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Lessons	
  learnt:	
  
The	
  reality	
  of	
  Inhala2on	
  Gx	
  Filings	
  	
  
©	
  Copyright	
  Aedestra	
  2015	
  
Philippe	
  Rogueda 	
   	
   	
   	
   	
   	
  30	
  March	
  2015	
  
Aedestra	
  Ltd
1	
  
Disclaimer	
  
The	
  informa9on	
  contained	
  in	
  this	
  presenta9on	
  is	
  privileged.	
  
	
  
This	
  presenta9on	
  contains	
  the	
  personal	
  opinions	
  and	
  thoughts	
  of	
  the	
  presenter	
  and	
  
may	
  not	
  be	
  assumed	
  to	
  represent	
  the	
  opinion	
  of	
  Aedestra	
  Ltd	
  nor	
  of	
  any	
  employer	
  or	
  
company	
  or	
  learned	
  society	
  with	
  whom	
  	
  the	
  presenter	
  might	
  be	
  or	
  might	
  have	
  been	
  
associated.	
  
	
  
Aedestra	
  Ltd	
  makes	
  no	
  representa9ons	
  to	
  the	
  accuracy	
  of	
  the	
  informa9on	
  contained	
  
therein.	
  
	
  
Aedestra	
  Ltd	
  declines	
  any	
  responsibility	
  on	
  the	
  use	
  of	
  the	
  informa9on	
  contained	
  in	
  
these	
  slides.	
  Aedestra	
  Ltd	
  does	
  not	
  recommend	
  any	
  course	
  of	
  ac9ons	
  resul9ng	
  
directly	
  or	
  indirectly	
  from	
  the	
  informa9on	
  presented	
  in	
  these	
  slides.	
  
©	
  Copyright	
  Aedestra	
  2015	
   2	
  
European	
  aspira2ons	
  
©	
  Copyright	
  Aedestra	
  2015	
   3	
  
In	
  vitro	
  BE	
  
PK	
  BE	
  
PD	
  BE	
  
The	
  orderly	
  stepwise	
  approach	
  of	
  
the	
  European	
  Union	
  
European	
  “perpetuum	
  mobile”	
  
©	
  Copyright	
  Aedestra	
  2015	
   4	
  
In	
  vitro	
  BE	
  
The	
  PK	
  study	
  merry	
  go	
  round	
  
PD	
  BE	
  PK	
  BE	
  X	
  
Some	
  famous	
  UK	
  Gx	
  products	
  
©	
  Copyright	
  Aedestra	
  2015	
   5	
  
u Salbutamol:	
  
	
  3	
  pMDI	
  
	
  6	
  DPI	
  
u Beclomethasone:	
  
	
  2	
  pMDI	
  
	
  4	
  DPI	
  
u  Most	
  of	
  these	
  products	
  were	
  not	
  filed	
  as	
  generics,	
  but	
  as	
  brands.	
  That	
  in	
  itself	
  is	
  quite	
  
revealing	
  of	
  the	
  difficul9es	
  in	
  crea9ng	
  generics	
  in	
  the	
  inhala9on	
  space.	
  
u  Only	
  one	
  product	
  seems	
  to	
  have	
  been	
  filed	
  on	
  in	
  vitro	
  data	
  in	
  Europe	
  
	
   	
   	
  	
  
	
   	
   	
   	
   	
  …	
  More	
  about	
  this	
  a	
  moment	
  
u Formoterol:	
  
	
  1	
  pMDI	
  
	
  4	
  DPI	
  
u Budesonide:	
  
	
  7	
  DPI	
  
©	
  Copyright	
  Aedestra	
  2015	
  
Salmeson	
  -­‐	
  Rolenium	
  -­‐	
  Elpen	
  
Flu9casone	
  pMDI	
  -­‐	
  Cipla	
  
Airflusal	
  -­‐	
  Forspiro	
  -­‐	
  Sandoz	
  
DuoResp	
  -­‐	
  Spiromax	
  -­‐	
  Teva	
  
Formoterol	
  DPI	
  -­‐	
  ELC	
  
1
2	
  
6	
  
5	
  
3	
  
4	
  
©	
  Copyright	
  Aedestra	
  2015	
   7	
  
1.	
  Rolenium:	
  the	
  challenger	
  
Branded	
  Gx	
  –	
  2	
  blisters	
  –	
  250/50	
  and	
  500/50	
  strengths.	
  
