CHMP News – November 2014
CHMP recommended ten new medicines for approval, two orphans among those
Ten new medicines have been recommended for approval at the November 2014 meeting of the Committee for Medicinal Products for Human Use (CHMP). The CHMP has recommended:
- granting a marketing authorisation for Cerdelga (eliglustat), an orphan medicine for the treatment of Gaucher disease type 1. For more information please see the press release in the grid below.
- The Committee also gave positive opinions for Exviera (dasabuvir) and Viekirax (ombitasvir + paritaprevir + ritonavir) for the treatment of chronic hepatitis C. Both products were reviewed under accelerated assessment and belong to a new generation of antiviral products for chronic hepatitis C infection that have high cure rates and have recently reshaped the treatment landscape for the disease.
- The orphan medicine Ofev (nintedanib) received a positive opinion for the treatment of idiopathic pulmonary fibrosis.
- Cosentyx (secukinumab) and Otezla (apremilast) were recommended by the CHMP as new treatment options for psoriasis.
- Senshio (ospemifene) received a positive opinion for the treatment of vulvar and vaginal atrophy and Zontivity (vorapaxar) was recommended for the reduction of atherothrombotic events.
- The CHMP also granted positive opinions for two new informed consent applications: Sevelamer carbonate Zentiva (sevelamer) for the control of hyperphosphataemia in adults receiving haemodialysis or peritoneal dialysis and Rasagiline ratiopharm (rasagiline) for the treatment of Parkinson’s disease.
Two recommendations on extensions of therapeutic indications
The Committee recommended extensions of indications for Inductos and Travatan.
Change to non-prescription status
The CHMP recommended a change in classification status from prescription to non-prescription for the emergency contraceptive ellaOne (ulipristal acetate). For more information, please see here.
Outcome of safety review
The CHMP concluded its review of Corlentor/Procoralan (ivabradine) and made recommendations aimed at reducing the risk of heart problems, including heart attack and bradycardia (excessively low heart rate), in patients taking the medicine for angina. Corlentor/Procoralan is used to treat symptoms of angina (chest pain due to problems with the blood flow to the heart) and to treat heart failure.
Update on Tecfidera
The CHMP discussed a fatal case of progressive multifocal leukoencephalopathy (PML) which was reported in a patient treated with Tecfidera (dimethyl fumarate), a medicine used for relapsing-remitting multiple sclerosis. This is the first case of PML, a rare viral brain infection with symptoms that can be similar to those of a multiple sclerosis attack, to be reported in association with Tecfidera. The fatal case of PML occurred after long-term treatment with the medicine in a patient experiencing severe long-term lymphopenia, a known possible side effect of Tecfidera.
The CHMP recommended that a letter is sent to healthcare professionals to alert them to the potential risk of PML and to allow them to inform their patients.
Withdrawals of applications
The application for a marketing authorisation for Egranli has been withdrawn.
For more information on the CHMP November 2014 meeting, please see on the EMA webpages, or here.