CTC Akademiska, Uppsala:
Our 12-bed, FIH unit, Akademiska, is perfectly located adjacent to the ICU, PET-centre and MRI-facilities at Uppsala University Hospital in Sweden.
Safety always comes first when planning, managing and running a FIH study. CTC has experience in setting up adaptive FIH umbrella protocols including single and multiple ascending dose cohorts, food and drug-drug interaction parts, and patient cohorts. We conduct approximately five FIH studies each year. Being a certified site for early precision QT-assessments (EPQT), we may incorporate this service into your FIH study and provide the possibility for a TQT waiver.
CTC Oscar, Uppsala:
This unit has 24 beds and is, together with CTC’s head office, located next to the Uppsala University hospital. At this research unit we offer Phase 0-IV studies, for example drug-drug interaction, thorough QT, and bioavailability and proof-of-concept studies.
CTC MTC, Uppsala:
This unit is located in proximity to Uppsala University Hospital. With 4 beds and a high capacity for out-patient visits, it is perfectly fitted for multi-centre trials conducted on-site or with a hybrid or virtual design.
CTC Karolinska, Stockholm:
This unit is located close to the Karolinska University Hospital and has 8 beds for conduct of phase I-IV trials and a high capacity for out-patients visits. At this site we have a mix of online staff for virtual visits, site staff for on-site visits as well as home care staff.
CTC Ebbepark, Linköping:
With 4 beds and a high capacity for out-patient visits, it is perfectly fitted for multi-centre trials conducted on-site or with a hybrid or virtual design.
CTC GoCo, Gothenburg (opens Oct 01):
Our newest clinic in located at GoCo Health Innovation City in Gothenburg. With 8 beds and a high capacity for out-patient visits, it is perfectly fitted for multi-centre trials conducted on-site or with a hybrid or virtual design.
Besides studies conducted by our in-house physicians, CTC’s Site Network also facilitates the conduct of clinical trials with external Principal Investigators who are given access to all benefits of using a professional research site with established systems and procedures – the ClinSmart Concept. Our team of Research Nurses assist with logistics, administration, patient recruitment and clinical conduct.