Filed	
  in	
  Greece	
  18	
  June	
  2009.	
  
First	
  EU	
  DCP	
  approval	
  30	
  Nov	
  2011	
  RMS	
  Sweden.	
  No	
  in	
  vitro	
  BE.	
  PK	
  BE.	
  PD	
  data.	
  
©	
  Copyright	
  Aedestra	
  2015	
   8	
  
Commercial	
  claims	
  –	
  ACI	
  data	
  
Flu9casone	
  FPF:	
  
Rolenium	
  	
  16±6%	
  
Sere9de	
  Diskus	
  23±13%	
  
	
  
ERS	
  2013	
  
Abstract	
  #	
  4967	
  
Pub	
  #	
  P714	
  
Elpen	
  commercial	
  lit.	
  
©	
  Copyright	
  Aedestra	
  2015	
   9	
  
Advanced	
  Drug	
  Delivery	
  Reviews	
  75(2014)	
  18–31	
  
Flow	
  dependence	
  of	
  Flu2casone	
  FPF	
  
©	
  Copyright	
  Aedestra	
  2015	
   10	
  
R.	
  Price	
  DDL	
  2013	
  
PK	
  study,	
  2	
  way	
  crossover,	
  single	
  dose	
  500/50	
  
©	
  Copyright	
  Aedestra	
  2015	
   11	
  
Rolenium	
  Approval	
  History	
  
u 18	
  June	
  2009:	
  Greece	
  –	
  What	
  data	
  was	
  presented?	
  
u 4	
  May	
  2011:	
  DCP,	
  RMS	
  Sweden,	
  CMS	
  Bulg.	
  Est.	
  Lat.	
  Lith.	
  Lux.	
  Rom.	
  Slv.	
  
	
   	
  -­‐No	
  In	
  Vitro	
  BE	
  
	
  	
  -­‐PK	
  efficacy	
  500/50,	
  with	
  charcoal,	
  60	
  Healthy	
  subj.,	
  
	
  extrapolated	
  to	
  250/50.	
  
	
  -­‐No	
  PK	
  safety,	
  in	
  vitro	
  bioavailability	
  knowledge	
  sufficient.	
  
	
  -­‐2	
  informa9ve	
  PD	
  studies	
  (500/50	
  &	
  250/50),	
  FEV1,	
  n=28	
  	
  
	
  
u 30	
  Nov	
  2011:	
  DCP,	
  RMS	
  Sweden,	
  CMS	
  Cze.	
  Ge.	
  Hu.	
  Icl.	
  It.	
  Pol.	
  Slk.	
  
	
  -­‐Same	
  as	
  4	
  May	
  2011	
  
	
  
u 13	
  March	
  2013:	
  DCP,	
  RMS	
  Sweden,	
  CMS	
  Fl.	
  Fr.	
  No.	
  Pol.	
  
	
   	
  DCP,	
  RMS	
  Sweden,	
  CMS	
  Au.	
  Bel.	
  Dk.	
  Ir.	
  Nl.	
  
	
   	
  -­‐2011	
  +	
  PK	
  	
  safety	
  250/50,	
  without	
  charcoal,	
  Asthma	
  pa9ents	
  
	
  
2	
  PK,	
  2	
  PD	
  studies	
  acknowledged	
  
Not	
  approved	
  in:	
  France,	
  UK,	
  Spain	
  
©	
  Copyright	
  Aedestra	
  2015	
   12	
  
2.	
  Flu2casone	
  pMDi:	
  luck	
  incarnate?	
  
u Flu9casone	
  pMDI	
  CIPLA	
  agains	
  Flixo9de	
  Evohaler.	
  
