Helmut Schütz. The Global Bioequivalence Harmonisation Initiative. 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 1

Similar documents
Modified Release: C min C τ. Modified Release

How to measure what happens in pharmacokinetics

Noncompartmental Analysis (NCA) in PK, PK-based Design

Helmut Schütz. BioBriges 2018 Prague, September

EMA/EGA. Session 1: orally administered Modified Release Products European Regulatory Requirements London 30 April 2015 Dr.

Noncompartmental Analysis (NCA) in PK, PK-based Design

Pharmacokinetic and Statistical Analysis of BE Data

How to design a pilot study

General Hurdles and Pitfalls in BE Studies

Introduction to Bioequivalence

Helmut Schütz. Satellite Short Course Budapest, 5 October

Pharmacokinetic and Statistical Analysis of BE Data

General Hurdles and Pitfalls in BE Studies

Interested parties (organisations or individuals) that commented on the draft document as released for consultation.

Revised European Guideline on PK and Clinical Evaluation of Modified Release Dosage Forms

Helmut Schütz. Statistics for Bioequivalence Pamplona/Iruña, 24 April

Establishing the Biostudy Statistical Design

Prasugrel hydrochloride film-coated tablets 5 mg and 10 mg product-specific bioequivalence guidance

The Predictive Power of Dissolution and Alternatives to Full Bioequivalence

Helmut Schütz. Training on Bioequivalence Kaunas, 5 6 December

Bioequivalence of MR Products. AGAH Conference on the New European Modified Release Guideline Bonn, June 15 th, 2015

Draft Agreed by Pharmacokinetics Working Party February Adoption by CHMP for release for consultation 1 April 2016

Session 1 : Orally Administered Modified Release Products

Scientific And Regulatory Background For The Revised Bioequivalence Requirements For NTI, Steep Exposure-Response, And Drugs With Complex PK Profiles

PHA5128 Dose Optimization II Case Study 3 Spring 2013

Basic Pharmacokinetics and Pharmacodynamics: An Integrated Textbook with Computer Simulations

Public Assessment Report Scientific discussion. Ibuprofen Idifarma 4 mg/ml solution for infusion. Ibuprofeno ES/H/0256/001/DC

NOTE FOR GUIDANCE ON TOXICOKINETICS: THE ASSESSMENT OF SYSTEMIC EXPOSURE IN TOXICITY STUDIES S3A

Comparison of GW (908) Single Dose and Steady-state Pharmacokinetics (PK): Induction Potential and AAG Changes (APV10013)

Year in review. Vit Perlik Director of Regulatory Science and Clinical Development

Public Assessment Report Scientific discussion. Ivabradine Grindeks 5 mg and 7.5 mg and filmcoated. Ivabradine hydrochloride ES/H/0375/ /DC

Pharmacometric Modelling to Support Extrapolation in Regulatory Submissions

Add-On n and Sequential Designs

DRAFT GUIDANCE DOCUMENT Comparative Bioavailability Standards: Formulations Used for Systemic Effects

Biopharmaceutics Lecture-11 & 12. Pharmacokinetics of oral absorption

PHA Spring First Exam. 8 Aminoglycosides (5 points)

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

Interested parties (organisations or individuals) that commented on the draft document as released for consultation.

Evaluation of a Scenario in Which Estimates of Bioequivalence Are Biased and a Proposed Solution: t last (Common)

BASIC PHARMACOKINETICS

6/7 Statistical Design and Analysis III. and Analysis II

5/6 Statistical Design and Analysis I. and Analysis I. Statistical Design. Helmut Schütz BEBAC. informa life sciences

Guidance Document. Comparative Bioavailability Standards: Formulations Used for System Effects

Multiple IV Bolus Dose Administration

Public Assessment Report. Scientific discussion. Metoprololsuccinat Actavis. Prolonged release tablets 25 mg, 50 mg, 100 mg and 200 mg

Decentralised Procedure. Public Assessment Report. Lorazepam-neuraxpharm 1/ 2,5 mg Schmelztabletten. Lorazepam DE/H/4558/ /DC

Application of IVIVCs in Formulation Development Douglas F Smith

Pharmacokinetic and absolute bioavailability studies in early clinical development using microdose and microtracer approaches.

Excipient Interactions Relevant For BCS Biowaivers Peter Langguth

Development of Canagliflozin: Mechanistic Absorption Modeling During Late-Stage Formulation and Process Optimization

Decentralised Procedure. Public Assessment Report. Metamizol Midas / Metamizol STADA / Mimetanal 500 mg Tabletten. Metamizole sodium monohydrate

Public Assessment Report. Scientific discussion. Mogilarta. (Telmisartan and hydrochlorothiazide) DK/H/2306/ /DC.

