WO2003103679A1 - Use of devazepide in combination with an opioid analgesic for potentiating the effect of the analgesic - Google Patents

Use of devazepide in combination with an opioid analgesic for potentiating the effect of the analgesic Download PDF

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Publication number
WO2003103679A1
WO2003103679A1 PCT/GB2003/002480 GB0302480W WO03103679A1 WO 2003103679 A1 WO2003103679 A1 WO 2003103679A1 GB 0302480 W GB0302480 W GB 0302480W WO 03103679 A1 WO03103679 A1 WO 03103679A1
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devazepide
opioid
analgesic
use according
day
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PCT/GB2003/002480
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French (fr)
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Karen Jackson
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Ml Laboratories Plc
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Priority to JP2004510798A priority Critical patent/JP2005533046A/en
Priority to AU2003246888A priority patent/AU2003246888A1/en
Priority to EP03757146A priority patent/EP1569654A1/en
Publication of WO2003103679A1 publication Critical patent/WO2003103679A1/en

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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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • 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
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
    • A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
    • 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
    • A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19—Carboxylic acids, e.g. valproic acid
    • A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4453—Non condensed piperidines, e.g. piperocaine only substituted in position 1, e.g. propipocaine, diperodon
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/485—Morphinan derivatives, e.g. morphine, codeine
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • 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
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/5513—1,4-Benzodiazepines, e.g. diazepam or clozapine

Definitions

  • This invention relates to a novel method of treatment and to a novel use of a medicament. 5
  • WO 99/18967 describes pharmaceutical compositions for treating chronic and neuropathic pain which comprises an analgesic amount of an opioid and an opioid potentiating amount of a CCK antagonist.
  • WO 5 '967 describes the use of both CCK-A (CCK-1) antagonists and CCK-B (CCK 2) antagonists, although it is described that, generally, CCK-B (CCK-2) antagonists are preferred.
  • page 2, lines 6 to 8 of WO '967 describes that CCK-A (CCK- 1) antagonists may be suitable, but only at relatively higher dosages.
  • CCK-A (CCK-1) antagonist which is mentioned is devazepide, which is 3 s-(-) 1 , 3 dihydro-3 -(2-indolecarbonylamino)- 1 -me thyl-5 -phenyl-2H- 1 ,4- benzodiazepin-2-one.
  • WO 99/18967 describes a pharmaceutical 5 formulation comprising a CCK antagonist, such as devazepide (Devacade®), an opioid and a biphasic carrier, comprising a glyceride derivative organic phase.
  • a CCK antagonist such as devazepide (Devacade®)
  • Devacade® devazepide
  • a biphasic carrier comprising a glyceride derivative organic phase.
  • the use of the CCK antagonist is intended to block the CCK receptors thereby reversing or preventing the development of opioid tolerance in patients and potentiating the analgesic effect of the opioid.
  • patients undergoing opioid therapy will receive a stable dose of an opioid.
  • a patient may also use an additional 'breakthrough pain' relieving dose of opioid therapy, as symptoms dictate.
  • the opioid dose may be reduced as much as 95% in some cases, in others as much as 75%.
  • the administration of a combination of an opioid and devazepide does not just retain the "pain level" experienced by a patient, but actually improves it, i.e. it is not just a case of opioid sparing or opioid potentiation, but the effect of the opioid is superpotentiated.
  • the analgesic sparing amount of devazepide will advantageously cause a reduction in the amount of analgesic administered to the patient.
  • the reduction may vary but may, for example, be a reduction of from 25% to 95% w/w of the amount of analgesic required in the absence of devazepide, more preferably from 25% to 75% w/w.
  • a reduced amount of analgesic of from 25% to 95% w/w may be administered.
  • a reduced amount of analgesic of from 25 to 75% w/w may be administered.
  • the opioid may be selected from those which are effective analgesics and particularly those which need to be administered at relatively high or increasing doses.
  • examples include morphine, or a salt thereof such as the sulphate, chloride or hydrochloride other analgesics such as, meperidine, pentazocine, dextropropoxyphene, pethidine, fentanyl, alfentanil, alphaprodine, dextromoramide, diphenoxylate, dipipanone, meptazinol, methadone, nalbuphine, phenadoxone, phenazocine, remifentanil, tramadol, or the 1,4-hydroxymorphinan opioid analgesics such as butorphanol, morphine-6-glucuronide, codeine, dihydrocodeine, diamorphine, buprenorphine, heroin (diacetylmorphine), hydrocodone (d
  • Naloxone is also included within the definition of an opioid.
  • analgesics which may be mentioned are hydromorphone, oxycodone, morphine, e.g. morphine sulphate and fentanyl.
  • the analgesic is morphine or morphine sulphate, hi a further preferred embodiment the opioid is fentanyl, or a salt thereof.
