AU6378299A

AU6378299A - A new composition

Info

Publication number: AU6378299A
Application number: AU63782/99A
Authority: AU
Inventors: John Evenden; Seth-Olov Thorberg
Original assignee: AstraZeneca AB
Current assignee: AstraZeneca AB
Priority date: 1998-09-16
Filing date: 1999-09-13
Publication date: 2000-04-03
Also published as: EP1113793A1; WO2000015220A1; CA2342233A1; SE9803158D0; JP2002524510A

Description

WO 00/15220 PCT/SE99/01599 A NEW COMPOSITION Field of the Invention 5 The present invention relates to a composition which comprises (R)-5-carbamoyl-8-fluoro 3-N,N-dicyclobutylamino-3,4-dihydro-2H-l-benzopyrans in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, and (+)-1-[3 (dimethylamino)propyl]-1-(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. The present invention to also relates to a process for the preparation of the inventive composition, pharmaceutical formulations containing said composition and to the use of said composition either by concomitant administration or by separate administration as an improvement of the treatment of affective disorders such as depression, anxiety, obsessive compulsive disorder (OCD), etc. 15 Background of the Invention Today, it is generally considered that antidepressants take 2-4 weeks to reach full clinical effect. In contrast, the side effects occur immediately. Thus, slow onset of action of 20 antidepressants leads to a vulnerable period for patients in which they experience the side effects, but not the therapeutic effects of drugs. There is often a heavy burden on the treating physician to persuade the patient to continue with the treatment during this period. Furthermore, in suicidal patients, as the onset of action is gradual,initiative may be regained without the experiencing of full reversal of symptoms, leaving a window of risk 25 for suicide and a frequent requirement for hospitalization. An antidepressant with fast onset of action would not only be beneficial due to the faster symptom reduction, but would also be more acceptable to patients and physicians and reduce the need for and duration of hospitalization. The same long period to reach full clinical effect has been shown in the treatment of other affective disorders such as anxiety and OCD. 30 WO 00/15220 PCT/SE99/01599 2 Prior art In WO 96/33710 is disclosed that the compound (R)-5-carbamoyl-8-fluoro-3-NN dicyclobutylamino-3,4-dihydro-2H-1-benzopyran which has high affinity to 5-HT receptors 5 and antagonizes 5-HTIA mediated responses induces a rapid improvement of depressed patients treated with serotonin reuptake inhibitors. Summary of the Invention 10 The present invention is directed to a new composition comprising of the specific 5 HT IAantagonist (R)-5-carbamoyl-8-fluoro-3-NN-disubstituted-amino-3,4-dihydro-2H-1 benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, and the specific 5-HT reuptake inhibitor (+)-1-[3-(dimethylamino)propyl] 1-(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a is pharmaceutically acceptable salt and/or solvate thereof. Said composition attains a faster onset of action and consequently, provides a more efficacious treatment of the patients suffering from affective disorders, particularly depression. It has been shown in animal studies that acute administration of selective 5-HT reuptake 20 inhibitors (SSRIs) decreases the electrical impulse propagation in 5-HT neurones via a negative feedback reaction probably mediated by collateral 5-HT axons releasing 5-HT in raph6 nuclei. By inhibiting the somatodendritic 5-HTIA autoreceptors in the raph6 nuclei the selective antagonists counteract the decrease in propagetion caused by 5-HT reuptake inhibitors. This indicates that a selective blockade of somatodendritic autoreceptor i.e. 5 25 HTIA antagonist may have a clinical potential to improve the efficacy of 5-HT reuptake inhibitors (SSRIs) and offer a new rationale for rapid onset of effect in the treatment of affective disorders, for instance the antidepressant actions.

