RoActemra (tocilizumab) vs Lagevrio (molnupiravir)

RoActemra (tocilizumab) vs Lagevrio (molnupiravir)

RoActemra (tocilizumab) is an immunosuppressive drug, specifically an interleukin-6 (IL-6) receptor antagonist, typically used for the treatment of rheumatoid arthritis and has been utilized in severe cases of COVID-19 to manage the immune system's overreaction. Lagevrio (molnupiravir), on the other hand, is an oral antiviral medication designed to directly inhibit the replication of SARS-CoV-2, the virus that causes COVID-19, and is used for treating mild to moderate COVID-19 in adults who are at risk for developing severe illness. When deciding between the two, it is crucial to consider the stage and severity of the disease, the patient's underlying health conditions, and the intended use—whether to modulate an overactive immune response or to directly target viral replication.

Difference between RoActemra and Lagevrio

Metric RoActemra (tocilizumab) Lagevrio (molnupiravir)
Generic name Tocilizumab Molnupiravir
Indications Rheumatoid arthritis, Systemic Juvenile Idiopathic Arthritis, Giant Cell Arteritis, COVID-19 (under emergency use authorization) Mild-to-moderate COVID-19 in adults at risk for severe disease
Mechanism of action Interleukin-6 (IL-6) receptor antagonist Oral antiviral that induces viral mutagenesis
Brand names RoActemra Lagevrio
Administrative route IV infusion, subcutaneous injection Oral
Side effects Upper respiratory tract infections, headache, hypertension, injection site reactions Diarrhea, nausea, dizziness
Contraindications Hypersensitivity to tocilizumab, active infections Hypersensitivity to molnupiravir, pregnancy, breastfeeding
Drug class Immunosuppressive drug, DMARD Antiviral
Manufacturer Roche Merck & Co. (developed in collaboration with Ridgeback Biotherapeutics)

Efficacy

Efficacy of RoActemra (Tocilizumab) for COVID-19

RoActemra, known generically as tocilizumab, is an immunosuppressive drug traditionally used to treat rheumatoid arthritis. However, during the COVID-19 pandemic, its efficacy in treating severe cases of the disease has been explored due to its action as an interleukin-6 (IL-6) receptor antagonist. Clinical studies have suggested that tocilizumab may reduce the risk of death among patients hospitalized with COVID-19, particularly those experiencing severe respiratory symptoms and systemic inflammation. It is hypothesized that by blocking IL-6, tocilizumab can mitigate the cytokine release syndrome (CRS) associated with severe COVID-19, thereby reducing the need for mechanical ventilation and improving survival rates.

The results from randomized controlled trials have shown that tocilizumab, when administered to hospitalized patients with COVID-19 who require oxygen and have evidence of inflammation, can improve outcomes. The RECOVERY trial, for instance, indicated that tocilizumab was beneficial when used alongside dexamethasone, another anti-inflammatory medication. However, it is important to note that the benefits of tocilizumab appear to be most pronounced in patients with rapid disease progression and elevated inflammatory markers.

Efficacy of Lagevrio (Molnupiravir) for COVID-19

Lagevrio, with the generic name molnupiravir, is an antiviral medication designed to treat mild to moderate COVID-19 in adults who are at risk of developing severe illness. Molnupiravir works by introducing errors into the SARS-CoV-2 virus' RNA, thereby inhibiting its ability to replicate. This mechanism has been shown to be effective in reducing the risk of hospitalization or death in patients with mild to moderate COVID-19 who are not hospitalized but have at least one risk factor for severe disease.

Clinical trials have demonstrated that early administration of molnupiravir can reduce the rate of hospitalization and death. The MOVe-OUT trial, a Phase 3 study, found that molnupiravir reduced the risk of hospitalization or death by approximately 30% when given within five days of symptom onset in non-hospitalized patients with mild to moderate COVID-19. While these results are promising, the efficacy of molnupiravir compared to other antiviral treatments and its role in the broader context of COVID-19 therapeutic strategies continue to be areas of active research and discussion.

Regulatory Agency Approvals

RoActemra
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
Lagevrio
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Therapeutic Goods Administration (TGA), Australia
  • Medicines & Healthcare products Regulatory Agency (MHRA), United Kingdom

Access RoActemra or Lagevrio today

If RoActemra or Lagevrio are not approved or available in your country (e.g. due to supply issues), you can access them via Everyone.org.

How it works

Make an enquiry

Choose the medicine you want to buy, answer a couple of questions, and upload your prescription to speed things up. We’ll get back to you within 24 hours.

Breeze through the paperwork

We'll guide you through the required documents for importing unapproved medicine, ensuring you have all the necessary information.

Get a personalized quote

We’ll prepare a quote for you, including medicine costs and any shipping, administrative, or import fees that may apply.

Receive your medicine

Accept the quote and we’ll handle the rest - sourcing and safely delivering your medicine.

Some text on this page has been automatically generated. Speak to your physician before you start a new treatment or medication.

Let's talk

If you have any questions, call us or send us a message through WhatsApp or email:

Contact us
LV 0