T4 potency, total impurities and microbial contamination, thus resulting in a preparation meeting all the acceptability criteria for pharmaceutical use. The use of the single dose container protected by an envelope defends the product from microbiological contamination; the specific alcohol-free and preservative-free formulation is particularly indicated for chronic use.

EXPERIMENTALS

[0044] The following acronyms are herein used: polyethylene (PE), polyethylene terephthalate (PET), ethylene vinyl alcohol copolymer resins (EVOH), polyvinyl chloride (PVC), polyvinylidene chloride (PVdC), polyvinyl acetate (PVA), cyclic olefin copolymers (COC), polyamides (PA), polystyrene (PS), and polycarbonate (PC).

Example 1: Water-ethanol-glycerol T4 solution (reference)

[0045] A reference formulation was prepared in accordance with example 1 of WO2013/072304. Accordingly, one liter of a water-alcohol solution containing 100 μg/mL of T4 was prepared as follows, using the qualitative/quantitative composition listed below:

TABLE-US-00001 i. T4 0.105 g ii. ethanol (96%) 243 g iii. glycerol (85%) 861 g

[0046] The T4 was solubilized in ethanol in a suitable dissolver apparatus, under continuous stirring at ambient temperature. When a clear solution free of visible non-solubilized residues was obtained, glycerol was added, and a homogenous, clear, colourless solution was obtained under gentle stirring at ambient temperature. The solution was filtered (0.8 μm), and was then ready for packaging. The final T4 concentration in solution was 100 μg/mL. Following the same method, further solutions were prepared having the final concentrations of 25 μg/mL, 50 μg/mL, 75 μg/mL.

[0047] The packaging arrangement was made according to example 3 of WO2013/072304 as follows: a single-dose container with a nominal volume of 1.10 mL made of one-component LDPE plastic (600 μm thick) was placed in a sealed sachet (PET/A1/PE). The characteristics of the sachet were as follows:

1. Stratified film with high gas and light barrier:
2. Polyethylene terephthalate: 12 μm film thickness (value to be considered±5-6%);
3. A1: 9 μm film thickness (value to be considered±5-6%);
4. Polyethylene: 50 μm film thickness (value to be considered±5-6%);
5. Overall thickness: 71 μm;
6. Oxygen permeability: 0.1-0.2 cc/m.sup.2/day; and
7. Water vapor permeability: 0.1-0.2 g/m.sup.2/day.

[0048] The oxygen permeability was measured in accordance with ASTM Standard D-3985. The water permeability was measured in accordance with ASTM Standard E-398. The prototypes were prepared on a laboratory scale, using an automatic pipette (Gilson P-1000) to fill disposable containers with 1.1 mL of the water-glycerol-ethanol solution previously described, after which the containers were sealed with a Pentaseal-lab benchtop sealing machine. They were then packaged in a hermetically sealed sachet of the type described above.

Example 2: Water-glycerol T4 solution

[0049] A number of solutions were prepared according to the previous reference Example 1, replacing the water-ethanol-glycerol solution described therein with the alcohol-free water-glycerol solution in accordance with the present invention. Accordingly, the following amounts of T4 hormone were dissolved in 1.222 g of glycerol 85%: 25 μg, 50 μg, 75 μg, and 100 μg, obtaining the respective final concentrations of: 25 μg/mL, 50 μg/mL, 75 μg/mL, and 100 μg/mL.

[0050] Packaging arrangement: a single-dose container with a nominal volume of 1.10 mL made of one-component LDPE plastic (600 μm thick) was placed in a sealed sachet (PET/A1/PE). Characteristics of sachet: Stratified film with high gas and light barrier: Polyethylene terephthalate: 12 μm layer thickness; A1,12 μm layer thickness; Polyethylene 45 μm layer thickness (all values to be considered±5-6%); Overall thickness: 69 μm.

Example 3: Storage stability studies

[0051] The packaged solutions obtained in the previous examples 1 and 2 were subjected to storage stability testing with the aim, in particular, to evaluate the extent of conversion of T4 in T3 during storage, under both normal or accelerated conditions. The sealed sachets were thus placed in suitable environmental test chambers, and immediately underwent a stability study under ICH conditions. The equipment used was calibrated and instantly monitored for correct operation. The following tables show the compared performances of the products obtained in Examples 1 and 2.

