Atovaquone With Radical ChemorADIotherapy in Locally Advanced NSCLC

PHASE1CompletedINTERVENTIONAL
Enrollment

21

Participants

Timeline

Start Date

December 7, 2020

Primary Completion Date

October 2, 2023

Study Completion Date

October 2, 2023

Conditions
Locally Advanced Non-Small Cell Lung Cancer
Interventions
DRUG

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).

DRUG

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.

RADIATION

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.

Trial Locations (3)

EH4 2XU

Western General Hospital, NHS Lothian, Edinburgh

SE1 9RT

Guy's and St Thomas', London

OX3 7LE

Churchill Hospital, Oxford University Hospitals, Oxford

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Cancer Research UK

OTHER

collaborator

National Institute for Health Research, United Kingdom

OTHER_GOV

collaborator

NHS Lothian

OTHER_GOV

collaborator

Oxford University Hospitals NHS Trust

OTHER

collaborator

NHS Research Scotland

OTHER

collaborator

Guy's and St Thomas' NHS Foundation Trust

OTHER

lead

University of Oxford

OTHER