FP7 Health Program supporting paediatric initiative: the DEEP multinational and multicultural experience Adriana Ceci DEEP Scientific Coordinator, and.

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Presentation transcript:

FP7 Health Program supporting paediatric initiative: the DEEP multinational and multicultural experience Adriana Ceci DEEP Scientific Coordinator, and member of PDCO-EMA

16 Partners 18 recruiting centres from 7 Countries: EU: Cyprus, Greece, Italy, (UK) non-EU: Albania, Egypt, Tunisia 16 Partners 18 recruiting centres from 7 Countries: EU: Cyprus, Greece, Italy, (UK) non-EU: Albania, Egypt, Tunisia A large research-driven network covering the ‘area’ to which the disease belongs to A large research-driven network covering the ‘area’ to which the disease belongs to DEEP is a 4-year multinational project aimed to make available reliable treatments to children with beta-thalassaemia, sickle cell disease and other congenital haemoglobinopathies which represent the most severe forms of anaemia in the world with specific reference to the Mediterranean Area DEEP - DE FERIPRONE E VALUATION IN P AEDIATRICS

The DEEP project: what’s new Starting from an old drug, the project aims to perform paediatric studies in order to develop a new liquid formulation specific for the paediatric population and a new paediatric indication A new Marketing Authorisation (PUMA) The Project develops around a full drug developmental Plan (PIP) approved by the European Agency- PDCO that includes: 1 post-marketing study o pharmacoeconomic study Liquid Formulation preparation 2 Clinical Trials: o PK trial providing appropriate dose definition (DEEP-1) o efficacy-safety multicentre, comparator controlled trial (DEEP-2) o long-term safety non-interventional study (DEEP-3)

Innovative approaches in CTs: DEEP-1 PK modeling/simulation study to define drug exposure and appropriate dosage of deferiprone for children aged < 6yrs Inclusion criteria based only on number on transfusional Fe intake without any age threshold First time comparison between the two oral available comparators: deferiprone vs deferasirox DEEP-2: the larger RCT in paediatric patients New, more reliable endpoint based on magnetic resonance: Cardiac MRI T2* included as co-primary endpoint for children above 10 year and liver MRI-R2 included to measure LIC instead of liver biopsy in all patients not requiring sedation. The DEEP project: what’s Innovative

Multi-ethnic population with different cultures and laws Multi-ethnic population with different cultures and laws Paediatric population (involves children of different ages) Paediatric population (involves children of different ages) ‘Registrative’ CTs with Economic burden Ethical stringent provisions GCP-ICH E11 obligations ‘Registrative’ CTs with Economic burden Ethical stringent provisions GCP-ICH E11 obligations A rare and disperse population involving different Rare Congenital Anaemia The DEEP Project: what’s Challenging

2.To implement a unique procedure and a unique CTA ‘trial submission package’ 3.To develop a ‘patients tailored approach’ involving children, families and association 1.To organize a ‘trials management plan and infrastructure’ including SOPs, data management, drug management, pharmacovigilance, monitoring, etc T HE DEEP MULTISTEPS APPROACH The DEEP strategy deals with COMPLEXITY

STEP 1: A COMPLEX ( AND EXPENSIVE ) ORGANISATIONAL INFRASTRUCTURE HAS BEEN SET UP The DEEP strategy deals with DIVERSITY

In EU Countries (Italy, Cyprus and Greece) the Competent Authority authorisation and the Ethics Committee approval is ruled by the Directive 2001/20/EC in terms of CTA form, IMP documents, insurance, informed consent Specific rules for the paediatric population PIP, EMA 2008 recommendations, ICH-E11, etc) In Albania specific rules on CTs are lacking; a special decision from the Ministry of Health is needed In Egypt the CTA is largely similar to Europe, but informed consent procedures are different (i.e. consent from only one parent is accepted- sending samples abroad is regulated) In Tunisia the Ministry of Health, the National and local ECs shall authorise a paediatric trial The legislative context: national rules in DEEP countries This ‘gold standard’ is to be applied in all centers modified according to the national rules

BOOKLET for the younger ones (under 6 years old) Patient-tailored communication model: 3 different BOOKLETS explaining CTs aims and procedures and what they are going to experience 2 different ASSENT FORMS Translated in the national language: available in Arabic, Albanian, French, English, Italian, Greek The DEEP strategy to deal with diversity STEP 3: P ATIENTS EMPOWERMENT IN DEEP

BOOKLET and ASSENT FORM for 6-10 years old children The DEEP strategy to deal with diversity STEP 3: P ATIENTS EMPOWERMENT IN DEEP

BOOKLET and ASSENT FORM for years old adolescents The DEEP strategy to deal with diversity STEP 3: P ATIENTS EMPOWERMENT IN DEEP

Recruitment and approval: the state of the art New formulation is available to the investigational sites and used in the trials DEEP-1 is concluding recruitment with success DEEP-2 approved by the 80% of the Ethics Committees and Competent Authorities and the recruitment is now starting DEEP-3 observational study is on-going DEEP is a succes story in the EUROMED perspective

DEEP is aimed to respond to a specific need from the European Union Policies and rules on Paediatric Medicines as stated in the Paediatric Regulation What makes DEEP project so special in the contest of FP7 Projects Framework? DEEP is responding to a real therapeutic need. This need is a common need in european and no-european MEDITERRANEA REGIONS Less than 30% of Medicines on the market are approved for children. Unapproved drugs are used ‘off-label’ because uncovered therapeutic needs.

Innovative approaches in CTs: DEEP-1 PK modeling/simulation study to define drug exposure and appropriate dosage of deferiprone for children aged < 6yrs Inclusion criteria based only on number on transfusional Fe intake without any age threshold First time comparison between the two oral available comparators: deferiprone vs deferasirox DEEP-2: the larger RCT in paediatric patients New, more reliable endpoint based on magnetic resonance: Cardiac MRI T2* included as co-primary endpoint for children above 10 year and liver MRI-R2 included to measure LIC instead of liver biopsy in all patients not requiring sedation. The DEEP project: based on scientist excellence located to European/no-European countries

FP7 application PIP application PUMA Applications Project considered on the basis of scientific excellence (no paediatric needs) No mention to the trials conduct Very few preclinical studies funded Research Consortia having no experiences in regulatory process A whole research & development plan requested. All paed. subsets should be covered Details of timing & measures including preclinical, formulation Efficacy, Safety Commercial Sponsor Intellectual Property DEEP demonstrate to be able

The lesson learnt from these projects  In response to the EC Research policies  Networking action: a very large scientific community is sharing competencies and skills.  Pubblic-private integration and support to SMEs  In response to the specific topic (Paediatric Medicines:  Development of Paediatric Plans (PIPs available for 15 Active Substances)  Consistent number of paediatric patients, also neonates, in the trials  An appropriate drug for treating iron overload in children  In response to the Scientific Community expectations  Innovative elements included in the trials: pharmacogenetic studies  New competencies acquired (Regulatory, trials managements, Ethics, Communication with parents/patients, etc)

Conclusions Is DEEP Research CONSORZIUM qualified to apply for? Excellent Science Industrial Leadership Societal Concerns Health, demographic change and wellbeing