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Investor Presentation
January 2018
2
Forward-Looking Statements
To the extent any statements made in this presentation contain information that is not historical, these statements are
forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section
21E of the Securities Exchange Act of 1934, as amended. We have based these forward-looking statements on our
current expectations and projections about future events. Our actual results could differ materially from those discussed
in, or implied by, these forward-looking statements.
Forward-looking statements are identified by words such as "believe," "anticipate," "expect," "intend," "plan," "will,"
"may" and other similar expressions. In addition, any statements that refer to expectations, projections or other
characterizations of future events or circumstances are forward-looking statements. Forward-looking statements
include, but are not necessarily limited to, risks and uncertainties, including the difficulty of predicting U.S. Food and
Drug Administration and Canadian Therapeutic Products Directorate approvals, acceptance and demand for new
pharmaceutical products, the impact of competitive products and pricing, new product development and launch,
reliance on key strategic alliances, availability of raw materials and finished products, the regulatory environment, tax
rate assumptions, the outcome of legal proceedings, fluctuations in operating results and other risks detailed from time
to time in the Company's filings with the Securities and Exchange Commission and the Ontario Securities Commission.
IntelGenx undertakes no obligation to update or revise any forward-looking statement.
3
2
3
• IntelGenx Corp. Founded
• TSX-V (IGX)1
• OTCQX (IGXT)1
• Market Capitalization
• Shares Issued
• Shares Fully Diluted
• Insider Beneficial Ownership
• Cash/Equivalent2
1)As of December 31, 2017
2)As of September 30, 2017
2003
CAD$1.00
US$0.81
CAD$66M
67M
71M
19%
US$6.9M
Analyst Coverage
Firm Analyst
H.C. Wainwright Swayampakula Ramakanth
Singular Research Greg Eisen
Company Snapshot
4
IntelGenx Drug Delivery Technology Platforms
Rapidly disintegrating films improving
drug performance and easing
administration
without the need for water
Oral Films
VersaFilm™
Mucoadhesive Tablets
Controlled-release tablets for oral
absorption over an extended time
period
AdVersa™
Specializing in Oral Drug Delivery
5
7
We are focused on areas where oral films are particularly well-suited:
Develop and commercialize products that provide therapeutic advantages to patients
leveraging oral films, such as:
• Reduced side effects
• Improved bioavailability
• Response time versus existing drugs
• Abuse resistant
• Convenience
• Lifecycle management
• Repurpose existing drugs for new indications using oral films
• “First-to-file” generic drugs where high technology barriers to
entry exist in reproducing branded films
VersaFilm Technology Focused on Four Growth Strategies
5
Operations
State-of-the-Art
Manufacture
Full Scale
Manufacturing
Finished Product
Testing
Cost Effective
Regulatory &
Quality
Dossiers in Multiple
Territories (EU, US)
Compliant to ICH,
GMP & ISO
Health Canada
Approved Mfg Site
A Comprehensive Service Portfolio
R&D
Formulation
Feasibility Study
Analytical Method
Development
Clinical trials
CTA/ IND Applications
Trial monitoring
IP
Patented Products &
Technologies
Patent Filings
FTO Opinions
7
• 17,000 sqft facility in Montreal fully GMP
compliant
• Health Canada certified – Drug Establishment
License (DEL) obtained in December 2017
• State-of-the-art manufacturing and packaging
equipment
• Plans for manufacturing
expansion underway
• Manufacturing expansion will
increase manufacturing
capacity 5-fold
State-of-the-Art Film Manufacturing Facility Established
Indication
Partnering
Status
Formulation
Development
Pilot
Study
Pivotal Study Filing Launch Partner
Migraine – Rizaport®
(Rizatriptan)
Available
ex-ES & SKR
Erectile Dysfunction
(Tadalafil) Available
Schizophrenia
(Loxapine) Available
Neurodegenerative Brain Diseases
(Montelukast) Available
Opioid Dependence
(Buprenorphine/ Naloxone)
Partnered
Undisclosed Partnered
Undisclosed Partnered
Undisclosed Partnered
Hypertension Partnered
CNS Partnered
Pain
(Dronabinol)
Available
ex-US/ CAN
8