	
  
u 2	
  strengths	
  approved	
  11	
  June	
  2013,	
  RMS	
  Sweden,	
  CMS	
  Ge,	
  Sp.	
  
u 2nd	
  approval:	
  25	
  Sept	
  14,	
  RMS	
  Sweden,	
  CMS	
  Fl,	
  Ge,	
  Hu,	
  It,	
  No,	
  Sp	
  
u No	
  in	
  vitro	
  BE,	
  2	
  PK	
  studies	
  acknowledged.	
  
u PK	
  studies	
  WO	
  charcoal:	
  
	
  -­‐32	
  subjects	
  
	
  -­‐28	
  subjects	
  with	
  spacer	
  
	
  
	
  
	
  
	
  
	
  
How	
  many	
  studies	
  were	
  necessary	
  to	
  fine	
  tune	
  this	
  formula2on?	
  
©	
  Copyright	
  Aedestra	
  2015	
   13	
  
3.	
  Airflusal:	
  normalised	
  data	
  
u Flu9casone	
  +	
  Salmeterol	
  DPI	
  
u 2	
  Strengths	
  approved	
  500/50	
  &	
  250/50	
  
u No	
  in	
  vitro	
  match	
  
u 3	
  PK	
  (W/Wo	
  Charcoal),	
  2	
  PD	
  (one	
  PIF)	
  
u PD	
  studies	
  (n=555)	
  and	
  PIF	
  study	
  (n=60)	
  
u Major	
  point	
  of	
  applica9on:	
  FPD	
  of	
  Flu9casone	
  was	
  normalised	
  to	
  yield	
  an	
  IVIV	
  
correla9on	
  with	
  Cmax,	
  and	
  achieve	
  Cmax	
  BE	
  
©	
  Copyright	
  Aedestra	
  2015	
   14	
  
	
  	
   AUC0-­‐tpg*h/ml	
   Cmax	
  pg/ml	
  
Test	
   328.57	
  ±	
  109.00	
   297.50	
  ±	
  111.29	
  
Reference	
   282.11	
  ±	
  90.83	
   265.69	
  ±	
  84.21	
  
Normalised	
  Ra9o	
  
(90%CI)	
  
1.1592	
  
(1.1243-­‐1.1952)	
  
1.1041	
  
(1.0574-­‐1.1528)	
  
Natural	
  Ra9o	
   1.1647	
   1.1197	
  
	
  	
   AUC0-­‐tpg*h/ml	
   Cmax	
  pg/ml	
  
Test	
   1083.11	
  ±	
  311.76	
   148.03	
  ±	
  45.16	
  
Reference	
   1166.84	
  ±	
  260.88	
   176.53	
  ±	
  49.99	
  
Normalised	
  
Ra9o(90%CI)	
  
0.9129	
  
(0.8791-­‐0.9479)	
  
0.8340	
  
(0.8022-­‐0.8671)	
  
Natural	
  Ra9o	
   0.9282	
   0.8386	
  
u Flu9casone,	
  PK,	
  2	
  x	
  50/500,	
  n=59.	
  
u Salmeterol,	
  PK,	
  2	
  x	
  50/500,	
  n=59.	
  
©	
  Copyright	
  Aedestra	
  2015	
   15	
  
4.	
  DuoResp:	
  11	
  clinical	
  studies	
  
2	
  strengths,	
  11	
  clinical	
  studies,	
  628	
  volunteers,	
  77	
  children,	
  20	
  years	
  in	
  the	
  making	
  
©	
  Copyright	
  Aedestra	
  2015	
   16	
  
Centralised	
  procedure:	
  seal	
  of	
  quality?	
  