Clinical Study Synopsis for Public Disclosure

The study listed may include approved and non-approved uses, formulations or treatment regimens. The results reported in any single study may not

Interchangeable Drug Products - Additional Criteria

Saliva Versus Plasma Bioequivalence of Rusovastatin in Humans: Validation of Class III Drugs of the Salivary Excretion Classification System

DE/H/0763/01-04 / MR DE/H/0764/01-04 / MR DE/H/0765/01-05 / MR

The science behind generic drugs

IPAC-RS/UF Orlando Inhalation Conference March 20, S.T. Horhota 1, C.B. Verkleij 2, P.J.G. Cornelissen 2, L. Bour 3, A. Sharma 3, M.

Understand the physiological determinants of extent and rate of absorption

Mutual Recognition Procedure. Public Assessment Report. Valproat Orion 300 / 500 mg Retardtabletten. Sodium valproate DE/H/1910/ /MR

Public Assessment Report Scientific discussion. Pramipexole Orion (pramipexole) SE/H/1672/01-07/DC

Two-Stage Designs in BE Studies. Two-Stage Designs in BE Studies

PHA Second Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

Adaptive and Innovative Study Designs to Accelerate Drug Development from First-In-Human to First-In-Patient

USING PBPK MODELING TO SIMULATE THE DISPOSITION OF CANAGLIFLOZIN

PHA Final Exam Fall 2006

INDIVIDUAL STUDY TABLE REFERRING TO PART OF THE DOSSIER

ANNEX I LIST OF THE NAMES, PHARMACEUTICAL FORM, STRENGTHS OF THE MEDICINAL PRODUCTS, ROUTE OF ADMINISTRATION, APPLICANTS IN THE MEMBER STATES

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

Decentralised Procedure. Public Assessment Report. Memantin Orion 10/20 mg Filmtabletten. Memantine hydrochloride DE/H/3653/ /DC

Public Assessment Report Scientific discussion. Ibuprofen 400 mg/100 ml solution for infusion & Ibuprofen 600 mg/100 ml solution for infusion

This clinical study synopsis is provided in line with Boehringer Ingelheim s Policy on Transparency and Publication of Clinical Study Data.

Prequalification Programme Bioequivalence Assessment Update. Dr. John Gordon

SYNOPSIS. Number of subjects: Planned: 22 Randomized: 23 Treated: 23. Evaluated: Pharmacodynamic: 22 Safety: 23 Pharmacokinetics: 22

Public Assessment Report. EU worksharing project paediatric data. Valcyte. Valganciclovir

Decentralised Procedure. Public Assessment Report. Nurofen Immedia 200mg Weichkapseln Ibuprofen DE/H/1482/001/DC

Current Challenges and Opportunities in Demonstrating Bioequivalence

Monica Edholm Medica Medic l a Pr oducts Agency

Supplementary Table 1: Summary of 33 Patients Treated with Abemaciclib in Dose Escalation

HIV and FDC aspects of two guidelines. Filip Josephson

PHA Final Exam. Fall On my honor, I have neither given nor received unauthorized aid in doing this assignment.

Section 5.2: Pharmacokinetic properties

Public Assessment Report Scientific discussion. Nicorette Pepparmint (nicotine) SE/H/904/01/DC

Absolute bioavailability and pharmacokinetic studies in early clinical development using microdose and microtracer approaches.

Clinical Study Synopsis for Public Disclosure

Multi-Group Studies in Bioequivalence.

Effect of Common Excipients on the Oral Drug Absorption of Biopharmaceutics Classification System Class 3 Drugs

Annex I. Scientific conclusions and grounds for refusal presented by the European Medicines Agency

(Invented) name Strength. Leflunomide Apotex 10 mg Tablet Oral use. Leflunomide Apotex 20 mg Tablet Oral use

Caveat: Validation and Limitations of Phenotyping Methods for Drug Metabolizing Enzymes and Transporters

Open Questions on Bioequivalence

Annex I. List of the names, pharmaceutical form, strengths of the medicinal products, route of administration, applicant in the Member States

DOSE SELECTION FOR CARCINOGENICITY STUDIES OF PHARMACEUTICALS *)

Clinical Study Synopsis for Public Disclosure

Prequalification Team Medicines (PQTm) Bioequivalence Assessment Update. Dr. John Gordon

Pharmacokinetics and bioavailability derived from various body fluids. Saliva samples instead of plasma samples

Modeling and Simulation to Support Development and Approval of Complex Products

ICH Topic S1C(R2) Dose Selection for Carcinogenicity Studies of Pharmaceuticals. Step 5

Decentralised Procedure. Public Assessment Report. Memantin AbZ 10 mg/20 mg Filmtabletten ; Starterpack

Transcription:

Primary and secondary PK metrics for evaluation of steady state studies, C min vs.c τ, relevance of C min /C τ or fluctuation for bioequivalence assessment Helmut Schütz 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 1