Robust Product Pipeline
Addressing Significant Market Opportunities
VersaFilmTMTablets
9
Leverages VersaFilm™ Technology
Oral Film Containing 10 mg Rizatriptan
European Marketing Approval – December 2015
 Definitive agreement signed July 2016 with Grupo
Juste for Spain & additional territories
 Definitive agreement signed Dec 2016 with
Pharmatronic for South Korea
 Actively pursuing several opportunities to open
new markets
Patent granted in April 2016 protecting Rizaport
505(b)(2) NDA resubmitted in November 2017
PDUFA date expected for H1/2018
For Migraines
10
• A high value, pleasantly flavored, and
convenient VersaFilm™ dosage form
of 2.5, 5, 10 and 20 mg tadalafil that
can be administered without water
• Pilot phase 1 clinical trial for safety and
pharmacokinetics has been successfully
completed, confirming bioequivalence
to Cialis® Tablets (Eli Lilly)
• 2 patent applications protecting
Tadalafil VersaFilm pending
13
For Erectile Dysfunction
11
• Tadalafil market in the US estimated at $1.7B
• Tadalafil substance patent expired, but orange
book ‘166 dosing patent still in force until April
2020
• IntelGenx’ exclusive license to ‘166 dosing
patent will allow entry of Tadalafil VersaFilm™
into the ED US market upon FDA approval,
potentially before the market entry of Cialis®
generic competitors
• Expected US FDA approval H2/2018
$1,703$1,429
$175
$11
$48
$18
US ED Market by Sales ($M)
Cialis
Viagra
Levitra
Staxyn
Stendra
Edex
Significant Market Opportunity
12
• Fast-acting loxapine oral film dosage
• For treatment of acute agitation and anxiety
attacks in non-institutionalized patients with
schizophrenia & bipolar 1 disorder
• Reduces risk of pulmonary side effects
and potential risk of violence and injury to
patients and caregivers
• US patent & PCT applications submitted
• Formulation optimization stage – results
expected H1/2018
For Schizophrenia & Bipolar 1 Disorder
13
• AdVersa® mucoadhesive tablet adheres to the oral mucosa and
releases the drug onto the site of application at a controlled rate
• Repurposing of synthetic THC dronabinol for use in pain
• Protected by several issued and pending patents
• Competitive advantages vs. Marinol® capsules (Abbvie)
Marinol® (dronabinol) capsule Dronabinol AdVersa®
Conventional oral dosage form AdVersa® mucoadhesive tablet
High rate of metabolization Limited first-pass metabolism
Limited bioavailability Improved bioavailability
Undesired psychoactivity
Reduced gastro-intestinal
exposure and side-effects
Limited shelf life Enhanced product stability
Dronabinol
20
Dronabinol Mucoadhesive Tablet
For Pain Management
14
• Licensing and development agreements entered for
four generic products
• IntelGenx granted Chemo exclusive worldwide license
to commercialize two generic tablets and U.S. license
for two generic oral films
• IntelGenx to receive upfront, milestone, R&D
revenues and share of profits – total value of 7 digits
• Combined total market of four products is >$7B
• Chemo making a strategic move into novel drug
delivery products with IntelGenx as its partner
• Partnership could result in numerous future
product agreements
About Chemo Group:
• Founded in 1978
• 5,000 employees
• Head office in Spain
• Revenues of $1.2B annually
• Markets over 300 products
• Operating in over 40 countries
• 20 state-of-the-art facilities
• 9 specialized R&D centers
Strategic Partnership with Chemo Group
15
2
2
Mild Cognitive Impairment
(MCI)
> 80 Mi persons
Dementia
> 30 Mi persons
Cognitive Disorder Stage and Prevalent
Population in nine major markets.
(Global Data, 2013 )
Neurodegenerative Clinical Changes
(Global Data, 2013)
Issues with word selection
Misplacing of belongings
Inability to recall recent events
Memory loss
Cognitive impairment
Functional decline
Drastic reduction in quality of life
Requires full-time support
1 Mood and personality changes
Poor judgment
Frequently getting lost
2 Difficulty recognizing family or friends
Inability to learn new concepts
Hallucinations, delusions, or paranoia
3 Inability to communicate
Poor swallowing function
Incontinence
Global Sales for AD by
Patients Category (Global
Data, 2013)
Currently approved treatments for brain degenerative diseases are limited, resulting
in unmet clinical needs, which translates into a promising market opportunity.
