US20090012180A1 - Titration of Tapentadol - Google Patents

Titration of Tapentadol Download PDF

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US20090012180A1
US20090012180A1 US12/106,695 US10669508A US2009012180A1 US 20090012180 A1 US20090012180 A1 US 20090012180A1 US 10669508 A US10669508 A US 10669508A US 2009012180 A1 US2009012180 A1 US 2009012180A1
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dose
administration
tapentadol
optional
interval
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Claudia Lange
Ferdinand Rombout
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Gruenenthal GmbH
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Gruenenthal GmbH
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Priority to US12/106,695 priority Critical patent/US20090012180A1/en
Assigned to GRUENENTHAL GMBH reassignment GRUENENTHAL GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LANGE, CLAUDIA
Assigned to GRUENENTHAL GMBH reassignment GRUENENTHAL GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ROMBOUT, FERDINAND
Publication of US20090012180A1 publication Critical patent/US20090012180A1/en
Priority to US14/945,289 priority patent/US20160074342A1/en
Priority to US15/369,257 priority patent/US20170079938A1/en
Priority to US16/439,135 priority patent/US11344512B2/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/0012—Galenical forms characterised by the site of application
    • A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids

Definitions

  • the present invention relates to a dosing regimen for the administration of the analgesic tapentadol, preferably as a prolonged release dosage form.
  • the dosing regimen achieves the desired analgesic effect while reducing or delaying the onset of side effects.
  • Tapentadol (CG5503), the chemical name for which is ( ⁇ )-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol, is a synthetic, centrally-acting analgesic that is effective for the treatment of moderate to moderately-severe acute or chronic pain.
  • the compound can be employed as the free base or its pharmaceutically acceptable salts and solvates. Preparation of the free base is known from EP-A 693 475.
  • analgesic therapeutic regimen that is both effective and well tolerated.
  • the two traditional categories of analgesics i.e. opioids and nonsteroidal anti-inflammatory drugs (NSAIDs)
  • opioids and nonsteroidal anti-inflammatory drugs are both effective but are associated with potentially serious side effects.
  • NSAIDs nonsteroidal anti-inflammatory drugs
  • Concerns regarding tolerance and dependence minimize the use of narcotics such as morphine and codeine for the treatment of acute or chronic pain.
  • Patients on chronic NSAID therapy risk severe gastrointestinal symptoms, including ulceration and bleeding which have been estimated to result in up to 20,000 deaths each year.
  • Tapentadol is an investigational, centrally acting analgesic with a dual mode of action consisting of p-opioid receptor (MOR) agonism and norepinephrine (NE) reuptake inhibition.
  • MOR p-opioid receptor
  • NE norepinephrine
  • the efficacy, safety, and pharmacokinetic profile of tapentadol indicate that the drug may be useful in treating acute as well as chronic pain.
  • tapentadol The activity of tapentadol is independent of metabolic activation and resides in a single enantiomer which readily crosses the blood-brain barrier; hence, tapentadol displays a rapid onset of action after administration.
  • the biotransformation of tapentadol by metabolic enzymes results in deactivation, i.e., tapentadol has no active metabolites, and the main metabolic pathway for elimination is phase II glucuronidation.
  • Phase I biotransformations such as hydroxylation and N-demethylation play only a minor role in the metabolic fate of tapentadol. Owing to the minor involvement of phase I metabolic pathways, tapentadol has a low potential for drug-drug interactions and interindividual variability (cf.
  • Tapentadol is well tolerated, however, nuisance adverse events such as somnolence can occur, e.g., during the initiation of treatment, which may lead to early discontinuation of the treatment.
  • the most frequently reported adverse events observed in clinical trials of tapentadol are associated with the central nervous system (e.g. somnolence, dizziness/vertigo, headache) and the gastrointestinal tract (e.g. constipation, nausea, vomiting) (cf. Weber H. et al. Journal of Pain 2006, 7, S3; Kleinert R. et al. Journal of Pain 2006, 7, 44).
  • somnolence is of particular concern, because drug-induced somnolence may have a negative effect on activities of daily living and impair the physical functioning of chronic pain patients. “Quality of Life” may suffer thereby.
  • the present invention relates to the use of tapentadol for the manufacture of a medicament comprising
  • tapentadol is used for the manufacture of a medicament, where dose a of tapentadol is administered during a first administration interval and dose b of tapentadol is administered during a second administration interval following said first administration interval, where dose a ⁇ dose b, for the treatment of pain.
  • tapentadol may be improved by initiating the treatment at a comparatively low dose of tapentadol and successively increasing the dose according to a titration regimen.
  • FIGS. 1 , 2 , 3 and 4 show preferred embodiments of the medicament according to the invention in form of blister packages.
  • FIGS. 5 and 6 show the effect of titration of tapentadol prolonged release (PR) on the occurrence of somnolence observed in clinical trials (examples E-1 and E-2 vs. comparative examples C-1 and C-2).
  • PR tapentadol prolonged release
  • FIG. 7 schematically illustrates a preferred titration regimen for tapentadol prolonged release (PR).
  • FIG. 8 shows the effect of titration of oxycodone controlled release (CR) on the occurrence of somnolence observed in clinical trials (example E-1 vs. comparative example C-1).
  • FIGS. 9 A/B show a mathematical analysis of the distribution of serum concentrations of tapentadol (ng/ml) after administration in comparative clinical trials (comparative examples C-1 and C-2).
  • FIGS. 10 A/B show a mathematical analysis of the distribution of serum concentrations of tapentadol (ng/ml) after administration in the clinical trials according to the invention (examples E-1 and E-2).
  • tapeentadol is intended to include ( ⁇ )-(1R,2R)-3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol, its pharmaceutically acceptable salts and solvates thereof.
  • Suitable pharmaceutically acceptable salts include salts of inorganic acids, such as hydrochloric acid (tapentadol HCl), hydrobromic acid and sulfuric acid, and salts of organic acids, such as methane sulfonic acid, fumaric acid, maleic acid, acetic acid, oxalic acid, succinic acid, malic acid, tartaric acid, mandelic acid, lactic acid, citric acid, glutamic acid, acetylsalicylic acid, nicotinic acid, aminobenoic acid, ⁇ -liponic acid, hippuric acid and asparaginic acid.
  • the preferred salt is the hydrochloride salt.
  • doses of tapentadol relate to the free base.
  • a pharmaceutically acceptable salt when used instead, its dose has to be adapted to the equivalent dose of the free base.
  • a dose of “200 mg” means an amount of 200 mg of the free base or any equivalent amount of a pharmaceutically acceptable salt or solvate corresponding to 200 mg of the free base (e.g. about 233 mg of the hydrochloride). If not expressly stated otherwise, doses are “per administration”, not “per day”.
  • Tapentadol is indicated for the treatment of moderate to severe acute and chronic pain.
  • Clinical studies have shown tapentadol prolonged release (PR) to be an effective treatment for chronic joint pain (osteoarthritis of the hip or knee) and low back pain.
  • tapentadol prolonged release (PR) is useful for the treatment of chronic cancer pain and chronic painful diabetic peripheral neuropathy (DPN).
  • DPN diabetic peripheral neuropathy
  • tapentadol immediate release (IR) is useful in the treatment of acute dental pain, acute pain after bunionectomy and acute pain after abdominal surgery.
  • ongoing studies are concerned with acute pain after hip replacement, acute pain after abdominal hysterectomy (visceral pain) and acute pain in patients waiting for joint replacement.
  • Tapentadol is well tolerated, however, nuisance adverse events can occur during initiation of treatment with tapentadol. These side effects may lead to early discontinuation of tapentadol therapy.
