EMA: Sirolimus product-specific GL [Regulatives / Guidelines]

posted by luvblooms  – India, 2013-11-19 14:00 (4597 d 04:53 ago) – Posting: # 11912
Views: 31,743

Dear HS and All

Sirolimus

❝ No strict dose-proportionality between 0.5 and 5 mg tablets.

❝ 0.5 and 5 mg tablets, 1 mg/ml solution (if similarity requirements not fulfilled). Single dose cross-overs in healthy subjects (fasting and fed state), parent in blood (achiral),

❝ AR 90.00–111.11% for AUCt (NTID) and 80.00–125.00% for for Cmax.


Have a small doubt that is there some typographic error or something in Sirolimus guidance?

If I am right, in EU Rapamune is available in following strengths (as per the SmPC approved/updated in Sep-13)

Rapamune® 0.5 mg coated tablets
Rapamune® 1 mg coated tablets
Rapamune® 2 mg coated tablets
Rapamune® 1 mg/ml oral solution

Now from where 5 mg strength came in picture?

Rapamune® 5 mg Tablets are only approved in Canada (not in US- was there earlier but not discontinued or EU)?

What if one wants to develop only two strengths 1mg and 2 mg?

Am I missing something over here or getting too paranoid? :confused:

~A happy Soul~

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