  • a method of treatment of a patient requiring analgesia which comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
  • analgesic will be an opioid analgesic.
  • devazepide in the manufacture of a medicament for the treatment of analgesia wherein the treatment comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
  • the devazepide and/or the opioid may be administered using any methods conventionally known per se.
  • such methods would include, but shall not be limited to, administration intravenously, intra-arterially, orally, intrathecally, intranasally, intrarectally, intramuscularly/subcutaneously, by inhalation and by transdermal patch.
  • the devazepide and/or opioid When the devazepide and/or opioid is administered intravenously, it may, for example, be as an intravenous bolus or a continuous intravenous infusion.
  • the devazepide and/or the opioid is administered subcutaneously, it may, for example, be by subcutaneous infusion.
  • the opioid and/or devazepide are administered intravenously or orally.
  • Oral administration is especially preferred.
  • the opioid and the devazepide will be administered using the same mode of administration.
  • the opioid when the opioid is administered intravenously then the devazepide will be administered intravenously also.
  • the opioid when the opioid is administered orally then the devazepide will be administered orally also.
  • the opioid may be administered by a transdermal patch.
  • the preferred opioid is fentanyl.
  • the composition may be made up into a capsule formulation, e.g. with a fill weight of 150 mg ⁇ 5% by weight or 300 mg ⁇ 5% by weight.
  • the capsule formulation may comprise 1.25mg devazepide, and 148.75 mg of a filler or other excipient, e.g. corn starch, i a further preferred embodiment, the capsule formulation may comprise 2.5mg devazepide, and 297.5 mg of a filler or other excipient, e.g. corn starch.
  • fillers may be selected from the group lactose, mannitol, talc, magnesium stearate, sodium chloride, potassium chloride, citric acid, spray-dried lactose, hydrolysed starches, directly compressible starch, macrocrystalline cellulose, cellulosics, sorbitol, sucrose, sucrose-based materials, icodextrin, calcium sulphate, dibasic calcium phosphate and dextrose.
  • a preferred filler is starch, e.g. corn starch.
  • the size of the devazepide and filler particles may be the same or different. However, in a preferred embodiment the sizes of the devazepide and filler particles will differ. Preferentially, the devazepide and/or the filler may be of reduced particle size, e.g. by milling.
  • the daily dosage of devazepide may vary depending upon, inter alia, the weight of the patient, the method of administration, etc. In patients that are suffering serious disorders, such as cancer patients, the weight of the patient may be very low and therefore the dosage of devazepide consequentially may be low.
  • the daily dosage of devazepide may be up to 0.7 mg/kg/day.
  • the daily dosage of devazepide may be from 25 ⁇ g/kg/day to 0.7 mg/kg/day, more preferably from 50 ⁇ g/kg/day to 0.5 mg/kg/day.
  • the daily dosage of devazepide may be from preferably 0.07 mg/kg/day to 0.7 mg/kg/day.
  • the daily dosage of devazepide may be from 0.07 mg/kg/day to 0.29 mg/kg/day.
  • the dosage of devazepide is preferably 50 ⁇ g/kg/day to 0.5 mg/kg/day.
  • the ratio of devazepide to dose of opioid may be varied.
  • the ratio devazepide to opioid may be from 2:1 to 1:200 w/w, preferably from 1 :2 to 1:40 w/w.
  • the dosage of the opioid analgesic administered may vary depending upon, inter alia, the nature of the opioid analgesic, the weight of the patient, the method of administration, etc.
  • the dosage of, e.g. an opioid, such as morphine may be from 5 to 2000mg daily.
  • a particular dosage which may be mentioned is from 10 to 240mg daily.
  • a daily dosage of morphine may be from 5 to lOOmg or occasionally up to 500mg.
  • the devazepide used in the method of the invention is the S enantiomer, preferentially, the S enantiomer wherein the level of R enantiomer, which may be present as an impurity, is not greater than 1.5% w/w.
  • Patients completed a pre-treatment period of at least two weeks duration. During pre-treatment the patients continued to take regular doses of strong opioids and breakthrough analgesics when required. All use of strong opioids and analgesics was recorded. Patients completed an assessment of their pain each evening prior to going to bed, using a pain questionnaire. Any adverse events and changes in concomitant medication were also recorded.
  • each patient received blinded treatments of devazepide 1.25mg, devazepide 5mg and placebo twice daily for two weeks with washout periods between each treatment, according to the following schedule.
  • Breakthrough analgesic product use included (in addition to the above) tramadol, diclofenac, dihydrocodeine, paracetamol, codeine, aspirin, ibuprofen, dextropropoxyphene, buprenorphine, pethidine, carbamazepine, and hydromorphone (and combination products containing the above, for example; AnadinTM (aspirin), AnadinTM extra (aspirin and paracetamol), co-codamol, co- dydramol, co-proxamol, and remedeine).