Alzheimer’s Disease
(AD)
1 Mild > 6.5 Mi persons
2 Moderate > 3.9 Mi persons
3 Severe > 2.1 Mi persons
Brain Degenerative Diseases
Sizeable Addressable Patient Population
16
 Improves Learning and Memory in aged animals
 Crosses the Blood-Brain Barrier in rats and humans
 Restores Blood Vessel Structural Integrity
 Returns Generation of New Neurons
 Restores Learning and Memory in a Model of
Lewy Body dementia
 Improves function in a number of models of acute
and chronic neurodegenerative diseases
Before
MMSE 13:
Moderate to Severe
Dementia
MMSE 22:
Mild Dementia
After 2 Months of
Montelukast
Note: MMSE = Mini-Mental State Examination; is a test to measure cognitive
impairment
Early Clinical EvidencePreclinical Demonstration
Montelukast Improves Cognitive Functions
& Structural Integrity of the Brain
17
Conclusions
The present results suggest that montelukast may alleviate the
cognitive decline associated with human aging. However, further
data, preferably based on controlled clinical trials, are required.
Source: Immunity and Ageing 2017: 14: 20
Evidence from Epidemiology / Comparative Effectiveness in Humans
Montelukast Protects Against Dementia
Phase I Clinical Study Results
18
0.0
100.0
200.0
300.0
400.0
500.0
600.0
0.00 5.00 10.00 15.00 20.00 25.00 30.00
Montelukastconcentration(ng/mL)
Time (hrs)
Montelukast Avg plasma profile
Test buccal film 10mg
Ref tablet 10mg
CSF ng/mL
avg at 3hrs 3.6
avg at 7hrs 4.2
CSF level measured for Buccal Film (avg of 8)
A Single-Dose, Non-Randomized, Open-Label, Two-Way, Pilot, Comparative Bioavailability Study of Montelukast 10 mg Oral Film
(Intelgenx Corp.) and Singulair® 10 mg Film-coated Tablet (Merck & Co., Inc., approved for Asthma in 1998) in Healthy Male and
Non-pregnant Female Volunteers under Fasting Conditions
Safety Results:
A total of 2 possibly related adverse events were reported
to the Buccal Film. A total of 2 subjects experienced
somnolence when taking the Buccal Film.
Phase IIa Clinical Study Design
• Study protocol approved by Health Canada
• Study Drug: 7.5mg montelukast buccal film and matching placebo
• Duration: 26 weeks
• Assessment of the treatment effect: S-STS, MMSE, ADCS-CGIC, ADCS-ADL and NPI-12
• Number of patients: 70 (35 per arm)
• Patients: ≥50 years of age with mild to moderate Alzheimer’s Disease and treated daily with donepezil,
rivastigmine or galanthamine for ≥3 months
• 8 Canadians sites currently committed; enrollment preparations ongoing
19
A randomized Phase IIa, multi-center, double-blind, placebo-controlled study to assess the
safety, feasibility, tolerability, and efficacy of a new buccal film of Montelukast in patients with
mild to moderate Alzheimer’s Disease
20
$M
3.7
3.3
5.2
0
1
2
3
4
5
6
First Nine Months 2017 First Nine Months 2016 2016 Full Year
Revenue
REVENUE ($M)
Financial Performance: Revenue
21
Net Comprehensive Income & Adjusted EBITDA ($M)
$M
27
-1.6
-1.5 -1.5
-0.85
-0.91
-0.3
-1.8
-1.6
-1.4
-1.2
-1
-0.8
-0.6
-0.4
-0.2
0
First Nine Months 2017 First Nine Months 2016 2016 Full Year
Net Income Adjusted EBITDA
Financial Performance: Income & EBITDA
22
Andre Godin, CPA, CA
Executive VP, CFO
• 25+ years biotech/pharma industry
experience
• Member of the Canadian Chartered
Professional Accountants and the
Canadian Institute of Chartered
Accountants
Nadine Paiement, M. Sc.
VP, Research & Development
• Co-inventor of IntelGenx Trilayer
Technology
• 15 years experience in product
development and technology
transfer
Stephen Kilmer
Investor Relations
• 20+ years experience in healthcare
IR and PR
• President of Kilmer Lucas, a health-
care only investor relations and
capital markets advisory company
Horst G. Zerbe, Ph. D.
Chairman, President & CEO
• 30+ years drug delivery / pharma
experience (Lohmann Therapy
Systems, 3M Pharmaceuticals,
Smartrix Technologies)
• Pioneer in development and
manufacturing of oral films and
transdermal products
• Numerous patents and scientific
publications
Dana Matzen, Ph.D.
