A LentiVector Platform Company, and a leader in gene and cell therapy. Annual General Meeting 23 May 2017

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Transcription:

A LentiVector Platform Company, and a leader in gene and cell therapy Annual General Meeting 23 May 2017

Forwardlooking statements This presentation does not constitute an offer to sell or a solicitation of offers to buy Ordinary Shares (the Securities ). Although reasonable care has been taken to ensure that the facts stated in this presentation are accurate and that the opinions Cohort expressed 2 Dose are fair and reasonable, Administrationthe contents 3 months of (UPDRS) this presentation 6 months (UPDRS) have not been 1 year (UPDRS) formally verified 2 years by(updrs) Oxford BioMedica plc (the Company ) or any other person. Accordingly, no representation or warranty, expressed or implied, 1, n=3 1x Original Mean 27% is made as to the fairness, accuracy, completeness Max. or up correctness to 30% ofmax. theup to information 50% and Max. up opinions to 44% contained in this presentation, and no reliance should be placed on such information or opinions. Further, the information in this presentation is2, not n=3complete and2xmay be changed. Original Neither the Company Mean 28% nor any of Mean its34% respective members, directors, officers or employees nor any other person accepts any liability whatsoever for any loss howsoever arising from any use of such information or opinions or otherwise arising in connection with this presentation. This presentation may contain forwardlooking statements that reflect the Company's current expectations regarding future events, its liquidity and results of operations and its future working capital requirements. Forwardlooking statements involve risks and uncertainties. Actual events could differ materially from those projected herein and depend on a number of factors, including the success of the Company's development strategies, the successful and timely completion of clinical studies, securing satisfactory licensing agreements for products, the ability of the Company to obtain additional financing for its operations and the market conditions affecting the availability and terms of such financing. 2

Strategy: Leveraging Our LentiVector Delivery Platform 1, n=3 1x Original Mean 27% Multiple income streams Partners Programmes Process development Max. fees up to 30% Process development incentives Bioprocessing revenues Royalties 2, n=3 2x Original Mean 28% OXB products via spin out or outlicence Development milestones Royalties Bioprocessing revenues Process development and bioprocessing Spin out or outlicense R&D Investment Technical Developments R&D Investment Early Stage/ preclinical LentiVector Platform IP patents and knowhow Facilities Expertise Quality systems 3

Operational highlights (1 of 2) Strong progress from LentiVector delivery platform and cell therapy partnerships Novartis collaboration progressing well with CTL019 close to launch 1, n=3 1x Original Mean 27% 2, n=3 2x Original Mean 28% Strategic alliance with Orchard Therapeutics to develop and supply lentiviral vectors for ex vivo treatments Immune Design collaboration extended, including licence to use lentiviral vector based products for in vivo treatments for cancer New R&D collaboration with Green Cross LabCell focused on gene modified natural killer (NK) cellbased therapies 200 litre bioreactor production process established with potential to increase yield and reduce cost per dose Transgene Repression in Vector Production (TRiP) system developed to enhance production titres of a broad range of gene therapy vectors 4

Operational highlights (2 of 2) Stateoftheart bioprocessing and laboratory facilities Major capacity expansion completed 1, n=3 1x Original Mean 27% MHRA approval granted for GMP manufacture Vector bioprocessing volume increased by 54% compared to 2015 2, n=3 2x Original Mean 28% Progress with proprietary product development Ground breaking longterm results seen from followup studies of patients treated with OXB101 (Parkinson s disease) and OXB201 (for wet AMD) OXB102 (for Parkinson s disease) and OXB202 (for corneal graft rejection) ready to start Phase I/II studies following outlicensing/spinout OXB302 (for solid tumours) preclinical proofofconcept achieved and ready for further development following outlicensing/spinout SR422459 (licensed to Sanofi for Stargardt disease) in Phase II development 5

Partnering

Oxford BioMedica is a leader in lentiviral vector technology Gene and cell therapy field set to grow into $ multibillion sector over next 510 years. Several products, particularly ex vivo, likely to 1, n=3 1x Original Mean 27% launch in next few years Lentiviral vectors are preferred choice for ex vivo therapies because they integrate into DNA of target cells with genetic payload replicating when cells divide 2, n=3 2x Original Mean 28% Increasing number of lentivirus clinical studies initiated during 2015 (30% yearonyear) Oxford BioMedica has unique combination of patents, know how, expertise and facilities in lentiviral vectors the LentiVector platform leading to partnerships and collaborations We expect more such partnerships in the future 7

Financial impact of growing Partnership activities 35 30 25 1, n=3 1x Original incentives, Mean 27% 20 15 2, n=3 2x Original Mean 28% 10 5 0 0.0 1.0 2.0 3.0 4.0 5.0 6.0 Gross income (1) ( m) 2014 2015 2016 Licences, grants Earnings Before Interest, Depreciation & H1 2014 H2 2014 Includes 6.1m Novartis upfronts Amortisation ( m) H1 H2 2015 2015 H1 2016 Bioprocess & Commercial Devevlopment H2 2016 30 25 20 15 10 5 0 5 10 Partnering segment ( m) Partnering segment 2015 2016 Gross income EBITDA Operating profit/loss Gross income received from partnership arrangements Now generating cash (2016 EBITDA 3.1m) Infrastructure in place to support further growth 8 1 Gross income = aggregate of revenue and other operating income