Keep in memory Whenever a theory appears to you as the only possible one, take this as a sign that you have neither understood the theory nor the problem which it was intended to solve. Karl R. Popper Even though it s applied science we re dealin with, it still is science! Leslie Z. Benet 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 2

Regulatory demands for study design in BE Design should allow accurate (unbiased) assessment of the treatment effect Carbamazepine (k a(r) 0.472 h 1, k a(t1) 0.94 h 1, k a(t2) 3.6 h 1 ). t ½ after first administration 43 h ( 10 h after full auto-induction) A rare [sic] example where MD is more sensitive to detect differences in the rate of absorption than SD first administration concentration (µg/ml) 5 4 3 2 Cmax T1/R = 105.0% Cmax T2/R = 110.0% R T1 T2 concentration (µg/ml) 6 5 4 3 2 fully induced, steady state (day 6) Cmax T1/R = 110.8% Cmax T2/R = 124.9% R T1 T2 1 1 0 0 24 48 72 96 120 144 168 time (h) 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 3 0 0 4 8 12 16 20 24 time (h)

Differences in the rate of absorption C max and C min are composite metrics Depend on the rate of absorption (i.e., formulation-specific) and the rate of (distribution and) elimination (i.e., drug-specific) In linear PK according to the superposition principle AUC 0 τ (steady state) = AUC 0 (single dose) However, due to drug- and regimen-specific accumulation the difference between products in their maximum conentrations is reduced in steady state C max (SD) is more sensitive to detect differences in the rate of absorption than C ss,max (MD) Prolonged (a.k.a. sustained, controlled, extended) release products Generally flip-flop PK (k a < k el ) C min more dependent on the rate of absorption than on elimination 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 4

Minimum concentration History Was never a primary PK metric in any regulation Alternative PK metrics for MR products were explored in the mid 1990s; C min was none of them (likely due to its high ISCV) As a primary PK metric The EMA s IR draft (2008) C τ,ss (termed C min,ss ); dropped in the final GL (2010) The EMA s MR draft (2013) C τ,ss ; widening of the acceptance criteria possible The EMA s MR GL (2014) Prolonged release products and multiphasic modified release products» With accumulation: C τ,ss ; widening of the acceptance criteria possible» With no risk of accumulation or those intended exclusively for once only use: MD not required 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 5

Minimum concentration (EMA s terminology) IR GL (draft 2008) C min,ss : minimum plasma concentration at steady state IR GL (comments on the draft 2010) By C min,ss we mean the concentration at the end of the dosage interval, i.e. C trough. IR GL (final 2010) C min,ss removed from required steady state PK metrics MR GL (2014) New formulations C min,ss (minimum concentration anywhere within the profile) Abridged applications (generics) C τ,ss C τ (together with partial AUCs) might waive MD if low accumulation 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 6

Minimum concentration (problems) C τ and C τ,ss Not to be confused with the last concentration >LLOQ (C z or C last ) Might require intra- or extrapolation if the sample is missing (e.g., vial broken in centrifugation) deviation from scheduled sampling at τ Might not be supported in standard NCA software Only implemented in the current release of Phoenix/WinNonlin (Certara 2017) As a single point metric high ISCV expected Esp. for products with low to moderate accumulation the highest ISCV of the entire profile Reference-scaling possible even within a single profile (two values of C τ,ss ) Model with two sequences: TTRR RRTT 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 7 concentration 100 80 60 40 20 0 0 6 12 18 24 time

EMA: Waiving of MD studies (generics) MD study not required for delayed release products MD study might be waived for prolonged and multiphasic modified release products Conditions SD with the highest strenght performed Low accumulation expected Mean AUC 0 τ covers at least 90% AUC 0, both for test and reference Additional PK metrics representing the shape of profiles demonstrate BE early and late partial AUC with pre-defined cut-off time cut-off = τ/2 or other if justified If at least one of the partial AUCs fails to demonstrate BE, the MD has to be performed If PK metrics in the MD study demonstrate BE, overrules failing one(s) of the SD study 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 8

EMA: Waiving of MD studies (generics) Proposal to waive the MD study based on BE of the additional PK metric C τ in the SD study * Three models (each with/without lag-time) Matrix type formulation (three absorption rate constants) Osmotic pump (zero- and first-order) Biphasic product (IR fraction first-order, MR fraction zero-order) Simulations Crossover 12 48 subjects Parameters CV 10, 15, 20% SD and MD * An alternative single dose parameter to avoid the need for steady-state studies on oral extended-release drug products. Eur J Pharmaceut Biopharmaceut. 2012;80(2):410 7. doi:10.1016/j.ejpb.2011.11.001 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 9