  • Titration of a therapeutic agent is sometimes used by practicing clinicians to minimize adverse events associated with centrally-acting agents such as antidepressants and anticonvulsants. Although titration may minimize the adverse side effects associated with a particular agent, it may also delay the onset of the effect of the agent as well.
  • a first aspect of the invention relates to the use of tapentadol for the manufacture of a medicament comprising:
  • At least one administration unit A containing dose a of tapentadol and
  • an “administration unit” may be composed of a single dosage form or of a group of dosage forms.
  • administration unit X comprises n X dosage forms, where n X is an integer ⁇ 1.
  • administration unit X comprises a single dosage form.
  • administration unit X comprises a group of dosage forms which are adapted and intended to be administered simultaneously.
  • “simultaneously” does not mean exactly at the same time, but approximately at the same time, e.g., within a period of up to five minutes, preferably up to one minute.
  • administration of dose x of tapentadol may be achieved either by administering administration unit X composed of a single dosage form containing dose x of tapentadol or by administering administration unit X composed of a group of n X dosage forms (with n X >1), the entirety of said group of n X dosage forms containing dose x of tapentadol, which group of n X dosage forms is adapted and intended to be administered simultaneously.
  • the invention relates to the use of tapentadol for the manufacture of a medicament comprising
  • administration unit A and administration unit B are solid.
  • tapentadol is used for the manufacture of a medicament, where dose a of tapentadol is administered during a first administration interval of at least one day and dose b of tapentadol is administered during a second administration interval of at least one day following said first administration interval, where dose a ⁇ dose b, for the treatment of pain, preferably of chronic pain.
  • dose a is within the range of from 10 to 90 wt-% of dose b, more preferably from 20 to 80 wt.-%, still more preferably from 45 to 70 wt.-%.
  • dose a is below the pharmaceutically effective pain treating dose of tapentadol.
  • the pharmaceutically effective pain treating dose of tapentadol may vary individually and can be determined by routine experimentation for a given subject. Usually, the minimum pharmaceutically effective pain treating dose will be above 50 mg twice daily (bid).
  • effective pain treatment is to be regarded as at least 5% decrease in pain in an individual, more preferably at least 10%, still more preferably at least 15% and most preferably at least 20% decrease in pain in an individual, taking into account that low serum concentrations of tapentadol suffice to show an effect in individuals that are relatively sensitive and higher serum concentrations of tapentadol are needed to show an effect in persons that are relatively unsensitive.
  • Preliminary clinical trials revealed that a significant pain treating effect is seen at serum concentrations in the range of from about 5 ng/ml (approximately ⁇ 2 mm visual analog scale (VAS) in a population mean) to about 300 ng/ml (approximately ⁇ 15 mm visual analog scale (VAS) in a population mean).
  • serum concentrations in the range of from about 5 ng/ml (approximately ⁇ 2 mm visual analog scale (VAS) in a population mean) to about 300 ng/ml (approximately ⁇ 15 mm visual analog scale (VAS) in a population mean).
  • the ratio of dose a:dose b ([mg]:[mg]) is selected from the group consisting of
  • administration unit A releases 50% of dose a in a shorter or in a longer time interval than administration unit B releases 50% of dose b.
  • suitable in vitro conditions e.g., release may be investigated according to the European Pharmacopoeia, paddle method, 100 Upm, artificial gastric juice.
  • administration unit A and administration unit B are adapted to be administered via different routes, which preferably are independently selected from the group consisting of orally, buccally, sublingually, transmucosally, intralumbally, intraperitoneally, transdermally, intraveneously, intramusculously, intragluteally, intracutaneously and subcutaneously. Most preferably, however, administration unit A and administration unit B are adapted to be administered via the same route, preferably orally.
  • the medicament further comprises at least one administration unit C containing dose c of tapentadol, where dose b ⁇ dose c.
  • dose a is within the range of from 10 to 65 wt.-% of dose c, more preferably from 20 to 55 wt.-%
  • dose b is within the range of from 35 to 90 wt.-% of dose c, more preferably from 45 to 80 wt.-%.
  • tapentadol is used for the manufacture of a medicament, where dose a of tapentadol is administered during a first administration interval of at least one day, dose b of tapentadol is administered during a second administration interval of at least one day following said first administration interval, and dose c of tapentadol is administered during a third administration interval of at least one day following said second administration interval, where dose a ⁇ dose b ⁇ dose c, for the treatment of pain, preferably of chronic pain.
  • the ratio of dose a:dose b:dose c ([mg]:[mg]:[mg]) is selected from the group consisting of
  • the medicament further comprises at least one administration unit D containing dose d of tapentadol, where dose c ⁇ dose d.
  • tapentadol is used for the manufacture of a medicament, where dose a of tapentadol is administered during a first administration interval of at least one day, dose b of tapentadol is administered during a second administration interval of at least one day following said first administration interval, dose c of tapentadol is administered during a third administration interval of at least one day following said second administration interval, and dose d of tapentadol is administered during a fourth administration interval of at least one day following said third administration interval, where dose a ⁇ dose b ⁇ dose c ⁇ dose d, for the treatment of pain, preferably of chronic pain.
  • dose a is within the range of from 10 to 55 wt.-% of dose d, more preferably 15 to 50 wt.-%
  • dose b is within the range of from 35 to 75 wt.-% of dose d, more preferably 40 to 70 wt.-%
  • dose c is within the range of from 60 to 95 wt.-% of dose d, more preferably 65 to 90 wt.-%.
  • the medicament further comprises at least one administration unit E containing dose e of tapentadol, where dose d ⁇ dose e.
  • tapentadol is used for the manufacture of a medicament, where dose a of tapentadol is administered during a first administration interval of at least one day, dose b of tapentadol is administered during a second administration interval of at least one day following said first administration interval, dose c of tapentadol is administered during a third administration interval of at least one day following said second administration interval, dose d of tapentadol is administered during a fourth administration interval of at least one day following said third administration interval, and dose e of tapentadol is administered during a fifth administration interval of at least one day following said fourth administration interval, where dose a ⁇ dose b ⁇ dose c ⁇ dose d ⁇ dose e, for the treatment of pain.
  • dose a is within the range of from 10 to 30 wt.-% of dose e, more preferably 15 to 25 wt.-%
  • dose b is within the range of from 30 to 50 wt.-% of dose e, more preferably 35 to 45 wt.-%
  • dose c is within the range of from 50 to 70 wt.-% of dose e, more preferably 55 to 65 wt.-%
  • dose d is within the range of from 70 to 90 wt.-% of dose e, more preferably 75 to 85 wt.-%.
  • the daily dose of tapentadol is within the range of from 20 to 550 mg, more preferably 30 to 530 mg and most preferably 40 to 520 mg.
  • administration unit A, administration unit B, optional administration unit C, optional administration unit D and optional administration unit E are adapted to be administered once daily (sid) each, and dose a, dose b, optional dose c, optional dose d and optional dose e are each independently within the range of from 20 to 550 mg, more preferably 30 to 530 mg and most preferably 40 to 520 mg.
  • administration unit A, administration unit B, optional administration unit C, optional administration unit D and optional administration unit E are adapted to be administered twice daily (bid) each, and dose a, dose b, optional dose c, optional dose d and optional dose e are each independently within the range of from 10 to 275 mg, more preferably 15 to 265 mg and most preferably 20 to 260 mg.
  • administration unit A, administration unit B, optional administration unit C, optional administration unit D and optional administration unit E are adapted to be administered thrice daily (tid) each, and dose a, dose b, optional dose c, optional dose d and optional dose e are each independently within the range of from 6 to 180 mg, more preferably 10 to 175 mg and most preferably 13 to 170 mg.
