The evolution of initial indications for new cancer medicines authorised in Europe from 1995 to 2023
dc.rights.license | CC-BY-NC-ND | |
dc.contributor.advisor | Bloem, Lourens | |
dc.contributor.author | Nonis, Cristheena | |
dc.date.accessioned | 2025-09-30T00:01:10Z | |
dc.date.available | 2025-09-30T00:01:10Z | |
dc.date.issued | 2025 | |
dc.identifier.uri | https://studenttheses.uu.nl/handle/20.500.12932/50448 | |
dc.description.sponsorship | Utrecht University | |
dc.language.iso | EN | |
dc.subject | Introduction: Despite the critical importance of therapeutic indications in optimising the benefit-risk balance of a medicine, thereby guiding clinical practice and ensuring patient safety, there is limited literature on how indication-setting has evolved over time and which factors have plays a role in that process. Objective: This study aimed to investigate the evolution of initial indications of cancer medicines authorized between January 1, 1995, and December 31, 2023. | |
dc.title | The evolution of initial indications for new cancer medicines authorised in Europe from 1995 to 2023 | |
dc.type.content | Master Thesis | |
dc.rights.accessrights | Open Access | |
dc.subject.courseuu | Drug Innovation | |
dc.thesis.id | 42229 |