21
Participants
Start Date
December 7, 2020
Primary Completion Date
October 2, 2023
Study Completion Date
October 2, 2023
Atovaquone Oral Suspension
Atovaquone, cisplatin and vinorelbine are all considered Investigational Medicinal Products (IMPs) in this trial due to the investigation of these drugs in a novel combination. Patients will be allocated one of four doses of atovaquone: 450 mg, 600 mg, 675 mg or 750 mg (all doses PO BD).
Standard of care chemotherapy
Atovaquone, cisplatin and vinorelbine are all considered Investigational Medicinal Products (IMPs) in this trial due to the investigation of these drugs in a novel combination. Patients will receive two 21-day cycles of cisplatin and vinorelbine chemotherapy, comprising 80 mg/m2 cisplatin on days 1 \& 22 of their CRT treatment and 15 mg/m2 vinorelbine on days 1, 8, 22 \& 29.
Standard of care radiotherapy
Thoracic radiotherapy will commence on day one of chemotherapy and be delivered in 66 Gy in 33 fractions, once daily, 5 days a week (Monday-Friday) for 6.5 weeks.
Western General Hospital, NHS Lothian, Edinburgh
Guy's and St Thomas', London
Churchill Hospital, Oxford University Hospitals, Oxford
Collaborators (1)
Cancer Research UK
OTHER
National Institute for Health Research, United Kingdom
OTHER_GOV
NHS Lothian
OTHER_GOV
Oxford University Hospitals NHS Trust
OTHER
NHS Research Scotland
OTHER
Guy's and St Thomas' NHS Foundation Trust
OTHER
University of Oxford
OTHER