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  1. Medical Information Right
  2. Taltz® (ixekizumab) Right
  3. Differences of the new and old Taltz® (ixekizumab) formulation
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Taltz ® (ixekizumab)

This information is intended for UK registered healthcare professionals only as a scientific exchange in response to your search for information. For current prescribing information for all Lilly products, including Summaries of Product Characteristics, Patient Information Leaflets and Instructions for Use, please visit: www.medicines.org.uk (England, Scotland, Wales) or www.emcmedicines.com/en-GB/northernireland/ (Northern Ireland).

Differences of the new and old Taltz® (ixekizumab) formulation

The new citrate-free formulation is without buffers and contains sucrose as tonicity agent.

UK_cFAQ_IXE469_CITRATE_FREE_FORMULATION_DIFFERENCE
UK_cFAQ_IXE469_CITRATE_FREE_FORMULATION_DIFFERENCE
en-GB

Formulation differences

The new citrate-free formulation of ixekizumab

  • does not contain any buffer; that is, it is
    • citrate free and contains
    • sucrose (80 mg/mL) as the tonicity agent.1

The original formulation contains

  • sodium citrate dihydrate (5.11 mg/mL) and
  • citric acid anhydrous (0.51 mg/mL) as buffers and
  • sodium chloride (11.69 mg/mL) as the tonicity agent.1 

The ingredients are the same for both the pre-filled pen and syringe.1 Please also see  All Taltz ingredients for all ingredients.  

This medicinal product contains less than 1 mmol sodium (23 mg) per 80 mg dose, that is to say essentially “sodium-free”.2

Ixekizumab is contraindicated in patients with serious hypersensitivity to the active substance or to any of the excipients.2

 All Taltz ingredients 1

Ingredients

Original Formulation

New Citrate-free Formulation

Purpose of Ingredient

Ixekizumab (active ingredient)

80 mg

80 mg

Active ingredient

Polysorbate 80

0.30 mg

0.30 mg

Stabilizer

Sodium citrate dihydrate

5.11 mg

-

Buffer

Citric acid anhydrous

0.51 mg

-

Buffer

Sodium chloride

11.69 mg

-

Tonicity agent

Sucrose

-

80 mg

Tonicity agent/ stabilizer

Sodium hydroxide

-

q.s. to pH 5.7

pH adjustment

Water for injection

q.s. to 1.0 mL

q.s. to 1.0 mL

Solvent/ vehicle

Abbreviations: q.s. = quantity sufficient

References

1Data on file, Eli Lilly and Company and/or one of its subsidiaries.

2Taltz [summary of product characteristics]. Eli Lilly and Company (Ireland) Limited, Ireland

Date of Last Review: 08 December 2021

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