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D l t fM D l dTil C bi ti MDI ith t Cf l ti Eff t Development of Mono Dual and Triple Combination pMDIs without Coformulation Effect Development of Mono Dual and Triple Combination pMDIs without Coformulation Effect Development of Mono, Dual, and Triple Combination pMDIs without Coformulation Effect Vidya Joshi David Lechuga Ballesteros Brad Flynn Reinhard Vehring Robert Schultz Brian Noga Vidya Joshi, David Lechuga-Ballesteros, Brad Flynn, Reinhard Vehring, Robert Schultz, Brian Noga, Vidya Joshi, David Lechuga Ballesteros, Brad Flynn, Reinhard Vehring, Robert Schultz, Brian Noga, RH i C i J HS k dS j KD i di R Harris Cummings Jason H Speck and Sarvajna K Dwivedi R. Harris Cummings, Jason H. Speck, and Sarvajna K. Dwivedi Pearl Therapeutics 200 Saginaw Drive Redwood City CA 94063 (USA) Pearl Therapeutics, 200 Saginaw Drive, Redwood City, CA 94063 (USA) Pearl Therapeutics, 200 Saginaw Drive, Redwood City, CA 94063 (USA) Ab t t Results Abstract Results Abstract Results C i MDI Eli i Cf l i Eff Clinical comparison of combination pMDI products for the Phospholipid microparticles associate ith API Cosuspension pMDI Eliminates Coformulation Effect: Clinical comparison of combination pMDI products for the Phospholipid microparticles associate with API Cosuspension pMDI Eliminates Coformulation Effect: treatment of asthma and COPD is complicated because in vitro i tl t f t bl i Aerosol performance is independent of other components in combination treatment of asthma and COPD is complicated because in vitro l f f h i i h bi i microcrystals to form a stable cosuspension Aerosol performance is independent of other components in combination aerosol performance of each active in the combination may not microcrystals to form a stable cosuspension aerosol performance of each active in the combination may not b i l t t th t f th i di id l t f be equivalent to that of the individual components or from SEM Images of Phospholipid Microparticles (left bi ti i hi h th d f f th SEM Images of Phospholipid Microparticles (left t ) dit i t t (l ft b tt d combinations in which the dose of one or more of the top) and interior nanostructure (left bottom and 35% 35% GP components is varied Cosuspension upon actuation (right) MF GP components is varied. 30% 30% MF GP 30% 30% Mi i d GP l (l ft Spray dried low density porous particles generate uniform and Micronized GP alone (left 25% ed 25% ed Spray dried low density porous particles generate uniform and vial) and micronized GP ere ere stable cosuspensions with micronized APIs across wide dose cosuspension with 20% ve 20% ve stable cosuspensions with micronized APIs, across wide dose cosuspension with h h li id 2 μm 20% co 20% co ranges for all principal classes of respiratory therapeutics in phospholipid 2 μm Rec 15% Rec ranges for all principal classes of respiratory therapeutics in d l d til bi ti ith l f f microparticles (right vial) 100 nm 15% FR 15% PR mono, dual and triple combinations, with aerosol performance of demonstrating formation of M GP mono, dual and triple combinations, with aerosol performance of h API bi id d t f th b t f demonstrating formation of d i ti l 10% % 10% % 100 nm each API being independent of the number or type of co- drug-microparticle 10% % suspended APIs ensembles that remain 5% 5% suspended APIs. associated even upon 5% 5% associated even upon t ti ( h actuation (as shown on 0% 0% Extensive in vitro characterization of Pearl’s triple combination picture on the right) Glycopyrrolate Phospholipid Inhaler Throat 1 2 3 4 5 6 7 Filter Inhaler USP 1 2 3 4 5 6 7 Filter Extensive in vitro characterization of Pearl s triple combination Glycopyrrolate Phospholipid Microparticles Inhaler Throat 1 2 3 4 5 6 7 Filter Inhaler USP Throat 1 2 3 4 5 6 7 Filter (F) MDIs containing a LAMA a LABA and an ICS and their crystals Microparticles Throat (F) MDIs, containing a LAMA, a LABA and an ICS, and their MF Monotherapy MF/GP Double Combination GP Monotherapy MF/GP Double Combination corresponding double and mono MDIs demonstrate remarkable pMDI with Micronized Active 4 Cosuspension pMDI MF Monotherapy MF/GP Double Combination GP Monotherapy MF/GP Double Combination corresponding double and mono MDIs, demonstrate remarkable h i l bili h i l bili d l f pMDI with Micronized Active Cosuspension pMDI MF/FF DoubleCombination MF/GP/FF Triple Combination GF/FF Double Combination