  • administration unit A comprises n A dosage forms
  • administration unit B comprises n B dosage forms
  • optional administration unit C comprises n C dosage forms
  • optional administration unit D comprises n D dosage forms
  • the n X dosage forms belonging to administration unit X are to be administered simultaneously, i.e. approximately at the same time.
  • n A ⁇ n B ⁇ optional n C ⁇ optional n D ⁇ optional n E .
  • the medicament according to the invention is adapted to administer tapentadol by initiating the treatment at a comparatively low dose of tapentadol (dose a), preferably at a dose of 25 mg ⁇ 5%, 50 mg ⁇ 5%, 75 mg ⁇ 5% or 100 mg ⁇ 5%, more preferably below the pharmaceutically effective pain treating dose of tapentadol, and successively increasing the dose according to a titration regimen (dose b, optional dose c, optional dose d and optional dose e).
  • initial dose a is administered not only once, but several times for several days, preferably twice daily (bid), during a certain period of time (first administration interval), e.g., during three days.
  • first administration interval e.g., during three days.
  • the increase of the dose of tapentadol according to the titration regimen may be realized by administering dose b, e.g., also during a period of three days (second administration interval), e.g., twice daily (bid).
  • second administration interval e.g., twice daily (bid).
  • consecutive dose b is administered
  • the further increase of the dose of tapentadol according to the titration regimen may optionally be realized by administering doses c, d and e of tapentadol, i.e. by administering administration units C, D and E during a third, fourth and fifth administration interval, respectively.
  • Patients may be allowed 1, 2 or more doses of tapentadol, e.g. 25 mg, at least 6 hours apart, as supplemental analgesia.
  • administration unit X may comprise n X dosage forms, two cases may be distinguished:
  • the dosage forms belonging to administration unit X may be identical or different and may be provided in the same package or in different packages.
  • the first dosage form may contain 100 mg of tapentadol and the second dosage form may contain 150 mg of tapentadol, or the first dosage form may contain 200 mg of tapentadol and the second dosage form may contain 50 mg of tapentadol, so that the entirety of the 2 dosage forms of administration unit X contains the required dose x of 250 mg of tapentadol.
  • the n X dosage forms may be provided in the same package or in different packages.
  • a first dosage form containing 200 mg of tapentadol may be taken from a first package and a second dosage form containing 50 mg of tapentadol may be taken from a second package and both dosage forms may be combined in order to form an administration unit containing a dose of 250 mg of tapentadol.
  • administration of an administration unit containing a dose of 150 mg of tapentadol may be realized by administering
  • the medicament according to the invention is provided in form of a packaging containing one or more administration units A, one or more administration units B, optionally one or more administration units C, optionally one or more administration units D and optionally one or more administration units E.
  • the medicament according to the invention may be provided in form of a blister packaging containing 36 identical dosage forms each containing, e.g., 50 mg ⁇ 5% of tapentadol.
  • six of the dosage forms in the blister packaging may be marked as administration units A and/or may be locally separated from the other dosage forms in the blister packaging.
  • dose b amounts to, e.g., 100 mg ⁇ 5% of tapentadol
  • twelve of the dosage forms in the blister packaging may be divided into six groups each group comprising two dosage forms.
  • Every group may be marked as administration unit B and/or may be locally separated from the other dosage forms in the blister packaging.
  • dose c amounts to, e.g., 150 mg ⁇ 5% of tapentadol
  • eighteen of the dosage forms in the blister packaging may be divided into six groups each group comprising three dosage forms. Every group may be marked as administration unit C and/or may be locally separated from the other dosage forms in the blister packaging.
  • This embodiment of the medicament according to the invention is further illustrated in FIGS. 2 and 3 .
  • six of the dosage forms in the blister packaging may each contain dose a, e.g., 50 mg ⁇ 5% of tapentadol, and may be marked as administration units A and/or may be locally separated from the other dosage forms in the blister packaging.
  • Another six of the dosage forms in the blister packaging may each contain dose b, e.g., 100 mg ⁇ 5% of tapentadol, and may be marked as administration unit B and/or may be locally separated from the other dosage forms in the blister packaging.
  • the remaining six of the dosage forms in the blister packaging may each contain dose c, e.g., 150 mg ⁇ 5% of tapentadol, and may be marked as administration unit C and/or may be locally separated from the other dosage forms in the blister packaging.
  • dose c e.g. 150 mg ⁇ 5% of tapentadol
  • administration unit C e.g. 150 mg ⁇ 5% of tapentadol
  • FIG. 4 This embodiment of the medicament according to the invention is further illustrated in FIG. 4 .
  • the medicament according to the invention comprises a plurality of administration units A, a plurality of administration units B, optionally a plurality of administration units C, optionally a plurality of administration units D and optionally a plurality of administration units E.
  • these administration units are adapted to be administered sequentially, preferably in alphabetical order.
  • the entirety of all administration units A (each comprising n A dosage forms) is adapted to be administered during a first administration interval and the entirety of all administration units B (each comprising n B dosage forms) is adapted to be administered during a second administration interval following the first administration interval, i.e. after the administration of the entirety of all administration units A has been completed.
  • the medicament is provided in form of a packaging comprising a plurality of administration units A, a plurality of administration units B, optionally a plurality of administration units C, optionally a plurality of administration units D and optionally a plurality of administration units E, which are adapted to be administered in sequential, alphabetical order, preferably twice daily (bid), so that all administration units A are adapted to be administered during a first administration interval, all administration units B are adapted to be administered during a second administration interval following the first administration interval, optionally all administration units C are adapted to be administered during a third administration interval following the second administration interval, optionally all administration units D are adapted to be administered during a fourth administration interval following the third administration interval, and optionally all administration units E are adapted to be administered during a fifth administration interval following the fourth administration interval.
  • a packaging comprising a plurality of administration units A, a plurality of administration units B, optionally a plurality of administration units C, optionally a plurality of administration units D and optionally a plurality of administration units
  • administration units A, administration units B, optional administration units C, optional administration units D and optional administration units E are each adapted to be administered once daily (sid), twice daily (bid) or thrice daily (tid), twice daily (bid) being particularly preferred.
  • the medicament comprises:
  • the medicament comprises
  • tapentadol is used in the manufacture of a medicament for the treatment of pain, wherein dose a of tapentadol is administered twice daily (bid) for ⁇ days; then dose b of tapentadol is administered twice daily (bid) for ⁇ days; then, optionally, dose c of tapentadol is administered twice daily (bid) for ⁇ days; then, optionally, dose d of tapentadol is administered twice daily for ⁇ days; and then, optionally, dose e of tapentadol twice daily for ⁇ days is administered; where a, b, c, d, e and ⁇ , ⁇ , ⁇ , ⁇ , ⁇ satisfy any requirement selected from the group of the above requirements P 1-9 , Q 1-9 , R 1-9 and S 1-9 .
  • the embodiments P 1 to P 9 are particularly useful for the treatment of chronic pain, especially due to osteoarthritis (hip or knee) or low back pain.
  • the embodiments Q 1 to Q 9 are particularly useful for the treatment of chronic pain, especially due to osteoarthritis (hip or knee), low back pain or painful diabetic peripheral neuropathy (DPN).
  • osteoarthritis hip or knee
  • DPN painful diabetic peripheral neuropathy
  • the embodiments R 1 to R 9 are particularly useful for the treatment of chronic pain, especially due to osteoarthritis (hip or knee) or low back pain.
  • the embodiments S 1 to S 9 are particularly useful for the treatment of chronic pain, especially chronic malignant tumor-related pain.
