Metopirone

Metopirone® Capsules 250mg

Metyrapone BP 250mg.

Excipient(s) with known effect

Each capsule contains 0.71 mg of sodium ethylparaben (E215) and 0.35 mg sodium propylparaben (E217).

For the full list of excipients, see section 6.1.

Yellowish-white, oblong, opaque, soft gelatin capsules printed 'HRA' on one side in red ink.

A diagnostic aid in the differential diagnosis of ACTH-dependent Cushing's syndrome. The management of patients with Cushing's syndrome.

In conjunction with glucocorticosteroids in the treatment of resistant oedema due to increased aldosterone secretion in patients suffering from cirrhosis, nephrosis and congestive heart failure.

Posology

Adults

For use as a diagnostic aid:

the patient must be hospitalised. Urinary 17- oxygenic steroid excretion is measured over 24 hours on each of 4 consecutive days. The first 2 days serve as a control period. On the third day, 750mg Metopirone (3 capsules) must be given at four-hourly intervals to give a total of 6 doses (ie 4.5g). Maximum urine steroid excretion may occur on the fourth day. If urinary steroid excretion increases in response to Metopirone, this suggests the high levels of circulatory cortisol are due to adrenocortical hyperplasia following excessive ACTH production rather than a cortisol- producing adrenal tumour.

For therapeutic use:

for the management of Cushing's syndrome, the dosage must be adjusted to meet the patient's requirements; a daily dosage from 250mg to 6g may be required to restore normal cortisol levels.

For the treatment of resistant oedema:

The usual daily dose of 3g (12 capsules) should be given in divided doses in conjunction with a glucocorticoid.

Children: Children should be given a smaller amount based upon 6 four- hourly doses of 15mg/kg, with a minimum dose of 250mg every four hours.

Elderly: Clinical evidence would indicate that no special dosage regimen is necessary.

Method of administration

The capsules should be taken with milk or after a meal, to minimise nausea and vomiting, which can lead to impaired absorption.

Primary adrenocorticol insufficiency.

Hypersensitivity to Metopirone or to any of the excipients. Pregnancy.

In relation to use as a diagnostic aid: anticonvulsants (eg phenytoin, barbiturates), anti-depressants and neuroleptics (eg amitriptyline, chlorpromazine), hormones that affect the hypothalamo-pituitary axis and anti-thyroid agents may influence the results of the Metopirone test. If these drugs cannot be withdrawn, the necessity of carrying out the Metopirone test should be reviewed.

If adrenocortical or anterior pituitary function is more severely compromised than indicated by the results of the test, Metopirone may trigger transient adrenocortical insufficiency. This can be rapidly corrected by giving appropriate doses of corticosteroids.

Long-term treatment with Metopirone can cause hypertension as the result of excessive secretion of desoxycorticosterone.

The ability of the adrenal cortex to respond to exogenous ACTH should be demonstrated before Metopirone is employed as a test, as Metopirone may induce acute adrenal insufficiency in patients with reduced adrenal secretory capacity, as well as in patients with gross hypopituitarism.

Patients with liver cirrhosis often show a delayed response to Metopirone, due to liver damage delaying the metabolism of cortisol.

In cases of thyroid hypofunction, urinary steroid levels may rise very slowly, or not at all, in response to Metopirone.

Patients with ectopic Cushing's syndrome are at risk from opportunistic infections such as Pneumocystis Jirovecii pneumonia (previously termed Pneumocystis carinii pneumonia) during Metopirone treatment. Appropriate prophylactic treatment may be considered in this population.

When Metopirone is used as ACTH suppression test a diminished response was observed during pregnancy.

Excipients

Sodium ethylparaben (E215) and sodium propylparaben (E217) may cause allergic reactions (possibly delayed).

This medicine contains less than 1 mmol sodium (23 mg) per capsule, that is to say essentially 'sodium free'.

Anticonvulsants (e.g. phenytoin, barbiturates), psychotropic drugs (e.g. amitriptyline, chlorpromazine, alprazolam), hormone preparations, corticosteroids, antithyroid agents and cyproheptadine may affect the results of the Metopirone test (see Section 4.4, Special warnings and precautions for use).

Metopirone may potentiate paracetamol (acetaminophen) toxicity in humans.

Pregnancy

Unless the potential benefit outweighs the risk to the foetus Metopirone should not be given to pregnant women, since the drug can impair the biosynthesis of foetal- placental steroids. Animal reproduction studies adequate to evaluate teratogenicity and postnatal development have not been conducted with Metopirone (see section 5.3 Preclinical safety data).

Breast-feeding

Since it is not known whether metyrapone passes into the breast milk, Metopirone should not be given to breast-feeding women.

Fertility

No data are available from animal reproduction studies.