  • a research programme has included a double blind, double dummy, randomised, crossover study of a single dose of either 1.25mg devazepide, 5.0 mg devazepide or placebo. Patients who took part in the study had pain with a neuropathic element, and were taking regular doses of strong opioids. Following completion of the study those patients who, in the opinion of their Clinical Investigator, had gained benefit from participation were given the opportunity to consent to continue receiving devazepide treatment for a period of up to six months. 2.2 Study design
  • the primary objective of this study was to compare descriptive and visual analogue scale (NAS) assessments of pain and pain relief in patients with neuropathic pain.
  • NAS descriptive and visual analogue scale
  • Figure 1 illustrates the trend with a weaker opioid, dihydrocodeine.
  • the patient(s) commenced on 120 mg dihydrocodeine per day.

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Abstract

There is described a method of treatment of a patient undergoing analgesic therapy which comprises the separate, simultaneous or sequential administration of a therapeutically effective amount of an analgesic and an analgesic sparing amount of devazepide. There is also described the use of devazepide in the manufacture of a medicament which reduces the dose required for administration of an opioid analgesic and superpotentiates the effect of the analgesic.

Description

SE OF DEVAZEPIDE IN COMBINATION WITH AN OPIOID ANALGESIC FOR POTENTIATING THE EFFECT OF THE ANALGESIC
This invention relates to a novel method of treatment and to a novel use of a medicament. 5
Fans, in Science 1984; 226:1215-1217 describes a reduction of morphine analgesia by endogenously released cholecystokinin. Thus, Faris suggests that concomitant administration of morphine and a specific CCK antagonist may allow reduction in the initial dose of morphine required and a reduction in the frequency of its 0 administration.
International Patent Application No. WO 99/18967 describes pharmaceutical compositions for treating chronic and neuropathic pain which comprises an analgesic amount of an opioid and an opioid potentiating amount of a CCK antagonist. WO 5 '967 describes the use of both CCK-A (CCK-1) antagonists and CCK-B (CCK 2) antagonists, although it is described that, generally, CCK-B (CCK-2) antagonists are preferred. Moreover, page 2, lines 6 to 8 of WO '967 describes that CCK-A (CCK- 1) antagonists may be suitable, but only at relatively higher dosages.
0 One specific CCK-A (CCK-1) antagonist which is mentioned is devazepide, which is 3 s-(-) 1 , 3 dihydro-3 -(2-indolecarbonylamino)- 1 -me thyl-5 -phenyl-2H- 1 ,4- benzodiazepin-2-one.
International Patent Application No. WO 99/18967 describes a pharmaceutical 5 formulation comprising a CCK antagonist, such as devazepide (Devacade®), an opioid and a biphasic carrier, comprising a glyceride derivative organic phase. The use of the CCK antagonist is intended to block the CCK receptors thereby reversing or preventing the development of opioid tolerance in patients and potentiating the analgesic effect of the opioid. 0 Generally, patients undergoing opioid therapy will receive a stable dose of an opioid. A patient may also use an additional 'breakthrough pain' relieving dose of opioid therapy, as symptoms dictate.
As hereinbefore described, International Patent Application No. WO 99/18967 discloses the administration of devazepide in combination with an opioid analgesic so as to potentiate the analgesic effect of the overall dose of the opioid. In practice the expected outcome would result in the analgesia, or the "pain level", experienced by a patient generally remaining the same, whilst the dosage of opioid administered to the patient is reduced or analgesia improving with the same dose of opioid. However, we have now found that in fact devazepide has a "superpotentiating" effect in combination with an opioid. Thus, in the present invention the use of devazepide can act to enable the overall dose of opioid to be reduced or minimised, concurrent with improved analgesia, i.e. an increase in the analgesia, or a lowering of "pain level", experienced by the patient. Indeed clinical studies have shown that the opioid dose may be reduced as much as 95% in some cases, in others as much as 75%. Thus, the administration of a combination of an opioid and devazepide does not just retain the "pain level" experienced by a patient, but actually improves it, i.e. it is not just a case of opioid sparing or opioid potentiation, but the effect of the opioid is superpotentiated.
Thus according to the invention we provide a method of treatment of a patient undergoing analgesic therapy by the administration of a therapeutically effective amount of an analgesically active medicament which method comprises the separate, simultaneous or sequential administration of an analgesic sparing amount of devazepide.
The analgesic sparing amount of devazepide will advantageously cause a reduction in the amount of analgesic administered to the patient. The reduction may vary but may, for example, be a reduction of from 25% to 95% w/w of the amount of analgesic required in the absence of devazepide, more preferably from 25% to 75% w/w.
Thus according to a further aspect of the invention we provide a method of treatment of a patient as hereinbefore described characterised in that a reduced amount of analgesic of from 25% to 95% w/w may be administered. In a preferred embodiment of the invention a reduced amount of analgesic of from 25 to 75% w/w may be administered.
