11 June 2019 EMA/PRAC/325596/2019 Inspections, Human Medicines Pharmacovigilance and Committees Division Pharmacovigilance Risk Assessment Committee (PRAC) Draft agenda for the meeting on 11-14 June 2019 Chair: Sabine Straus – Vice-Chair: Martin Huber 11 June 2019, 13:00 – 19:30, room 1/C 12 June 2019, 08:30 – 19:30, room 1/C 13 June 2019, 08:30 – 19:30, room 1/C 14 June 2019, 08:30 – 16:00, room 1/C Organisational, regulatory and methodological matters (ORGAM) 27 June 2019, 09:00-12:00, room 6/D, via teleconference Health and safety information In accordance with the Agency’s health and safety policy, delegates are to be briefed on health, safety and emergency information and procedures prior to the start of the meeting. Disclaimers Some of the information contained in this agenda is considered commercially confidential or sensitive and therefore not disclosed. With regard to intended therapeutic indications or procedure scopes listed against products, it must be noted that these may not reflect the full wording proposed by applicants and may also change during the course of the review. Additional details on some of these procedures will be published in the PRAC meeting highlights once the procedures are finalised. Of note, this agenda is a working document primarily designed for PRAC members and the work the Committee undertakes. Note on access to documents Some documents mentioned in the agenda cannot be released at present following a request for access to documents within the framework of Regulation (EC) No 1049/2001 as they are subject to on- going procedures for which a final decision has not yet been adopted. They will become public when adopted or considered public according to the principles stated in the Agency policy on access to documents (EMA/127362/2006, Rev. 1). Official address Domenico Scarlattilaan 6 ● 1083 HS Amsterdam ● The Netherlands Address for visits and deliveries Refer to www.ema.europa.eu/how-to-find-us Send us a question Go to www.ema.europa.eu/contact Telephone +31 (0)88 781 6000 An agency of the European Union © European Medicines Agency, 2019. Reproduction is authorised provided the source is acknowledged. Table of contents 1. Introduction 13 1.1. Welcome and declarations of interest of members, alternates and experts .......... 13 1.2. Agenda of the meeting on 11-14 June 2019 ......................................................... 13 1.3. Minutes of the previous meeting on 13-16 May 2019 ........................................... 13 2. EU referral procedures for safety reasons: urgent EU procedures 13 2.1. Newly triggered procedures ................................................................................. 13 2.2. Ongoing procedures ............................................................................................. 13 2.3. Procedures for finalisation.................................................................................... 13 2.4. Planned public hearings ....................................................................................... 13 3. EU referral procedures for safety reasons: other EU referral procedures 13 3.1. Newly triggered procedures ................................................................................. 13 3.1.1. Leuprorelin (NAP) .................................................................................................... 13 3.2. Ongoing procedures ............................................................................................. 14 3.3. Procedures for finalisation.................................................................................... 14 3.4. Re-examination procedures .................................................................................. 14 3.5. Others .................................................................................................................. 14 4. Signals assessment and prioritisation 14 4.1. New signals detected from EU spontaneous reporting systems ............................ 14 4.1.1. Azacitidine – VIDAZA (CAP) ...................................................................................... 14 4.1.2. Durvalumab – IMFINZI (CAP) .................................................................................... 14 4.1.3. Pembrolizumab – KEYTRUDA (CAP) ............................................................................ 15 4.2. New signals detected from other sources ............................................................. 15 4.3. Signals follow-up and prioritisation ...................................................................... 