TABLE-US-00002 TABLE 1 T4 solutions 25 μg/mL-Stability Data under Long Term Conditions (25° C. ± 2° C./60% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance limit 3 m 6 m 9 m 12 m 18 m Sample (%) (%) (%) (%) (%) (%) Example 1 ≤2.5 0.3 0.5 0.8 1.0 1.5 (reference) Example 2 ≤2.5% 1.0 0.7 0.7 0.7 1.1 (invention)

TABLE-US-00003 TABLE 2 T4 solutions 25 μg/mL - Stability Data under Intermediate Term Conditions (30° C. ± 2° C./65% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance Sample limit (%) 3 m (%) 6 m (%) 9 m (%) 12 m(%) Example 1 ≤2.5 0.3 0.5 0.8 1.0 (reference) Example 2 ≤2.5% 0.7 0.9 1.3 0.8 (invention)

TABLE-US-00004 TABLE 3 T4 solutions 50 μg/mL-Stability Data under Long Term Conditions (25° C. ± 2° C./60% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance limit 3 m 6 m 9 m 12 m 18 m Sample (%) (%) (%) (%) (%) (%) Example 1 ≤2.5 0.5 1.2 1.3 1.5 2.1 (reference) Example 2 ≤2.5% 0.5 0.7 0.8 0.9 1.4 (invention)

TABLE-US-00005 TABLE 4 T4 solutions 50 μg/mL - Stability Data under Intermediate Term Conditions (30° C. ± 2° C./65% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance Sample limit (%) 3 m (%) 6 m (%) 9 m (%) 12 m(%) Example 1 ≤2.5 1.1 1.8 2.0 2.4 (reference) Example 2 ≤2.5% 0.6 1.2 1.7 2.2 (invention)

TABLE-US-00006 TABLE 5 T4 solutions 75 μg/mL-Stability Data under Long Term Conditions (25° C. ± 2° C./60% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance limit 3 m 6 m 9 m 12 m 18 m Sample (%) (%) (%) (%) (%) (%) Example 1 ≤2.5 1.1 1.0 1.2 1.4 1.8 (reference) Example 2 ≤2.5% 0.5 0.8 0.9 1.0 1.5 (invention)

TABLE-US-00007 TABLE 6 T4 solutions 75 μg/mL - Stability Data under Intermediate Term Conditions (30° C. ± 2° C./65% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance Sample limit (%) 3 m (%) 6 m (%) 9 m (%) 12 m(%) Example 1 ≤2.5 1.3 2.2 2.4 2.6 (reference) Example 2 ≤2.5% 0.7 1.3 1.8 2.3 (invention)

TABLE-US-00008 TABLE 7 T4 solutions 100 μg/mL-Stability Data under Long Term Conditions (25° C. ± 2° C./60% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance limit 3 m 6 m 9 m 12 m 18 m Sample (%) (%) (%) (%) (%) (%) Example 1 ≤2.5 0.5 1.0 1.3 1.5 2.2 (reference) Example 2 ≤2.5% 0.5 0.8 0.8 1.0 1.4 (invention)

TABLE-US-00009 TABLE 8 T4 solutions 100 μg/mL - Stability Data under Intermediate Term Conditions (30° C. ± 2° C./65% ± 5% R.H.): percent of T4.fwdarw.T3 conversion Acceptance Sample limit (%) 3 m (%) 6 m (%) 9 m (%) 12 m(%) Example 1 ≤2.5 1.1 1.9 2.4 2.8 (reference) Example 2 ≤2.5% 0.7 1.4 1.9 2.2 (invention)

Example 4: Binary experiments with glycerol and water

[0052] In binary experiments, T4 solutions were prepared in glycerol:water mixtures with 30:70 w/w, 50:50 w/w, 70:30 w/w and 85:1.5 w/w ratios. T4 was also dissolved in 100% pure glycerol. The behaviour of such T4 preparations was investigated by assessing T4 solubility, as well as chemical and microbiological stability.

[0053] The results of T4 solubility and chemical stability in accelerated conditions (40° C.±2° C./75%±5% R.H.) are reported in the tables below. T4 was added in all preparations at the highest intended concentration of 200 μg/mL. The preparations were stirred up to 40 minutes at room temperature.

TABLE-US-00010 TABLE 9 T4 solubility and chemical stability in accelerated conditions (40° C. ± 2° C./75% ± 5% R.H.) Aspect Preparations T0 2 Days 15 Days 1 Month Glycerol:Water Slightly Presence of a N/A N/A 30:70 opalescent precipitate dispersion Glycerol:Water Apparent clear Slightly N/A N/A 50:50 and colourless opalescent solution dispersion Glycerol:Water Clear and Clear and Clear and Clear and 70:30 colourless colourless colourless colourless solution solution solution solution after 40 min Glycerol:Water Clear and Clear and Clear and Clear and 85:15 colourless colourless colourless colourless solution solution solution solution after 30 min Glycerol Clear and Clear and Clear, N/A colourless colourless slightly solution solution yellow solution N/A = Not available

[0054] Chemical stability data of T4 dissolved in glycerol:water mixtures with 70:30 w/w, 85:15 w/w ratios and 100% glycerol are given in the following table.

