Joint Formulary & PAD

Bimekizumab - Psoriasis

I agree that in using this database I understand that this platform only provides guidance on local prescribing policy and that all prescribing decisions are ultimately the responsibility of the clinician.

Status 1

Red
Formulations :
  • Subcutaneous injection (sc)
Associated Icons :
Restrictions / Comments :

PAD Profile

ChemicalSubstance :
Bimekizumab
Indication :
Psoriasis
Group Name :
Keywords :
Biologic, immunosuppressant, interleukin (IL) 17RA inhibitor, DMARD, bDmard, Disease modulating, Dermatology,
Brand Names Include :
Bimzelx
Important Information :
Latest Additions Date From :
Latest Additions Date To :
Guidelines :
Supporting Documents :
2

Committee Recommendations (2)

The Surrey Heartland Integrated Care System Area Prescribing Committee have agreed to adopt the SERMOG high-cost drugs pathway.for adiults with psoriasis

The Surrey Heartlands integrated care system Area Prescribing Committee (APC) approve bimekizumab as a treatment option for the treatment of severe plaque psoriasis in line with NICE TA723. 
Increased frequency of dosing is agreed for those patients with a body weight ≥ 120 kg who did not achieve complete skin clearance during induction.

Bimekizumab for this indication will be considered as RED on the traffic light status (treatment should be initiated and continued by specialist clinicians).

Increased frequency of dosing is agreed for those patients with a body weight ≥ 120 kg who did not achieve complete skin clearance during induction.
Primary care prescribers should be aware that their patient is receiving this medicine and ensure that this is recorded on the patient’s medication screen as a hospital-only drug in line with guidance on the PAD. This will also alert the prescriber to potential side effects and interactions with other medicines prescribed in primary care. It will also ensure that GP records, which are accessed by other healthcare providers, are a true and accurate reflection of the patient’s medication.”