WO 00/15220 PCT/SE99/01599 3 The compound (R)-5-carbamoyl-8-fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H-1 benzopyran in the form of the free base, and pharmaceutically acceptable salts thereof as disclosed herein is described in WO 95/11891, as a selective 5-HT1 A receptor antagonist. 5 The enantiomer (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5 phthalancarbonitrile disclosed herein, and which is stated to be a 5-HT reuptake inhibitor is described in US 4,943,590. The (R)-5-carbamoyl-8-fluoro-3-N.N-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran is 10 in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. Both organic and inorganic acids can be employed to form nontoxic pharmaceutically acceptable acid addition salts of the compounds of this invention. Illustrative acids are sulfuric, nitric, phosphoric, oxalic, hydrochloric, formic, hydrobromic, citric, acetic, lactic, tartaric, dibenzoyltartaric, diacetyltartaric, pamoic, ethanedisulfonic, sulfamic, succinic, 15 propionic, glycollic, malic, gluconic, pyruvic, phenylacetic, 4-aminobenzoic, anthranilic, salicylic, 4-aminosalicylic, 4-hydroxybenzoic, 3,4-dihydroxybenzoic, 3,5 dihydroxybenzoic, 3-hydroxy-2-naphthoic, nicotinic, methanesulfonic, ethanesulfonic, hydroxyethanesulfonic, benzenesulfonic, p-toluenesulfonic, sulfanilic, naphthalenesulfonic, ascorbinic, cyclohexylsulfamic, fumaric, maleic and benzoic acids. These salts are readily 20 prepared by methods known in the art. The (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran possesses a high affinity to the specific subgroup of 5-HTIA receptor in the CNS and acts as an antagonist on that 5-HTIA receptor, and as also shows favourable bioavailability after 25 oral administration. The composition according to the present invention may exist in one pharmaceutical formulation comprising of (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4 dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable 30 salt and/or solvate thereof, and (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5- WO 00/15220 PCT/SE99/01599 4 phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. Alternatively, the composition may exist in two different pharmaceutical formulations, one for (R)-5-carbamoyl-8-fluoro-3-N, N-dicyclobutylamino 3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable 5 salt and/or solvate thereof and one for (+)-1- [ 3 -(dimethylamino)propyl]-1-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. The pharmaceutical formulation may be in the form of tablets or capsules, powders, mixtures, solutions or other suitable pharmaceutical formulation forms such as patches and nasal formulations. 10 The composition of the present invention can be prepared by that (R)-5-carbamoyl-8 fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is incorporated into the same pharmaceutical formulation as (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5 is phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof by e.g. mixing in a conventional way. The present invention also includes a method of improving the onset of therapeutic action by concomitant administration of a composition comprising (R)-5-carbamoyl-8-fluoro-3 20 NN-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof and (+)-1-[3-(dimethylamino) propyl]-1-(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. 25 A further embodiment of the present invention is a kit containing a dosage unit of (R)-5 carbamoyl-8-fluoro-3-N,N-dicyclbutylamino-3,4-dihydro-2H- 1 -benzopyrans in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, and a dosage unit of (+)-1-[3-(dimethylamino)propyl]-I-(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, 30 optionally with instructions for use.