In the method of the invention a variety of opioids may be used. Thus, the opioid may be selected from those which are effective analgesics and particularly those which need to be administered at relatively high or increasing doses. Examples include morphine, or a salt thereof such as the sulphate, chloride or hydrochloride other analgesics such as, meperidine, pentazocine, dextropropoxyphene, pethidine, fentanyl, alfentanil, alphaprodine, dextromoramide, diphenoxylate, dipipanone, meptazinol, methadone, nalbuphine, phenadoxone, phenazocine, remifentanil, tramadol, or the 1,4-hydroxymorphinan opioid analgesics such as butorphanol, morphine-6-glucuronide, codeine, dihydrocodeine, diamorphine, buprenorphine, heroin (diacetylmorphine), hydrocodone (dihydrocodeinone), hydromorphone (dihydromorphinone), levorphanol, metopon (methyldihydromorphinone), oxycodone (dihydrohydroxycodeinone), oxymorphone (dihydrohydroxymorphinone); or a salt of any of the aforementioned. Naloxone is also included within the definition of an opioid. Especially preferred analgesics which may be mentioned are hydromorphone, oxycodone, morphine, e.g. morphine sulphate and fentanyl. In a preferred embodiment of the invention the analgesic is morphine or morphine sulphate, hi a further preferred embodiment the opioid is fentanyl, or a salt thereof.
According to a further feature of the invention we provide a method of treatment of a patient requiring analgesia which comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
hi a preferred aspect of the invention the analgesic will be an opioid analgesic.
According to a further aspect of the invention we provide the use of devazepide in the manufacture of a medicament which reduces the dose of the analgesic and superpotentiates the analgesic effect.
We further provide the use of devazepide in the manufacture of a medicament for the treatment of analgesia wherein the treatment comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
hi the method of the invention the devazepide and/or the opioid may be administered using any methods conventionally known per se. Thus, such methods would include, but shall not be limited to, administration intravenously, intra-arterially, orally, intrathecally, intranasally, intrarectally, intramuscularly/subcutaneously, by inhalation and by transdermal patch. When the devazepide and/or opioid is administered intravenously, it may, for example, be as an intravenous bolus or a continuous intravenous infusion. When the devazepide and/or the opioid is administered subcutaneously, it may, for example, be by subcutaneous infusion. Preferably, the opioid and/or devazepide are administered intravenously or orally. Oral administration is especially preferred. Preferentially, the opioid and the devazepide will be administered using the same mode of administration. Thus, for example, when the opioid is administered intravenously then the devazepide will be administered intravenously also. Similarly, when the opioid is administered orally then the devazepide will be administered orally also. However, it is within the scope of the invention for either the opioid to be administered orally and the devazepide to be administered intravenously or vice versa, hi a further preferred embodiment the opioid may be administered by a transdermal patch. When a transdermal patch is used, the preferred opioid is fentanyl.
According to a further aspect of the invention we provide the use of devazepide in the manufacture of a pharmaceutical composition as hereinbefore described.
Thus, for example, in one embodiment of the invention the composition may be made up into a capsule formulation, e.g. with a fill weight of 150 mg ± 5% by weight or 300 mg ± 5% by weight. In the one preferred embodiment, the capsule formulation may comprise 1.25mg devazepide, and 148.75 mg of a filler or other excipient, e.g. corn starch, i a further preferred embodiment, the capsule formulation may comprise 2.5mg devazepide, and 297.5 mg of a filler or other excipient, e.g. corn starch.
Thus, such fillers may be selected from the group lactose, mannitol, talc, magnesium stearate, sodium chloride, potassium chloride, citric acid, spray-dried lactose, hydrolysed starches, directly compressible starch, macrocrystalline cellulose, cellulosics, sorbitol, sucrose, sucrose-based materials, icodextrin, calcium sulphate, dibasic calcium phosphate and dextrose. A preferred filler is starch, e.g. corn starch.
When the composition of the invention includes a filler, the size of the devazepide and filler particles may be the same or different. However, in a preferred embodiment the sizes of the devazepide and filler particles will differ. Preferentially, the devazepide and/or the filler may be of reduced particle size, e.g. by milling.
Thus, in the method of the invention the daily dosage of devazepide may vary depending upon, inter alia, the weight of the patient, the method of administration, etc. In patients that are suffering serious disorders, such as cancer patients, the weight of the patient may be very low and therefore the dosage of devazepide consequentially may be low. Thus the daily dosage of devazepide may be up to 0.7 mg/kg/day. Preferably, the daily dosage of devazepide may be from 25 μg/kg/day to 0.7 mg/kg/day, more preferably from 50 μg/kg/day to 0.5 mg/kg/day. For oral administration the daily dosage of devazepide may be from preferably 0.07 mg/kg/day to 0.7 mg/kg/day. More preferably, for oral administration the daily dosage of devazepide may be from 0.07 mg/kg/day to 0.29 mg/kg/day. For intravenous administration the dosage of devazepide is preferably 50 μg/kg/day to 0.5 mg/kg/day.