	
  
u Dossier	
  received	
  29	
  Jan	
  2013,	
  posi9ve	
  opinion	
  20	
  Feb	
  2014	
  
u 3	
  strengths	
  submired,	
  2	
  approved:	
  160/4.5	
  &	
  320/9	
  
u Asthma	
  and	
  COPD	
  
u Children	
  and	
  adolescent	
  excluded	
  
u 8	
  scien9fic	
  mee9ngs:	
  
24	
  Sept,	
  6	
  Nov,	
  8	
  Dec	
  2009;	
  9	
  April,	
  22	
  April,	
  18	
  Nov	
  2010;	
  22	
  Sept	
  2011;	
  16	
  Feb	
  2012	
  
u No	
  in-­‐vitro	
  BE	
  
u 9	
  PK	
  studies	
  submired	
  (3	
  strengths)	
  and	
  2	
  PD	
  (one	
  safety	
  study	
  in	
  children)	
  
©	
  Copyright	
  Aedestra	
  2015	
   17	
  
In	
  vitro	
  data	
  –	
  Middle	
  strength	
  
DUORESP	
   SYMBICORT	
   T/R	
  
L/min	
   40	
   60	
   90	
   40	
   60	
   90	
   40	
   60	
   90	
  
%	
  LC	
  
BUDESONIDE	
  
TD	
   94.78	
   97.08	
   99.94	
   70.73	
   85.52	
   93.94	
   1.34	
   1.14	
   1.06	
  
IP+PS	
   59.25	
   53.81	
   50.02	
   37.16	
   35.47	
   37.73	
   1.59	
   1.52	
   1.33	
  
FPD	
   31.07	
   38.39	
   44.21	
   29.19	
   45.23	
   51.47	
   1.06	
   0.85	
   0.86	
  
MMAD	
   2.41	
   2.2	
   2.09	
   2.58	
   2.25	
   2.01	
   0.93	
   0.98	
   1.04	
  
GSD	
   1.86	
   1.94	
   1.98	
   1.78	
   1.83	
   1.95	
   1.04	
   1.06	
   1.02	
  
	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  	
  FORMOTEROL	
  
TD	
   88.04	
   91.15	
   96.76	
   69.9	
   84.53	
   93.86	
   1.26	
   1.08	
   1.03	
  
IP+PS	
   57.27	
   51.85	
   49.29	
   37.43	
   35.38	
   38.61	
   1.53	
   1.47	
   1.28	
  
FPD	
   27.54	
   35.51	
   42.44	
   27.93	
   43.95	
   50.19	
   0.99	
   0.81	
   0.85	
  
MMAD	
   2.39	
   2.18	
   2.11	
   2.63	
   2.3	
   2.08	
   0.91	
   0.95	
   1.01	
  
GSD	
   1.86	
   1.9	
   2.01	
   1.78	
   1.84	
   1.94	
   1.04	
   1.03	
   1.04	
  
©	
  Copyright	
  Aedestra	
  2015	
   18	
  
Spiromax	
  PIF	
  studies	
  
©	
  Copyright	
  Aedestra	
  2015	
   19	
  
5.	
  Formoterol	
  DPI:	
  a	
  rare	
  case	
  of	
  in	
  vitro	
  filing	
  
	
  
u RMS	
  Sweden,	
  CMS	
  France	
  
u Authorisa9on	
  granted:	
  12	
  Dec.	
  2014	
  
©	
  Copyright	
  Aedestra	
  2015	
   20	
  
Formoterol	
  DPI:	
  a	
  rare	
  case	
  of	
  in	
  vitro	
  filing	
  
u Ref:	
  Foradil,	
  Aerolizer	
  
	
  
u In	
  vitro	
  BE	
  only	
  
	
  Same	
  device	
  design	
  
	
  Same	
  cri9cal	
  dimension	
  
	
  Same	
  handling	
  
	
  Same	
  device	
  resistance	
  
	
  
u Special	
  request:	
  PIF	
  and	
  FIVC	
  study	
  on	
  20	
  subjects	
  REF	
  &	
  TEST	
  
	
   	
   	
  REF 	
  TEST	
  
	
  FIVC	
  (L) 	
  2.2 	
  2.1	
  	
  
	
  PIF	
  (L/min) 	
  101.23 	
  102.65	
  
	
  
u Let’s	
  study	
  its	
  in	
  vitro	
  performance!	
  
