Indication: TAVNEOS (avacopan) is indicated as an adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody...
Read moreIndication: TAVNEOS (avacopan) is indicated as an adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (granulomatosis with polyangiitis [GPA] and microscopic polyangiitis [MPA]) in combination with standard therapy including glucocorticoids. TAVNEOS does not eliminate glucocorticoid use.
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The HCPs appearing in these videos were compensated for their participation.
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Induction patient case study
Watch a case study of a patient receiving induction therapy presented by rheumatologist Dr. John Stone. In this case study, Dr. Stone explains his experience using TAVNEOS® to induce remission in a real-life patient case.
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Induction therapy case study
Watch a case study of a patient receiving induction therapy presented by rheumatologist Dr. John Stone. In this case study, Dr. Stone explains his experience using TAVNEOS® to induce remission in a real-life patient case.
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Persistent symptoms case study
Watch a case study of a patient with persistent severe active symptoms presented by nephrologist Dr. Suneel Udani. In this case study, Dr. Udani reviews a real-life case he had in which a patient with persistent severe active MPA was treated using TAVNEOS®.
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Achieving and sustaining remission in severe active AAV (GPA & MPA)
Join rheumatologist Dr. Adam Kilian and nephrologist Dr. Reza Zonozi as they discuss challenges during diagnosis and management of severe active AAV (GPA and MPA), as well as how adding TAVNEOS® could help your patients achieve and sustain remission.
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Adding TAVNEOS® in patients with persistent severe active disease
Join rheumatologist Dr. Adam Kilian as he shares his approach treating a hypothetical patient with severe active GPA following initial induction therapy.
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Adding TAVNEOS® in newly diagnosed patients with severe active GPA or MPA
Join nephrologist Dr. Reza Zonozi as he shares his approach to management of severe active MPA in a newly diagnosed patient. Hear his perspective on the benefits of adding TAVNEOS®, right from the start, to help appropriate patients achieve and sustain remission following diagnosis.
Licensed healthcare professionals can download the Patient Enrollment Form/Quick Start and Samples Request Form to help their appropriate patients get started on TAVNEOS®
If you’ve decided TAVNEOS® is right for your patient, you can find access and clinical resources below
This guide provides patients (and caregivers) with accessible insights into how adding TAVNEOS® to their treatment plan may help achieve and sustain remission.
With clear emphasis throughout on the importance of their doctor and suggested questions for productive conversations.
The brochure helps patients and their caregivers understand what to expect from the time they make the decision to start TAVNEOS® to the time their medication is received. It provides important information about the TAVNEOS® program and reminders on what to expect during the insurance review process until first shipment.
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Serious hypersensitivity to avacopan or to any of the excipients.
Hepatotoxicity: Serious cases of hepatic injury have been observed in patients taking TAVNEOS, including life-threatening events. Obtain liver test panel before initiating TAVNEOS, every 4 weeks after start of therapy for 6 months and as clinically indicated thereafter. Monitor patients closely for hepatic adverse reactions, and consider pausing or discontinuing treatment as clinically indicated (refer to section 5.1 of the Prescribing Information). TAVNEOS is not recommended for patients with active, untreated, and/or uncontrolled chronic liver disease (e.g., chronic active hepatitis B, untreated hepatitis C, uncontrolled autoimmune hepatitis) and cirrhosis. Consider the risks and benefits before administering this drug to a patient with liver disease.
Serious Hypersensitivity Reactions: Cases of angioedema occurred in a clinical trial, including 1 serious event requiring hospitalization. Discontinue immediately if angioedema occurs and manage accordingly. TAVNEOS must not be readministered unless another cause has been established.
Hepatitis B Virus (HBV) Reactivation: Hepatitis B reactivation, including life-threatening hepatitis B, was observed in the clinical program. Screen patients for HBV. For patients with evidence of prior infection, consult with physicians with expertise in HBV and monitor during TAVNEOS therapy and for 6 months following. If patients develop HBV reactivation, immediately discontinue TAVNEOS and concomitant therapies associated with HBV reactivation, and consult with experts before resuming.
Serious Infections: Serious infections, including fatal infections, have been reported in patients receiving TAVNEOS. The most common serious infections reported in the TAVNEOS group were pneumonia and urinary tract infections. Avoid use of TAVNEOS in patients with active, serious infection, including localized infections. Consider the risks and benefits before initiating TAVNEOS in patients with chronic infection, at increased risk of infection, or who have been to places where certain infections are common.
The most common adverse reactions (≥5% of patients and higher in the TAVNEOS group vs. prednisone group) were nausea, headache, hypertension, diarrhea, vomiting, rash, fatigue, upper abdominal pain, dizziness, blood creatinine increased, and paresthesia.
Avoid co-administration of TAVNEOS with strong and moderate CYP3A4 enzyme inducers. Reduce TAVNEOS dose when co-administered with strong CYP3A4 enzyme inhibitors to 30 mg once daily. Consider dose reduction of CYP3A4 substrates when coadministering TAVNEOS. Co-administration of avacopan and 40 mg simvastatin increases the systemic exposure of simvastatin. While taking TAVNEOS, limit simvastatin dosage to 10 mg daily (or 20 mg daily for patients who have previously tolerated simvastatin 80 mg daily for at least one year without evidence of muscle toxicity). Consult the concomitant CYP3A4 substrate product information when considering administration of such products together with TAVNEOS.
TAVNEOS is available as a 10 mg capsule.
TAVNEOS (avacopan) is indicated as an adjunctive treatment of adult patients with severe active anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis (granulomatosis with polyangiitis [GPA] and microscopic polyangiitis [MPA]) in combination with standard therapy including glucocorticoids. TAVNEOS does not eliminate glucocorticoid use.
Please see Full Prescribing Information and Medication Guide for TAVNEOS.
To report a suspected adverse event, call 1-833-828-6367. You may report to the FDA directly by visiting www.fda.gov/medwatch or calling 1-800-332-1088.
important safety information Contraindications Serious hypersensitivity to avacopan or to any of the excipients.
Warnings and Precautions Hepatotoxicity: Serious cases of hepatic injury have been observed in patients taking TAVNEOS, including life-threatening events. Obtain liver test panel before initiating TAVNEOS, every 4 weeks after start of therapy for 6 months and as clinically...