September 01, 2014 5:09 PM ET

Biotechnology

Company Overview of Biosceptre International Limited

Company Overview

Biosceptre International Limited, a biotechnology company, develops and commercializes antibody technologies for applications in the diagnosis and treatment of cancer. It develops a range of polyclonal, monoclonal, and domain antibodies for use in IVDs, topical therapeutics, in vivo imaging diagnostics, systemic therapeutics, and vaccines. The company was founded in 2000 and is based in North Ryde, Australia.

Suite 3.08

56 Delhi Road

North Ryde, NSW 2113

Australia

Founded in 2000

Phone:

61 2 9889 1202

Fax:

61 2 9887 4777

Key Executives for Biosceptre International Limited

Chief Executive Officer and Executive Director
Group Chief Financial Officer and Executive Director
Chief Scientist
Scientific Director
Research Director
Compensation as of Fiscal Year 2014.

Biosceptre International Limited Key Developments

Biosceptre Announces Positive Phase I Results for BIL-010T to Treat Basal Cell Carcinoma

Biosceptre announced positive results from its Phase I trial to assess the safety and tolerability of BIL-010t (formerly known as BSCT (Anti-nf-P2X(7)) 10% Ointment), a topically administered, highly purified sheep antibody therapy, to treat Basal Cell Carcinoma (BCC). The Phase I trial, conducted in the US, was an open-label, single-arm, multicentre study, to assess safety, tolerability, and levels of anti-drug antibodies in the patients' serum. The study enrolled 21 male and female patients, with a BCC lesion histologically confirmed within the previous four weeks, who self-applied the BIL-010t ointment for 28 days. The results showed that BIL-010t was both safe and well tolerated, with very high levels of patient compliance. The only reported side effect, associated with treatment, was mild to moderate localised skin reactions. Levels of BIL-010t were generally undetectable in patients' blood serum, and gave no evidence of immunogenicity in the majority of patients. Although efficacy was not a prescribed endpoint of the trial, it was noted that 65% of patients (13 out of 20) who completed the study had decreases in the size of their BCC lesions. The reductions ranged from 10% to 56% reduction in the size of the BCC during the course of treatment.

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Recent Private Companies Transactions

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