VP, Business & Corporate
Development
• 15 years experience in
pharmaceutical product licensing
• Prev. Director, BD at Paladin
• Completed 13 transaction,
7 new product launches
Rodolphe Obeid, M. Eng. Ph.D.
Senior Director Operations
• 5+ years experience in
manufacturing & scale-up of oral film
products
• Previously Director, R&D and
Process Development at IntelGenx
• Author and co-author of numerous
scientific papers, patents, book
chapters, and scientific
communications
Strengthened Management Team
40 Employees, including 10 with Ph.D.’s
Simona Surdila, M.Eng., MSc.
Senior Director, Quality Operations
• 30 years , Global Pharma/ Biotech/
Medical Device Industry experience
• Numerous Awards for New
Launches & Technology transfer,
QBD
• PDA speaker & Coach : Aseptic
Process/Transdermal Design, Data
Integrity
Lou Panini, M. Sc.
Senior Director, PP & Supply Chain
Management .
• 35 + years Pharma experience
(Pfizer, KEATA, Apotex Inc. in
Global SCM
• Managing Global Strategic Projects
• Solid track record of Talent
development
23
1. History
• Leader in oral film development and manufacturing with 30+ years experience
2. Formulation Team
• Strong in applying biopharmaceutical aspects to formulation development
• Top quality scientists: highly creative, focused on problem solving & innovative approaches
• Experienced in developing films for oral (GI), sublingual & buccal absorption
3. Clearly Defined Corporate Strategy And Business Model
• Focus on drug repurposing, lifecycle management, patient benefits, and FTF generics
• Provider of comprehensive pharmaceutical services to industry partners
4. Competitive Manufacturing Capabilities
• First in Canada
• New, Health Canada approved, state-of-the-art manufacturing facility
• Offering one-stop-shopping to our partners with lean operations keeping costs down
• Customized manufacturing equipment
The IntelGenx Advantage
24
30
Thank You!
www.IntelGenx.com
Contact Info:
Stephen Kilmer André Godin Dana Matzen, Ph.D.
Investor Relations Executive VP & CFO VP Corp & BD
+1-514-331-7440 ext. 232 +1-514-331-7440 ext. 203 +1-514-331-7440 ext. 220
Stephen@intelgenx.com Andre@intelgenx.com Dana@intelgenx.com
IntelGenx Corporate Offices
6420 Abrams
Saint-Laurent (Quebec)
H4S 1Y2 Canada
www.intelgenx.com

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Company pres jpm final 01 09-2018-updated

  • 2. 2 Forward-Looking Statements To the extent any statements made in this presentation contain information that is not historical, these statements are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended. We have based these forward-looking statements on our current expectations and projections about future events. Our actual results could differ materially from those discussed in, or implied by, these forward-looking statements. Forward-looking statements are identified by words such as "believe," "anticipate," "expect," "intend," "plan," "will," "may" and other similar expressions. In addition, any statements that refer to expectations, projections or other characterizations of future events or circumstances are forward-looking statements. Forward-looking statements include, but are not necessarily limited to, risks and uncertainties, including the difficulty of predicting U.S. Food and Drug Administration and Canadian Therapeutic Products Directorate approvals, acceptance and demand for new pharmaceutical products, the impact of competitive products and pricing, new product development and launch, reliance on key strategic alliances, availability of raw materials and finished products, the regulatory environment, tax rate assumptions, the outcome of legal proceedings, fluctuations in operating results and other risks detailed from time to time in the Company's filings with the Securities and Exchange Commission and the Ontario Securities Commission. IntelGenx undertakes no obligation to update or revise any forward-looking statement.
