Overview

This is a summary of the European public assessment report (EPAR) for Scenesse. It explains how the Agency assessed the medicine to recommend its authorisation in the EU and its conditions of use. It is not intended to provide practical advice on how to use Scenesse.

For practical information about using Scenesse, patients should read the package leaflet or contact their doctor or pharmacist.

Scenesse is an implant used to treat patients with erythropoietic protoporphyria (EPP), a rare disease that causes intolerance to light.

In patients with EPP, exposure to light can lead to symptoms such as pain and swelling of the skin, which prevent patients from being able to spend time outdoors or in places with bright light. Scenesse is used to help prevent or reduce these symptoms so that these patients can lead more normal lives.

Because the number of patients with EPP is low, the disease is considered ‘rare’, and Scenesse was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 8 May 2008.

Scenesse contains the active substance afamelanotide.

Scenesse is only prescribed by specialist doctors in recognised centres for treating EPP and should only be used by doctors who have been properly trained.

One Scenesse implant is injected under the patient’s skin once every 2 months, before and during periods of high sunlight exposure, e.g. from spring to autumn. The number of implants per year depends on how much protection from the sun is needed. Three implants per year are recommended; the maximum number is 4. Patients should be observed for allergic reactions for 30 minutes after the injection of each implant.

For more information on how to use Scenesse, see the summary of product characteristics (also part of the EPAR).

The active substance in Scenesse, afamelanotide, is similar to a hormone in the body known as alpha-melanocyte stimulating hormone, which stimulates the production of a brown-black pigment in the skin. This pigment, known as eumelanin, is produced during exposure to sunlight to block the penetration of light into cells.

Patients with EPP have high levels of a substance called protoporphyrin IX in the body. Protoporphyrin IX is phototoxic and, when exposed to light, causes the painful reactions seen with this condition. By stimulating the production of eumelanin in the skin, Scenesse reduces the penetration of light through the skin, thus helping to prevent the painful reactions.

Scenesse has been shown in a study to lead to an increase in the amount of time patients can spend in sunlight. In the study, involving 93 patients with EPP, patients were treated with either Scenesse or a placebo (a dummy treatment) over a six?month period. Daily records of exposure to sunlight between 10 am and 6 pm showed that patients treated with Scenesse spent on average 116 hours in direct sunlight without experiencing pain during the six?month period compared with 61 hours for patients treated with placebo.

The most common side effects seen in studies with Scenesse were nausea (feeling sick), headache and reactions at the implant site (such as discoloration, pain and redness). These affected around 1 in 5 patients and were generally mild in severity.

Scenesse must not be used in patients with reduced liver or kidney function. For the full list of all side effects and restrictions with Scenesse, see the package leaflet.

The Agency’s Committee for Medicinal Products for Human Use (CHMP) decided that Scenesse’s benefits are greater than its risks and recommended that it be given marketing authorisation. The CHMP noted that Scenesse led to an increase in the amount of time patients could spend in direct sunlight without experiencing pain. Although the additional time spent in sunlight was small, the Committee considered the possible improvements in quality of life, the unmet medical need in patients with EPP, and the mild side effects seen during short-term treatment with the medicine in deciding to recommend approval for Scenesse in the EU. The Committee also consulted individual patients and experts on their experience with Scenesse.

Scenesse has been authorised under ‘exceptional circumstances’. This is because it has not been possible to obtain complete information about the benefits of Scenesse, in part due to the rarity of the disease. Every year, the European Medicines Agency will review any new information that becomes available and this summary will be updated as necessary.

Since Scenesse has been approved under exceptional circumstances, the company that markets Scenesse will provide longer-tem data on the benefits and safety of the medicine from an EU registry of patients taking the medicine.

A risk management plan has been developed to ensure that Scenesse is used as safely as possible. Based on this plan, safety information has been included in the summary of product characteristics and the package leaflet for Scenesse, including information on the appropriate precautions to be followed by healthcare professionals and patients.

In addition, the company that markets Scenesse will ensure that doctors receive educational material and are trained in how to use the medicine. Doctors will also be given information on the EU registry.

Further information can be found in the Scenesse : EPAR - Risk-management-plan summary.

The European Commission granted a marketing authorisation valid throughout the European Union for Scenesse on 22 December 2014.

For more information about treatment with Scenesse, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.

Scenesse : EPAR - Summary for the public

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Scenesse : EPAR - Risk-management-plan summary

Product information

Scenesse : EPAR - Product Information

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Latest procedure affecting product information: IAIN/0040

04/01/2022

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This medicine’s product information is available in all official EU languages.
Select 'available languages' to access the language you need.

Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

Scenesse : EPAR - All Authorised presentations

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Product details

Name of medicine
Scenesse
Active substance
afamelanotide
International non-proprietary name (INN) or common name
afamelanotide
Therapeutic area (MeSH)
Protoporphyria, Erythropoietic
Anatomical therapeutic chemical (ATC) code
D02BB02

Pharmacotherapeutic group

Emollients and protectives

Therapeutic indication

Prevention of phototoxicity in adult patients with erythropoietic protoporphyria (EPP).

Authorisation details

EMA product number
EMEA/H/C/002548

Additional monitoring

This medicine is under additional monitoring, meaning that it is monitored even more intensively than other medicines. For more information, see Medicines under additional monitoring.

Exceptional circumstances

This medicine was authorised under exceptional circumstances, because the applicant was unable to provide comprehensive data on the efficacy and safety of the medicine under normal conditions of use. This can happen because the condition to be treated is rare or because collection of full information is not possible or is unethical. For more information, see Pre-authorisation guidance.

Orphan

This medicine was designated an orphan medicine. This means that it was developed for use against a rare, life-threatening or chronically debilitating condition or, for economic reasons, it would be unlikely to have been developed without incentives. For more information, see Orphan designation.

Marketing authorisation holder
Clinuvel Europe Limited

10 Earlsfort Terrace
Dublin 2 D04 T380
Ireland

Opinion adopted
23/10/2014
Marketing authorisation issued
22/12/2014
Revision
9

Assessment history

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

Scenesse : EPAR - Public assessment report

CHMP summary of positive opinion for Scenesse

Topics

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