In particular, the ratio of devazepide to dose of opioid may be varied. Thus, the ratio devazepide to opioid may be from 2:1 to 1:200 w/w, preferably from 1 :2 to 1:40 w/w.
In the method of the invention the dosage of the opioid analgesic administered may vary depending upon, inter alia, the nature of the opioid analgesic, the weight of the patient, the method of administration, etc. Thus, for example, the dosage of, e.g. an opioid, such as morphine, may be from 5 to 2000mg daily. A particular dosage which may be mentioned is from 10 to 240mg daily. A daily dosage of morphine may be from 5 to lOOmg or occasionally up to 500mg.
The devazepide used in the method of the invention is the S enantiomer, preferentially, the S enantiomer wherein the level of R enantiomer, which may be present as an impurity, is not greater than 1.5% w/w.
The invention will now be illustrated by way of example only.
Example 1
Clinical Crossover Study
A multi-centre, double blind placebo controlled crossover study was designed to investigate devazepide as adjunctive therapy to strong opioids in patients with moderate or severe neuropathic pain. 1.1 Rationale for Study Design
The study was conducted to observe the effects of two different doses for devazepide (1.25mg b.d. and 5mg b.d.) in patients when given as an adjunct to strong opioids. Previous studies have shown devazepide is well tolerated at levels up to 5mg bd. This study was designed to further investigate the analgesic effect and the safety and toxicity of devazepide compared to placebo when administered twice daily for two weeks.
1.2 Pre-treatment
Patients completed a pre-treatment period of at least two weeks duration. During pre-treatment the patients continued to take regular doses of strong opioids and breakthrough analgesics when required. All use of strong opioids and analgesics was recorded. Patients completed an assessment of their pain each evening prior to going to bed, using a pain questionnaire. Any adverse events and changes in concomitant medication were also recorded.
1.3 Treatment
Following the two-week pre-treatment period, each patient received blinded treatments of devazepide 1.25mg, devazepide 5mg and placebo twice daily for two weeks with washout periods between each treatment, according to the following schedule.
Table I Treatment Schedule
Figure imgf000008_0001
On each day of treatment, assessment of pain, general activity and sleep interference were made by the patients and recorded on diary cards. At the end of each treatment period, the patient rated overall pain relief using a descriptive scale, and the opinion of both the patient and investigator of that treatment was recorded. All concomitant medication use (including strong opioid and breakthrough analgesic use) and adverse events were recorded throughout the study. Blood samples were collected at screening and at the end of each treatment for safety monitoring.
1.4 Results
Of the 62 patients screened, 41 completed the study according to the protocol. There were 18 (44%) women and 23 (56%) men, who had a mean (range) age of 48.6 (23.2 to 70.7) years. Patients were stabilised on moφhine (34), oxycodone (2), fentanyl (3), methadone (1), hydromorphone (1) and diamorphine (1); with one patient taking both morphine and fentanyl. Breakthrough analgesic product use included (in addition to the above) tramadol, diclofenac, dihydrocodeine, paracetamol, codeine, aspirin, ibuprofen, dextropropoxyphene, buprenorphine, pethidine, carbamazepine, and hydromorphone (and combination products containing the above, for example; Anadin™ (aspirin), Anadin™ extra (aspirin and paracetamol), co-codamol, co- dydramol, co-proxamol, and remedeine).
The analysis of specific use of breakthrough analgesia as opposed to regular opioid use was not possible because patients were taking a variety of different analgesic drugs (including opioids) in addition to their regular opioid. It was also difficult to define breakthrough analgesia in those patients who were using the same opioid for both regular use and for breakthrough analgesia (latter to control breakthrough pain). For this reason, all analgesic medication was included in the determination of a total dose for the treatment period, irrespective of whether it was used as regular stable medication or for breakthrough pain. The results are illustrated in Table H
Table II : Analgesic use expressed as a percentage of pre-treatment use
SUM OF DAILY DOSE
PATIENT DRUG UNITS Devazepide Devazepide placebo pre NUMBER 1.25mg 5mg treatment ap06/05 morphine mg 104 100 104 100% tramadol mg 79 54 79 100% ggOl/01 co-codamol tablets 106 78 67 100% fentanyl mcg/h 100 67 83 100% gg03/03 morphine mg 55 93 97 100% ng02/02 diclofenac mg 17 50 50 100% morphine mg 87 84 87 100% ng05/05 morphine mg 104 100 104 100% paracetamol mg 48 14 43 100% sj 03/03 morphine mg 93 97 93 100% morphine ml 13 5 42 100% sj 10/73 dihydrocodeine mg 100 50 100 100% morphine mg 100 98 100 100% paracetamol mg 75 50 100 100%
Example 2
2.1 Clinical assessment study
A research programme has included a double blind, double dummy, randomised, crossover study of a single dose of either 1.25mg devazepide, 5.0 mg devazepide or placebo. Patients who took part in the study had pain with a neuropathic element, and were taking regular doses of strong opioids. Following completion of the study those patients who, in the opinion of their Clinical Investigator, had gained benefit from participation were given the opportunity to consent to continue receiving devazepide treatment for a period of up to six months. 2.2 Study design
This continuation study was a multicentre, open label study of devazepide at twice daily doses of 1.25mg, 2.5mg and 5.0 mg.