Lessons	
  learnt	
  
©	
  Copyright	
  Aedestra	
  2015	
   21	
  
Products	
   In	
  Vitro	
  BE	
   PK/PD	
  studies	
   PIF	
  studies	
  
Rolenium	
   ✗	
   4	
   ✓	
  
Seroflo	
  pMDI	
   ✗	
   2	
  !!	
   ✓	
  
Airflusal	
   ✗	
   5	
   ✓	
  
DuoResp	
   ✗	
   11	
   ✓	
  
Formoterol	
  DPI	
   ✓	
   ✗	
   ✓	
  
When	
  mul9ple	
  strengths	
  are	
  available,	
  the	
  lower	
  strength	
  seems	
  
impossible	
  to	
  match	
  and	
  file.	
  
Lessons	
  learnt	
  
©	
  Copyright	
  Aedestra	
  2015	
  
u In	
  vitro	
  filing	
  is	
  possible	
  in	
  the	
  EU.	
  It	
  is	
  the	
  excep9on	
  rather	
  than	
  the	
  norm.	
  
u In	
  vitro	
  filing	
  requires	
  same	
  device,	
  formula9on,	
  API,	
  groupings.	
  Further	
  
requirements:	
  PIF	
  study,	
  Handling	
  studies,	
  knowledge	
  of	
  bioavailability	
  of	
  API/
Formula9on.	
  A	
  stage	
  by	
  stage	
  match	
  is	
  difficult,	
  groupings	
  will	
  be	
  accepted	
  when	
  
jus9fied.	
  
	
  
u Some	
  countries	
  are	
  more	
  recep9ve	
  to	
  in	
  vitro	
  filing	
  than	
  others.	
  
u Most	
  products	
  will	
  be	
  approved	
  aver	
  PK	
  studies.	
  Study	
  the	
  reference	
  product	
  in	
  
depth.	
  How	
  many	
  PK	
  studies	
  will	
  you	
  conduct?	
  
u Do	
  not	
  assume	
  a	
  linear	
  development:	
  in	
  vitro	
  followed	
  by	
  PK.	
  This	
  is	
  a	
  very	
  naïve	
  
approach.	
  
u The	
  variety	
  of	
  PK	
  studies	
  presented	
  and	
  their	
  jus9fica9ons	
  show	
  the	
  complexity	
  of	
  
the	
  inhala9on	
  field,	
  and	
  the	
  recep9veness	
  of	
  regulatory	
  authori9es.	
  
22	
  
The	
  most	
  likely	
  filing	
  scenario	
  
©	
  Copyright	
  Aedestra	
  2015	
   23	
  
In	
  vitro	
  BE	
  
PK	
  BE	
  
+	
  
Aim	
  to	
  achieve	
  PK	
  
	
  
In	
  Vitro	
  BE	
  is	
  nigh	
  
impossible	
  
©	
  Copyright	
  Aedestra	
  2015	
  
www.inhalationasia.org
Follow	
  us	
  on	
  
24	
  
With	
  compliments	
  
	
  
AEDESTRA	
  Ltd	
  
©	
  Copyright	
  Aedestra	
  2015	
   25	
  

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ADA APS talk 4 APS 4 April 15

