Tagrisso (osimertinib) vs Rybrevant (amivantamab-vmjw)

Tagrisso (osimertinib) vs Rybrevant (amivantamab-vmjw)

Tagrisso (osimertinib) is an oral, third-generation, irreversible EGFR tyrosine kinase inhibitor specifically designed to treat non-small cell lung cancer (NSCLC) with certain EGFR mutations. Rybrevant (amivantamab-vmjw) is a bispecific antibody, administered through intravenous infusion, that targets EGFR and MET receptors and is used for NSCLC with EGFR exon 20 insertion mutations. The choice between these two medications would depend on the specific EGFR mutation present in a patient's cancer, their overall health, and treatment goals, which should be determined in consultation with an oncologist.

Difference between Tagrisso and Rybrevant

Metric Tagrisso (osimertinib) Rybrevant (amivantamab-vmjw)
Generic name Osimertinib Amivantamab-vmjw
Indications Non-small cell lung cancer (NSCLC) with specific EGFR mutations Non-small cell lung cancer (NSCLC) with EGFR exon 20 insertion mutations
Mechanism of action EGFR tyrosine kinase inhibitor Bispecific antibody targeting EGFR and MET receptors
Brand names Tagrisso Rybrevant
Administrative route Oral Intravenous
Side effects Diarrhea, rash, dry skin, nail toxicity, stomatitis, decreased appetite Infusion-related reactions, skin rash, paronychia, musculoskeletal pain, dyspnea
Contraindications Hypersensitivity to osimertinib or any component of the formulation Hypersensitivity to amivantamab, polysorbate 80, or any component of the formulation
Drug class Tyrosine kinase inhibitor Bispecific antibody
Manufacturer AstraZeneca Janssen Biotech, Inc.

Efficacy

Tagrisso (Osimertinib) Efficacy in Lung Cancer

Tagrisso (osimertinib) is a third-generation, irreversible epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) that has shown significant efficacy in the treatment of non-small cell lung cancer (NSCLC) with specific EGFR mutations. Clinical trials have demonstrated that osimertinib is particularly effective in patients with NSCLC harboring EGFR T790M mutations, which are a common mechanism of resistance to earlier-generation EGFR TKIs. In the AURA3 study, osimertinib significantly improved progression-free survival (PFS) compared to platinum-based chemotherapy in patients with T790M mutation-positive NSCLC who had progressed after first-line EGFR TKI therapy.

Moreover, the FLAURA trial established osimertinib as a first-line treatment option for NSCLC patients with EGFR mutations (exon 19 deletions or exon 21 L858R mutations). In this study, osimertinib not only improved PFS but also showed a survival benefit compared to first-generation EGFR TKIs. The efficacy of osimertinib in improving overall survival highlights its role as a preferred treatment for patients with advanced EGFR-mutated NSCLC.

Rybrevant (Amivantamab-vmjw) Efficacy in Lung Cancer

Rybrevant (amivantamab-vmjw) is a bispecific antibody that targets both the EGFR and MET receptors and has been approved for the treatment of adults with NSCLC with EGFR exon 20 insertion mutations, whose disease has progressed on or after platinum-based chemotherapy. This approval was based on the results of the CHRYSALIS study, which demonstrated that amivantamab-vmjw led to a significant clinical response in a population of patients with few treatment options.

The CHRYSALIS trial showed that amivantamab-vmjw had a manageable safety profile and provided durable responses in patients with NSCLC harboring EGFR exon 20 insertion mutations. The efficacy of Rybrevant in this patient population is particularly noteworthy as these mutations are typically resistant to conventional EGFR TKIs, and patients have limited treatment options. The introduction of amivantamab-vmjw offers a new therapeutic avenue for these patients, with the potential to improve outcomes in a challenging subset of lung cancer.

Regulatory Agency Approvals

Tagrisso
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA
  • Health Canada
  • Therapeutic Goods Administration (TGA), Australia
  • Medsafe (NZ)
Rybrevant
  • European Medical Agency (EMA), European Union
  • Food and Drug Administration (FDA), USA

Access Tagrisso or Rybrevant today

If Tagrisso or Rybrevant 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
US 0