2.3 Study Objective
The primary objective of this study was to compare descriptive and visual analogue scale (NAS) assessments of pain and pain relief in patients with neuropathic pain.
2.4 Methods
At the end of the previous randomised trial, patients received 1.25mg devazepide twice daily for an initial period of one week. After this initial one week period, the dose of devazepide was reviewed and increased, if necessary, to 2.5 mg twice daily and thereafter to 5.0 mg twice daily as required. Devazepide treatment was continued for a period of up to six months.
During the study patients were required to remain on regular doses of opioids at a dose prescribed by the investigator.
2.5 Study assessments
Patients were assessed at clinic visits at week 1, week 2 (dose escalation) and thereafter at routine monthly clinic visits.
At weekly intervals for the first eight weeks and at monthly intervals thereafter, patients recorded pain and global pain relief using NAS and descriptive pain questionnaires. The questionnaires were returned to the Investigator at the monthly visits. At each clinic visit the Investigator assessed safety and the patients' pain relief, reviewed the dosage, and decided if devazepide treatment should be continued.
2.6 Results
Seventeen patients elected to stay on devazepide by entering the continuation study and received devazepide at 1.25mg, 2.5mg or 5.0 mg twice daily for up to 26 weeks.
Of these patients, ten appeared to achieve long-term pain relief (5 - 26 weeks) with devazepide. Despite the requirement to remain on stable, regular doses of opioids at the dose prescribed by the investigator, several patients reduced markedly reduced their daily opioid dose.
Figure 1 illustrates the trend with a weaker opioid, dihydrocodeine. The patient(s) commenced on 120 mg dihydrocodeine per day.

Claims

1. The use of devazepide in the manufacture of a medicament which reduces the dose required for administration of an opioid analgesic and superpotentiates the effect of the analgesic.
2. The use of devazepide in the manufacture of a medicament for the treatment of analgesia wherein the treatment comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
3. The use according to claims 1 or 2 characterised in that the amount of analgesic required by a patient is reduced by an amount of from 25% to 95% by weight of the amount of analgesic required in the absence of devazepide.
4. The use according to claim 3 characterised in that the amount of analgesic required by a patient is reduced by an amount of from 25% to 75% by weight of the amount of analgesic required in the absence of devazepide.
5. The use according to claim 1 or 2 characterised in that the opioid is selected from those which need to be administered at relatively high or increasing doses.
6. The use according to claims 1 or 2 characterised in that the analgesic is an opioid.
7. The use according to claims 1 or 2 characterised in that the analgesic is selected from the group morphine, or a salt thereof such as the sulphate, chloride or hydrochloride other analgesics such as, meperidine, pentazocine, dextropropoxyphene, pethidine, fentanyl, alfentanil, alphaprodine, dextromoramide, diphenoxylate, dipipanone, meptazinol, methadone, nalbuphine, phenadoxone, phenazocine, remifentanil, tramadol, or the 1,4-hydroxymorphinan opioid analgesics such as butorphanol, morphine-6-glucuronide, codeine, dihydrocodeine, diamorphine, buprenoφhine, heroin (diacetylmorphine), hydrocodone
(dihydrocodeinone), hydromorphone (dihydromorphinone), levorphanol, metopon (methyldihydromoφhinone), oxycodone (dihydrohydroxycodeinone), oxymoφhone (dihydrohydroxymoφhinone); or a salt of any of the aforementioned.
8. The use according to claim 6 characterised in that the opioid is naloxone.
9. The use according to claim 7 characterised in that the analgesic is selected from the group hydromoφhone, oxycodone, moφhine, and fentanyl or a salt thereof.
10. The use according to claim 9 characterised in that the opined is fentanyl or a salt thereof.
11. The use according to claim 9 characterised in that the analgesic is moφhine or moφhine sulphate.
12. The use according to claim 6 characterised in that the ratio of devazepide to opioid is from 2:1 to 1 :400 w/w.
13. The use according to claim 12 characterised in that the ratio of devazepide to opioid is from 2:1 to 1:200 w/w.
14. The use according to claim 13 characterised in that the ratio of devazepide to opioid is from 1 :2 to 1 :40 w/w.
15. The use according to claims 1 or 2 characterised in that the devazepide and/or the opioid may be administered using a method selected from administration intravenously, intra-arterially, orally, infrathecally, intranasally, intrarectally, intramuscularly/subcutaneously, by inhalation and by transdermal patch.
