Basic Information
EMA regulatory identification and product classification information
EMA Identifiers
Overview Summary
Comprehensive product overview and regulatory summary
On 13 December 2024, the European Commission withdrew the marketing authorisation for Alofisel (darvadstrocel) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Takeda Pharma A/S, which notified the European Commission of its decision to permanently stop the marketing of the product in the EU.
Alofisel was granted marketing authorisation in the EU on 23 March 2018 for the treatment of complex perianal fistulas. The European Public Assessment Report (EPAR) for Alofisel is updated to indicate that the marketing authorisation is no longer valid.
Active Substances (1)
darvadstrocel
Documents (12)
Alofisel : EPAR - Public assessment report
April 3, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP summary of positive opinion for Alofisel
December 15, 2017
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Alofisel : EPAR - Procedural steps taken and scientific information after authorisation
May 29, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
Alofisel : Orphan maintenance assessment report (initial authorisation)
April 3, 2018
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Alofisel : EPAR - Public assessment report
April 3, 2018
INITIAL_MARKETING_AUTHORISATION_DOCUMENTS
Alofisel-H-C-004258-II-0051-G : EPAR - Assessment report - Variation
March 26, 2025
CHANGES_SINCE_INITIAL_AUTHORISATION
Alofisel : Orphan maintenance assessment report (initial authorisation)
April 3, 2018
CHANGES_SINCE_INITIAL_AUTHORISATION
CHMP summary of positive opinion for Alofisel
December 15, 2017
CHANGES_SINCE_INITIAL_AUTHORISATION
Alofisel : EPAR - Product information
April 3, 2018
DRUG_PRODUCT_INFORMATION
Alofisel : EPAR - All Authorised presentations
April 3, 2018
AUTHORISED_PRESENTATIONS
Alofisel : EPAR - Summary for the public
April 3, 2018
OVERVIEW_DOCUMENT
Alofisel : EPAR - Risk-management-plan summary
July 29, 2019
RISK_MANAGEMENT_PLAN_SUMMARY
Overview Q&A (8)
Question
How is Alofisel used?
Answer
Alofisel should be given only by specialist doctors experienced in the diagnosis and treatment of the condition for which it is used. The medicine can only be obtained with a prescription.
Alofisel is given just once. The patient is given an anaesthetic (either to put the patient to sleep or to numb the treatment area). After preparing the fistulas for treatment in an operating room, the contents of two vials (each containing 30 million cells) are injected around the internal openings and two further vials through the external openings into the walls of the fistula.
For further information, see the package leaflet.
Question
How does Alofisel work?
Answer
Alofisel is made up of ‘mesenchymal stem cells’ from the fat tissue of a donor. To make this medicine, the cells are selected and cultivated in the laboratory to increase their number. When injected into the walls of the fistula, these cells can help to reduce inflammation and support the growth of new tissue. This encourages the fistula to heal and close.
Question
What benefits of Alofisel have been shown in studies?
Answer
One main study, involving 212 patients with Crohn’s disease and complex anal fistulas, found Alofisel more effective than placebo (a dummy treatment) 24 weeks after treatment. Treatment with conventional or biological medicines had not worked in these patients. The main measure of effectiveness, called ‘combined remission’, was the closing of abnormal external openings together with lack of fluid collections of more than 2 cm associated with internal passages (since these are likely to re-open the fistula). Of the patients treated with Alofisel, combined remission occurred in almost 50% of patients (53 out of 107); this compared with 34% of patients (36 out of 105) receiving placebo.
Question
What are the risks associated with Alofisel?
Answer
The most common side effects with Alofisel (which may affect up to 1 in 10 people) are anal abscess (a swollen area with a collection of pus), proctalgia (anal pain), anal fistula and pain during treatment.
Alofisel must not be used in patients with hypersensitivity (allergy) to bovine serum (the clear liquid in blood from cattle) or to any of the ingredients of Alofisel.
Question
Why is Alofisel approved?
Answer
The European Medicines Agency decided that Alofisel’s benefits are greater than its risks and recommended that it be approved for use in the EU. Alofisel is of value in the treatment of complex anal fistulas that have not responded well to other treatments. Data on the safety of Alofisel are limited but they provide enough information on the pattern of side effects.
Question
What measures are being taken to ensure the safe and effective use of Alofisel?
Answer
The company that markets Alofisel will provide educational material for healthcare professionals on how to give the medicine correctly and on the possibility of passing on an infection to the patient. The company will also complete a study to continue to collect information on the effectiveness and safety of Alofisel.
Recommendations and precautions to be followed by healthcare professionals and patients for the safe and effective use of Alofisel have also been included in the summary of product characteristics and the package leaflet.
Question
Other information about Alofisel
Answer
The European Commission granted a marketing authorisation valid throughout the European Union for Alofisel on 23 March 2018.
For more information about treatment with Alofisel, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist.
Question
What is Alofisel and what is it used for?
Answer
Alofisel is a medicine that is used to treat complex anal fistulas in adults with Crohn’s disease (an inflammatory condition of the gut) when a conventional or biological medicine has not worked well enough.
Fistulas are abnormal passages between the lower parts of the gut and the skin near the anus. Complex fistulas are those with several abnormal passages and openings, or with passages that go deep inside the body, or where there are other complications such as collection of pus.
Alofisel contains the active substance darvadstrocel, which comprises stem cells removed from fat tissue of adult donors. It is a type of advanced therapy medicine called a ‘somatic cell therapy product’. This is a type of medicine that contains cells or tissues that have been modified so that they can be used to cure, diagnose or prevent a disease.
Because the number of patients with anal fistula is low, the disease is considered ‘rare’, and Alofisel was designated an ‘orphan medicine’ (a medicine used in rare diseases) on 8 October 2009.
