10-Q – Quarterly report [Sections 13 or 15(d)]

Burzynski Research Institute has filed a 10-Q – Quarterly report [Sections 13 or 15(d)] with the U.S. Securities and Exchange Commission .

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(Press release, PolyTherics, OCT 15, 2013, View Source [SID:1234505303])

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(Press release, NBE Therapeutics, OCT 15, 2013, View Source;titolo=nbe-therapeutics-has-been-awarded-and-is-coordinating-a-eur-14-mio-european-research-for-smes-grant [SID:1234503547])

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AstraZeneca oncology portfolio strengthened as MedImmune acquisition of Spirogen boosts antibody-drug conjugate capability

On October 15, 2013 AstraZeneca reported that MedImmune has acquired Spirogen, a privately-held biotech company focused on antibody-drug conjugate technology for use in oncology (Press release AstraZeneca, OCT 15, 2014, View Source;astrazeneca-oncology-portfolio-strengthened [SID:1234500456]).
MedImmune has also entered into a collaboration agreement with ADC Therapeutics to jointly develop two of ADC Therapeutics’ antibody-drug conjugate programmes in preclinical development. MedImmune will also make an equity investment in ADC Therapeutics, which has an existing licensing agreement with Spirogen.
MedImmune will acquire 100 per cent of Spirogen’s shares for an initial consideration of $200 million and deferred consideration of up to $240 million based on reaching predetermined development milestones. Existing out-licensing agreements and associated revenue streams are excluded from this acquisition.
MedImmune will also pay $20 million for an equity investment in ADC Therapeutics, which will be matched by Auven Therapeutics, the majority shareholder in both ADC Therapeutics and Spirogen. The collaboration agreement will include an upfront payment with predetermined development milestones for two programmes from a defined list and a cost- and profit-sharing arrangement with MedImmune representing the majority share. ADC Therapeutics will also have the option to co-promote one of the products in the US.
Antibody-drug conjugates are a clinically-validated cancer drug technology that offers both high potency and selective targeting of cancer cells. Spirogen’s proprietary pyrrolobenzodiazepine (PBD) technology attaches highly potent cytotoxic agents, or ‘warheads’ to specific cancer-targeting antibodies using biodegradable ‘linkers’. This targeting optimises the delivery of the cancer drug to the tumour cells only and provides the greatest degree of tumour killing while minimising the toxicity to the patient.

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BioInvent and Bayer extend and broaden collaboration for the discovery and development of therapeutic antibodies

On October 14, 2013 BioInvent reported that it has signed an extension to its 2008 license agreement with Bayer Pharma AG for the development of antibodies from BioInvent’s n-CoDeR libraries (Press release BioInvent, OCT 14, 2013, http://www.bioinvent.com/investors/press-releases/release.aspx?releaseid=817483 [SID:1234500560]). Under the terms of the extension, Bayer will broaden its access to BioInvent’s discovery and development technology platform.
BioInvent will receive an undisclosed license fee to cover new projects plus success-based milestone payments and royalties on products already in development.
The n-CoDeR libraries contain more than 20 billion (2 x 1010) highly diverse, fully human antibody fragments that have been created using BioInvent’s patented approach, generating antibodies with high affinity and selectivity.

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