Abraxis BioScience Limited

Rosanne House , Parkway , Welwyn Garden City , Herts , AL8 6HG
Telephone: +44 (0) 207 081 0850
E-mail: abraxismedical@idispharma.com
Customer Care direct line: +44 (0) 5603 141 956
Summary of Product Characteristics last updated on the eMC: 20/08/2009
SPC Abraxane 5 mg/ml powder for suspension for infusion

When a pharmaceutical company changes an SPC or PIL, a new version is published on the eMC. For each version, we show the dates it was published on the eMC and the reasons for change.

Updated on 20/08/2009 and displayed until Current
Reasons for adding or updating:
  • Change to section 4.8 - Undesirable Effects
  • Change to section 5.2 - Pharmacokinetic Properties
  • Change to section 4.5 - Interaction with other medicinal products and other forms of interaction
  • Change to section 6. 3 - Shelf Life
  • Change to section 6. 4 - Special Precautions for Storage
  • Change to section 7 - Marketing Authorisation Holder
  • Change to section 10 date of revision of the text
  • Addition of link to EMEA website
  • Change to section 4.4 - Special warnings and precautions for Use
Date of revision of text on the SPC:   01-Aug-2009
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



In Section 4.4 Special Warnings and Precautions for Use
An additional warning has been added advising that Abraxane should not be substituted for or with other paclitaxel formulations.

In Section 4.5 Interactions with other medicinal products and other forms of interaction

The examples of drugs known to inhibit either CYP2C8 or CYP3A4 have been expanded to include ketoconazole and other imidazole antifungals, erythromycin, fluoxetine, gemfibrozil, cimetidine, ritonavir, saquinavir, indinavir, and nelfinavir)

 

In Section 4.8 Undesirable effects Table 1 has been updated to include the following effects:

bone marrow supression (very common)

severe hypersensitivity (rare)

keratitis (uncommon)

arrhythmia, supraventricular tachycardia (common)

bradycardia, cardiac arrest (rare)

pulmonary emboli, pulmonary thromboembolism (uncommon)

nail pigmentation, nail changes (common)

radiation pneumonitis (rare)

Additionally, hyperbilirubinaemia has been removed from the hepatobiliary disorders SOC and appears as increased bilirubin in the Investigations SOC

 

In Section 5.2 Pharmacokinetic properties the following information has been added:

 

In a repeat dose study with 12 patients receiving Abraxane administered intravenously at the approved dose, intrapatient variability in systemic paclitaxel exposure (AUCinf) was 19% (range = 3.21%-27.70%). There was no evidence for accumulation of paclitaxel with multiple treatment courses.

 

The protein binding of paclitaxel following Abraxane was evaluated by ultrafiltration. The fraction of free paclitaxel was significantly higher with Abraxane (6.2%) than with solvent-based paclitaxel (2.3%). This resulted in significantly higher exposure to unbound paclitaxel with Abraxane compared with solvent-based paclitaxel, even though the total exposure is comparable.  This is possibly due to paclitaxel not being trapped in Cremophor EL micelles as with solvent-based paclitaxel.

 

In Section 6.3 Shelf life

The shelf-life of the unopened vials has been increased from 2 to 3 years.

For the storage of the reconstituted solution in the vial, where health care practitioners were advised to store the vials in the original carton in order to protect the product from light, a clarifying statement has been added: "Alternative light-protection may be used in the clean room."

 

In Section 6.4 Special precautions for storage

For the unopened vials the following text has been added:

"This medicinal product does not require any special temperature storage conditions"

 

In Section 7 Marketing Authorisation Holder the address has been updated

Updated on 21/04/2009 and displayed until 20/08/2009
Reasons for adding or updating:
  • Change to section 4.2 - Posology and method of administration
  • Change to section 4.4 - Special warnings and precautions for Use
  • Change to section 5.2 - Pharmacokinetic Properties
Date of revision of text on the SPC:   01-Apr-2009
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company



In section 4.2, the text relating to doses for patients with hepatic impairment has been clarified.

 

In section 4.4, under hepatic impairment, the following caution has been added

"Because the toxicity of paclitaxel can be increased with hepatic impairment, administration of Abraxane in patients with hepatic impairment should be performed with caution."
Additionally, physicians are advised to contemplate a dose reduction in patients whose blood bilirubin exceeds twice the limit of normal, since paclitaxel clearance is decreased in patients with high bilirubin levels.

 

In section 5.2, Figure 1 shows the relationship between paclitaxel clearance and blood bilirubin following administration of Abraxane to patients with hepatic impairment.

Updated on 12/01/2009 and displayed until 21/04/2009
Reasons for adding or updating:
  • New SPC for new product
Date of revision of text on the SPC:  
Legal Category:   POM
Black Triangle (CHM):   NO

Free-text change information supplied by the pharmaceutical company

None provided

Active Ingredients/Generics

 
   paclitaxel albumin


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