Key Counseling Points for Bimekizumab in Plaque Psoriasis
Bimekizumab is a highly effective dual IL-17A/F inhibitor that should be recommended for patients with moderate-to-severe plaque psoriasis, particularly those with relevant skin involvement impacting quality of life or extensive disease. 1
Mechanism of Action and Efficacy
- Bimekizumab is a humanized IgG1 monoclonal antibody that selectively inhibits both interleukin-17A and interleukin-17F 2
- Clinical efficacy highlights to discuss with patients:
- Superior to adalimumab and secukinumab in achieving complete skin clearance 3, 4
- Rapid onset of action with significant improvement often seen within 4 weeks 4
- High rates of complete skin clearance (PASI 100) maintained through 96 weeks of treatment 5
- Effective for difficult-to-treat areas including scalp, nails, and palmoplantar psoriasis 1
Dosing and Administration
- Initial dosing: 320 mg administered subcutaneously at weeks 0,4,8,12, and 16 2
- Maintenance dosing: 320 mg every 8 weeks (may require every 4 weeks in some patients) 6
- Self-administered subcutaneous injection using prefilled syringe or autoinjector 2
- Higher dosing may be required for patients weighing ≥120 kg due to lower plasma concentrations 2
Safety Considerations
Common Side Effects
- Upper respiratory tract infections
- Oral candidiasis (more common than with other biologics)
- Diarrhea
- Hypertension 3
Important Safety Warnings
- Increased risk of infections, particularly oral candidiasis (predominantly mild to moderate) 4
- Tuberculosis screening required before initiating therapy
- Live vaccines should not be given during treatment
- Inactivated vaccines appear to maintain normal immune response 2
Monitoring Requirements
- Baseline tuberculosis screening before initiating therapy
- Regular assessment of treatment response and adverse events
- No specific laboratory monitoring requirements, but general health monitoring recommended
Immunogenicity
- Anti-drug antibodies may develop in approximately 45% of patients with plaque psoriasis
- Neutralizing antibodies occur in approximately 16% of patients
- Current evidence suggests antibodies do not significantly impact efficacy or safety 2
Special Considerations
- May be particularly beneficial for patients with:
- Avoid in patients with active infections
- Similar efficacy in both TNF-naïve and TNF-experienced populations 1
Practical Aspects
- Store in refrigerator (2-8°C/36-46°F)
- Allow to reach room temperature before injection (approximately 30 minutes)
- Rotate injection sites
- Dispose of used needles/syringes properly