Treatments for coronavirus (COVID-19)

The NHS is offering new antibody and antiviral treatments to people with coronavirus (COVID-19) who are at highest risk of becoming seriously ill. People eligible should have been directly contacted and sent a PCR test to use, if needed.

From 10 February, a positive lateral flow test (LFT) can also be used to access the treatments. Find out more on the NHS.uk website on treatments for coronavirus, the page will be updated with the new process from 10 February.

2 types of COVID-19 treatment are available:

Sotrovimab is a biological medicine. It is also known as a neutralising monoclonal antibody (nMAb).

Molnupiravir is an antiviral medicine.

These treatments can help some people manage their COVID-19 symptoms and reduce the risk of becoming seriously ill.

Who can have a COVID-19 treatment

Treatments for COVID-19 are for people aged 12 and over who:

  • are at highest risk of getting seriously ill from COVID-19 (eligibility mentioned in table below)
  • have symptoms of COVID-19 that started within the last 5 days
  • have tested positive for COVID-19 by LFT within the last 5 days

Eligibility Criteria for nMAB/Antiviral Treatment 

Down’s syndrome 

All patients with Down’s syndrome 

Sickle cell disease 

All patients with a diagnosis of sickle cell disease 

Patients with a solid cancer 

  • Active metastatic cancer and active solid cancers (at any stage)  
  • All patients receiving chemotherapy within the last 3 months  
  • Patients receiving group B or C chemotherapy 3-12 months prior  
  • Patients receiving radiotherapy within the last 6 months  

Patients with a haematologic malignancy 

  • Allogeneic haematopoietic stem cell transplant (HSCT) recipients in the last 12 months or active graft vs host disease (GVHD) regardless of time from transplant 
  • Autologous HSCT recipients in the last 12 months 
  • Individuals with haematological malignancies who have 
    • received chimaeric antigen receptor (CAR)-T cell therapy in the last 24 months, or 
    • anti-CD20 monoclonal antibody therapy in the last 12 months 
  • Individuals with chronic B-cell lymphoproliferative disorders receiving systemic treatment or radiotherapy within the last 3 months 
  • Individuals with chronic B-cell lymphoproliferative disorders with hypogammaglobulinaemia or reduced peripheral B cell counts 
  • Individuals with acute leukaemias and clinically aggressive lymphomas who are receiving chemotherapy or within 3 months of completion at the time of vaccination 
  • Individuals with haematological malignancies who have received anti-CD38 monoclonal antibody or B-cell maturation agent (BCMA) targeted therapy in the last 6 months 
  • Individuals with chronic B-cell lymphoproliferative disorders not otherwise described above 

Patients with renal disease 

  • Renal transplant recipients (including those with failed transplants within the past 12 months), particularly those who: 
    • Received B cell depleting therapy within the past 12 months (including alemtuzumab, rituximab [anti-CD20], anti-thymocyte globulin) 
    • Have an additional substantial risk factor which would in isolation make them eligible for nMABs or oral antivirals 
    • Not been vaccinated prior to transplantation 
  • Non-transplant patients who have received a comparable level of immunosuppression 
  • Patients with chronic kidney stage (CKD) 4 or 5 (an eGFR less than 30 ml/min/1.73m2) without immunosuppression 

Patients with liver disease 

  • Patients with cirrhosis Child’s-Pugh class B and C (decompensated liver disease). 
  • Patients with a liver transplant 
  • Liver patients on immune suppressive therapy (including patients with and without liver cirrhosis) 
  • Patients with cirrhosis Child’s-Pugh class A who are not on immune suppressive therapy (compensated liver disease) 

Patients with immune-mediated inflammatory disorders (IMID) 

  • IMID treated with rituximab or other B cell depleting therapy in the last 12 months 
  • IMID with active/unstable disease on corticosteroids, cyclophosphamide, tacrolimus, cyclosporin or mycophenolate. 
  • IMID with stable disease on either corticosteroids, cyclophosphamide, tacrolimus, cyclosporin or mycophenolate. 
  • IMID patients with active/unstable disease including those on biological monotherapy and on combination biologicals with thiopurine or methotrexate 

Primary immune deficiencies 

  • Common variable immunodeficiency (CVID) 
  • Undefined primary antibody deficiency on immunoglobulin (or eligible for Ig) 
  • Hyper-IgM syndromes 
  • Good’s syndrome (thymoma plus B-cell deficiency) 
  • Severe Combined Immunodeficiency (SCID) 
  • Autoimmune polyglandular syndromes/autoimmune polyendocrinopathy, candidiasis, ectodermal dystrophy (APECED syndrome) 
  • Primary immunodeficiency associated with impaired type I interferon signalling 
  • X-linked agammaglobulinaemia (and other primary agammaglobulinaemias) 

HIV/AIDs 

  • Patients with high levels of immune suppression, have uncontrolled/untreated HIV (high viral load) or present acutely with an AIDS defining diagnosis 
  • On treatment for HIV with CD4 <350 cells/mm3 and stable on HIV treatment or CD4>350 cells/mm3 and additional risk factors (e.g. age, diabetes, obesity, cardiovascular, liver or renal disease, homeless, those with alcohol-dependence) 

Solid organ transplant recipients 

All recipients of solid organ transplants not otherwise specified above 

Rare neurological conditions 

  • Multiple sclerosis 
  • Motor neurone disease 
  • Myasthenia gravis 
  • Huntington’s disease 
If you are eligible and have not been contacted by NHS

Any patients that have not been identified centrally and test positive either on LFT or PCR test should contact us or 111 and ask for a referral into CMDU. The CMDU team will then contact the patient as soon as possible to triage them and refer them on for assessment if necessary. 

Page Updated: 11.02.2022