Product image of Omvoh (Mirikizumab) supplied by GNH India

Omvoh

Active Ingredient:
Mirikizumab
Origin:
EU

Omvoh (Mirikizumab)

Mirikizumab, the active ingredient in Omvoh, is a monoclonal antibody presented as a 100 mg/mL solution for intravenous infusion use. It targets inflammatory pathways and is indicated for the treatment of moderate to severe ulcerative colitis in adult patients. GNH India supplies Omvoh as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and specialty clinics worldwide.

GNH India supplies Omvoh as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and specialty clinics worldwide.

Manufacturer / TM Owner

Eli Lilly Nederland B.V.

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Indications & Clinical Uses

Omvoh is a selective interleukin‑23 (IL‑23) inhibitor used in inflammatory bowel disease management.

  • Ulcerative colitis: reduces signs and symptoms, achieving clinical remission in many patients.
  • Crohn’s disease (investigational): evaluated for induction of remission in clinical trials.
  • Pouchitis: studied as a potential therapy for inflammation of the ileal pouch.
  • Rheumatoid arthritis (exploratory): assessed in early‑phase studies for disease activity reduction.

How It Works

  • Mirikizumab binds selectively to the p19 subunit of interleukin‑23, blocking its interaction with the IL‑23 receptor. This inhibition prevents downstream activation of the JAK‑STAT signaling cascade, reducing the production of pro‑inflammatory cytokines such as IL‑17 and IL‑22, and thereby modulating the immune response that drives chronic intestinal inflammation.

Side Effects

Adverse reactions reported with mirikizumab are generally mild to moderate, but serious events can occur.

Common Side Effects

  • Injection site reactions: redness, swelling, or pain at the infusion site.
  • Upper respiratory tract infection: nasopharyngitis or mild sinusitis.
  • Headache: transient and often mild.
  • Fatigue: general feeling of tiredness.
  • Nausea: occasional mild gastrointestinal upset.
  • Diarrhea: loose stools without infection.

Serious or Rare Side Effects

  • Severe infections: including opportunistic bacterial, fungal or viral infections.
  • Hypersensitivity reactions: anaphylaxis, urticaria, or angioedema.
  • Hepatotoxicity: elevated liver enzymes indicating liver stress.
  • Inflammatory bowel disease flare: paradoxical worsening of disease activity.
  • Malignancy risk: potential increased risk of certain cancers with long‑term immunosuppression.
  • Cardiovascular events: rare cases of myocardial infarction or stroke.

Precautions & Warnings

When prescribing mirikizumab, clinicians should assess patient history and monitor for specific safety concerns.

  • Infection screening: evaluate for active or latent infections before initiation.
  • Vaccination status: update vaccines, avoiding live vaccines during therapy.
  • Liver function: monitor transaminases and bilirubin periodically.
  • Gastrointestinal monitoring: watch for signs of disease flare or new abdominal symptoms.
  • Pregnancy and lactation: weigh potential benefits against unknown fetal risks.
  • Store at 2‑8 °C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Mirikizumab may interact with other agents that affect immune function or infection risk.

Major Interactions (Avoid)

  • Live vaccines: concurrent administration can cause severe infection.
  • Systemic immunosuppressants (e.g., high‑dose corticosteroids): may amplify infection risk.

Moderate Interactions (Monitor Closely)

  • Antifungal agents (e.g., azoles): may require infection surveillance.
  • Antiviral therapies (e.g., hepatitis B prophylaxis): monitor viral load.
  • Antibiotics: use judiciously, observing for opportunistic infections.

Frequently Asked Questions

Omvoh contains mirikizumab, a monoclonal antibody indicated for the treatment of moderate to severe ulcerative colitis in adults. It works by targeting specific immune pathways that drive intestinal inflammation, helping to achieve clinical remission and improve quality of life.

Mirikizumab selectively binds to the p19 subunit of interleukin‑23, blocking its interaction with the IL‑23 receptor. This inhibition stops downstream signaling that leads to the production of pro‑inflammatory cytokines, thereby reducing the inflammatory response in the gut mucosa.

The dosing regimen for Omvoh is determined by the prescribing clinician based on the patient’s condition, weight, and response to therapy. Healthcare professionals follow the approved labeling and adjust the infusion schedule as needed.

Safety data for mirikizumab in pregnancy and lactation are limited. The drug should only be used if the potential benefit justifies the potential risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To place an order, submit an enquiry on the Omvoh product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, confirming trade or institutional credentials before providing pricing, availability, shipping details, and necessary import documentation.

Omvoh (mirikizumab) is one of several IL‑23 inhibitors approved for inflammatory bowel disease. Compared with alternatives such as ustekinumab or risankizumab, mirikizumab targets the p19 subunit specifically, which may offer distinct efficacy and safety profiles, though head‑to‑head comparative data are limited.

Omvoh should be stored at 2‑8 °C (refrigerated) in its original packaging, protected from light. It must not be frozen or shaken, and any vial that has been kept outside the recommended temperature range should be discarded.

Omvoh is supplied as a sterile solution for intravenous infusion. The infusion is typically administered by a healthcare professional in a clinical setting, following the recommended infusion rate and monitoring guidelines outlined in the product label.

Serious risks include severe infections, hypersensitivity reactions such as anaphylaxis, liver enzyme elevations, and a potential increased risk of malignancies with long‑term immunosuppression. Patients should be monitored regularly for signs of infection, liver dysfunction, and any unexpected symptoms.

Omvoh is contraindicated in patients with known hypersensitivity to mirikizumab or any excipients in the formulation. Caution is also advised for individuals with active serious infections, uncontrolled liver disease, or those who are pregnant or breastfeeding without a clear benefit‑risk justification.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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