BioLineRx (BLRX) 6-K Third Quarter 2013 Earnings Presentation

Exhibit 1

Third Quarter 2013
Earnings Presentation

November 13, 2013

This presentation contains "forward-looking statements."
These statements include words like "may," "expects,"
"believes," “plans,” “scheduled," and "intends," and describe
opinions about future events. These forward-looking
statements involve known and unknown risks and
uncertainties that may cause the actual results, performance
or achievements of BioLineRx to be materially different from
any future results, performance or achievements expressed or
implied by such forward-looking statements.

2

Forward Looking Statements

3

Pipeline

Chief Executive Officer
Kinneret Savitsky, Ph.D.

4

Update on Operations and Selected Programs

Highlights of BioLineRx’s Quarterly Activities

•Progress in key clinical programs:

–BL-1040 - Recruitment on track for CE Mark registration trial

–BL-5010 - On schedule to begin EU pivotal study by end of this year

–BL-8040 - Partial phase 2 results expected by end of this year

–BL-7010 - All approvals received to start phase 1/2 trial by end of this year

•Partnership discussions

–BL-5010 - advanced discussions with potential partners

–BL-7040- initial co-development discussions

–BL-9020 - advanced discussions with optimization and manufacturing partners

•Appointment of Dr. BJ Bormann to Board of Directors

5

PROGRESS ON KEY PROGRAMS

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BL-1040: First-In-Class Myocardial Implant for
Prevention of Ventricular Remodeling Following AMI

Continued progress in pivotal trial:

–Pivotal CE-mark registration trial continuing
to progress at full steam

–Over 55 sites recruiting (including 14 sites
in the U.S.)

–Approximately 306 patients in total to be
recruited

–Results expected in 2014

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Substantial progress on many fronts:

• Received orphan drug designation by FDA

• Ongoing phase 2 study:

•All eight sites now open

•Memorial Sloan Kettering Cancer Center joined
the study

•Partial results to be announced by end of year

• Received patent allowance from USPTO through 2029
  as method of obtaining stem cells

• Additional trials for other hematological indications
  expected to commence in first half of 2014

• Publication in British Journal of Hematology of positive
  pre-clinical results for BL-8040 in treatment of
  thrombocytopenia

BL-8040: Best-in-Class CXCR4 Antagonist

for Treatment of Hematological Cancers

9

BL-5010: Novel Formulation for

Non-Surgical Removal of skin Lesions

Positioned for Commercial Success:

• Pivotal CE-mark study in seborrheic keratosis expected
  to begin by end of year

• Submissions made to regulatory authorities in Germany;
  approval already granted by ethical committees

• Study results expected mid-2014, pending approval from
  German Federal Institute for Drugs and Medical Devices
  (BfArM)

• CE mark by end of 2014

• Additional pivotal trial(s) in actinic keratosis and other
  indications planned for 2014

• In meaningful discussions with interested potential
  partners

10

BL-7010:Novel Gliadin Binding
Polymer for Celiac Disease

Great potential in a fast growing market:

•    Received all regulatory approvals to start phase
     1/2 study by end of 2013

•32-patients at world-leading site in Finland for
celiac disease research

•Single and repeated ascending dose study

•Results expected in mid-2014

•Efficacy study planned to commence by end
of 2014

•Made oral presentation of BL-7010 at 15th
International Celiac Disease Symposium

•Exploring multiple commercialization
pathways for product to maximize opportunity

•Significantly increased interest in celiac
disease by pharma industry

11

HCV Programs

BL-8020:

•    Novel HCV therapy in midst of Phase 1/2
     clinical trial

•Primary endpoint of study is effect of 16-
week combination therapy with Ribavirin and
BL-8020

•Received USPTO patent

BL-8030:

•NS3/4A inhibitor - demonstrated high genetic
barrier to development of resistant variant

•    Partnered with CTTQ

•Chemistry studies and pre-clinical
development advancing on-track with CTTQ

12

Chief Financial & Operating Officer
Philip A. Serlin, CPA, MBA

12

Third Quarter 2013 Financial Overview

Financial Overview (based on nine-month data)
(in USD at 30-Sep-13 exchange rate)

•Research and development

•Total R&D expenses decreased $1.9 million to $11.3 million in 2013 period

•2013 includes $1.7 million one-time reversal of OCS liability

•“Normalized” R&D decreased by $0.2 million

•Decrease resulted primarily from:

•Lower expenses in 2013 associated with the CLARITY trial

•Partially offset by significant increase in spending on other clinical-stage projects

•Sales and marketing

•S&M expenses were $0.7 million for both 2013 and 2012 periods

13

Financial Overview (based on nine-month data)
(in USD at 30-Sep-13 exchange rate)

•General and administrative

•G&A increased $0.2 million to $2.8 million in 2013 period

•Increase resulted primarily from one-time expense for professional services.

•Non-operating income

•Non-operating increased $1.9 million to $2.6 million in 2013 period

•Increase primarily due to fair-value adjustment related to warrant liability

•Financial income/expenses

•Net financial expenses were $0.9 million for the 2013 period, compared to net
financial income of $1.2 million for the 2012 period

•Changes results primarily from changes in the average exchange rate of NIS to
USD, since we hold net assets in USD

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Financial Overview (based on nine-month data)
(in USD at 30-Sep-13 exchange rate)

•Cash and burn rate information

•Cash and short-term deposits amounted to $20.3 million at 30-Sep-13

•Our burn rate is ~$12 million per year (~$1 million per month)

•Cash expected to last into mid-2015, without regard to any upfront or milestone
payments from current/potential partners

•Analyst Coverage

•Aegis Capital Corporation - Raghuram Selvaraju

•Roth Capital Partners, LLC - Robert Hazlett

•Analyst/Investor Day

•November 21, 2013 from 9:00 am to 11:45 am in NYC

•Presentations from BioLineRx’s senior management team

•Keynote presentation by Dr. BJ Bormann, BioLineRx Director

•Several KOLs will be speaking in reference to selected programs

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BL-8020 (HCV) phase I/II initiation

BL-8020 (HCV) partial results

BL-8040 (AML) partial results

BL-7010 (Celiac Disease) pilot study initiation

BL-8040 (AML) topline results

BL-7010 (Celiac Disease) pivotal study initiation

BL-5010 (Skin Lesions) pivotal EU study initiation

BL-1040 (AMI) pivotal CE mark study results

BL-5010 (Skin Lesions) EU study topline results

BL-7040 (IBD) phase II POC study results

BL-7010 (Celiac Disease) topline results

2013-14 Clinical and Commercial Milestones

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BL-8030 (HCV) collaboration deal with Chinese

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QUESTIONS?