Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 25-28 January 2016

Six medicines, of which two have been fast-tracked, receive positive opinions from the Committee

The European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) recommended six new medicines for marketing authorisation at its January 2016 meeting.

The CHMP recommended granting a marketing authorisation, under accelerated assessment, for Empliciti (elotuzumab) for the treatment of multiple myeloma. Empliciti is to be used in combination with lenalidomide and dexamethasone for the treatment of patients who have received at least one prior therapy. Empliciti has an orphan designation. For more details, please refer to the press release in the grid below.

The Committee recommended granting a marketing authorisation for Coagadex (factor X), for the treatment of factor X deficiency, a rare inherited bleeding disorder. Coagadex has an orphan designation and was reviewed under accelerated assessment. For more details, please refer to the press release in the grid below.

Uptravi (selexipag) was recommended by the Committee for the treatment of pulmonary arterial hypertension. Uptravi has an orphan designation.

Three generic medicines received a positive opinion from the Committee: Amlodipine-Valsartan Mylan (amlodipine/valsartan) for the treatment of essential hypertension, Rasagiline Mylan (rasagiline) for the treatment of idiopathic Parkinson's disease and Zonisamide Mylan (zonisamide) for the treatment of partial seizures, with or without secondary generalisation.

Two recommendations on extensions of therapeutic indications

The Committee recommended extensions of indication for Revlimid and Revolade.

Request for re-examination of CHMP recommendation

The applicant for Dropcys (mercaptamine hydrochloride) has requested a re-examination of the CHMP's negative opinion for this medicine adopted at the December 2015 meeting. Upon receipt of the grounds of the request for re-examination, the CHMP will re-examine this opinion and issue a final opinion.

Review of metformin-containing medicines started

The CHMP has started a review of all metformin-containing medicines. Metformin, alone or in combination with other medicines, is widely used for treating type 2 diabetes. This review was requested by the Dutch medicines agency (the Medicines Evaluation Board, MEB) following a routine evaluation which showed that the prescribing information of these medicines varies in its advice on how the medicine should be used in patients with reduced kidney function. For more information, please see the start of referral document in the grid below.

Update on Ebola

The CHMP has adopted a final scientific opinion following its review of experimental Ebola treatments. The final report includes information on nine experimental medicines intended for the treatment of people infected with the Ebola virus: BCX4430, Brincidofovir, Favipiravir, TKM-Ebola, AVI-7537, ZMapp, Anti-Ebola F(ab')2, GS-5734 and Ebotab. The assessment report for this review will be published shortly.

Withdrawal of application

An application for marketing authorisation for Aripiprazole Mylan (aripiprazole) has been withdrawn. A question-and-answer document on this withdrawal is available below.

Agenda and minutes

The agenda of the January 2016 meeting is published on EMA's website. Minutes of the December 2015 CHMP meeting will be published next week.

CHMP statistics

Key figures from the January 2016 CHMP meeting are represented in the graphic below.

More information on this, and all other outcomes of the CHMP's January 2016 meeting, is available in the grid below.

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Positive recommendations on new medicines

Name of medicine	Uptravi
INN	selexipag
Marketing-authorisation applicant	Actelion Registration Ltd
Therapeutic indication	Treatment of pulmonary arterial hypertension
More information	Summary of opinion for Uptravi

Positive recommendations on new generic medicines

Name of medicine	Amlodipine-Valsartan Mylan
INN	amlodipine / valsartan
Marketing-authorisation applicant	Mylan S.A.S.
Therapeutic indication	Treatment of essential hypertension
More information	Summary of opinion for Amlodipine-Valsartan Mylan

Name of medicine	Rasagiline Mylan
INN	rasagiline
Marketing-authorisation applicant	Mylan S.A.S.
Therapeutic indication	Treatment of idiopathic Parkinson's disease
More information	Summary of opinion for Rasagiline Mylan

Name of medicine	Zonisamide Mylan
INN	zonisamide
Marketing-authorisation applicant	Mylan S.A.S.
Therapeutic indication	Treatment of partial seizures, with or without secondary generalisation
More information	Summary of opinion for Zonisamide Mylan

Positive recommendations on extensions of therapeutic indications

Start of referral

Outcome of arbitration procedure

Withdrawal of application

Name of medicine	Aripiprazole Mylan
INN	aripiprazole
More information	Questions and answers on Aripiprazole Mylan

Other updates

Opinions on annual re-assessments, renewals of marketing authorisations and accelerated assessment procedures

Opinions on safety variations

Start of Community reviews

Scientific advice and protocol assistance

Guidelines and concept papers adopted

Organisational matters