  • administration unit A administration unit B, optional administration unit C, optional administration unit D and optional administration unit E and the dosage forms belonging to said administration units, respectively, each
  • dose a, dose b, optional dose c, optional dose d and optional dose e are independently selected so that the mean serum concentration of tapentadol is at least 0.1 ng/ml, more preferably at least 1.0 ng/ml, still more preferably at least 2.0 ng/ml, most preferably at least 5.0 ng/ml and in particular at least 10 ng/ml at any point in time during the administration interval(s), except during an initial phase of up to one, two or three days.
  • the mean serum concentration of tapentadol is within the range of from 0.1 to 10,000 ng/ml, more preferably 1.0 to 9,000 ng/ml, still more preferably 2.0 to 8,000 ng/ml, yet more preferably 3.0 to 5,000 ng/ml, most preferably 4.0 to 500 ng/ml and in particular 5.0 to 300 ng/ml at any point in time during the administration interval(s), except during an initial phase of up to one, two or three days.
  • the mean serum concentration of tapentadol is at least 15 ng/ml or at least 20 ng/ml, more preferably at least 25 ng/ml or at least 30 ng/ml, still more preferably at least 35 ng/ml or at least 40 ng/ml, most preferably at least 45 ng/ml or at least 50 ng/ml and particularly at least 55 ng/ml or at least 60 ng/ml.
  • a person skilled in the art knows how to measure the serum concentration of tapentadol and its metabolites. In this context it can be referred to e.g. T. M. Tschentke et al., Drugs of the Future, 2006, 31(12), 1053.
  • tapentadol is used in the manufacture of a medicament for the treatment of pain, by administration of which medicament
  • tapentadol is used in the manufacture of a medicament for the treatment of pain, by administration of which medicament
  • tapentadol is used in the manufacture of a medicament for the treatment of pain, by administration of which medicament
  • tapentadol is used in the manufacture of a medicament for the treatment of pain, wherein
  • the margins of the serum concentrations C ⁇ , C ⁇ , C ⁇ , C ⁇ , C ⁇ in the above tables, instead of ⁇ 75%, are ⁇ 67%, more preferably ⁇ 50%, still more preferably ⁇ 40% or ⁇ 35%, most preferably ⁇ 30% or ⁇ 25% and in particular ⁇ 20%, ⁇ 15%, ⁇ 10% or ⁇ 5%.
  • tapentadol When, for example, tapentadol is administered during a second administration interval of ⁇ days following a first administration interval, after 24 hours providing a mean serum concentration C ⁇ of tapentadol, this means that 24 hours after having initiated the second administration interval, the mean serum concentration has reached the value C ⁇ .
  • the mean serum concentration has reached the value C ⁇ .
  • about 24 hours are needed to achieve steady state conditions within a given administration interval when increasing (or decreasing) the dose of tapentadol from the dose administered during the preceding administration interval to the dose administered during the next administration interval.
  • Administration units A and B and the optionally present administration units C, D and E of the medicament according to the invention may each comprise 1 or more dosage forms, which in turn may contain, besides tapentadol, additives and/or auxiliary substances.
  • Suitable additives and/or auxiliary substances in the context of this invention include all those substances known to persons skilled in the art for preparing galenical formulations.
  • the choice of these auxiliary substances and the amounts thereof to be employed depend on whether the administration unit/dosage form is to be administered orally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally or locally.
  • Formulations in the form of tablets, chewable tablets, coated tablets, capsules, granules, drops, juices or syrups are suitable for oral administration, and solutions, suspensions, easily reconstitutable dry formulations and sprays are suitable for parenteral, topical and inhalatory administration. Suppositories for use in the rectum are a further possibility.
  • the use in a depot in dissolved form, a carrier film or a patch, optionally with the addition of agents which promote penetration through the skin, are examples of suitable forms for percutaneous administration.
  • auxiliary substances and additives for the oral administration units/dosage forms include disintegrating agents, lubricants, binders, fillers, mold release agents, optionally solvents, flavorings, sugars, in particular carrier agents, diluents, dyestuffs, antioxidants etc.
  • disintegrating agents lubricants, binders, fillers, mold release agents, optionally solvents, flavorings, sugars, in particular carrier agents, diluents, dyestuffs, antioxidants etc.
  • lubricants binders
  • fillers fillers
  • mold release agents optionally solvents
  • flavorings flavorings
  • sugars in particular carrier agents
  • diluents diluents
  • dyestuffs dyestuffs
  • antioxidants antioxidants etc.
  • waxes and fatty acid esters can be used, and for compositions for parental administration carrier substances, preservatives, suspension auxiliaries etc.
  • the dosage forms comprise preferably 0.05 wt.-% to 99.5 wt.-% of tapentadol, more preferably 0.1 to 90 wt.-%, still more preferably 0.5 to 80 wt.-%, most preferably 1.0 to 50 wt.-% and in particular 5.0 to 20 wt.-%.
  • Auxiliary substances can be, for example: water, ethanol, 2-propanol, glycerol, ethylene glycol, propylene glycol, polyethylene glycol, polypropylene glycol, glucose, fructose, lactose, sucrose, dextrose, molasses, starch, modified starch, gelatine, sorbitol, inositol, mannitol, microcrystalline cellulose, methylcellulose, carboxymethyl cellulose, cellulose acetate, shellac, cetyl alcohol, polyvinylpyrrolidone, paraffins, waxes, naturally occurring and synthetic gums, gum acacia, alginates, dextran, saturated and unsaturated fatty acids, stearic acid, magnesium stearate, zinc stearate, glyceryl stearate, sodium lauryl sulfate, edible oils, sesame oil, coconut oil, groundnut oil, soya bean oil, lecithin, sodium lactate, polyoxy
  • administration units/dosage forms according to the invention may be controlled release, delayed release, prolonged release/extended release, sustained release, repeat-action release, etc. Prolonged release administration units/dosage forms are preferred.
  • administration units/dosage forms according to the invention are prepared with the aid of means, devices, methods and processes which are well-known in the prior art of pharmaceutical formulation, such as are described, for example, in “Remington's Pharmaceutical Sciences”, ed. A. R. Gennaro, 17th ed., Mack Publishing Company, Easton, Pa. (1985), in particular in part 8 , chapter 76 to 93.
  • tapentadol can be granulated with a pharmaceutical carrier, e.g. conventional tablet constituents, such as maize starch, lactose, sucrose, sorbitol, talc, magnesium stearate, dicalcium phosphate or pharmaceutically acceptable gums, and pharmaceutical diluents, such as e.g. water, in order to form a solid composition which comprises tapentadol in homogeneous distribution.
  • a pharmaceutical carrier e.g. conventional tablet constituents, such as maize starch, lactose, sucrose, sorbitol, talc, magnesium stearate, dicalcium phosphate or pharmaceutically acceptable gums
  • pharmaceutical diluents such as e.g. water
  • Homogeneous distribution is understood here as meaning that tapentadol is uniformly distributed over the entire composition, so that this can easily be divided into unit dose forms, such as tablets, pills or capsules, having the same activity.
  • the solid composition is then divided into unit dose forms.
  • the administration units according to the invention can also be coated or compounded in another manner in order to provide a dose form with delayed release.
  • Suitable coating compositions are, inter alia, polymeric acids and mixtures of polymeric acids with materials such as e.g. shellac, cetyl alcohol and/or cellulose acetate.
  • Tapentadol can be released in a delayed or prolonged or sustained manner from administration units/dosage forms which can be used orally, rectally or percutaneously.
  • Corresponding formulations in particular in the form of a “twice daily (bid)” preparation which has to be taken only twice a day (bid), are particularly preferred for the indication according to the invention (cf. US-A-2005-58706).
