MedPath
EMA Approval

Orgalutran

H01CC01

ganirelix

Pituitary and hypothalamic hormones and analogues

Basic Information

EMA regulatory identification and product classification information

EMA Identifiers

ATC CodeH01CC01
EMA European Classification

Overview Summary

Comprehensive product overview and regulatory summary

This is a summary of the European public assessment report (EPAR) for Orgalutran. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Orgalutran.

Authorisations (1)

EMEA/H/C/000274

N.V. Organon,Kloosterstraat 6,5349 AB Oss,The Netherlands

Authorised

May 16, 2000

Active Substances (1)

ganirelix

Documents (10)

Orgalutran : EPAR - Summary for the public

October 1, 2006

OVERVIEW_DOCUMENT

Orgalutran : EPAR - Steps taken after authorisation when a cutoff date has been used

October 20, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Orgalutran : EPAR - Scientific Discussion

October 20, 2005

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Orgalutran : EPAR - Procedural steps taken before authorisation

October 20, 2005

INITIAL_MARKETING_AUTHORISATION_DOCUMENTS

Orgalutran : EPAR - Product information

February 28, 2008

DRUG_PRODUCT_INFORMATION

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

February 28, 2008

CHANGES_SINCE_INITIAL_AUTHORISATION

Orgalutran : EPAR - Risk management plan

May 30, 2024

RISK_MANAGEMENT_PLAN_SUMMARY

Orgalutran : EPAR - Scientific Discussion

October 20, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Orgalutran : EPAR - Procedural steps taken before authorisation

October 20, 2005

CHANGES_SINCE_INITIAL_AUTHORISATION

Orgalutran : EPAR - All Authorised presentations

October 20, 2005

AUTHORISED_PRESENTATIONS

Overview Q&A (9)

Question

How is Orgalutran used?

Answer

Treatment with Orgalutran should be carried out by a doctor who has experience in this type of fertility treatment.

Orgalutran is given as a single 0.25-mg injection under the skin once a day. Treatment should start on day 5 or 6 after the start of ovarian stimulation with follicle-stimulating hormone (FSH) or corifollitropin alfa (a modified FSH). When treatment should start depends on how well the ovaries are responding to stimulation. Treatment with Orgalutran should be continued up to the day that there are enough large follicles (small sacs in the ovary that hold the eggs).

Orgalutran is preferably given into the upper leg. The patient or her partner may give the injections themselves, if they have been trained and have access to expert advice. For further information on how to use Orgalutran, see the package leaflet.

Question

How does Orgalutran work?

Answer

The active substance in Orgalutran, ganirelix, blocks the receptors for a natural hormone called gonadotrophin-releasing hormone (GnRH). GnRH controls the secretion of another hormone called luteinising hormone (LH), which causes ovulation (the release of eggs during the menstrual cycle). During fertility treatment, ovarian stimulation is normally used to make the ovaries produce more than one egg. A few days later, a hormone called human chorionic gonadotrophin (hCG) is given to trigger ovulation, and the eggs are then harvested. By blocking the effect of GnRH, Orgalutran stops the production of LH, and therefore prevents premature ovulation.

Question

Other information about Orgalutran

Answer

The European Commission granted a marketing authorisation valid throughout the European Union for Orgalutran to N.V. Organon on 17 May 2000. The marketing authorisation is valid for an unlimited period.

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

Question

Why has Orgalutran been approved?

Answer

The CHMP decided that Orgalutran’s benefits are greater than its risks and recommended that it be given marketing authorisation.

Question

What is Orgalutran?

Answer

Orgalutran is a solution for injection in a prefilled syringe. Each syringe contains 0.25 mg of the active substance, ganirelix.

Question

What is Orgalutran used for?

Answer

Orgalutran is used to prevent premature ovulation (early release of eggs from the ovary) in women having fertility treatment and who are having ovarian stimulation (stimulation of the ovaries so that they produce more eggs). In premature ovulation, the ovaries release eggs that may be immature and not suitable for use in techniques such as in-vitro fertilisation.

The medicine can only be obtained with a prescription.

Question

How has Orgalutran been studied?

Answer

The ability of Orgalutran to prevent premature ovulation has been studied in three main studies involving 1,335 women. Orgalutran was compared with buserelin, leuprorelin, and triptorelin (GnRH agonists: another group of medicines used to prevent premature ovulation, which work by stimulating the receptor for GnRH to such an extent that the body stops making LH). The main measures of effectiveness were the number of eggs that could be harvested and the number of women who became pregnant.

Question

What benefit has Orgalutran shown during the studies?

Answer

After treatment with Orgalutran, the average number of eggs that could be harvested was between 7.9 and 11.6 per woman. Between 20% and 31% of the women became pregnant. Overall, the values for the GnRH agonists were slightly higher.

Question

What is the risk associated with Orgalutran?

Answer

In studies, the most common side effect with Orgalutran (seen in more than 1 patient in 10) was a skin reaction at the injection site, mainly redness with or without swelling. For the full list of all side effects reported with Orgalutran, see the package leaflet.

Orgalutran should not be used in people who may be hypersensitive (allergic) to ganirelix, to any of the other ingredients, to GnRH or to other GnRH analogues (medicines that have a similar structure to GnRH and modify the activity of GnRH in the body). It must not be used by women who are pregnant or breast-feeding, or in women with moderate or severe kidney or liver disease. For the full list of restrictions, see the package leaflet.

Sometimes, the ovaries can over-respond to stimulation. This is called ‘ovarian hyperstimulation syndrome’. Doctors and patients must be aware of this possibility.

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