Is Corifollitropin alfa registered with the SFDA?

The SFDA human drug list (edition 4-2026, as published by the Council of Health Insurance) lists 1 valid registration of Corifollitropin alfa, including ELONVA 150 mcg Solution For Injection (150 µg, Solution for injection, SAR 2168.40).

Is Corifollitropin alfa authorised in the European Union?

EMA lists 1 centrally authorised medicine containing Corifollitropin alfa: Elonva.

Active substance

Corifollitropin alfa

SFDA 2
EMA 1

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade name	Strength	Form · route	Pack	Public price	Type	Company	Status
ELONVA 150 mcg Solution For Injection	150 µg	Solution for injection · Subcutaneous use	1 Pre-filled syringe	SAR 2168.40	NCE · Prescription	N.V. Organon	Valid
ELONVA 100 mcg Solution For Injection	100 µg	Solution for injection · Subcutaneous use	1 Pre-filled syringe	SAR 1436.35	NCE · Prescription	N.V. Organon	Withdrawn by MAH · Not Marketed

EMA European Union — centrally authorised medicines

Elonva Organon N.V. · Authorised · authorised 25 Jan 2010 · ATC G03GA09

Therapeutic indication (EMA)

Controlled Ovarian Stimulation (COS) in combination with a GnRH antagonist for the development of multiple follicles in women participating in an Assisted Reproductive Technology (ART) program. Elonva is indicated for the treatment of adolescent males (14 to less than 18 years and older) with hypogonadotropic hypogonadism, in combination with human Chorionic Gonadotropin (hCG).

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.