  • 1. Lessons  learnt:   The  reality  of  Inhala2on  Gx  Filings     ©  Copyright  Aedestra  2015   Philippe  Rogueda            30  March  2015   Aedestra  Ltd 1  
  • 2. Disclaimer   The  informa9on  contained  in  this  presenta9on  is  privileged.     This  presenta9on  contains  the  personal  opinions  and  thoughts  of  the  presenter  and   may  not  be  assumed  to  represent  the  opinion  of  Aedestra  Ltd  nor  of  any  employer  or   company  or  learned  society  with  whom    the  presenter  might  be  or  might  have  been   associated.     Aedestra  Ltd  makes  no  representa9ons  to  the  accuracy  of  the  informa9on  contained   therein.     Aedestra  Ltd  declines  any  responsibility  on  the  use  of  the  informa9on  contained  in   these  slides.  Aedestra  Ltd  does  not  recommend  any  course  of  ac9ons  resul9ng   directly  or  indirectly  from  the  informa9on  presented  in  these  slides.   ©  Copyright  Aedestra  2015   2  
  • 3. European  aspira2ons   ©  Copyright  Aedestra  2015   3   In  vitro  BE   PK  BE   PD  BE   The  orderly  stepwise  approach  of   the  European  Union  
  • 4. European  “perpetuum  mobile”   ©  Copyright  Aedestra  2015   4   In  vitro  BE   The  PK  study  merry  go  round   PD  BE  PK  BE  X  
  • 5. Some  famous  UK  Gx  products   ©  Copyright  Aedestra  2015   5   u Salbutamol:    3  pMDI    6  DPI   u Beclomethasone:    2  pMDI    4  DPI   u  Most  of  these  products  were  not  filed  as  generics,  but  as  brands.  That  in  itself  is  quite   revealing  of  the  difficul9es  in  crea9ng  generics  in  the  inhala9on  space.   u  Only  one  product  seems  to  have  been  filed  on  in  vitro  data  in  Europe                    …  More  about  this  a  moment   u Formoterol:    1  pMDI    4  DPI   u Budesonide:    7  DPI  
  • 6. ©  Copyright  Aedestra  2015   Salmeson  -­‐  Rolenium  -­‐  Elpen   Flu9casone  pMDI  -­‐  Cipla   Airflusal  -­‐  Forspiro  -­‐  Sandoz   DuoResp  -­‐  Spiromax  -­‐  Teva   Formoterol  DPI  -­‐  ELC   1 2   6   5   3   4  
  • 7. ©  Copyright  Aedestra  2015   7   1.  Rolenium:  the  challenger   Branded  Gx  –  2  blisters  –  250/50  and  500/50  strengths.   Filed  in  Greece  18  June  2009.   First  EU  DCP  approval  30  Nov  2011  RMS  Sweden.  No  in  vitro  BE.  PK  BE.  PD  data.  
  • 8. ©  Copyright  Aedestra  2015   8   Commercial  claims  –  ACI  data   Flu9casone  FPF:   Rolenium    16±6%   Sere9de  Diskus  23±13%     ERS  2013   Abstract  #  4967   Pub  #  P714   Elpen  commercial  lit.  
  • 9. ©  Copyright  Aedestra  2015   9   Advanced  Drug  Delivery  Reviews  75(2014)  18–31   Flow  dependence  of  Flu2casone  FPF  
  • 10. ©  Copyright  Aedestra  2015   10   R.  Price  DDL  2013   PK  study,  2  way  crossover,  single  dose  500/50  