EMA: Waiving of MD studies (generics) Proposal to waive the MD study based on BE of the additional PK metric C τ in the SD study Results ISCV Conventional PK metrics 20 30% C τ (SD) and C τ,ss (MD) 30 40% Inclusion of C τ in the required PK metrics of the SD study is predictive of MD performance Higher sample size in the SD study required in order to maintain power AAPS Clinical Pharmacology and Translational Research Section s Outstanding Manuscript Award in Modeling and Simulation (2012) 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 10

EMA: Waiving of MD studies (generics) Proposal challenged based on real data * Review of all studies of prolonged release products submitted to the Spanish Agency since 2000 Outcome (SD and MD) of six cases where the MD study failed on C min,ss Authors concluded that [ ] in [ ] six cases [ ] the multiple dose study was the only design able to detect the differences and, therefore, it was essential when comparing the in vivo performance of prolonged release products. Regarding the predictive value of C τ, one case [ ] shows that it is predictive of the bioequivalence failure of C min,ss, but in the other five cases, the results are not predictive or as sensitive as C max,ss or C min,ss. * Investigation on the need of multiple dose bioequivalence studies for prolonged-release generic products. Int J Pharm. 2012;423(2):321 5. doi:10.1016/j.ijpharm.2011.11.022 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 11

EMA: Waiving of MD studies (generics) Proposal challenged based on real data Critical review of the review Cases where the MD study passed on C min,ss were not reported Impossible the assess the false positive rate Outcome (SD and MD) of six cases where the MD study failed on C min,ss In five of six cases C τ (SD) correctly predicted the result of C min,ss In cases 6 and 11 the ISCV after MD increased which is uncommon In case 7 both SD and MD failed but the deviation of the PE from 100% reversed (SD 125%, MD 84%). Coding error? None of the studies were sufficiently powered to show BE of C τ and C min,ss (median 11.84%, quartiles 3.25 13.35%) Point estimate (90% CI) 160 140 120 100 80 6 7 8 9 10 11 Case # (SD, MD) 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 12

EMA: Waiving of MD studies (generics) Proposal supported by real data Critical review of the review All studies failing on C min,ss (MD) failed on C τ (SD) as well Insufficient power as expected since at the time of submission C min was not a strict requirement (even if designed for an expected GMR of 95%, only three of the twelve studies would have a power of 80%) The one case passing C τ (SD) and failing C min,ss (MD) was extremely underpowered in MD and therefore, inconclusive Contrary to their conclusions authors confirmed by real cases that C τ (SD) is indeed a reliable predictor of multiple dose performance of prolonged release formulations The findings do not refute but rather support the simulation study 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 13

EMA: Waiving of MD studies (generics) Harmonisation Option to waive the MD study based on low extent of accumulation Health Canada EMA 20% extrapolated AUC 10% extrapolated AUC Accumulation ratio of 1.1111 very unlikely to meet with prolonged release products * MD studies are generally not required in other jurisdictions Pharmacovigilance is not very sensitive but obviously no problems with safety or efficacy are evident even in countries with a high market share of generic products Accumulation ratio 1.5 1.4 1.3 1.2 1.1 1.0 1.1111 1.2500 0 5 10 15 20 25 30 % extrapolated AUC (SD) * Proposal for defining the relevance of drug accumulation derived from single dose study data for modified release dosage forms. Biopharm Drug Dis. 2015;36:93 103. doi:10.1002/bdd.1923 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 14

Secondary shape metrics % Peak-to-Trough Fluctuation (PTF) (C max,ss C min,ss ) /C av,ss, where C av,ss = AUC 0 τ /τ Variability generally lower than the one of C max,ss Swing (C max,ss C min,ss ) /C min,ss Might show extreme variability (esp. if low accumulation) Plateau Time (t 75% ), Peak Occupancy Time (POT-25) Time span during which concentrations are within 25% of C max Mandatory in Russia and the Eurasian Economic Union Half Value Duration (HVD), Peak Occupancy Time (POT-50) Time span during which concentrations are within 50% of C max More stable than t 75% /POT-25 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 15

Relevance of additional PK metrics Currently limited data available on any Proposal at the EUFEPS Open Discussion Forum on the Revised European Guideline on Pharmacokinetic and Clinical Evaluation of Modified Release Dosage Forms (Bonn, June 2013) Science-based regulations Applicants should analyze studies with the suggested new PK metrics in an exploratory (!) manner and submit results to agencies BE should be assessed only by conventional PK metrics like in the previous GL After a limited time frame (e.g., two years) the data could be assessed for their sensitivity and included in the GL if deemed necessary 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 16

Primary and secondary PK metrics for evaluation of steady state studies, C min vs.c τ, relevance of C min /C τ or fluctuation for bioequivalence assessment Thank You! Helmut Schütz BEBAC Consultancy Services for Bioequivalence and Bioavailability Studies 1070 Vienna, Austria helmut.schuetz@bebac.at 12 April 2018 [Session II: Necessity of multiple dose studies in BE testing] 17