Products

Products Pipeline Proprietary and Partnered Product Indication PreClinical Phase I Phase I/II Phase II Phase III Approval OXB Proprietary Products OXB102 Parkinson s disease 1, OXB202 n=3 Corneal 1x graft rejection Original Mean 27% OXB302 Cancer, multiple 2, OXB201 n=3 Wet AMD 2x Original Mean 28% OXB301 Cancer (multiple) 3, OXB n=3partnered products 2x Enhanced Mean 26% SAR422459 SAR421869 Partners Products Stargardt disease Usher syndrome 1B To be spun out or outlicensed Development milestones and royalties CTL019 CTL019 2nd CART CMB305 LV305 ADASCID MPS IIIA Undisclosed Undisclosed r/r ALL r/r DLBCL Cancer (multiple) Advanced, relapsed or metastatic sarcoma NYESO1 expressing cancers ADA severe combined immunodeficiency Sanfilippo A syndrome Undisclosed Undisclosed (Projected H2 2017) Process development and bioprocessing revenues, and royalties 10

InHouse Programmes OXB102 (Parkinson s disease) OXB101 showed encouraging efficacy and longterm duration of benefit OXB102 in latestage preparations for Phase I/II clinical study 1, n=3 1x Original Mean 27% 2, n=3 2x Original Mean 28% OXB202 (prevention of corneal graft rejection) OXB202 in latestage preparations for Phase I/II clinical study Tech transfer to clinical site to start once funding secured OXB302 (CART 5T4) Preclinical studies completed, demonstrating proofofconcept Highlights include: CART 5T4 cells can kill tumour cells derived from colorectal cancer and mesothelioma in a test tube (in vitro) T cells taken from patients with ovarian cancer can be reprogrammed with the 5T4 CAR construct and respond (in vitro) to their own tumour cells, resulting in tumour cell death In industry standard animal model (in vivo) 5T4 CART cells can treat established ovarian cancer Outlicensing and spinout opportunities being explored for priority products 11

Partners programmes Novartis CTL019 BLA for r/r ALL accepted by FDA (March 2017),granted priority review Novartis plan to file in EU in late 2017 DLBCL granted FDA Breakthrough Therapy designation 1, n=3 1x Original Mean 27% Submissions for r/r DLBCL in US and EU planned in Q4 2017 Analyst CTL019 consensus forecasts blockbuster product 2, n=3 2x Original Mean 28% USD Millions Novartis 2 nd CART programme underway Orchard Therapeutics Development and supply of lentiviral vectors for ADASCID underway Immune Design LV305 and CMB305 (combination of LV305 and G305 prime boost agent) in Phase I/II studies in cancers expressing NYESO1 antigen LV305 activates the immune system against a tumour by generating cytotoxic T cells (CTLs) against specific tumourassociated antigens Green Cross LabCell Research collaboration focusing on identifying and developing gene modified natural killer (NK) cellbased therapeutics for treatment of lifethreatening diseases such as cancer 12

R&D

Proprietary R&D Activity Inhouse Product Discovery/Research providing a flow of new product opportunities 1, n=3 1x Original Mean 27% Technical developments continuous improvement of the LentiVector platform 2, n=3 2x Original Mean 28% Cell Mean and 34% vector Mean engineering 29% projects to Several ocular orphan diseases programmes CNS orphan disease programme Respiratory orphan disease programme Genemodified NK cell therapeutics with Green Cross LabCell for cancer improve bioprocessing yield for example: TRiP system development Packaging & producer cell lines Analytical methods improvements to improve efficiency and effectiveness of testing Scaleup bioprocessing Serum free Suspension 200 L bioreactor Innovation and optimisation to build longterm value a key competitive advantage to durably maintain leadership in the field 14

Summary

Potential catalysts over next 12 months Novartis progress Data from adult r/r DLBCL study (expected Q2 2017) Confirmation of OXB commercial supply agreement for CTL019 vector 1, n=3 1x Original Mean 27% 2, n=3 2x Original Mean 28% FDA approval of CTL019 for r/r ALL and product launch Submission of DLBCL for approval LentiVector delivery platform Approval to supply lentiviral vector for commercial use Further contracts with new and existing partners giving us longterm economic interest in partners product candidates Established 200L bioreactor serumfree suspension platform to produce lentiviral vectors at significantly lower cost per dose Inhouse products Spin out / outlicense of inhouse product candidates 16

Summary: A Leading Gene and Cell Therapy Company 1 1, n=3 1x Original Mean 27% 2, n=3 2x Original Mean 28% Gene and cell therapy is predicted to grow into a multibillion US$ sector over the next 510 years 2 Lentiviral vectors have unique advantages for cell and gene therapy 3 OXB s soughtafter LentiVector gene delivery platform for both in vivo and ex vivo lentiviral vector products 4 OXB has worldclass bioprocessing facilities and collaboration trackrecord in the field 5 OXB s product interests include proprietary pipeline assets to be spun out or outlicensed and an economic interest in partners products 17 1 Clive Glover, GE Healthcare Sales of cell and gene therapy will reach $10 billion by 2021, October 2015.

Contact Us Oxford BioMedica plc Windrush Court Transport Way Oxford OX4 6LT John Dawson, CEO Tim Watts, CFO Tel: +44 (0) 1865 783 000 enquiries@oxfordbiomedica.co.uk www.oxfordbiomedica.co.uk