  • 11. ©  Copyright  Aedestra  2015   11   Rolenium  Approval  History   u 18  June  2009:  Greece  –  What  data  was  presented?   u 4  May  2011:  DCP,  RMS  Sweden,  CMS  Bulg.  Est.  Lat.  Lith.  Lux.  Rom.  Slv.      -­‐No  In  Vitro  BE      -­‐PK  efficacy  500/50,  with  charcoal,  60  Healthy  subj.,    extrapolated  to  250/50.    -­‐No  PK  safety,  in  vitro  bioavailability  knowledge  sufficient.    -­‐2  informa9ve  PD  studies  (500/50  &  250/50),  FEV1,  n=28       u 30  Nov  2011:  DCP,  RMS  Sweden,  CMS  Cze.  Ge.  Hu.  Icl.  It.  Pol.  Slk.    -­‐Same  as  4  May  2011     u 13  March  2013:  DCP,  RMS  Sweden,  CMS  Fl.  Fr.  No.  Pol.      DCP,  RMS  Sweden,  CMS  Au.  Bel.  Dk.  Ir.  Nl.      -­‐2011  +  PK    safety  250/50,  without  charcoal,  Asthma  pa9ents     2  PK,  2  PD  studies  acknowledged   Not  approved  in:  France,  UK,  Spain  
  • 12. ©  Copyright  Aedestra  2015   12   2.  Flu2casone  pMDi:  luck  incarnate?   u Flu9casone  pMDI  CIPLA  agains  Flixo9de  Evohaler.     u 2  strengths  approved  11  June  2013,  RMS  Sweden,  CMS  Ge,  Sp.   u 2nd  approval:  25  Sept  14,  RMS  Sweden,  CMS  Fl,  Ge,  Hu,  It,  No,  Sp   u No  in  vitro  BE,  2  PK  studies  acknowledged.   u PK  studies  WO  charcoal:    -­‐32  subjects    -­‐28  subjects  with  spacer             How  many  studies  were  necessary  to  fine  tune  this  formula2on?  
  • 13. ©  Copyright  Aedestra  2015   13   3.  Airflusal:  normalised  data   u Flu9casone  +  Salmeterol  DPI   u 2  Strengths  approved  500/50  &  250/50   u No  in  vitro  match   u 3  PK  (W/Wo  Charcoal),  2  PD  (one  PIF)   u PD  studies  (n=555)  and  PIF  study  (n=60)   u Major  point  of  applica9on:  FPD  of  Flu9casone  was  normalised  to  yield  an  IVIV   correla9on  with  Cmax,  and  achieve  Cmax  BE  
  • 14. ©  Copyright  Aedestra  2015   14       AUC0-­‐tpg*h/ml   Cmax  pg/ml   Test   328.57  ±  109.00   297.50  ±  111.29   Reference   282.11  ±  90.83   265.69  ±  84.21   Normalised  Ra9o   (90%CI)   1.1592   (1.1243-­‐1.1952)   1.1041   (1.0574-­‐1.1528)   Natural  Ra9o   1.1647   1.1197       AUC0-­‐tpg*h/ml   Cmax  pg/ml   Test   1083.11  ±  311.76   148.03  ±  45.16   Reference   1166.84  ±  260.88   176.53  ±  49.99   Normalised   Ra9o(90%CI)   0.9129   (0.8791-­‐0.9479)   0.8340   (0.8022-­‐0.8671)   Natural  Ra9o   0.9282   0.8386   u Flu9casone,  PK,  2  x  50/500,  n=59.   u Salmeterol,  PK,  2  x  50/500,  n=59.  
  • 15. ©  Copyright  Aedestra  2015   15   4.  DuoResp:  11  clinical  studies   2  strengths,  11  clinical  studies,  628  volunteers,  77  children,  20  years  in  the  making  
  • 16. ©  Copyright  Aedestra  2015   16   Centralised  procedure:  seal  of  quality?     u Dossier  received  29  Jan  2013,  posi9ve  opinion  20  Feb  2014   u 3  strengths  submired,  2  approved:  160/4.5  &  320/9   u Asthma  and  COPD   u Children  and  adolescent  excluded   u 8  scien9fic  mee9ngs:   24  Sept,  6  Nov,  8  Dec  2009;  9  April,  22  April,  18  Nov  2010;  22  Sept  2011;  16  Feb  2012   u No  in-­‐vitro  BE   u 9  PK  studies  submired  (3  strengths)  and  2  PD  (one  safety  study  in  children)  