WO 00/15220 PCT/SE99/01599 5 Pharmaceutical formulations According to the present invention the compounds in the composition will normally be 5 administered orally, rectally, transdermally, nasally or by injection, in the form of pharmaceutical formulations comprising the active ingredient either as a free base, a solvate e.g. a hydrate or a pharmaceutically acceptable non-toxic acid addition salt, e.g. the hydrochloride, hydrobromide, lactate, acetate, phosphate, sulfate, sulfamate, citrate, tartrate, oxalate and the like in a pharmaceutically acceptable dosage form. The dosage 10 form may be a solid, semisolid or liquid formulation. Usually the active substances will constitute between 0.1 and 99% by weight of the formulation, more specifically between 0.5 and 20% by weight for formulations intended for injection and between 0.2 and 50% by weight for formulations suitable for oral administration. is The pharmaceutical formulation comprises the active ingredients, optionally in association with adjuvants, diluents, excipients and/or inert carriers. To produce pharmaceutical formulations of the composition of the invention in the form of dosage units for oral application, the selected compounds may be mixed with a solid 20 excipient, e.g. lactose, saccharose, sorbitol, mannitol, starches such as potato starch, corn starch or amylopectin, cellulose derivatives, a binder such as gelatin or poly vinylpyrrolidone, disintegrants e.g. sodium starch glycolate, cross-linked PVP and cross caramellose sodium; and a lubricant such as magnesium stearate, calcium stearate, polyethylene glycol, waxes, paraffin, and the like, and an antisticking agent such as talc or 25 colloidal silicon dioxide, and then compressed into tablets. If coated tablets are required, the cores, prepared as described above, may be coated with a polymer known to the man skilled in the art e.g. HPMC, HC or other cellulose derivatives or PVP, wherein the polymer is dissolved in water or a readily volatile organic solvent or mixture of organic solvents. Alternatively, the tablets can be coated with a concentrated sugar solution which 30 may contain e.g. gum arabic, gelatine, talcum, titanium dioxide, and the like. Dyestuffs WO 00/15220 PCT/SE99/01599 6 may be added to these coatings for instance in order to readily distinguish between tablets' containing different active substances or different amounts of the active compounds. For the formulation of soft gelatin capsules, the active substances may be admixed with s e.g. a vegetable oil or polyethylene glycol. Hard gelatine capsules may contain granules of the active substances using any of the above mentioned excipients for tablets e.g. lactose, saccharose, sorbitol, mannitol, starches (e.g. potato starch, corn starch or amylopectin), cellulose derivatives, plasticizers, polyetheneglycole, waxes, lipids or gelatin. Also liquids or semisolids of the drug can be filled into hard gelatin capsules. 10 Dosage units for rectal application can be solutions or suspensions or can be prepared in the form of suppositories comprising the active substances in a mixture with a neutral fatty base, or gelatin rectal capsules comprising the active substances in admixture with veget able oil or paraffin oil. Liquid formulations for oral application may be in the form of is solutions, syrups or suspensions, for example solutions containing from about 0.2% to about 20% by weight of the active substances herein described, the balance being sugar and a mixture of ethanol, water, glycerol and propylene glycol. Optionally such liquid formulations may contain colouring agents, flavouring agents, saccharin and carboxymethyl-cellulose as a thickening agent or other excipients known to a person 20 skilled in the art. Solutions for parenteral applications by injection can be prepared in an aqueous solution of a water-soluble pharmaceutically acceptable salt of the active substances, preferably in a concentration of from about 0.5% to about 10% by weight. These solutions may also 25 contain stabilizing agents and/or buffering agents and may conveniently be provided in various dosage unit ampoules. Suitable daily doses of the active compounds in the composition of the invention in therapeutic treatment of humans are about 0.01-100 mg/kg bodyweight for peroral 30 administration and 0.001-100 mg/kg bodyweight for parenteral administration. The daily WO 00/15220 PCT/SE99/01599 7 doses of the active ingredient (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4 dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof may very well differ from the daily doses of the active ingredient (+)-l-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5-phthalancarbonitrile in the form of 5 the free base, or a pharmaceutically acceptable salt and/or solvate thereof but the doses can also be the same for both of the active ingredients. Medical and Pharmaceutical Use io In a further aspect the present invention provides the use of the composition of (R)-5 carbamoyl-8-fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof and (+)-1-[3 (dimethylamino)propyll- 1 -(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, and the use in the is treatment of 5-hydroxytryptamine mediated disorders, such as affective disorders. Examples of affective disorders are disorders in the CNS such as mood disorders (depression, major depressive episodes, dysthymia, seasonal affective disorder, depressive phases of bipolar disorder), anxiety disorders (obsessive compulsive disorder, panic disorder with/without agoraphobia, social phobia, specific phobia, generalized anxiety 20 disorder, posttraumatic stress disorder), personality disorders (disorders of impulse control, trichotellomania) and sleep disorders. Other disorders in the CNS such as eating disorders(obesity, anorexia, bulimia), premenstrual syndrome, sexual disturbances, alcoholism, tobacco abuse, autism, attention deficit, hyperactivity disorder, migraine, memory disorders (age associated memory impairment, presenile and senile dementia such 25 as Alzheimer's disease), pathological aggression, schizophrenia, endocrine disorders (e g hyperprolactinaemia), stroke, dyskinesia, Parkinson's disease, thermoregulatory disorders, pain and hypertension may also be treated with the combination described herein. Examples of other hydroxytryptamine mediated disorders are urinary incontinence, vasospasm and growth control of tumors (e g lung carcinoma) and it may be possible to 30 treat those with the combination described herein as well.

