INDiGO-Select: profiling and selecting your optimal clinical development candidate

An educational webinar on mitigating risk of failure in drug development

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View our webinar on INDiGO-Select, our characterisation package to increase the knowledge on new chemical entities that are approaching the development phase.

INDiGO-Select is focused on the lead molecule chemistry, its physical-chemical properties and preclinical DMPK and safety profile, as to minimise the risk of failure during transition into the subsequent development stages, thus maximising probability of success and minimising overall development costs and timelines.

The webinar covers a description of the approach, showing the main benefits and case studies where this approach was successfully applied, leading to a 100% track record in identifying liabilities – no programmes stopped due to tox or developability issues.


About the speakers

pagliaruscoSabrina Pagliarusco | Manager, Integrated Development Programmes

Senior Scientific Project Leader with over 20 years' experience in the pharmaceutical industry. Strong experience in Pre-Clinical Drug Development mainly from candidate selection up to market drug approval. Accountable for the scientific management of drug development integrated projects defined as multi- departmental and potentially multi-sites work packages including CMC and Pre-clinical functions, leading overall scientific strategy development and facilitating technical problems solving and solutions implementation.

Extensive knowledge and background in the design and execution of Pre-clinical studies (as well as in the interpretation of generated data), tailored to needs of each development phase depending on the specific indication accordingly to regulatory (ICH and FDA) requirements. Experience in review of and contributions to regulatory submissions of Investigator's Brochure, IND, CTD, IMPD and registration dossiers to support NDA/MAA drug submission.

 

Tosini FedericoFederico Tosini | Senior Scientific Project Leader

Prior to joining Aptuit in April 2017, Federico was principal scientist and formulation lead at Novartis Global Development in Switzerland. He previously held different roles with increasing responsibility at Novartis Pharma and Chiesi Farmaceutici.

Federico has more than 12 years’ experience in the pharmaceutical industry, acquired within pharma companies at global level and he combines a solid knowledge of drug product development, especially on inhalation products, with project leadership skills.

He has been a member and leader of several formulation and validation projects that led to market product launches.

Accountable for the scientific management of drug development integrated projects defined as multi- departmental and potentially multi-sites work packages including CMC and Pre-clinical functions, leading overall scientific strategy development and facilitating technical problems solving and solutions implementation.

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