  • Delayed or prolonged or sustained release of tapentadol may be achieved by administration units/dosage forms which contain tapentadol in a matrix, which contains e.g. 1 to 80% by weight, in particular 5 to 80 by weight, of one or more hydrophilic or hydrophobic polymers as pharmaceutically acceptable matrix forming agents and which comprise cellulose ethers and/or cellulose esters having a viscosity (determined using a Pharm. Eu. capillary viscosimeter) of 3,000 to 150,000 mPa s in a 2% by weight aqueous solution at 20° C. as pharmaceutically acceptable matrix forming agents.
  • a matrix which contains e.g. 1 to 80% by weight, in particular 5 to 80 by weight, of one or more hydrophilic or hydrophobic polymers as pharmaceutically acceptable matrix forming agents and which comprise cellulose ethers and/or cellulose esters having a viscosity (determined using a Pharm. Eu. capillary viscosimeter) of 3,000
  • Preferred pharmaceutically acceptable matrix forming agents include polyethylene oxide having a molecular mass of more than 0.5 mio g/mol, cellulose ethers and/or cellulose esters having a viscosity between 10,000, in particular 50,000 mPa s, and 150,000 mPa s in a 2% by weight aqueous solution at 20° C.
  • Particularly suitable pharmaceutically acceptable matrix forming agents may be selected from the group consisting of hydroxypropylmethyl celluloses (HPMC), hydroxyethyl celluloses, hydroxypropyl celluloses (HPC), methyl celluloses, ethyl celluloses and carboxymethyl celluloses and are selected, in particular, from the group consisting of HPMCs, hydroxyethyl celluloses and HPCs.
  • HPMCs having a viscosity of approximately 100,000 mPa s, measured in a 2% by weight aqueous solution at 20° C. are most preferred.
  • the administration units/dosage forms according to the invention can exist both as a simple tablet and as a coated tablet, for example as a film tablet or dragee.
  • the tablets are typically round and biconvex, but oblong tablet shapes which allow the tablet to be divided are also possible.
  • Granules, spheroids, pellets or microcapsules which are poured into sachets or capsules or may be compressed to disintegrating tablets are also possible within the scope of the invention.
  • tapentadol can be contained in a conventional matrix of microcrystalline cellulose and optionally further pharmaceutical auxiliaries such as binders, fillers, glidants, lubricants and flow regulators, which are covered or coated with a material controlling the slow release of tapentadol in an aqueous medium.
  • suitable coating agents include, for example, water-insoluble waxes and polymers such as polymethacrylates (Eudragit or the like) or water-insoluble celluloses, in particular ethyl cellulose.
  • the coating material can optionally also contain water-soluble polymers such as polyvinyl pyrrolidone, water-soluble celluloses such as hydroxypropylmethyl cellulose or hydroxypropyl cellulose, other water-soluble agents such as Polysorbate 80 or hydrophilic pore-forming agents such as polyethylene glycol, lactose or mannitol.
  • water-soluble polymers such as polyvinyl pyrrolidone, water-soluble celluloses such as hydroxypropylmethyl cellulose or hydroxypropyl cellulose, other water-soluble agents such as Polysorbate 80 or hydrophilic pore-forming agents such as polyethylene glycol, lactose or mannitol.
  • an osmotically driven release system can also be used to achieve a slow release.
  • Embodiments and examples of the actual production of osmotically driven release systems can be found in U.S. Pat. No. 4,765,989, U.S. Pat. No. 4,783,337, and U.S. Pat. No. 4,612,008.
  • a further aspect of the invention relates to a kit comprising at least one administration unit A, at least one administration unit B, optionally at least one administration unit C, optionally at least one administration unit D and optionally at least one administration unit E, as defined above.
  • the kit according to the invention preferably comprises a packaging containing a plurality of administration units A each comprising n A dosage forms, a plurality of administration units B each comprising n B dosage forms, optionally a plurality of administration units C each comprising n C dosage forms, optionally a plurality of administration units D each comprising n D dosage forms, and optionally a plurality of administration units E each comprising n D dosage forms, where n A , n B , optional n C , optional n D and optional n E are preferably independently of one another 1, 2, 3, 4 or 5.
  • n X dosage form(s) belonging to a particular administration unit X are grouped and/or marked and/or locally separated from the other administration units and dosage forms, respectively, that are contained in the packaging (cf. FIGS. 2 and 3 ).
  • the dosage forms that belong to administration unit(s) A differ from the dosage forms that belong to administration unit(s) B, which in turn differ from the dosage forms that belong to administration unit(s) C, and so on.
  • n C optional
  • n D optional
  • n E 1 or 2 (cf. FIG. 4 ).
  • the kit according to the invention comprises a plurality of administration units and dosage forms, respectively, suitable for administering dose a of tapentadol twice daily (bid) for ⁇ days, then dose b of tapentadol twice daily (bid) for ⁇ days, then optionally dose c of tapentadol twice daily (bid) for ⁇ days, then optionally dose d of tapentadol twice daily for ⁇ days, and then optionally dose e of tapentadol twice daily for ⁇ days, where a, b, c, d, e and ⁇ , ⁇ , ⁇ , ⁇ , ⁇ satisfy any requirement selected from the group of the above requirements P 1-9 , Q 1-9 , R 1-9 and S 1-9 .
  • Still another aspect of the invention relates to a pharmaceutical oral dosage form containing tapentadol, which comprises a notch that divides the dosage form into at least two portions and mechanically weakens the dosage form so that it may be manually broken at the notch along a predetermined site of fracture (breaking notch).
  • the dosage form is preferably adapted to be administered twice daily (bid) and tapentadol is embedded in a retard matrix. The matrix ensures that delayed release of tapentadol from the dosage form is not diminished when breaking the administration unit at the notch.
  • the notch may be linear or assume the shape of a cross. When the notch is linear, the dosage form may be broken into two halves, which preferably have about the same shape, size and content of tapentadol.
  • the dosage form When the notch assumes the shape of a cross, the dosage form may be broken into two halves and each have in turn may be broken into two quarts, which preferably have about the same shape, size and content of tapentadol.
  • the dosage form contains 40 to 260 mg of tapentadol.
  • each halve contains about 20 to about 130 mg of tapentadol and each quart contains about 10 to about 65 mg of tapentadol respectively.
  • the dosage form according to the invention may be used to realize a titration regimen.
  • the dosage form according to the invention may contain a total of 200 mg ⁇ 5% of tapentadol.
  • each dosage form is manually broken and only a halve containing about 100 mg ⁇ 5% of tapentadol is administered. After the first administration interval, the dosage form is not broken anymore, but administered as such.
  • the individual fragments of the dosage form according to the invention that are obtained when the dosage form is broken along the notch preferably each contain a dose of tapentadol that corresponds to any of doses a, doses b, doses c, doses d, and doses e, respectively, as defined supra.
  • a further aspect of the invention relates to a method of treating pain which comprises administering to one in need thereof tapentadol according to a titration regimen, preferably by means of the medicament according to the invention.
  • tapentadol is administered once daily (sid), twice daily (bid), or thrice daily (tid), twice daily (bid) being particularly preferred.
  • each regimen may be divided into a titration phase and a continuous phase.
  • titration means that after a certain administration interval, the dose of tapentadol is increased (or decreased) until the optimal dose is reached.
  • the regimen may be static (forced) or dynamic.
  • the regimen is dynamic, i.e. the dose is successively increased until the optimal, pharmaceutically effective dose for the individual subject has been reached.
  • the optimal dose may vary individually and also depends upon the type and degree of pain to be treated.
  • the optimal dose is defined as the dose providing a meaningful improvement of pain with acceptable side effects in the patient's perception (maximum therapeutic benefit).
  • the regimen results in a lower incidence or severity of side effects, such as somnolence.
  • the subject monitors the achievement of amelioration of pain and the occurrence of side effects caused by the current dose of tapentadol.