WO 00/15220 PCT/SE99/01599 8 Pharmacology Potentiation of the 5 HT IA autoreceptor blocking effekt of 5-HT of (+)-1-[3 5 (dimethylamino)propyl]-1-(p-fluorophenyl)-5-phtalancarbonitrile by using of (R)-5 carbamoyl-8-fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran. Materials and methods Animals 1o The studies were carried out in male Sprague-Dawley rats (290-450g; B&K Universal, Sollentuna, Sweden). The animals were housed for at least 3 weeks after arrival until used in the experiments. Methods is The studies were carried out by means of intra-cerebral microdialysis in awake rats. To assess any putative regional differences between dorsal and median rapheinnervated 5-HT projection areas, dialysis probes were simultaneously implanted both into the frontal cortex (FCx) and dorsal hippocampus (DH). 20 Microdialysis The rats were anaesthetised with a mixture of ketamine HCl (67 mg/kg intraperitoneal (IP); Ketalar , Park-Davis) and xylazine HCI (13 mg/kg IP; Rompun , Bayer-Leverkusen). U shaped microdialysis probes (total dialysis fibre length 4 mm, OD 220pm) were stereotaxically implanted in the frontal cortex (FCx) and dorsal hippocampus (DH); probe 25 tips at AP +3.5, ML -3.0, DV -4.2 and -4.3, ML +2.5, DV -4.2, respectively, vs. bregma and dura surface (Paxinos, et al, in The Rat Brain in Stereotaxic Coordinates, 2nd Ed., Academic Press, San Diego (1996)). The microdialysis studies were performed in conscious animals after a 40-48 h recovery period, during which they were kept individually. Food and water were allowed ad libitum in the plastic cages subsequently 30 used in the experimental sessions. On the day of the experiment, the probe inlets were WO 00/15220 PCT/SE99/01599 9 connected to a syringe perfusion pump (CMA/100; CMA Microdialysis AB, Sweden), delivering artificial CSF (Hjorth, S., J. Neurochem. 60:776-779 (1993)) at a speed of 1.3gl/min. Twenty-min dialysate fractions were collected from the probe outlet tubing, and immediately analysed for 5-HT and 5-HIAA by standard HPLC-EC methods. After the 5 perfusion was commenced, a period of 2-3 h was allowed to establish stable baseline dialysate levels of 5-HT, prior to drug treatment(s).

Claims

1. A composition comprising of (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4 dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically acceptable 5 salt and/or solvate thereof, and (+)-l-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5 phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof.

2. Use of the composition according to claim 1 for the manufacture of a medicament for 10 the treatment of 5-HT mediated disorders.

3. The use according to claim 2 for the manufacture of a medicament for the treatment of affective disorders. is

4. The use according to claim 3 for the manufacture of a medicament for the treatment of mood disorders.

5. The use according to claim 4 for the manufacture of a medicament for the treatment of depression. 20

6. A method for the treatment of 5-HT mediated disorders by administering to a patient suffering therefrom the composition defined in claim 1.

7. The method according to claim 6 for the treatment of affective disorders. 25

8. The method according to claim 7 for the treatment of mood disorders.

9. The method according to claim 8 for the treatment of depression. WO 00/15220 PCT/SE99/01599 11

10. A method of improving the onset of therapeutic action by concomitant administration of a composition defined in claim 1.

11. A pharmaceutical formulation wherein the active ingredients are those in the 5 composition defined in claim 1, optionally in association with adjuvants, excipients and/or inert carriers.

12. A pharmaceutical formulation according to claim 11 wherein (R)-5-carbamoyl-8 fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran in the form of the free base, io or a pharmaceutically acceptable salt and/or solvate thereof is concomitantly administered with (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof.

13. A pharmaceutical formulation according to any one of claims 11-12 for use in the is treatment of 5-HT mediated disorders.

14. A pharmaceutical formulation according to any one of claims 11-12 for use in the treatment of affective disorders. 20

15. A pharmaceutical formulation according to any one of claims 11-12 for use in the treatment of mood disorders.

16. A pharmaceutical formulation according to any one of claims 11-12 for use in the treatment of depression. 25

17. A process for the preparation of the composition according to claim 1 whereby (R)-5 carbamoyl-8-fluoro-3-N,N-dicycl0butylamino-3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is incorporated into the same pharmaceutical formulation as (+)-1-[3-(dimethylamino)propyl]-1-(p- WO 00/15220 PCT/SE99/01599 12 fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof.