15 4.3.1. Dipeptidyl peptidase-4 (DPP-4) inhibitors: alogliptin – VIPIDIA (CAP) - EMEA/H/C/002182/SDA/011; linagliptin – TRAJENTA (CAP) - EMEA/H/C/002110/SDA/017; saxagliptin – ONGLYZA (CAP) - EMEA/H/C/001039/SDA/043; sitagliptin – JANUVIA (CAP) - EMEA/H/C/000722/SDA/038, RISTABEN (CAP) - EMEA/H/C/001234/SDA/016, TESAVEL (CAP) - EMEA/H/C/000910/SDA/032, XELEVIA (CAP) - EMEA/H/C/000762/SDA/037; vildagliptin – GALVUS (CAP) - EMEA/H/C/000771/SDA/047, JALRA (CAP) - EMEA/H/C/001048/SDA/031, XILIARX (CAP) - EMEA/H/C/001051/SDA/031; Glucagon-like peptide-1 (GLP-1) receptor agonists: albiglutide – EPERZAN; dulaglutide – TRULICITY (CAP) - EMEA/H/C/002825/SDA/012; exenatide – BYDUREON (CAP) - EMEA/H/C/002020/SDA/026, BYETTA (CAP) - EMEA/H/C/000698/SDA/046; liraglutide – SAXENDA (CAP) - EMEA/H/C/003780/SDA/018, VICTOZA (CAP) - EMEA/H/C/001026/SDA/037; lixisenatide – LYXUMIA (CAP) - EMEA/H/C/002445/SDA/015; semaglutide – OZEMPIC (CAP) – EMEA/H/C/004174/SDA/006 ..................................................................................... 15 4.3.2. Loperamide (NAP) ................................................................................................... 16 4.3.3. Propylthiouracil (NAP) .............................................................................................. 16 4.3.4. Rivaroxaban - XARELTO (CAP) - EMEA/H/C/000944/SDA/045 ....................................... 16 Pharmacovigilance Risk Assessment Committee (PRAC) EMA/PRAC/325596/2019 Page 2/77 4.3.5. Secukinumab - COSENTYX (CAP) - EMEA/H/C/003729/SDA/006 .................................... 16 4.3.6. Sulfasalazine (NAP).................................................................................................. 16 4.3.7. Temozolomide - TEMODAL (CAP) - EMEA/H/C/000229/SDA/042 .................................... 17 4.3.8. Topiramate (NAP) .................................................................................................... 17 5. Risk management plans (RMPs) 17 5.1. Medicines in the pre-authorisation phase ............................................................. 17 5.1.1. Azacitidine - EMEA/H/C/005300 ................................................................................. 17 5.1.2. Bortezomib - EMEA/H/C/005074 ................................................................................ 17 5.1.3. Cefiderocol - EMEA/H/C/004829 ................................................................................ 17 5.1.4. Clopidogrel, acetylsalicylic acid - EMEA/H/C/004996 .................................................... 17 5.1.5. Emapalumab - EMEA/H/C/004386, Orphan ................................................................. 18 5.1.6. Fostamatinib - EMEA/H/C/005012 .............................................................................. 18 5.1.7. Lacosamide - EMEA/H/C/005243 ............................................................................... 18 5.1.8. Netarsudil - EMEA/H/C/004583 ................................................................................. 18 5.1.9. Omadacycline tosilate - EMEA/H/C/004715 ................................................................. 18 5.1.10. Quizartinib - EMEA/H/C/004468, Orphan .................................................................... 18 5.1.11. Replication-competent live recombinant vesicular stomatitis virus (rVSVΔG-ZEBOV-GP, live attenuated) expressing the envelope glycoprotein of the Ebolavirus-Zaire Kikwit strain - EMEA/H/C/004554 ................................................................................................... 18 5.1.12. Rituximab - EMEA/H/C/005387 ................................................................................. 19 5.1.13. Rituximab - EMEA/H/C/004807 ................................................................................. 19 5.2. Medicines in the post-authorisation phase – PRAC-led procedures ....................... 19 5.2.1. Adalimumab - HULIO (CAP) - EMEA/H/C/004429/II/0009 ............................................. 19 5.2.2. Apremilast - OTEZLA (CAP) - EMEA/H/C/003746/II/0023 ............................................. 19 5.2.3. Cobimetinib - COTELLIC (CAP) - EMEA/H/C/003960/II/0016 ......................................... 19 5.2.4. Deferasirox - EXJADE (CAP) - EMEA/H/C/000670/II/0064 ............................................. 20 5.2.5. Guselkumab - TREMFYA (CAP) - EMEA/H/C/004271/II/0013 ......................................... 20 5.2.6. Human normal immunoglobulin - KIOVIG (CAP) - EMEA/H/C/000628/II/0091 ................. 20 5.2.7. Lenvatinib - KISPLYX (CAP) - EMEA/H/C/004224/II/0024 ............................................. 20 5.2.8. Ponatinib - ICLUSIG (CAP) - EMEA/H/C/002695/II/0051, Orphan .................................. 21 5.2.9. Rilpivirine - EDURANT (CAP) - EMEA/H/C/002264/II/0034 ............................................ 21 5.2.10. Safinamide - XADAGO (CAP) - EMEA/H/C/002396/II/0031 ............................................ 21 5.3. Medicines