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TACI-Fc Fusion Protein (Dual APRIL and BLyS Inhibitor)

Telitacicept (APRIL/BLyS Dual Inhibitor — SLE/IgA Nephropathy)

Brand names: Tai Ai (泰爱) — China; RC18 — global trials

Telitacicept is a recombinant fusion protein biologic investigated and used for systemic lupus erythematosus and IgA nephropathy.

Dosing — being independently re-sourced

ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.

Clinical monograph

How it works

It is a TACI-Fc fusion protein that binds and neutralises both B-lymphocyte stimulator (BLyS/BAFF) and a proliferation-inducing ligand (APRIL), suppressing the survival and maturation of B cells and plasma cells that drive autoantibody production.

Prescribing in practice

  • By suppressing B-cell-mediated immunity it increases the risk of infection, so active serious infection should be treated before starting and patients monitored for infection during therapy.
  • Injection-site reactions and hypersensitivity can occur; it is given by subcutaneous injection.
  • Avoid live vaccines during treatment and review immunisation status before starting.

Monitoring

Monitor for signs of infection and infusion- or injection-related reactions, along with disease activity and relevant immunological markers.

Counselling the patient

  • Report fever or other signs of infection promptly.
  • Do not have live vaccines while on treatment and discuss any planned vaccinations with your team.
  • Report any rash, swelling or reaction at the injection site or signs of an allergic reaction.

Evidence & guidelines

Benefit in systemic lupus erythematosus and IgA nephropathy has been reported in randomised controlled trials, with evolving regulatory and guideline positions.

Reference: Wang et al. Arthritis Rheumatol 2021 (Phase 2 SLE trial); Phase 3 TELLUS-SC and TELESCOPE trials (ongoing); China NMPA Approval 2021; Tak et al. Ann Rheum Dis 2023 (IgAN review); Confirm identity and dosing against the manufacturer SPC (eMC) and NICE. Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).

Related

Curated clinical cross-links plus same-class fallbacks.