MF/GP/FF Triple Combination chemical stability, physical stability and aerosol performance as MF/FF DoubleCombination MF/GP/FF Triple Combination GF/FF Double Combination MF/GP/FF Triple Combination chemical stability, physical stability and aerosol performance as d b tt th th t ffi i t bi ti MDI good as or better than the most efficient combination pMDIs 35% tl il bl 35% FF currently available. Cos spension pMDI Eliminates Microni ed API PSD Effects FF 0 seconds 5 seconds 0 seconds 15 seconds 30 seconds 30% Cosuspension pMDI Eliminates Micronized API PSD Effects FF 0 seconds 5 seconds 0 seconds 15 seconds 30 seconds Clinical experience with a LAMA and LABA combination 25% d Clinical experience with a LAMA and LABA combination 25% ed demonstrates that Pearl’s cosuspension technology has the 20% ere demonstrates that Pearl s cosuspension technology has the Table 3 Micronized drug PSD by laser diffraction Equivalent performance for all actives in combination 20% ove potential of becoming the next generation combination pMDI Table 3. Micronized drug PSD by laser diffraction Equivalent performance for all actives in combination eco potential of becoming the next generation combination pMDI regardless of dose or physicochemical properties 15% Re product platform (1-3) Micronized regardless of dose or physicochemical properties FF product platform (1 3). Micronized D x 10 (μm) x 50 (μm) x 90 (μm) Span 10% %F Drug 10 50 90 T bl 1 Fi ti l f ti (FPF) d MMAD f th i di id l t 10% % MF 04 11 28 22 Table 1. Fine particle fraction (FPF) and MMADs of the individual components MF 0.4 1.1 2.8 2.2 f ICS/LAMA/LABA til bi ti di d bl bi ti 5% GP 05 13 30 18 of an ICS/LAMA/LABA triple combination, corresponding double combinations Materials and Methods GP 0.5 1.3 3.0 1.8 FF 06 19 41 18 and single component pMDIs 0% Materials and Methods FF 0.6 1.9 4.1 1.8 and single component pMDIs 0% Materials and Methods P l f l ti i MDI f ltd ith Actives in FPF (%) MMAD (μm) Inhaler USP 1 2 3 4 5 6 7 Filter Pearl formulations are suspension pMDIs formulated with Actives in FPF (%) MMAD (μm) Throat (F) micronized actives such as FF (at 5 μg/actuation) GP (at 36 Combination MF GP FF MF GP FF h / bl b micronized actives such as FF (at ~5 μg/actuation), GP (at ~36 Combination MF GP FF MF GP FF FF Monotherapy MF/FF DoubleCombination Conclusions μg / actuation) and MF (at ~50 μg/actuation) cosuspended with MF/GP/FF 59 59 63 35 35 30 GF/FF Double Combination MF/GP/FF Triple Combination Conclusions μg / actuation), and MF (at ~50 μg/actuation) cosuspended with MF/GP/FF 59 59 63 3.5 3.5 3.0 GF/FF Double Combination MF/GP/FF Triple Combination Conclusions spray-dried low density microparticles in a hydrofluoroalkane MF/GP 56 56 3.7 3.8 spray-dried low density microparticles in a hydrofluoroalkane MF/GP 56 56 3.7 3.8 MF/FF 57 60 35 31 Figure 1 Aerodynamic PSD of MF GP and FF in Pearl The Pearl cosuspension pMDI platform enables : (HFA) propellant MF/FF 57 60 3.5 3.1 Figure 1. Aerodynamic PSD of MF, GP, and FF in Pearl C i MDI i i l t dl f th b d The Pearl cosuspension pMDI platform enables : (HFA) propellant. GP/FF 60 62 34 28 Cosuspension pMDIs is equivalent regardless of the number and GP/FF 60 62 3.4 2.8 type of drugs in the formulation and tolerates variability in particle Th i ti l ti h h li id d li hl id MF 54 36 type of drugs in the formulation and tolerates variability in particle Seamless transition from mono to dual to triple These microparticles contain phospholipid and calcium chloride MF 54 3.6 size distribution of the micronized drug (shown in Table 3.) Seamless transition from mono to dual to triple These microparticles contain phospholipid and calcium chloride i th ti f 2 1 d t i th d t t GP 57 37 size distribution of the micronized drug (shown in Table 3.) combinations in the ratio of 2:1 and are present in the product at a GP 57 3.7 combinations concentration of 300 μg/actuation FF 61 30 concentration of ~300 μg/actuation. FF 61 3.0 Cosuspension pMDI enables long term physical D li f i t lli API ith th f ll i Average 57 58 62 36 36 30 Cosuspension pMDI enables long term physical Delivery of microcrystalline API with the following Average 57 58 62 3.6 3.6 3.0 stability of partially soluble actives Delivery of microcrystalline API with the following f t t i l il bl Stability was assessed by storing the triple combination MDIs at RSD (%) 3 3 2 23 45 37 stability of partially soluble