  • the subject decides whether the dose of tapentadol is
  • tapentadol is administered twice daily (bid) at a constant first (initial) dose for a first administration interval.
  • tapentadol is administered twice daily (bid) at a constant second dose for a second administration interval, with the proviso that the second dose is higher than the first dose.
  • the titration phase may be terminated, i.e. administration of tapentadol may be continued twice daily (bid) at said constant second dose, thereby initiating the continuous phase.
  • the titration phase is terminated by the fact that the dose of tapentadol that was administered during the second administration interval is no further increased (or decreased).
  • the titration phase may continue, i.e. tapentadol is administered twice daily (bid) at a constant third dose for a third administration interval, with the proviso that the third dose is higher than the second dose.
  • the titration phase may be terminated, i.e. administration of tapentadol may be continued twice daily (bid) at said constant third dose, thereby initiating the continuous phase.
  • the titration phase may continue, i.e. tapentadol is administered twice daily (bid) at a constant fourth dose for a fourth administration interval.
  • the dose may be either further increased or decreased, depending on the individual needs of the subject.
  • the titration phase encompasses at least 2 administration intervals, preferably 3, 4 or 5 administration intervals, at which different doses of tapentadol are administered, preferably twice daily (bid), resulting in biphasic, triphasic, tetraphasic and pentaphasic regimens, respectively.
  • the titration phase of the dosing regimen comprises at least 1, 2, 3, 4, 5, 6 or 7 days, more preferably at least 14 days, still more preferably 7 to 28 days, most preferably 14 to 28 days and in particular 14 to 21 days.
  • the dosing regimen is biphasic (two consecutive administration intervals), comprises 1, 2, 3, 4, 5, 6 or 7 to 28 days, more preferably 7 to 21 days and most preferably 7 to 14 days
  • the dose of tapentadol at the first administration interval is within the range of from 50 mg ⁇ 5% to 100 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the second administration interval is within the range of from 100 mg ⁇ 5% to 150 mg ⁇ 5%, preferably twice daily (bid).
  • the second administration interval commences 2 to 11, more preferably 3 to 7 days after initiation of administration of tapentadol.
  • the dosing regimen is triphasic (three consecutive administration intervals), comprises 1, 2, 3, 4, 5, 6 or 7 to 28 days, more preferably 7 to 21 days and most preferably 7 to 14 days
  • the dose of tapentadol at the first administration interval is within the range of from 25 mg ⁇ 5% to 100 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the second administration interval is within the range of from 50 mg ⁇ 5% to 150 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the third administration interval is within the range of from 100 mg ⁇ 5% to 200 mg ⁇ 5%, preferably twice daily (bid).
  • the second administration interval commences 2 to 11, more preferably 3 to 7 days after initiation of administration of tapentadol
  • the third administration interval commences 5 to 22, more preferably 6 to 14 days after initiation of administration of tapentadol.
  • the dosing regimen is tetraphasic (four consecutive administration intervals), comprises 1, 2, 3, 4, 5, 6 or 7 to 28 days, more preferably 7 to 21 days and most preferably 14 to 21 days
  • the dose of tapentadol at the first administration interval is within the range of from 25 mg ⁇ 5% to 100 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the second administration interval is within the range of from 50 mg ⁇ 5% to 150 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the third administration interval is within the range of from 100 mg ⁇ 5% to 200 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the fourth administration interval is within the range of from 150 mg ⁇ 5% to 250 mg ⁇ 5%, preferably twice daily (bid).
  • the second administration interval commences 2 to 11, more preferably 3 to 7 days after initiation of administration of tapentadol
  • the third administration interval commences 5 to 16, more preferably 6 to 14 days after initiation of administration of tapentadol
  • the fourth administration interval commences 8 to 22, more preferably 9 to 14 days after initiation of administration of tapentadol.
  • the dosing regimen is pentaphasic (five consecutive administration intervals), comprises 1, 2, 3, 4, 5, 6 or 7 to 28 days, more preferably 7 to 21 days and most preferably 14 to 21 days
  • the dose of tapentadol at the first administration interval is within the range of from 25 mg ⁇ 5% to 50 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the second administration interval is within the range of from 50 mg ⁇ 5% to 100 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the third administration interval is within the range of from 100 mg ⁇ 5% to 150 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the fourth administration interval is within the range of from 150 mg ⁇ 5% to 200 mg ⁇ 5%, preferably twice daily (bid)
  • the dose of tapentadol at the fifth administration interval is within the range of from 200 mg ⁇ 5% to 250 mg ⁇ 5%, preferably twice daily (bid)
  • the second administration interval commences 2 to 11, more preferably
  • the individual doses that are to be administered may be administered by a single administration unit containing the entire dose or by a plurality of administration units each containing a portion of said entire dose.
  • a dose of 100 mg tapentadol may be administered either by a tablet containing 100 mg or by two tablets each containing 50 mg.
  • the method for treating pain, preferably of chronic pain, according to the invention follows a titration regimen.
  • the method comprises administering to one in need thereof
  • the first administration interval and the second administration interval last independently of one another at least 1 day, more preferably at least 2 days and in particular at least 3 days.
  • tapentadol is administered orally.
  • tapentadol is administered twice daily (bid).
  • dose a is within the range of from 10 to 90 wt.-% of dose b, more preferably from 20 to 80 wt.-%, still more preferably from 45 to 70 wt.-%.
  • the method according to the invention further comprises orally administering dose c of tapentadol once daily (sid), twice daily (bid) or thrice daily (tid) during a third administration interval following the second administration interval, where dose b ⁇ dose c.
  • dose a is within the range of from 10 to 65 wt.-% of dose c, more preferably from 20 to 55 wt.-%
  • dose b is within the range of from 35 to 90 wt.-% of dose c, more preferably from 45 to 80 wt.-%.
  • the method according to the invention further comprises orally administering dose d of tapentadol once daily (sid), twice daily (bid) or thrice daily (tid) during a fourth administration interval following the third administration interval, where dose c ⁇ dose d (or where dose c>dose d).
  • dose a is within the range of from 10 to 55 wt.-% of dose d, more preferably 15 to 50 wt.-%
  • dose b is within the range of from 35 to 75 wt.-% of dose d, more preferably 40 to 70 wt.-%
  • dose c is within the range of from 60 to 95 wt.-% of dose d, more preferably 65 to 90 wt.-%.
  • the method according to the invention further comprises orally administering dose e of tapentadol once daily (sid), twice daily (bid) or thrice daily (tid) during a fifth administration interval following the fourth administration interval, where dose d ⁇ dose e (where dose d>dose e).
  • dose a is within the range of from 10 to 30 wt.-% of dose e, more preferably 15 to 25 wt.-%
  • dose b is within the range of from 30 to 50 wt.-% of dose e, more preferably 35 to 45 wt.-%
  • dose c is within the range of from 50 to 70 wt.-% of dose e, more preferably 55 to 65 wt.-%
  • dose d is within the range of from 70 to 90 wt.-% of dose e, more preferably 75 to 85 wt.-%.
  • the first administration interval, second administration interval, optional third administration interval, optional fourth administration interval and optional fifth administration interval comprise independently of one another 1 to 21 days, more preferably 2 to 14 days.
  • the method according to the invention comprises administering
  • the number of administrations per day is harmonized, i.e. when during the first administration interval tapentadol is administered twice daily (bid), during the second administration interval tapentadol is preferably also administered twice daily (bid), i.e. neither once daily (sid) nor thrice daily (tid).
  • dose a, dose b, optional dose c, optional dose d and optional dose e are independently selected so that the daily dose of tapentadol on every day of every administration interval is within the range of from 20 to 550 mg, more preferably 30 to 530 mg and most preferably 40 to 510 mg.