  • 3. 3 2 3 • IntelGenx Corp. Founded • TSX-V (IGX)1 • OTCQX (IGXT)1 • Market Capitalization • Shares Issued • Shares Fully Diluted • Insider Beneficial Ownership • Cash/Equivalent2 1)As of December 31, 2017 2)As of September 30, 2017 2003 CAD$1.00 US$0.81 CAD$66M 67M 71M 19% US$6.9M Analyst Coverage Firm Analyst H.C. Wainwright Swayampakula Ramakanth Singular Research Greg Eisen Company Snapshot
  • 4. 4 IntelGenx Drug Delivery Technology Platforms Rapidly disintegrating films improving drug performance and easing administration without the need for water Oral Films VersaFilm™ Mucoadhesive Tablets Controlled-release tablets for oral absorption over an extended time period AdVersa™ Specializing in Oral Drug Delivery
  • 5. 5 7 We are focused on areas where oral films are particularly well-suited: Develop and commercialize products that provide therapeutic advantages to patients leveraging oral films, such as: • Reduced side effects • Improved bioavailability • Response time versus existing drugs • Abuse resistant • Convenience • Lifecycle management • Repurpose existing drugs for new indications using oral films • “First-to-file” generic drugs where high technology barriers to entry exist in reproducing branded films VersaFilm Technology Focused on Four Growth Strategies
  • 6. 5 Operations State-of-the-Art Manufacture Full Scale Manufacturing Finished Product Testing Cost Effective Regulatory & Quality Dossiers in Multiple Territories (EU, US) Compliant to ICH, GMP & ISO Health Canada Approved Mfg Site A Comprehensive Service Portfolio R&D Formulation Feasibility Study Analytical Method Development Clinical trials CTA/ IND Applications Trial monitoring IP Patented Products & Technologies Patent Filings FTO Opinions
  • 7. 7 • 17,000 sqft facility in Montreal fully GMP compliant • Health Canada certified – Drug Establishment License (DEL) obtained in December 2017 • State-of-the-art manufacturing and packaging equipment • Plans for manufacturing expansion underway • Manufacturing expansion will increase manufacturing capacity 5-fold State-of-the-Art Film Manufacturing Facility Established
  • 8. Indication Partnering Status Formulation Development Pilot Study Pivotal Study Filing Launch Partner Migraine – Rizaport® (Rizatriptan) Available ex-ES & SKR Erectile Dysfunction (Tadalafil) Available Schizophrenia (Loxapine) Available Neurodegenerative Brain Diseases (Montelukast) Available Opioid Dependence (Buprenorphine/ Naloxone) Partnered Undisclosed Partnered Undisclosed Partnered Undisclosed Partnered Hypertension Partnered CNS Partnered Pain (Dronabinol) Available ex-US/ CAN 8 Robust Product Pipeline Addressing Significant Market Opportunities VersaFilmTMTablets
  • 9. 9 Leverages VersaFilm™ Technology Oral Film Containing 10 mg Rizatriptan European Marketing Approval – December 2015  Definitive agreement signed July 2016 with Grupo Juste for Spain & additional territories  Definitive agreement signed Dec 2016 with Pharmatronic for South Korea  Actively pursuing several opportunities to open new markets Patent granted in April 2016 protecting Rizaport 505(b)(2) NDA resubmitted in November 2017 PDUFA date expected for H1/2018 For Migraines
  • 10. 10 • A high value, pleasantly flavored, and convenient VersaFilm™ dosage form of 2.5, 5, 10 and 20 mg tadalafil that can be administered without water • Pilot phase 1 clinical trial for safety and pharmacokinetics has been successfully completed, confirming bioequivalence to Cialis® Tablets (Eli Lilly) • 2 patent applications protecting Tadalafil VersaFilm pending 13 For Erectile Dysfunction
  • 11. 11 • Tadalafil market in the US estimated at $1.7B • Tadalafil substance patent expired, but orange book ‘166 dosing patent still in force until April 2020 • IntelGenx’ exclusive license to ‘166 dosing patent will allow entry of Tadalafil VersaFilm™ into the ED US market upon FDA approval, potentially before the market entry of Cialis® generic competitors • Expected US FDA approval H2/2018 $1,703$1,429 $175 $11 $48 $18 US ED Market by Sales ($M) Cialis Viagra Levitra Staxyn Stendra Edex Significant Market Opportunity
  • 12. 12 • Fast-acting loxapine oral film dosage • For treatment of acute agitation and anxiety attacks in non-institutionalized patients with schizophrenia & bipolar 1 disorder • Reduces risk of pulmonary side effects and potential risk of violence and injury to patients and caregivers • US patent & PCT applications submitted • Formulation optimization stage – results expected H1/2018 For Schizophrenia & Bipolar 1 Disorder