TABLE-US-00011 TABLE 10 T4 dissolved in glycerol:water mixtures with 70:30 w/w, 85:15 w/w ratios and 100% glycerol 15 1 T0 DAYS MONTH GLYCEROL:WATER T4 106% 101.2%  97.2% 70:30 T3 0.10 0.56% 0.48% T2 <0.072 <0.072 <0.072 T3 reverse <0.014 <0.014 <0.014 triac <0.054 <0.054 <0.054 tetrac <0.134 <0.134 <0.134 Single <0.022% 0.055%  0.21% unknown imp. Total 0.10% 0.61% 0.69% impurities GLYCEROL:WATER T4 101.5% .sup. 98% 95.2% 85:15 T3 0.099% 0.44% 0.41% T2 <0.072 <0.072 <0.072 T3 reverse <0.014 <0.014 <0.014 triac <0.054 <0.054 <0.054 tetrac <0.134 <0.134 <0.134 Single <0.022% 0.41% 0.21% unknown imp. Total 0.10% 1.26% 0.62% impurities GLYCEROL T4 101.3% 67.6% 57.5% 100% T3 0.081% 0.14% 0.11% T2 <0.072 <0.072 <0.072 T3 reverse 0.13 0.12% <0.014 triac <0.054 <0.054 <0.054 tetrac <0.134 0.46% 0.40% Single 0.092%  3.4% 2.91% unknown imp. Total 0.37% 4.87% 3.96% impurities

[0055] Challenge test data of T4 dissolved in glycerol:water mixtures with 70:30 w w, 85:15 w/w ratios and 100% glycerol are given in the following table.

TABLE-US-00012 CHALLENGE TEST GLYCEROL:WATER complies 70:30 GLYCEROL:WATER complies 85:15 GLYCEROL complies 100%

[0056] T4 solubility and T4 chemical and microbiological stability in accelerated stability studies were monitored in order to reach an optimal balance of drug product characteristics. Glycerin:water ratios as low as 30:70 w/w and 50:50 did not guarantee the target T4 solubility, i.e., T4 concentrations as high as 200 μg/mL were not achievable since a precipitate or an opalescent dispersion was observed. When T4 was dissolved in 100% glycerol, a significant reduction of T4 assay (<70%) was observed after 15 days at 40° C.±2° C./75%±5% R.H.

[0057] The final selected formulation was a T4 solution in 85% glycerol w/w. In this mixture, T4 was freely soluble up to 200 μg/mL and was chemically stable in accelerated conditions. The outcome of the challenge test indicated that this solution was also microbiologically stable.

[0058] Although 70% glycerol showed T4 solubility and chemical stability similar to those observed with 85% glycerol, this latter concentration was selected for the product development. In fact, a slightly higher percentage of glycerol appeared to improve the solubilization rate of T4, and it is expected to better preserve T4 from precipitation at the higher concentrations and warrant microbiological stability.

[0059] Stability testing at 5° C., 25° C./60% R.H., 30° C./65% R.H. and 40° C./75% R.H. according to ICH conditions is currently ongoing on development batches of oral solutions of T4 dissolved in 85% glycerol at concentrations of 25, 50 and 100 μg/mL. After 9-month storage, this formulation is stable at all strengths at all of the above conditions.

[0060] It can be seen that all the tested samples in accordance with the invention, at substantially all doses, storage times and storage conditions, showed a consistent reduction of conversion in T4 to T3. The aims of the present invention are thus met.

[0061] Other objects, advantages and embodiments of the various aspects of the present invention will be apparent to those who are skilled in the field of the invention and are within the scope of the description. For example, but without limitation, structural or functional elements might be rearranged, or method steps reordered, consistent with the present invention. Similarly, features or methods may comprise a single instance or step, or a plurality of separate instances or steps. The features of the invention described in various embodiments are not meant to limit the possible types of elements that may be used in embodiments of aspects of the present invention, and other elements that may accomplish similar tasks may be implemented as well. Similarly, principles according to the present invention, and methods and systems that embody them, could be applied to other examples, which, even if not specifically described here in detail, would nevertheless be within the scope of the present invention.