  • the method according to the invention comprises orally administering
  • subjects initiate treatment with tapentadol, orally administered twice daily (bid), at a dose of 50 mg ⁇ 5%. After 3 days the dose is increased to 100 mg ⁇ 5%. This is the minimum dose to be continued with.
  • upward titration may then occur at a minimum of 3-day intervals (6 consecutive doses) in increments of 50 mg ⁇ 5%.
  • the maximum dose allowed is preferably 250 mg ⁇ 5%.
  • downward titration (preferably not below the minimum dose) is also permitted using the same decrements without a time restriction.
  • subjects initiate treatment with tapentadol, orally administered twice daily (bid), at a dose of 50 mg ⁇ 5%. After 3 days the dose is increased to 100 mg ⁇ 5%. This is the minimum dose to be continued with. The subject remains on the 100 mg ⁇ 5% dose for the next 4 days. Thereafter, to the discretion of the subject, upward titration may occur at a minimum of 3-day intervals (6 consecutive doses) in increments of 50 mg ⁇ 5%. The maximum dose allowed is preferably 250 mg ⁇ 5%. To the discretion of the subject, downward titration (preferably not below the minimum dose) is also permitted using the same decrements without a time restriction.
  • the two foregoing embodiments are particularly useful for the treatment of chronic pain, especially due to osteoarthritis (hip or knee), low back pain, painful diabetic peripheral neuropathy (DPN) and malignant pain.
  • osteoarthritis hip or knee
  • DPN painful diabetic peripheral neuropathy
  • subjects initiate treatment with tapentadol, orally administered twice daily (bid), at a dose of 100 mg ⁇ 5%. This is the minimum dose to be continued with.
  • upward titration may then occur at a minimum of 3-day intervals (6 consecutive doses) in increments of 50 mg ⁇ 5%.
  • the maximum dose allowed is preferably 250 mg ⁇ 5%.
  • downward titration (preferably not below the minimum dose) is also permitted using the same decrements without a time restriction.
  • This embodiment is particularly useful for the treatment of chronic pain, especially chronic malignant tumor-related pain.
  • the usual initial dose is 50 mg of tapentadol prolonged release (PR) twice daily (bid).
  • Patients are individually titrated to the optimal individual dose, which is defined as the dose providing a meaningful improvement of pain with acceptable side effects in the patient's perception (maximum therapeutic benefit).
  • Upward titration may occur at intervals in increments of 50 mg tapentadol prolonged release (PR) twice daily (bid).
  • Downward titration should use the same decrements.
  • the dose used should be the lowest dose that provides pain relief.
  • Tapentadol may be administered with or without food.
  • the usual initial dose is 50 mg of tapentadol prolonged release (PR) twice daily (bid).
  • Patients are individually titrated to the optimal individual dose, which is defined as the dose providing a meaningful improvement of pain with acceptable side effects in the patient's perception (maximum therapeutic benefit).
  • Upward titration may occur at a minimum of 3-day intervals (6 consecutive doses) in increments of 50 mg tapentadol prolonged release (PR) twice daily (bid).
  • Downward titration using the same decrements can be performed without a time restriction.
  • the dose used should be the lowest dose that provides pain relief.
  • the maximum dose is 250 mg tapentadol prolonged release (PR) twice daily (bid). Tapentadol may be administered with or without food.
  • dose a, dose b, optional dose c, optional dose d and optional dose e are independently selected so that the mean serum concentration of tapentadol is within the range of from 0.1 to 10,000 ng/ml, more preferably 1.0 to 9,000 ng/ml, still more preferably 2.0 to 8,000 ng/ml, most preferably 3.0 to 1,000 ng/ml and in particular 5.0 to 300 ng/ml at any point in time, except the initial phase of one, two or three days.
  • the margins of the serum concentrations C ⁇ , C ⁇ , C ⁇ , C ⁇ , C ⁇ in the above tables, instead of ⁇ 75%, are ⁇ 67%, more preferably ⁇ 50%, still more preferably ⁇ 40% or ⁇ 35%, most preferably ⁇ 30% or ⁇ 25% and in particular ⁇ 20%, ⁇ 15%, ⁇ 10% or ⁇ 5%.
  • about 24 hours are needed to achieve steady state conditions within a given administration interval when increasing (or decreasing) the dose of tapentadol from the dose administered during the preceding administration interval to the dose administered during the next administration interval.
  • the overall dosing regimen typically comprises a titration phase followed by a continuous phase.
  • the overall dosing regimen includes at least 10 consecutive days, more preferably at least 20 consecutive days, still more preferably at least 30 consecutive days, yet more preferably at least 50 consecutive days, most preferably at least 70 consecutive days and in particular at least 90 consecutive days.
  • the overall administration is terminated after the titration phase and the subsequent continuous phase have been completed, i.e., after the continuous phase preferably no second titration phase (e.g., downward titration, drug tapering) is supplemented.
  • the administration of tapentadol is preferably terminated at once, i.e. from the full dose (last regular dose) at the continuous phase down to zero without any intermediate doses.
  • the titration of tapentadol is effective in reducing discontinuations due to adverse effects while maintaining the analgesic properties of the compound. This is particularly true in the case of patients who previously had difficulty tolerating an analgesic because of side effects such as somnolence. This result is based on the cumulative proportion of patients who discontinued use of the agent due to adverse side effects.
  • a randomized, double-blind, parallel-group study that compares the efficacy and safety of two titration regimens of tapentadol prolonged release (25 mg-50 mg-100 mg and 100 mg-150 mg-200 mg) given orally twice daily (bid) and tramadol prolonged release (100 mg-150 mg-200 mg) p.o. bid to placebo in patients with moderate to severe chronic pain due to chronic low back pain.
  • PK/PD modeling and simulation were used to investigate if dose titration would bring a benefit for the development of adverse events.
  • the estimation of advantage of dose titration was based on somnolence as an indicator for typical opioid related adverse events. It was also one of the adverse events most commonly occurring and therefore enabling a modeling and simulation with enough reliability.
  • a population PK model was build over all studies using NONMEM V level 1.1 and a population PK/PD model was build for somnolence for studies of examples E-1 and E-2. Simulations were performed using Trial Simulator 2.1, taking into account the PK/PD model for somnolence established for the data from the studies of examples E-1 and E-2 and the population PK model without covariates for all 4 studies.
  • FIG. 5 (Tapentadol—observations of somnolence versus concentration with a 2 degree polynomial fitting) and FIG. 6 (Tapentadol—observations of somnolence versus concentration with a 6 degree polynomial fitting) clearly show that despite the dosages and concentrations being clearly lower in the studies of comparative examples C-1 and C-2, adverse events occurred typically at a much lower concentration compared to the studies of examples E-1 and E-2 in which dose titration was used.
  • FIG. 7 shows a schematic illustration of the titration regimen used for tapentadol in the clinical studies.
  • the population PK model together with the relationship between concentrations and somnolence was used to simulate 2000 patients, 1000 patients with dose titration (1 week 58 mg, 1 week 116 mg, 2 weeks 233 mg tapentadol HCl) and 1000 patients without dose titration (4 weeks at 233 mg). It was simulated what the probability in both designs would be when the subject was asked whether he had somnolence three times a day for seven days during the 4 th week of treatment. Drop outs were not taken into account in the simulation procedures.
  • FIG. 8 (oxycodone—observations of somnolence versus concentration with a linear fitting) indicates that when administering oxycodone according to the titration regimen of example E-1, there is no comparable effect on the suppression of somnolence.
  • FIGS. 9 A/B show a mathematical analysis of the distribution of concentrations of tapentadol (ng/ml) after administration in the comparative clinical trials (comparative examples C-1 and C-2).