  • 17. ©  Copyright  Aedestra  2015   17   In  vitro  data  –  Middle  strength   DUORESP   SYMBICORT   T/R   L/min   40   60   90   40   60   90   40   60   90   %  LC   BUDESONIDE   TD   94.78   97.08   99.94   70.73   85.52   93.94   1.34   1.14   1.06   IP+PS   59.25   53.81   50.02   37.16   35.47   37.73   1.59   1.52   1.33   FPD   31.07   38.39   44.21   29.19   45.23   51.47   1.06   0.85   0.86   MMAD   2.41   2.2   2.09   2.58   2.25   2.01   0.93   0.98   1.04   GSD   1.86   1.94   1.98   1.78   1.83   1.95   1.04   1.06   1.02                                  FORMOTEROL   TD   88.04   91.15   96.76   69.9   84.53   93.86   1.26   1.08   1.03   IP+PS   57.27   51.85   49.29   37.43   35.38   38.61   1.53   1.47   1.28   FPD   27.54   35.51   42.44   27.93   43.95   50.19   0.99   0.81   0.85   MMAD   2.39   2.18   2.11   2.63   2.3   2.08   0.91   0.95   1.01   GSD   1.86   1.9   2.01   1.78   1.84   1.94   1.04   1.03   1.04  
  • 18. ©  Copyright  Aedestra  2015   18   Spiromax  PIF  studies  
  • 19. ©  Copyright  Aedestra  2015   19   5.  Formoterol  DPI:  a  rare  case  of  in  vitro  filing     u RMS  Sweden,  CMS  France   u Authorisa9on  granted:  12  Dec.  2014  
  • 20. ©  Copyright  Aedestra  2015   20   Formoterol  DPI:  a  rare  case  of  in  vitro  filing   u Ref:  Foradil,  Aerolizer     u In  vitro  BE  only    Same  device  design    Same  cri9cal  dimension    Same  handling    Same  device  resistance     u Special  request:  PIF  and  FIVC  study  on  20  subjects  REF  &  TEST        REF  TEST    FIVC  (L)  2.2  2.1      PIF  (L/min)  101.23  102.65     u Let’s  study  its  in  vitro  performance!  
  • 21. Lessons  learnt   ©  Copyright  Aedestra  2015   21   Products   In  Vitro  BE   PK/PD  studies   PIF  studies   Rolenium   ✗   4   ✓   Seroflo  pMDI   ✗   2  !!   ✓   Airflusal   ✗   5   ✓   DuoResp   ✗   11   ✓   Formoterol  DPI   ✓   ✗   ✓   When  mul9ple  strengths  are  available,  the  lower  strength  seems   impossible  to  match  and  file.  
  • 22. Lessons  learnt   ©  Copyright  Aedestra  2015   u In  vitro  filing  is  possible  in  the  EU.  It  is  the  excep9on  rather  than  the  norm.   u In  vitro  filing  requires  same  device,  formula9on,  API,  groupings.  Further   requirements:  PIF  study,  Handling  studies,  knowledge  of  bioavailability  of  API/ Formula9on.  A  stage  by  stage  match  is  difficult,  groupings  will  be  accepted  when   jus9fied.     u Some  countries  are  more  recep9ve  to  in  vitro  filing  than  others.   u Most  products  will  be  approved  aver  PK  studies.  Study  the  reference  product  in   depth.  How  many  PK  studies  will  you  conduct?   u Do  not  assume  a  linear  development:  in  vitro  followed  by  PK.  This  is  a  very  naïve   approach.   u The  variety  of  PK  studies  presented  and  their  jus9fica9ons  show  the  complexity  of   the  inhala9on  field,  and  the  recep9veness  of  regulatory  authori9es.   22  
  • 23. The  most  likely  filing  scenario   ©  Copyright  Aedestra  2015   23   In  vitro  BE   PK  BE   +   Aim  to  achieve  PK     In  Vitro  BE  is  nigh   impossible  
  • 24. ©  Copyright  Aedestra  2015   www.inhalationasia.org Follow  us  on   24  
  • 25. With  compliments     AEDESTRA  Ltd   ©  Copyright  Aedestra  2015   25