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Statement in Advance of AGM

  • Biocompatibles now trading profitably
  • Increase in 2010 revenue and cash guidance
  • Cosmetic dermal filler bead investment programme on track

Farnham UK, 16 June 2010: Biocompatibles International plc (LSE:BII), the medical technology company, will today hold its Annual General Meeting.

The Chairman, Gerry Brown, will make the following comments:

“Biocompatibles has made a strong start to the year. The Board expects that in August, the Company will report a profit after interest and tax for the first half of 2010 and thereafter expects the Company to remain in profit.

The Oncology Products Division is trading ahead of Board expectations, as a result of strong Bead Products’ sales in each of the three main geographic markets - the United States, Europe and Asia. Conditions in the Brachytherapy market remain challenging.

In the Licensing Division, CellMed is also making good progress. The GLP-1 Diabetes clinical programme is on plan, and the €4million manufacturing investment plan is on track to deliver a significant increase in Novabel®1 production from early 2011.

The Company is increasing its guidance for 2010 revenue from £28-32million to £31-34million and on 2010 closing cash from £25million to £26million.

The Company will provide guidance on profit expectations for the full year of 2010, with the announcement of the half-yearly results, in August 2010; and 2011 sales and profit guidance, early in 2011.

The Board was pleased to pay the 2010 dividend of 6.25p per share on 28 May, representing an increase of 25% over the 2009 dividend.

These are exciting times for Biocompatibles.”

-Ends-

1Novabel is a registered trademark of Merz Pharmaceuticals GmbH, Biocompatibles’ licencee.

Contact:

Biocompatibles
Crispin Simon, Chief Executive
Ian Ardill, Finance Director
+44 (0) 1252 732732
   
Anna Keeble +44 (0) 7879 818876

 

Regulatory notices and product safety data

Worldwide (excluding USA)

Bead Block™ is CE marked and indicated for the treatment of a variety of hypervascular tumours (including Uterine Fibroids) and arteriovenous malformations (AVMs). For full prescribing information please refer to Bead Block instructions for use.

DC Bead® is CE marked and is indicated for the treatment of malignant hypervascular tumours and loading with doxorubicin drug. DC Bead® is also indicated for loading with irinotecan for the treatment of metastatic colorectal cancer (mCRC). Both indications may not be available in your territory. For full prescribing information please refer to DC Bead instructions for use.

DC BeadM1™ is indicated for loading with irinotecan for the treatment of metastatic colorectal cancer (mCRC). For full prescribing information please refer to DC Bead M1 instructions for use.

USA

In the USA, Bead Block™ is indicated for the treatment of hypervascular tumors and arteriovenous malformations (AVMs). For full prescribing information please refer to Bead Block USA Instructions for use.

LC Bead™ is cleared by the FDA for the embolization of hypervascular tumors and arteriovenous malformations (AVMs). For full prescribing information please refer to LC Bead instructions for use.

LC Bead M1™ is cleared by the FDA for the embolization of hypervascular tumors and arteriovenous malformations (AVMs). For full prescribing information please refer to LC Bead M1 instructions for use.

DC Bead is not currently available for sale or distribution in the USA. Both indications may not be available in your territory. 

DC Bead M1 is not currently available for sale or distributions in the USA. 

Canada

DC Bead® with doxorubicin is indicated for trans-arterial chemoembolization (TACE) of unresectable hepatocellular carcinoma (HCC). DC Bead are also intended to be loaded with irinotecan for the purpose of embolization of vessels supplying malignant colorectal cancer metastasised to the liver (mCRC), and delivery of a local, controlled, sustained dose of irinotecan to the mCRC. For full prescribing information please refer to DC Bead Canada Instructions for Use 

DC BeadM1 is primarily intended as an embolic agent to treat vessels supplying malignant colorectal cancer metastasised to the liver (mCRC). DC BeadM1 is also compatible with irinotecan, which can be loaded prior to embolisation and then, as a secondary action, elute a local, controlled and sustained dose to the mCRC after embolisation. For full prescribing information please refer to DC BeadM1 Canada Instructions for Use  

Tawain

DC Bead is approved by the Department of Health and is intended to be loaded with Mayne (Hospira) doxorubicin HCI for the purpose of embolisation of vessels supplying malignant hypervascularised tumour(s), and delivery of a local, controlled, sustained dose of doxorubicin.  DC Bead is also indicated for the embolisation of nidus vessels without medication.  Approved size ranges in Taiwan are 300-500µm and 500-700µm.

Hong Kong

PRECISION Bead™ is indicated for the delivery of Doxorubicin, a chemotherapeutic agent for the treatment of malignant hypervascular tumours, where Trans Arterial Embolisation (TAE) is not contraindicated.