18. A process for the preparation of the composition according to claim I whereby (R)-5 5 carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4-dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is in a one pharmaceutical formulation is combined with (+)-1-[3-(dimethylamino)propyl]-1-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is in a different pharmaceutical formulation. 10

19. A kit containing a dosage unit of (R)-5-carbamoyl-8-fluoro-3-N,N-dicyclobutylamino 3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, and a dosage unit of (+)-1-[3-(dimethylamino)propyl]-1-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically is acceptable salt and/or solvate thereof, optionally with instructions for use. WO 00/15220 PCT/SE99/01599 13 AMENDED CLAIMS [received by the International Bureau on 15 February 2000 (15.02.00); original claims 1-19 replaced by amended claims 1-22 (3 pages)] 1. A composition comprising of (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino-3,4 dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable 5 salt and/or solvate thereof, and (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5 phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. 2. Use of the composition according to claim 1 for the manufacture of a medicament for i0 the treatment of 5-HT mediated disorders. 3. The use according to claim 2 for the manufacture of a medicament for the treatment of affective disorders. 15 4. The use according to claim 3 for the manufacture of a medicament for the treatment of mood disorders. 5. The use according to claim 4 for the manufacture of a medicament for the treatment of depression.

20 6. The use according to claim 2 in the manufacture of a medicament in the prevention or in the treatment of urinary incontinence. 7. A method for the treatment of 5-HT mediated disorders by administering to a patient 25 suffering therefrom the composition defined in claim 1. 8. The method according to claim 7 for the treatment of affective disorders. 9. The method according to claim 8 for the treatment of mood disorders. 30 AMENDED SHEET (ARTICLE 19) WO 00/15220 PCT/SE99/01599 14 10. The method according to claim 9 for the treatment of depression. 11. A method according to claim 7 for the prevention or the treatment of urinary incontinence. 5 12. A method of improving the onset of therapeutic action by concomitant administration of a composition defined in claim 1. 13. A pharmaceutical formulation wherein the active ingredients are those in the 10 composition defined in claim 1, optionally in association with adjuvants, excipients and/or inert carriers. 14. A pharmaceutical formulation according to claim 13 wherein (R)-5-carbamoyl-8 fluoro-3-NN-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran in the form of the free 15 base, or a pharmaceutically acceptable salt and/or solvate thereof is concomitantly administered with (+)-1-[3-(dimethylamino)propyl]-1-(p-fluorophenyl)-5 phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof. 20 15. A pharmaceutical formulation according to any one of claims 13-14 for use in the treatment of 5-HT mediated disorders. 16. A pharmaceutical formulation according to any one of claims 13-14 for use in the treatment of affective disorders. 25 17. A pharmaceutical formulation according to any one of claims 13-14 for use in the treatment of mood disorders. 18. A pharmaceutical formulation according to any one of claims 13-14 for use in the 30 treatment of depression. AMENDED SHEET (ARTICLE 19) WO 00/15220 PCT/SE99/01599 15 19. A pharmaceutical formulation according to any one of claims 13-14 for use in the treatment of urinary incontinence. s 20. A process for the preparation of the composition according to claim I whereby (R)-5 carbamoyl-8-fluoro-3-N,N-dicycl0butylamino-3,4-dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is incorporated into the same pharmaceutical formulation as (+)-1-[3-(dimethylamino)propyl]-1-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically 10 acceptable salt and/or solvate thereof.

21. A process for the preparation of the composition according to claim 1 whereby (R)-5 carbamoyl-8-fluoro-3-N,N-dicyclobutylamino-3,4-dihydro-2H-1-benzopyran in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is in a one 15 pharmaceutical formulation is combined with (+)-1-[3-(dimethylamino)propyl]-1-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof is in a different pharmaceutical formulation.

22. A kit containing a dosage unit of (R)-5-carbamoyl-8-fluoro-3-NN-dicyclobutylamino 20 3,4-dihydro-2H- 1 -benzopyran in the form of the free base, or a pharmaceutically accept able salt and/or solvate thereof, and a dosage unit of (+)-1-[3-(dimethylamino)propyl]-l-(p fluorophenyl)-5-phthalancarbonitrile in the form of the free base, or a pharmaceutically acceptable salt and/or solvate thereof, optionally with instructions for use. AMENDED SHEET (ARTICLE 19)