  • 13. 13 • AdVersa® mucoadhesive tablet adheres to the oral mucosa and releases the drug onto the site of application at a controlled rate • Repurposing of synthetic THC dronabinol for use in pain • Protected by several issued and pending patents • Competitive advantages vs. Marinol® capsules (Abbvie) Marinol® (dronabinol) capsule Dronabinol AdVersa® Conventional oral dosage form AdVersa® mucoadhesive tablet High rate of metabolization Limited first-pass metabolism Limited bioavailability Improved bioavailability Undesired psychoactivity Reduced gastro-intestinal exposure and side-effects Limited shelf life Enhanced product stability Dronabinol 20 Dronabinol Mucoadhesive Tablet For Pain Management
  • 14. 14 • Licensing and development agreements entered for four generic products • IntelGenx granted Chemo exclusive worldwide license to commercialize two generic tablets and U.S. license for two generic oral films • IntelGenx to receive upfront, milestone, R&D revenues and share of profits – total value of 7 digits • Combined total market of four products is >$7B • Chemo making a strategic move into novel drug delivery products with IntelGenx as its partner • Partnership could result in numerous future product agreements About Chemo Group: • Founded in 1978 • 5,000 employees • Head office in Spain • Revenues of $1.2B annually • Markets over 300 products • Operating in over 40 countries • 20 state-of-the-art facilities • 9 specialized R&D centers Strategic Partnership with Chemo Group
  • 15. 15 2 2 Mild Cognitive Impairment (MCI) > 80 Mi persons Dementia > 30 Mi persons Cognitive Disorder Stage and Prevalent Population in nine major markets. (Global Data, 2013 ) Neurodegenerative Clinical Changes (Global Data, 2013) Issues with word selection Misplacing of belongings Inability to recall recent events Memory loss Cognitive impairment Functional decline Drastic reduction in quality of life Requires full-time support 1 Mood and personality changes Poor judgment Frequently getting lost 2 Difficulty recognizing family or friends Inability to learn new concepts Hallucinations, delusions, or paranoia 3 Inability to communicate Poor swallowing function Incontinence Global Sales for AD by Patients Category (Global Data, 2013) Currently approved treatments for brain degenerative diseases are limited, resulting in unmet clinical needs, which translates into a promising market opportunity. Alzheimer’s Disease (AD) 1 Mild > 6.5 Mi persons 2 Moderate > 3.9 Mi persons 3 Severe > 2.1 Mi persons Brain Degenerative Diseases Sizeable Addressable Patient Population
  • 16. 16  Improves Learning and Memory in aged animals  Crosses the Blood-Brain Barrier in rats and humans  Restores Blood Vessel Structural Integrity  Returns Generation of New Neurons  Restores Learning and Memory in a Model of Lewy Body dementia  Improves function in a number of models of acute and chronic neurodegenerative diseases Before MMSE 13: Moderate to Severe Dementia MMSE 22: Mild Dementia After 2 Months of Montelukast Note: MMSE = Mini-Mental State Examination; is a test to measure cognitive impairment Early Clinical EvidencePreclinical Demonstration Montelukast Improves Cognitive Functions & Structural Integrity of the Brain
  • 17. 17 Conclusions The present results suggest that montelukast may alleviate the cognitive decline associated with human aging. However, further data, preferably based on controlled clinical trials, are required. Source: Immunity and Ageing 2017: 14: 20 Evidence from Epidemiology / Comparative Effectiveness in Humans Montelukast Protects Against Dementia
  • 18. Phase I Clinical Study Results 18 0.0 100.0 200.0 300.0 400.0 500.0 600.0 0.00 5.00 10.00 15.00 20.00 25.00 30.00 Montelukastconcentration(ng/mL) Time (hrs) Montelukast Avg plasma profile Test buccal film 10mg Ref tablet 10mg CSF ng/mL avg at 3hrs 3.6 avg at 7hrs 4.2 CSF level measured for Buccal Film (avg of 8) A Single-Dose, Non-Randomized, Open-Label, Two-Way, Pilot, Comparative Bioavailability Study of Montelukast 10 mg Oral Film (Intelgenx Corp.) and Singulair® 10 mg Film-coated Tablet (Merck & Co., Inc., approved for Asthma in 1998) in Healthy Male and Non-pregnant Female Volunteers under Fasting Conditions Safety Results: A total of 2 possibly related adverse events were reported to the Buccal Film. A total of 2 subjects experienced somnolence when taking the Buccal Film.
