* receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. * participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) * groups 1, 2 and 3 only: prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). * administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. * any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting \<14 days). * any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. * history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. * any history of angioedema. * any history of anaphylaxis. * pregnancy, lactation or willingness/intention to become pregnant during the study. * history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). * history of any organic central nervous system disorder or any functional disorder involving neurological symptoms * history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). * bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin * history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or * history of antiphospholipid syndrome * prior receipt of unfractionated heparin * history of heparin induced thrombocytopenia * any other serious chronic illness requiring hospital specialist supervision. * chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). * chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). * nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). * seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). * suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. * suspected or known injecting drug abuse in the 5 years preceding enrolment. * any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. * any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. * groups 1, 2 and 3 only: living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). * groups 1, 2 and 3 only: membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

* receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. * participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) * groups 1, 2 and 3 only: prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). * administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. * any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting \<14 days). * any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. * history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. * any history of angioedema. * any history of anaphylaxis. * pregnancy, lactation or willingness/intention to become pregnant during the study. * history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). * history of any organic central nervous system disorder or any functional disorder involving neurological symptoms * history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). * bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin * history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or * history of antiphospholipid syndrome * prior receipt of unfractionated heparin * history of heparin induced thrombocytopenia * any other serious chronic illness requiring hospital specialist supervision. * chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). * chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). * nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). * seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). * suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. * suspected or known injecting drug abuse in the 5 years preceding enrolment. * any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. * any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. * groups 1, 2 and 3 only: living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). * groups 1, 2 and 3 only: membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - groups 1, 2 and 3 only: prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of any organic central nervous system disorder or any functional disorder involving neurological symptoms - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin - history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or - history of antiphospholipid syndrome - prior receipt of unfractionated heparin - history of heparin induced thrombocytopenia - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - groups 1, 2 and 3 only: living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - groups 1, 2 and 3 only: membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - groups 1, 2 and 3 only: prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of any organic central nervous system disorder or any functional disorder involving neurological symptoms - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin - history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or - history of antiphospholipid syndrome - prior receipt of unfractionated heparin - history of heparin induced thrombocytopenia - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - groups 1, 2 and 3 only: living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - groups 1, 2 and 3 only: membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin - history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or - history of antiphospholipid syndrome - prior receipt of unfractionated heparin - history of heparin induced thrombocytopenia - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 28 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture, or continuous anticoagulation e.g. with warfarin - history of confirmed major thrombotic event (including cerebral venous sinus thrombosis, deep vein thrombosis, pulmonary embolism), or - history of antiphospholipid syndrome - prior receipt of unfractionated heparin - history of heparin induced thrombocytopenia - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 30 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture. - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).

- receipt or planned receipt of any vaccine other than the study intervention within 30 days before and after each study vaccination. - participation in covid-19 prophylactic drug trials for the duration of the study. (note: participation in covid-19 treatment trials is allowed in the event of hospitalisation due to covid-19. the study team should be informed as soon as possible.) - prior receipt of an investigational or licensed vaccine likely to impact on interpretation of the trial data (e.g. adenovirus vectored vaccines, any coronavirus vaccines). - administration of immunoglobulins and/or any blood products within the three months preceding the planned administration of the vaccine candidate. - any confirmed or suspected immunosuppressive or immunodeficient state, including hiv infection; asplenia; recurrent severe infections and use of immunosuppressant medication within the past 6 months, except topical steroids or short-term oral steroids (course lasting <14 days). - any autoimmune conditions, except mild psoriasis, well-controlled autoimmune thyroid disease, vitiligo or stable coeliac disease not requiring immunosuppressive or immunomodulatory therapy. - history of allergic disease or reactions likely to be exacerbated by any component of chadox1 ncov-19. - any history of angioedema. - any history of anaphylaxis. - pregnancy, lactation or willingness/intention to become pregnant during the study. - history of cancer (except basal cell carcinoma of the skin and cervical carcinoma in situ). - history of serious psychiatric condition likely to affect participation in the study (e.g. ongoing severe depression, history of admission to an in-patient psychiatric facility, recent suicidal ideation, history of suicide attempt, bipolar disorder, personality disorder, alcohol and drug dependency, severe eating disorder, psychosis, use of mood stabilisers or antipsychotic medication). - bleeding disorder (e.g. factor deficiency, coagulopathy or platelet disorder), or prior history of significant bleeding or bruising following im injections or venepuncture. - any other serious chronic illness requiring hospital specialist supervision. - chronic respiratory diseases, including mild asthma (resolved childhood asthma is allowed). - chronic cardiovascular disease (including hypertension), gastrointestinal disease, liver disease (except gilberts syndrome), renal disease, endocrine disorder (including diabetes) and neurological illness (excluding migraine). - nasal pathology (e.g. congenital abnormalities such as an abnormal septum or polyps, previous cauterisation, rhinoplasty or nasal surgery of any kind, recurrent epistaxis). - seriously overweight (bmi≥40 kg/m2) or underweight (bmi≤18 kg/m2). - suspected or known current alcohol abuse as defined by an alcohol intake of greater than 42 units every week. - suspected or known injecting drug abuse in the 5 years preceding enrolment. - any clinically significant abnormal finding on screening biochemistry, haematology blood tests or urinalysis. - any other significant disease, disorder or finding which may significantly increase the risk to the volunteer because of participation in the study, affect the ability of the volunteer to participate in the study or impair interpretation of the study data. - living in the same household as any vulnerable groups at risk of severe covid-19 disease (as per phe guidance). - membership of any group identified by jcvi at the time of enrolment as being eligible for priority vaccination (i.e. ahead of the typical member of the individual's age cohort).