actives features not previously available : Stability was assessed by storing the triple combination MDIs at RSD (%) 3 3 2 2.3 4.5 3.7 40°C/75%RH foil overwrapped with desiccant for 6 months and Range 54-59 56-60 60-63 3.5-3.7 3.4-3.8 2.8-3.1 40 C/75%RH, foil overwrapped with desiccant for 6 months, and Range 54 59 56 60 60 63 3.5 3.7 3.4 3.8 2.8 3.1 M t F t (ICS) Gl lt (LAMA) F t l F t (LABA) 14 No coformulation effect (mono = double = triple) testing the product for physical (particle morphology by SEM and Mometasone Furoate (ICS); Glycopyrrolate (LAMA); Formoterol Fumarate (LABA): 14 -No coformulation effect (mono = double = triple) testing the product for physical (particle morphology by SEM and S G) ( FPF: Fine particle mass from stages 3 to filter of NGI divided by NGI delivered dose; MMAD = Mass 12 Physical stability for partially soluble APIs in HFA aPSD using NGI) and chemical attributes (drug content and FPF: Fine particle mass from stages 3 to filter of NGI divided by NGI delivered dose; MMAD = Mass d d 12 -Physical stability for partially soluble APIs in HFA aPSD using NGI) and chemical attributes (drug content and d d ti ) Median Aerodynamic Diameter -Dose size solubility density independent degradation). 10 g) -Dose, size, solubility, density independent Table 2 Physicochemical properties of compounds in cosuspension (μg performance Table 2. Physicochemical properties of compounds in cosuspension 8 P ( Double cosuspension = Mono cosuspension = Triple cosuspension performance GP Double cosuspension Mono cosuspension Triple cosuspension 6 ss I it d li i l f fP l Mas In vitro and clinical performance of Pearl 4 M cosuspension pMDIs meet the requirements to cosuspension pMDIs meet the requirements to 2 become the next generation platform for drug delivery 2 become the next generation platform for drug delivery 0 to the lungs in major disease areas 0 Ihl Th t 1 2 3 4 5 6 7 Filt to the lungs in major disease areas. Inhaler Throat 1 2 3 4 5 6 7 Filter References Release MMAD 3 m %FPF 64% References Release , MMAD: 3μm , %FPF: 64% References 3 mo at 40 C/75%RH MMAD: 3μm %FPF: 63% 1 Orevillo CJ St Rose E Fischer T Alameda P Reisner C A novel glycopyrrolate metered dose 3 mo at 40 C/75%RH, MMAD: 3μm , %FPF: 63% 1. Orevillo CJ, St Rose E, Fischer T, Alameda P, Reisner C. A novel glycopyrrolate metered dose inhaler formulation demonstrates superior bronchodilator efficacy relative to placebo and 6 mo at 40 C/75%RH, MMAD: 3.2μm , %FPF: 59% inhaler formulation demonstrates superior bronchodilator efficacy relative to placebo and comparable efficacy and safety to Spiriva® Handihaler® in patient with COPD Am J Respir Crit comparable efficacy and safety to Spiriva® Handihaler® in patient with COPD Am. J. Respir . Crit. Care Med 2010; 181: A4450 Figure 2: Aerodynamic PSD of GP in a triple combination Spray-dried phospholipid/CaCl 2 porous particle Care Med., 2010; 181: A4450. 2 Marjason J Orevillo CJ St Rose E Ferguson GT Vehring R Joshi V Dwivedi S Reisner C Figure 2:. Aerodynamic PSD of GP in a triple combination Spray dried phospholipid/CaCl 2 porous particle 2. Marjason J, Orevillo CJ, St Rose E, Ferguson GT, Vehring R, Joshi V, Dwivedi S, Reisner C. A t f ft d h ki ti fil f l fi d bi ti f l lt d cosuspension pMDI shows stable aerosol performance after 0, 3, ICS crystal LAMA crystal LABA crystal Assessment of safety and pharmacokinetic profile of a novel fixed combination of glycopyrrolate and f t l HFA MDI i h lth lt A J R i C it C Md 2010 181 A4455 cosuspension pMDI shows stable aerosol performance after 0, 3, d6 th t t 40°C/75%RH ICS crystal LAMA crystal LABA crystal formoterol HFA pMDI in healthy volnteers Am. J. Respir . Crit. Care Med., 2010; 181: A4455. 3Qi DF GT O ill CJ L k A St R A Fi h T G k HRi CA and 6 months storage at 40°C/75%RH. 3. Quinn D, Ferguson GT., Orevillo CJ, Luckey A, St Rose A, Fischer T, Granko H, Reisner C. A novel formoterol fumarate metered dose inhaler formulation demonstrates comparable bronchodilator efficacy relative to Foradil® Aerolizer® and favorable safety outcomes in patients with COPD. Am. J. Respir . Crit. Care Med., 2010; 181: A4458. 4. . Dellamary, LA, Tarara, TE, Smith, DJ, Woelk, CH, Adractas, A, Costello, ML, Gill, H, Weers, J G. Hollow porous particles in metered dose inhalers, Pharm. Res., 2000; 17: 168-174. Presented on May 8 th at RDD 2011 Berlin Germany Presented on May 8 th , at RDD 2011, Berlin, Germany