  • 19. Phase IIa Clinical Study Design • Study protocol approved by Health Canada • Study Drug: 7.5mg montelukast buccal film and matching placebo • Duration: 26 weeks • Assessment of the treatment effect: S-STS, MMSE, ADCS-CGIC, ADCS-ADL and NPI-12 • Number of patients: 70 (35 per arm) • Patients: ≥50 years of age with mild to moderate Alzheimer’s Disease and treated daily with donepezil, rivastigmine or galanthamine for ≥3 months • 8 Canadians sites currently committed; enrollment preparations ongoing 19 A randomized Phase IIa, multi-center, double-blind, placebo-controlled study to assess the safety, feasibility, tolerability, and efficacy of a new buccal film of Montelukast in patients with mild to moderate Alzheimer’s Disease
  • 20. 20 $M 3.7 3.3 5.2 0 1 2 3 4 5 6 First Nine Months 2017 First Nine Months 2016 2016 Full Year Revenue REVENUE ($M) Financial Performance: Revenue
  • 21. 21 Net Comprehensive Income & Adjusted EBITDA ($M) $M 27 -1.6 -1.5 -1.5 -0.85 -0.91 -0.3 -1.8 -1.6 -1.4 -1.2 -1 -0.8 -0.6 -0.4 -0.2 0 First Nine Months 2017 First Nine Months 2016 2016 Full Year Net Income Adjusted EBITDA Financial Performance: Income & EBITDA
  • 22. 22 Andre Godin, CPA, CA Executive VP, CFO • 25+ years biotech/pharma industry experience • Member of the Canadian Chartered Professional Accountants and the Canadian Institute of Chartered Accountants Nadine Paiement, M. Sc. VP, Research & Development • Co-inventor of IntelGenx Trilayer Technology • 15 years experience in product development and technology transfer Stephen Kilmer Investor Relations • 20+ years experience in healthcare IR and PR • President of Kilmer Lucas, a health- care only investor relations and capital markets advisory company Horst G. Zerbe, Ph. D. Chairman, President & CEO • 30+ years drug delivery / pharma experience (Lohmann Therapy Systems, 3M Pharmaceuticals, Smartrix Technologies) • Pioneer in development and manufacturing of oral films and transdermal products • Numerous patents and scientific publications Dana Matzen, Ph.D. VP, Business & Corporate Development • 15 years experience in pharmaceutical product licensing • Prev. Director, BD at Paladin • Completed 13 transaction, 7 new product launches Rodolphe Obeid, M. Eng. Ph.D. Senior Director Operations • 5+ years experience in manufacturing & scale-up of oral film products • Previously Director, R&D and Process Development at IntelGenx • Author and co-author of numerous scientific papers, patents, book chapters, and scientific communications Strengthened Management Team 40 Employees, including 10 with Ph.D.’s Simona Surdila, M.Eng., MSc. Senior Director, Quality Operations • 30 years , Global Pharma/ Biotech/ Medical Device Industry experience • Numerous Awards for New Launches & Technology transfer, QBD • PDA speaker & Coach : Aseptic Process/Transdermal Design, Data Integrity Lou Panini, M. Sc. Senior Director, PP & Supply Chain Management . • 35 + years Pharma experience (Pfizer, KEATA, Apotex Inc. in Global SCM • Managing Global Strategic Projects • Solid track record of Talent development
  • 23. 23 1. History • Leader in oral film development and manufacturing with 30+ years experience 2. Formulation Team • Strong in applying biopharmaceutical aspects to formulation development • Top quality scientists: highly creative, focused on problem solving & innovative approaches • Experienced in developing films for oral (GI), sublingual & buccal absorption 3. Clearly Defined Corporate Strategy And Business Model • Focus on drug repurposing, lifecycle management, patient benefits, and FTF generics • Provider of comprehensive pharmaceutical services to industry partners 4. Competitive Manufacturing Capabilities • First in Canada • New, Health Canada approved, state-of-the-art manufacturing facility • Offering one-stop-shopping to our partners with lean operations keeping costs down • Customized manufacturing equipment The IntelGenx Advantage
  • 24. 24 30 Thank You! www.IntelGenx.com Contact Info: Stephen Kilmer André Godin Dana Matzen, Ph.D. Investor Relations Executive VP & CFO VP Corp & BD +1-514-331-7440 ext. 232 +1-514-331-7440 ext. 203 +1-514-331-7440 ext. 220 Stephen@intelgenx.com Andre@intelgenx.com Dana@intelgenx.com IntelGenx Corporate Offices 6420 Abrams Saint-Laurent (Quebec) H4S 1Y2 Canada www.intelgenx.com