16. The use according to claim 15 characterised in that the devazepide and/or the opioid is administered intravenously.
17. The use according to claim 16 characterised in that the intravenous administration is by intravenous bolus or a continuous intravenous infusion.
18. The use according to claim 15 characterised in that the devazepide and/or the opioid is administered subcutaneously.
19. The use according to claim 18 characterised in that the subcutaneous administration is as a subcutaneous infusion.
20. The use according to claim 15 characterised in that the opioid and/or devazepide are administered intravenously or orally.
21. The use according to claim 20 characterised in that the opioid and/or devazepide are administered orally.
22. The use according to claim 15 characterised in that the opioid and the devazepide will be administered using the same mode of administration.
23. The use according to claim 22 characterised in that the opioid is administered orally and the devazepide is administered orally.
24. The use according to claim 15 characterised in that the opioid is administered by transdermal patch.
25. The use according to claim 24 characterised in that the opioid is fentanyl, or a salt thereof.
26. The use according to claim 1 characterised in that the daily dosage of devazepide is up to 0.7 mg/kg/day.
27. The use according to claim 26 characterised in that the daily dosage of devazepide is from 25 μg/kg/day to 0.7 mg/kg/day.
28. The use according to claim 27 characterised in that the daily dosage of devazepide is from 50 μg/kg/day to 0.5 mg/kg/day.
29. The use according to claim 26 characterised in that the dosage of devazepide is an oral dosage.
30. The use according to claim 29 characterised in that the devazepide is administered orally and the daily dosage of devazepide is from 0.07 mg/kg/day to 0.29 mg/kg/day.
31. The use according to claim 26 characterised in that the devazepide is administered intravenously at a dosage of from 50 μg/kg/day to 0.5 mg/kg/day.
32. The use according to claim 6 characterised in that the dosage of the opioid is from 5 to 2000mg daily.
33. The use according to claim 32 characterised in that the dosage of the opioid is from 10 to 240 mg daily.
34. The use according to claim 33 characterised in that the dosage of the opioid is from 5 to lOOmg daily.
35. The use according to claims 1 or 2 characterised in that the devazepide is provided as a composition incoφorating a filler or other excipient.
36. The use according to claim 35 characterised in that the composition is filled into a capsule.
37. The use according to claim 36 characterised in that the capsule is a gelatin capsule.
38. The use according to claim 36 characterised in that the capsule has a fill weight of 150 mg ± 5% by weight or 300 mg ± 5% by weight.
39. The use according to claim 36 characterised in that the capsule formulation comprises 1.25mg devazepide or 2.5 mg devazepide.
40. The use according to claim 39 characterised in that the 1.25 mg or 2.5 mg of devazepide is delivered at least twice daily.
41. The use according to claims 1 or 2 characterised in that the devazepide used in the method of the invention is substantially the S enantiomer.
42. The use according to claim 41 characterised in that the level of R enantiomer, which may be present as an impurity, is not greater than 1.5% w/w.
43. A method of treatment of a patient undergoing analgesic therapy which comprises the separate, simultaneous or sequential administration of a therapeutically effective amount of an analgesic and an analgesic sparing amount of devazepide.
44. A method of treatment of a patient requiring analgesia which comprises the administration of a therapeutically effective amount of an analgesic whilst minimising the amount of the analgesic by the separate, simultaneous or sequential administration of a therapeutically effective amount of devazepide.
45. A method according to claims 43 or 44 characterised in that the method comprises the administration of a therapeutically effective amount of an analgesic with a supeφotentiating amount of devazepide.
46. A method according to claims 43 or 44 characterised in that the amount of analgesic required by a patient is reduced by an amount of from 25% to 95% by weight of the amount of analgesic required in the absence of devazepide.
47. A method according to claim 46 characterised in that the amount of analgesic required by a patient is reduced by an amount of from 25% to 75% by weight of the amount of analgesic required in the absence of devazepide.
48. A method according to claim 43 or 44 characterised in that the opioid is selected from those which need to be administered at relatively high or increasing doses.
