ELONVA Solution for injection Ref.[7198] Active ingredients: Corifollitropin alfa

Source: European Medicines Agency (EU)  Revision Year: 2022  Publisher: N.V. Organon, Kloosterstraat 6, 5349 AB Oss, The Netherlands

Product name and form

Elonva 100 micrograms solution for injection.

Elonva 150 micrograms solution for injection.

Pharmaceutical Form

Solution for injection (injection).

Clear and colourless aqueous solution.

Qualitative and quantitative composition

Elonva 100 micrograms solution for injection: Each pre-filled syringe contains 100 micrograms of corifollitropin alfa* in 0.5 mL solution for injection.

Elonva 150 micrograms solution for injection: Each pre-filled syringe contains 150 micrograms of corifollitropin alfa* in 0.5 mL solution for injection.

* corifollitropin alfa is a glycoprotein produced in Chinese Hamster Ovary (CHO) cells by recombinant DNA technology.

Excipient(s) with known effect: This medicinal product contains less than 1 mmol sodium (23 mg) per injection, that is to say essentially ‘sodium-free’.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Corifollitropin alfa

Corifollitropin alfa is designed as a sustained follicle stimulant with the same pharmacodynamic profile as (rec)FSH, but with a markedly prolonged duration of FSH activity. Corifollitropin alfa does not display any intrinsic LH/hCG activity.

List of Excipients

Sodium citrate
Sucrose
Polysorbate 20
Methionine
Sodium hydroxide (for pH adjustment)
Hydrochloric acid (for pH adjustment)
Water for injections

Pack sizes and marketing

Elonva is supplied in pre-filled luerlock syringes of 1 mL (type I hydrolytic glass), closed with a bromobutyl elastomer plunger and a tip cap. The syringe is equipped with an automatic safety system to prevent needle stick injuries after use and is packed together with a sterile injection needle. Each pre-filled syringe contains 0.5 mL solution for injection.

Elonva is available in pack sizes of 1 pre-filled syringe.

Marketing authorization holder

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

Marketing authorization dates and numbers

EU/1/09/609/001
EU/1/09/609/002

Date of first authorisation: 25 January 2010
Date of latest renewal: 22 August 2014

Drugs

Drug Countries
ELONVA Austria, Australia, Brazil, Cyprus, Estonia, Spain, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Turkey

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