  • FIGS. 10 A/B show a mathematical analysis of the distribution of concentrations of tapentadol (ng/ml) after administration in the clinical trials according to the invention (examples E-1 and E-2).
  • IR 50 or 100 mg/dose; maximum 600 mg/day
  • oxycodone IR 10 or 15 mg/dose; maximum 90 mg/day
  • COWS Clinical Opioid Withdrawal Score
  • SOWS Subjective Opioid Withdrawal Score
  • the mean total SOWS score 2 to 4 days after last study drug intake, was lower for the tapentadol IR group (6.9) than the oxycodone IR group (8.7).
  • the corresponding P value revealed no significant difference between the treatment groups.
  • 5 or more days after last study drug intake the mean total SOWS score was 6.3 for the tapentadol IR group and 7.0 for the oxycodone IR group (no significant difference).

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US20110077656A1 (en) * 2009-09-25 2011-03-31 Sand Paul M Methods and devices for treating a structural bone and joint deformity
US20120225951A1 (en) * 2011-03-04 2012-09-06 Gruenenthal Gmbh Parenteral Administration of Tapentadol
US20120309840A1 (en) * 2011-04-05 2012-12-06 Gruenenthal Gmbh Treatment of Pain Associated with Trigeminal Neuralgia
US20130116334A1 (en) * 2010-06-30 2013-05-09 Gruenenthal Gmbh Treatment of Irritable Bowel Syndrome
US8652141B2 (en) 2010-01-21 2014-02-18 Tarsus Medical Inc. Methods and devices for treating hallux valgus
US8696719B2 (en) 2010-06-03 2014-04-15 Tarsus Medical Inc. Methods and devices for treating hallux valgus
EP2845625A1 (en) 2013-09-04 2015-03-11 Grünenthal GmbH Tapentadol for use in the treatment of fibromyalgia and chronic fatigue syndrome
US9446008B2 (en) 2011-03-04 2016-09-20 Gruenenthal Gmbh Semisolid aqueous pharmaceutical composition containing tapentadol
US9642801B2 (en) 2008-10-30 2017-05-09 Gruenenthal Gmbh And potent tapentadol dosage forms
US9980927B2 (en) 2011-04-29 2018-05-29 Gruenenthal Gmbh Use of tapentadol for inhibiting and/or treating depression and anxiety
US10398657B2 (en) 2011-04-05 2019-09-03 Gruenenthal Gmbh Method of inhibiting chronification of pain
US10898452B2 (en) 2016-09-23 2021-01-26 Gruenenthal Gmbh Stable formulation for parenteral administration of Tapentadol
US11013701B2 (en) 2015-03-27 2021-05-25 Grünenthal GmbH Stable formulation for parenteral administration of tapentadol
US11547678B2 (en) 2011-03-04 2023-01-10 Gruenenthal Gmbh Aqueous pharmaceutical formulation of tapentadol for oral administration

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EP2566461A2 (de) * 2010-05-05 2013-03-13 Ratiopharm GmbH Festes tapentadol in nicht-kristalliner form
EP3653600A1 (en) * 2010-07-23 2020-05-20 Grünenthal GmbH Salts or co-crystals of 3-(3-dimethylamino-1-ethyl-2-methyl-propyl)-phenol
CN101948397A (zh) * 2010-09-07 2011-01-19 天津泰普药品科技发展有限公司 镇痛药他喷他多重要中间体的制备方法
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WO2017148595A1 (en) 2016-02-29 2017-09-08 Grünenthal GmbH Titration of cebranopadol
EP4121013A1 (en) 2020-03-16 2023-01-25 Grünenthal GmbH Scored tablet
EP4308061A1 (en) * 2021-03-17 2024-01-24 Actelion Pharmaceuticals Ltd. Pharmaceutical dosage system
WO2022234076A1 (en) * 2021-05-07 2022-11-10 Grünenthal GmbH Tapentadol for treating neuropathic pain in covid-19 patients

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Cited By (20)

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US9642801B2 (en) 2008-10-30 2017-05-09 Gruenenthal Gmbh And potent tapentadol dosage forms
US20100211071A1 (en) * 2009-02-13 2010-08-19 Lettmann Jason W Methods and devices for treating hallux valgus
US8870876B2 (en) 2009-02-13 2014-10-28 Tarsus Medical Inc. Methods and devices for treating hallux valgus
US8277459B2 (en) 2009-09-25 2012-10-02 Tarsus Medical Inc. Methods and devices for treating a structural bone and joint deformity
US8795286B2 (en) 2009-09-25 2014-08-05 Tarsus Medical Inc. Methods and devices for treating a structural bone and joint deformity
US20110077656A1 (en) * 2009-09-25 2011-03-31 Sand Paul M Methods and devices for treating a structural bone and joint deformity
US8652141B2 (en) 2010-01-21 2014-02-18 Tarsus Medical Inc. Methods and devices for treating hallux valgus
US8696719B2 (en) 2010-06-03 2014-04-15 Tarsus Medical Inc. Methods and devices for treating hallux valgus
US20130116334A1 (en) * 2010-06-30 2013-05-09 Gruenenthal Gmbh Treatment of Irritable Bowel Syndrome
US20210212967A1 (en) * 2010-06-30 2021-07-15 Gruenenthal Gmbh Treatment of Irritable Bowel Syndrome
US11547678B2 (en) 2011-03-04 2023-01-10 Gruenenthal Gmbh Aqueous pharmaceutical formulation of tapentadol for oral administration
US20120225951A1 (en) * 2011-03-04 2012-09-06 Gruenenthal Gmbh Parenteral Administration of Tapentadol
US9446008B2 (en) 2011-03-04 2016-09-20 Gruenenthal Gmbh Semisolid aqueous pharmaceutical composition containing tapentadol
US10813891B2 (en) 2011-04-05 2020-10-27 Grünenthal GmbH Method of inhibiting chronification of pain
US10398657B2 (en) 2011-04-05 2019-09-03 Gruenenthal Gmbh Method of inhibiting chronification of pain
US20120309840A1 (en) * 2011-04-05 2012-12-06 Gruenenthal Gmbh Treatment of Pain Associated with Trigeminal Neuralgia
US9980927B2 (en) 2011-04-29 2018-05-29 Gruenenthal Gmbh Use of tapentadol for inhibiting and/or treating depression and anxiety
EP2845625A1 (en) 2013-09-04 2015-03-11 Grünenthal GmbH Tapentadol for use in the treatment of fibromyalgia and chronic fatigue syndrome
US11013701B2 (en) 2015-03-27 2021-05-25 Grünenthal GmbH Stable formulation for parenteral administration of tapentadol
US10898452B2 (en) 2016-09-23 2021-01-26 Gruenenthal Gmbh Stable formulation for parenteral administration of Tapentadol

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US20160074342A1 (en) 2016-03-17
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JP2018030864A (ja) 2018-03-01
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DK2148670T3 (da) 2012-03-12
EP3603630A1 (en) 2020-02-05
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PL2148670T3 (pl) 2012-04-30
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US11344512B2 (en) 2022-05-31
ATE534378T1 (de) 2011-12-15
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CA2683786A1 (en) 2008-10-30
US20190290603A1 (en) 2019-09-26
ES2378255T3 (es) 2012-04-10
CN101730530A (zh) 2010-06-09
US20170079938A1 (en) 2017-03-23
SI2148670T1 (sl) 2012-03-30
KR20150027840A (ko) 2015-03-12
EP2148670A1 (en) 2010-02-03
CA2683786C (en) 2021-10-26
KR20180004839A (ko) 2018-01-12
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AU2008241013A1 (en) 2008-10-30
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