49. A method according to claims 43 or 44 characterised in that the analgesic is an opioid.
50. A method according to claims 43 or 44 characterised in that the analgesic is selected from the group moφhine, or a salt thereof such as the sulphate, chloride or hydrochloride, other analgesics such as, meperidine, pentazocine, dextropropoxyphene, pethidine, fentanyl, alfentanil, alphaprodine, dextromoramide, diphenoxylate, dipipanone, meptazinol, methadone, nalbuphine, phenadoxone, phenazocine, remifentanil, tramadol, or the 1,4-hydroxymoφhinan opioid analgesics such as butoφhanol, moφhine-6-glucuronide, codeine, dihydrocodeine, diamoφhine, buprenoφhine, heroin (diacetylmoφhine), hydrocodone
(dihydrocodeinone), hydromoφhone (dihydromoφhinone), levoφhanol, metopon (methyldihydromoφhinone), oxycodone (dihydrohydroxycodeinone), oxymoφhone (dihydrohydroxymoφhinone); or a salt of any of the aforementioned.
51. A method according to claim 49 characterised in that the opioid is naloxone.
52. A method according to claim 50 characterised in that the analgesic is selected from the group hydromoφhone, oxycodone, moφhine, and fentanyl or a salt thereof.
53. A method according to claim 52 characterised in that the opined is fentanyl or a salt thereof.
54. A method according to claim 53 characterised in that the analgesic is moφhine or moφhine sulphate.
55. A method according to claim 49 characterised in that the ratio of devazepide to opioid is from 2:1 to 1:400 w/w.
56. A method according to claim 55 characterised in that the ratio of devazepide to opioid is from 2:1 to 1:200 w/w.
57. A method according to claim 56 characterised in that the ratio of devazepide to opioid is from 1 :2 to 1 :40 w/w.
58. A method according to claims 43 or 44 characterised in that the devazepide and/or the opioid may be administered using a method selected from administration intravenously, intra-arterially, orally, infrathecally, intranasally, intrarectally, intramuscularly/subcutaneously, by inhalation and by transdermal patch.
59. A method according to claim 58 characterised in that the devazepide and/or the opioid is administered intravenously.
60. A method according to claim 59 characterised in that the intravenous administration is by intravenous bolus or a continuous intravenous infusion.
61. A method according to claim 58 characterised in that the devazepide and/or the opioid is administered subcutaneously.
62. A method according to claim 61 characterised in that the subcutaneous administration is as a subcutaneous infusion.
63. A method according to claim 58 characterised in that the opioid and/or devazepide are administered intravenously or orally.
64. A method according to claim 63 characterised in that the opioid and/or devazepide are administered orally.
65. A method according to claim 58 characterised in that the opioid and the devazepide will be administered using the same mode of administration.
66. A method according to claim 59 characterised in that the opioid is administered orally and the devazepide is administered orally.
67. A method according to claim 58 characterised in that the opioid is administered by transdermal patch.
68. A method according to claim 67 characterised in that the opioid is fentanyl, or a salt thereof.
69. A method according to claim 43 characterised in that the daily dosage of devazepide is up to 0.7 mg/kg/day.
70. A method according to claim 69 characterised in that the daily dosage of devazepide is from 25 μg/kg/day to 0.7 mg/kg/day.
71. A method according to claim 70 characterised in that the daily dosage of devazepide is from 50 μg/kg/day to 0.5 mg/kg/day.
72. A method according to claim 69 characterised in that the dosage of devazepide is an oral dosage.
73. A method according to claim 72 characterised in that the devazepide is administered orally and the daily dosage of devazepide is from 0.07 mg/kg/day to 0.29 mg/kg/day.
74. A method according to claim 69 characterised in that the devazepide is administered intravenously at a dosage of from 50 μg/kg/day to 0.5 mg/kg/day.
75. A method according to claim 49 characterised in that the dosage of the opioid is from 5 to 2000mg daily.
76. A method according to claim 75 characterised in that the dosage of the opioid is from 10 to 240 mg daily.
77. A method according to claim 76 characterised in that the dosage of the opioid is from 5 to lOOmg daily.
78. A method according to claims 43 or 44 characterised in that the devazepide is provided as a composition incoφorating a filler or other excipient.
79. A method according to claim 78 characterised in that the composition is filled into a capsule.
80. A method according to claim 79 characterised in that the capsule is a gelatin capsule.
81. A method according to claim 79 characterised in that the capsule has a fill weight of 150 mg ± 5% by weight or 300 mg ± 5% by weight.
82. A method according to claim 79 characterised in that the capsule formulation comprises 1.25mg devazepide or 2.5 mg devazepide.
83. A method according to claim 82 characterised in that the 1.25 mg or 2.5 mg of devazepide is delivered at least twice daily.
84. A method according to claims 43 or 44 characterised in that the devazepide used in the method of the invention is substantially the S enantiomer.
85. A method according to claim 84 characterised in that the level of R enantiomer, which may be present as an impurity, is not greater than 1.5% w/w.
86. A method or a use substantially as described with reference to the accompanying examples.
PCT/GB2003/002480 2002-06-10 2003-06-10 Use of devazepide in combination with an opioid analgesic for potentiating the effect of the analgesic WO2003103679A1 (en)

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