Fexeric, common name-ferric citrate coordination …

1 30 July 2015 EMA/CHMP/535898/2015 Committee for Medicinal Products for Human Use (CHMP) Assessment report Fexeric ferric citrate coordination complex Procedure No. EMEA/H/C/003776/0000 Note Assessment report as adopted by the CHMP with all information of a commercially confidential nature deleted. 30 Churchill Place Canary Wharf London E14 5EU United Kingdom An agency of the European Union Telephone +44 (0)20 3660 6000 Facsimile +44 (0)20 3660 5520 Send a question via our website Table of contents 1. Background information on the procedure.

2 8 Submission of the dossier .. 8 Steps taken for the assessment of the product .. 9 2. Scientific discussion .. 10 Introduction .. 10 Quality aspects .. 12 12 Active Substance .. 13 Finished Medicinal Product .. 14 Discussion on chemical, pharmaceutical and biological 16 Conclusions on the chemical, pharmaceutical and biological aspects .. 17 Recommendations for future quality development .. 17 Non-clinical aspects .. 17 17 Pharmacology .. 17 Pharmacodynamic drug interactions .. 19 Pharmacokinetics.

3 19 Toxicology .. 21 Ecotoxicity/environmental risk assessment .. 23 Discussion on non-clinical aspects .. 23 Conclusion on the non-clinical aspects .. 24 Clinical aspects .. 24 24 Pharmacokinetics .. 27 Pharmacodynamics .. 29 Discussion on clinical pharmacology .. 31 Conclusions on clinical pharmacology .. 31 Clinical efficacy .. 32 Dose response studies .. 32 Main studies .. 34 Discussion on clinical efficacy .. 59 Conclusions on the clinical efficacy .. 61 Clinical safety .. 61 Discussion on clinical safety.

4 70 Conclusions on the clinical safety .. 73 Risk Management Plan .. 74 Pharmacovigilance .. 82 Product information .. 82 User consultation .. 82 Assessment report EMA/CHMP/535898/2015 Page 2/86 Additional monitoring .. 82 3. Benefit-Risk Balance .. 82 4. Recommendations .. 85 Assessment report EMA/CHMP/535898/2015 Page 3/86 List of abbreviations A/G albumin/globulin ratio Alb albumin ALP alkaline phosphatase ALT alanine aminotransferase APTT activated partial thromboplastin time AST aspartate aminotransferase AUC area under the serum concentration-time curve BET Brunauer Emmett Teller CHMP Committee for Medicinal Products for Human use CPMP Committee for Proprietary Medicinal Products CKD chronic kidney disease CKD 5D CKD dialysis (stage) CKD ND CKD non-dialysis (stages)

5 Cmax peak concentration CNS central nervous system Creat Creatinine DG day of gestation DMT-1 divalent metal ion transporter 1 DNA deoxyribonucleic acid DRF dose range finding EAP Efficacy assessment period, Efficacy analysis population EC European Commission EDTA Ethylenediaminetetraacetic acid ESA erythropoiesis stimulating agent ESKD End stage renal disease EU European Union GC Gas chromatography GGT gamma-glutamyl transpeptidase GI Gastrointestinal Assessment report EMA/CHMP/535898/2015 Page 4/86 GIT gastrointestinal tract GCP Good Clinical Practice GI gastrointestinal GLP good laboratory practice GMP Good manufacturing practice HD Haemodialysis HDPE high density polyethylene HED human equivalent dose HGB Haemoglobin HP

6 Hyperphosphatemia HPLC High performance liquid chromatography HPT hyperphosphatemia ICH International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use ICP-MS Inductively coupled plasma mass spectrometry ICP-OES Inductively coupled plasma optical emission spectrometry intramuscular intraperitoneal IPC In-process control IR Infrared IUPAC international union of pure and applied chemistry ITT intent-to-treat IV intravenous KF Karl Fischer titration KRX (KRX-0502) ferric citrate complex (a special construct of ferric citrate (formulation proposed for marketing))

7 , Fexeric Kt/V Dialysis adequacy measure LoD Loss on drying MAH Marketing authorisation holder MCH mean corpuscular haemoglobin MCHC mean corpuscular haemoglobin concentration Assessment report EMA/CHMP/535898/2015 Page 5/86 MCV mean corpuscular volume MPV mean platelet volume MRHD maximum recommended human dose MTD maximum tolerated dose NMR Nuclear magnetic resonance NOAEL no observed adverse effect level NOEL no observed effect level OECD organisation for economic co-operation and development P phosphorus Pi inorganic phosphorus PCE polychromatic erythrocyte PCS Potentially clinically significant PD parenteral dialysis PDE Permitted daily exposure Ph.

8 Eur. European Pharmacopoeia PT prothrombin time PTH parathyroid hormone QTc corrected qt interval RBC red blood cell count RDW red cell distribution width RES reticuloendothelial system RH relative humidity Subcutaneous SmPC Summary of product characteristics SP (SAP) Safety assessment period (safety analysis population) Tbili total bilirubin TG Triglycerides TIBC total iron binding capacity tmax time to peak concentration TP total protein TEAE treatment-emergent adverse event Assessment report EMA/CHMP/535898/2015 Page 6/86 TSAT transferrin saturation UIBC unsaturated iron binding capacity USAN united states adopted name UV Ultraviolet WBC leucocyte count XRPD X-ray powder diffraction Assessment report EMA/CHMP/535898/2015 Page 7/86 1.

9 Background information on the procedure Submission of the dossier The applicant Keryx Biopharma UK Ltd. submitted on 7 March 2014 an application for Marketing Authorisation to the European Medicines Agency (EMA) for Fexeric, through the centralised procedure under Article 3 (2) (a) of Regulation (EC) No 726/2004. The eligibility to the centralised procedure was agreed upon by the EMA/CHMP on 30 May 2013. The applicant applied for the following indication: Fexeric is indicated for the control of hyperphosphataemia in adult patients with chronic kidney disease.

10 The legal basis for this application refers to: Article of Directive 2001/83/EC -complete and independent application. The applicant indicated that ferric citrate coordination complex was considered to be a new active substance. The application submitted is composed of administrative information, complete quality data, non-clinical and clinical data based on applicants own tests and studies and bibliographic literature substituting/supporting certain tests or studies. Information on Paediatric requirements Pursuant to Article 7 of Regulation (EC) No 1901/2006, the application included an EMA Decision P/0183/2013 on the agreement of a paediatric investigation plan (PIP) and on the granting of a (product-specific) waiver.