Patients should be warned of the potential hazards of driving or operating machinery if they experience side effects such as dizziness and sedation.

Adverse drug reactions (Table 1) are ranked under heading of frequency, the most frequent first, using the following convention: very common (≥1/10); common (≥1/100, <1/10); uncommon (≥1/1,000, <1/100); rare (≥1/10,000, <1/1,000) very rare (<1/10,000), not known (cannot be estimated from the available data). Within each frequency grouping, adverse reactions are ranked in order of decreasing seriousness.

Table 1. Adverse drug reactions

Reporting of suspected adverse reactions

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via:

United Kingdom

Yellow Card Scheme

Website: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.

Signs and symptoms: The clinical picture of acute Metopirone poisoning is characterised by gastrointestinal symptoms and acute adrenocortical insufficiency. Laboratory findings: hyponatraemia, hypochloraemia, hyperkalaemia. In patients under treatment with insulin or oral antidiabetics, the signs and symptoms of acute poisoning with Metopirone may be aggravated or modified.

Treatment: There is no specific antidote. Immediate treatment is essential in the management of metyrapone overdose, patients should be referred to hospital urgently for immediate medical attention. Treatment with activated charcoal may be considered if the overdose has been taken within 1 hour. In addition to general measures, a large dose of hydrocortisone should be administered at once, together with iv saline and glucose. This should be repeated as necessary in accordance with the patient's clinical condition. For a few days, blood pressure and fluid and electrolyte balance should be monitored.

Pharmacotherapeutic group: Diagnostic agent, test for pituitary function, ATC code: V04CD01.

Metopirone inhibits the enzyme responsible for the 11β-hydroxylation stage in the biosynthesis of cortisol and to a lesser extent, aldosterone. The fall in plasma concentration of circulating glucocorticoids stimulates ACTH secretion, via the feedback mechanism which accelerates steroid biosynthesis. As a result, 11- desoxycortisol, the precursor of cortisol, is released into the circulation, metabolised by the liver and excreted in the urine. Unlike cortisol, 11-desoxycortisol does not suppress ACTH secretion and its urinary metabolites may be measured.

These metabolites can easily be determined by measuring urinary 17- hydroxycorticosteroids (17-OHCS) or 17-ketogenic steroids (17-KGS). Metopirone is used as a diagnostic test on the basis of these properties, with plasma 11- desoxycortisol and urinary 17-OHCS measured as an index of pituitary ACTH responsiveness. Metopirone may also suppress biosynthesis of aldosterone, resulting in mild natriuresis.

Metyrapone is rapidly absorbed and eliminated from the plasma. Peak plasma levels usually occur one hour after ingestion of Metopirone; after a dose of 750mg Metopirone, plasma drug levels average 3.7µg/ml. Plasma drug levels decrease to a mean value of 0.5µg/ml 4 hours after dosing. The half-life of elimination of Metopirone from the plasma is 20 to 26 minutes.

Metyrapol, the reduced form of metyrapone, is the main active metabolite. Eight hours after a single oral dose, the ratio of metyrapone to metyrapol in the plasma is 1:1.5. Metyrapol takes about twice as long as metyrapone to be eliminated in the plasma.

Seventy-two hours after a first daily dose of 4.5g Metopirone (750mg every 4 hours), 5.3% of the total dose was excreted in the urine as metyrapone (9.2% in free form and 90.8% conjugated with glucuronic acid), and 38.5% in the form of metyrapol (8.1% in free form and 91.9% conjugated with glucuronic acid).

Pre-clinical data for Metopirone (metyrapone) reveal no special hazard for humans based on conventional studies of single and repeated dose toxicity. Metopirone was not mutagenic with or without metabolic activation in three strains of bacteria.

Animal reproduction studies adequate to evaluate teratogenicity and postnatal development have not been conducted with Metopirone. Currently, there are no available non-clinical studies conducted to investigate the genotoxicity, or carcinogenic potential of Metopirone.

Effects in pre-clinical studies were observed only at exposures considered sufficiently in excess of the maximum human exposure indicating little relevance to clinical use.

Capsule contents: Glycerin, polyethylene glycol 400, polyethylene glycol 4000 and water.

Capsule shell: Sodium ethylparaben (E215), ethyl vanillin, gelatin, glycerin 85%, p-methoxy acetophenone, sodium propylparaben (E217) and titanium oxide (E171).

None stated.

3 years

Store below 25°C. Keep the bottle tightly closed to protect the product from moisture.

High density polyethylene bottles of 100 capsules with child resistant polypropylene closure.

None stated.

HRA Pharma Rare Diseases

200 avenue de Paris

92320 CHATILLON

France

PL 51757/0001

25 June 1998

01 April 2020