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OMLYCLO (Celltrion Healthcare Australia Pty Ltd)

Product name
OMLYCLO
Date registered
Evaluation commenced
Decision date
Approval time
200 (255 working days)
Active ingredients
Omalizumab
Registration type
New biosimilar medicine
Indication

Allergic Asthma

Children 6 to < 12 years of age

In children aged 6 to <12 years, Omlyclo is indicated as add-on therapy to improve asthma control in patients with severe allergic asthma who have documented exacerbations despite daily high dose inhaled corticosteroids, and who have immunoglobulin E levels corresponding to the recommended dose range (see Table 1 in Section 4.2 DOSE AND METHOD OF ADMINISTRATION).

Adults and adolescents ≥ 12 years of age

Omlyclo is indicated for the management of adult and adolescent patients with moderate to severe allergic asthma, who are already being treated with inhaled steroids, and who have serum immunoglobulin E levels corresponding to the recommended dose range (see Table 1 in Section 4.2 DOSE AND METHOD OF ADMINISTRATION).

Chronic rhinosinusitis with nasal polyps (CRSwNP)

Omlyclo is indicated as add-on treatment in adult patients (18 years of age and above) for the treatment of severe CRSwNP with inadequate response to intranasal corticosteroids.

Recommended dosing is determined by serum immunoglobulin E levels and body weight corresponding to the recommended dose range in the Product Information (see Section 4.2 DOSE AND METHOD OF ADMINISTRATION) .

Chronic Spontaneous Urticaria (CSU)

Omlyclo is indicated for adults and adolescents (12 years of age and above) with chronic spontaneous urticaria who remain symptomatic despite H1 antihistamine treatment.

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