MedPath
EMA Approval

Circadin

N05CH01

melatonin

Psycholeptics

melatonin

Sleep Initiation and Maintenance Disorders

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeN05CH01
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine.

If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

Authorisations (2)

EMEA/H/C/000695

RAD Neurim Pharmaceuticals EEC SARL,4 rue de Marivaux,75002 Paris,France

Authorised

June 29, 2007

EMEA/H/C/000695

RAD Neurim Pharmaceuticals EEC SARL,4 rue de Marivaux,75002 Paris,France

Authorised

June 29, 2007

Active Substances (1)

melatonin

Documents (12)

Circadin : EPAR - Procedural steps taken and scientific information after authorisation

May 5, 2025

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - Procedural steps taken and scientific information after authorisation (archive)

April 23, 2009

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - Summary for the public

July 10, 2007

OVERVIEW_DOCUMENT

Circadin : EPAR - Procedural steps taken before authorisation

July 10, 2007

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Circadin : EPAR - Scientific Discussion

July 10, 2007

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Circadin-H-C-695-P46-0019 : EPAR - Assessment Report

February 12, 2015

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - All Authorised presentations

July 10, 2007

AUTHORISED_PRESENTATIONS

Circadin : EPAR - Product Information

March 9, 2023

DRUG_PRODUCT_INFORMATION

Circadin-H-C-PSUSA-00001963-201409 : EPAR - Scientific conclusions and grounds recommending the variation to the terms of the marketing authorisation

August 12, 2015

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - Scientific Discussion

July 10, 2007

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - Procedural steps taken before authorisation

July 10, 2007

CHANGES_SINCE_INITIAL_AUTHORISATION

Circadin : EPAR - Procedural steps taken and scientific information after authorisation

May 5, 2025

CHANGES_SINCE_INITIAL_AUTHORISATION

Overview Q&A (9)

Question

Other information about Circadin

Answer

The European Commission granted a marketing authorisation valid throughout the European Union for Circadin to Neurim Pharmaceuticals EEC Limited on 29 June 2007.

Question

How is Circadin used?

Answer

The recommended dose of Circadin is one tablet a day, taken one to two hours before bedtime and after food. This dose can be continued for up to 13 weeks.

Question

How does Circadin work?

Answer

The active substance in Circadin, melatonin, is a naturally occurring hormone, which is normally produced by a gland in the brain called the pineal gland. Melatonin is involved in coordinating the body’s sleep cycle by acting on cells in specific areas of the brain and helping to bring about sleep. Its levels in the blood normally increase after the onset of darkness and peak in the middle of the night. Older people may produce less melatonin, leading to the development of insomnia. By replacing the hormone, Circadin increases blood levels of melatonin, helping them to sleep. Because Circadin tablets release melatonin slowly over a few hours, they mimic the natural production of melatonin in the body.

Question

What benefit has Circadin shown during the studies?

Answer

Circadin was more effective than placebo at improving quality of sleep and the patients’ ability to function normally on the following day. When the results of all three studies were looked at together, 32% of the patients taking Circadin (86 out of 265) reported a significant improvement in symptoms after three weeks, compared with 19% of those taking placebo (51 out of 272).

The additional study showed that Circadin was more effective than placebo for at least 13 weeks.

Question

Why has Circadin been approved?

Answer

The CHMP decided that, although Circadin has only been shown to have a small effect in a relatively small number of patients, its benefits are greater than its risks. The Committee recommended that Circadin be given marketing authorisation.

Question

How has Circadin been studied?

Answer

Circadin has been compared with placebo (a dummy treatment) in three main studies involving a total of 681 patients aged over 55 years with primary insomnia. The main measure of effectiveness was the number of patients who reported a significant improvement in their quality of sleep and ability to function normally on the following day, after three weeks of treatment. The patients assessed the severity of their symptoms using a standard questionnaire.

An additional study compared the effects of Circadin and placebo for up to six months.

Question

What is Circadin?

Answer

Circadin is a medicine that contains the active substance melatonin. It is available as white prolonged-release tablets (2 mg). ‘Prolonged-release’ means that melatonin is released slowly from the tablet over a few hours.

Question

What is Circadin used for?

Answer

Circadin is used on its own for the short-term treatment of primary insomnia (poor quality of sleep) in patients aged 55 years or over. ‘Primary’ means that the insomnia does not have any identified cause, including any medical, mental or environmental cause.

The medicine can only be obtained with a prescription.

Question

What is the risk associated with Circadin?

Answer

Side effects with Circadin are not common. However, the following side effects are seen in between 1 and 10 patients in 1,000: irritability, nervousness, restlessness, insomnia, abnormal dreams, anxiety, migraine, lethargy (lack of energy), psychomotor hyperactivity (restlessness with increased activity), dizziness, somnolence (sleepiness), hypertension (high blood pressure), abdominal pain (stomach ache), dyspepsia (heartburn), mouth ulcers, dry mouth, hyperbilirubinaemia (high blood levels of bilirubin, a breakdown product of red blood cells, which can cause yellowing of the skin and eyes), dermatitis (skin inflammation), night sweats, pruritus (itching), rash, dry skin, pain in the extremities (arms and legs), symptoms of the menopause, asthenia (weakness), chest pain, glycosuria (sugar in the urine), proteinuria (protein in the urine), abnormal liver function tests and increased weight. For the full list of all side effects reported with Circadin, see the package leaflet.

Circadin can cause drowsiness, so it should be used with caution if this could pose a risk to safety, including in people who need to drive or use machines. Patients should avoid alcohol before, during and after taking Circadin.

Circadin should not be used in people who may be hypersensitive (allergic) to melatonin or any of the other ingredients.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Circadin - EMA Approval | MedPath