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Page 1: Dl tfM Dl dTilC bitiMDI - sites.ualberta.cavehring/PE Page/Conference Files/RDD... · Dl tfM Dl dTilC bitiMDI ith t Cf lti Eff t Development of Mono Dual and Triple Combination pMDIs

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Spi

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in p

atie

nt w

ith C

OP

D A

m. J

. Res

pir.

Crit

. C

are

Med

2010

;181

:A44

50Fi

gure

2:A

erod

ynam

icP

SD

ofG

Pin

atri

ple

com

bina

tion

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y-dr

ied

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phol

ipid

/CaC

l 2po

rous

part

icle

Car

e M

ed.,

2010

; 181

: A44

50.

2M

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son

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tRos

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uson

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ived

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Figu

re 2

:. A

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ynam

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a tr

iple

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phos

phol

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/CaC

l 2po

rous

par

ticle

2. M

arja

son

J, O

revi

llo C

J, S

t Ros

e E

, Fer

guso

n G

T, V

ehrin

g R

, Jos

hi V

, Dw

ived

i S, R

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. A

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alth

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lnte

ers

Am

. J. R

espi

r. C

rit. C

are

Med

., 2

010;

181

: A44

55.

3Q

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TO

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mon

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age

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Qui

nn D

, Fer

guso

n G

T., O

revi

llo C

J, L

ucke

yA

, St R

ose

A, F

isch

er T

, Gra

nko

H, R

eisn

er C

. A

nove

l for

mot

erol

fum

arat

e m

eter

ed d

ose

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ler f

orm

ulat

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onst

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onch

odila

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lativ

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adil®

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and

favo

rabl

e sa

fety

out

com

es in

pat

ient

s w

ith C

OP

D. A

m. J

. Res

pir.

Crit

. Car

e M

ed.,

2010

; 181

: A44

58.

4. .

Del

lam

ary,

LA

, Tar

ara,

TE

, Sm

ith, D

J, W

oelk

, CH

, Adr

acta

s, A

, Cos

tello

, ML,

Gill,

H, W

eers

, J G

. y,

,,

,,

,,

,,

,,

,,

,,

Hol

low

por

ous

parti

cles

in m

eter

ed d

ose

inha

lers

, Pha

rm. R

es.,

2000

; 17:

168

-174

.P

rese

nted

onM

ay8t

hat

RD

D20

11B

erlin

Ger

man

yp

p,

,;

Pre

sent

ed o

n M

ay 8

th, a

t RD

D 2

011,

Ber

lin, G

erm

any