12 July 2018 EMA/482350/2018 Corr. Information Management Division
Applications for new human medicines under evaluation by the Committee for Medicinal Products for Human Use July 2018
This document lists information on applications for centralised marketing authorisation for human medicines that the European Medicines Agency has received for evaluation. It includes the international non-proprietary names (INN) and therapeutic areas for all new innovative medicines under evaluation by the Committee for Medicinal Products for Human Use (CHMP). For generic and biosimilar medicines, it includes the INN (active moiety only, with no information on salt, ester or derivative) and therapeutic area. This list only includes information for medicines whose applications have been validated at the time the report was compiled. The information in this report was compiled on 12 July 2018. Information on designated orphan medicines that are being assessed for marketing authorisation is also available in the monthly reports of the Committee for Orphan Medicinal Products (COMP). Information in bold corresponds to new entries in the monthly list. Entries are removed from this list once the medicine has received a positive or negative opinion from the CHMP or when the applicant has withdrawn the application. The Agency publishes information on these opinions and withdrawn applications on its website. Information on CHMP opinions is also published in the monthly CHMP highlights.
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Based on the ATC therapeutic sub-group. Correction: Angiotensin II (acetate) application was first recorded as being reviewed under EMA’s accelerated assessment programme, which is not the case. i
Non-orphan generic and biosimilar medicinal products International non-proprietary name /
Therapeutic area
i
Common Name
Total number of applications
Adalimumab
Immunosuppressants
2
Ambrisentan
Antihypertensives
2
Atazanavir
Antivirals for systemic use Antineoplastic medicines Other nervous system medicines Antineoplastic medicines Other therapeutic medicines Antineoplastic medicines
Applications for new human medicines under evaluation by the ...
Jul 12, 2018 - by the Committee for Medicinal Products for Human Use. July 2018. This document lists information on applications for centralised marketing ...
Dec 2, 2016 - Send a question via our website www.ema.europa.eu/contact ... non-proprietary names (INN) and therapeutic areas for all new ... also available in the monthly reports of the Committee for Orphan Medicinal Products (COMP).
May 3, 2017 - Send a question via our website www.ema.europa.eu/contact ... non-proprietary names (INN) and therapeutic areas for all new ... also available in the monthly reports of the Committee for Orphan Medicinal Products (COMP).
Aug 3, 2016 - Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5555 ... non-proprietary names (INN) and therapeutic areas for all new innovative medicines under evaluation ... Sex hormones and modulators of the genital system.
Mar 8, 2018 - Treatment of uterine fibroids. Haematology. New medicines authorised. ⢠Adynovi (rurioctocog alfa pegol). Treatment and prevention of bleeding in patients with haemophilia A. New information on authorised medicines. ⢠Feraccru (ferr
Treatment of cystine crystal deposits in the eye. New information on authorised medicines. Lucentis (ranibizumab) - change in indication. Treatment of visual ...
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