IntelGenx Reports 2012 Annual Results and Provides Operational Update

IntelGenx Reports 2012 Annual Results and Provides Operational Update

NDA for Rizatriptan Anti-Migraine VersaFilm(TM) to be Filed by the End of This

SAINT LAURENT, Quebec, March 18, 2013 (GLOBE NEWSWIRE) -- IntelGenx Corp.
(TSX-V:IGX) (OTCQX:IGXT) (the "Company") today announced financial results for
its fiscal year ended December 31, 2012 and provided an update on operational

"We ended 2012 with cash exceeding $2 million, no debt, and our first
FDA-approved product, Forfivo XL, having been successfully launched in the USA
by Edgemont Pharmaceuticals," stated Dr. Horst G. Zerbe, President and CEO of
IntelGenx. "As we enter 2013, we have received payment of the $1.0 million
milestone invoiced to Edgemont at the end of the fourth quarter of 2012, and
we look forward to receiving royalty income from Forfivo XL whilst we pursue
licensing opportunities for the rest of the world. We will also continue to
focus our attention on achieving FDA approval of the remaining products in our
pipeline, with a 505(b)(2) NDA submission for our anti-migraine VersaFilm
product on track to be filed by the end of March 2013, as previously

Corporate Development Update

Anti-migraine VersaFilm™ (rizatriptan)

In May 2012, we announced the completion of the pivotal bioequivalence study
for a novel oral thin-film formulation of Rizatriptan, the active drug in
Maxalt-MLT® orally disintegrating tablets. The study results indicate that the
product is safe, and that the 90% confidence intervals of the three relevant
parameters Cmax, AUC(0-t) and AUC(0-infinity) are well within the acceptance
range for bioequivalency.

In November 2012 we announced the successful conclusion of a pre-New Drug
Application ("NDA") meeting with the U.S. Food and Drug Administration related
to our VersaFilm™ formulation of Rizatriptan. The purpose of the meeting was
to receive confirmation from FDA regarding the adequacy of the clinical,
non-clinical and CMC data for our proposed 505(b)(2) NDA submission, which we
are on track to file by the end of the first quarter of 2013.

Maxalt-MLT® is a leading branded anti-migraine product manufactured by Merck &
Co. Our thin-film formulation of Rizatriptan has been developed in accordance
with the co-development and commercialization agreement with RedHill Biopharma
Ltd. using IntelGenx' proprietary immediate release "VersaFilm™" drug delivery

Erectile Dysfunction VersaFilm™ (tadalafil)

Subsequent to the end of the year, in February 2013 we successfully completed
a pilot bioequivalence study on our erectile dysfunction VersaFilm™ product.
In a previous study, we had already demonstrated that we are able to formulate
a bioequivalent product. In the recently completed study, we showed that we
were additionally able to develop a faster formulation with a significantly
shorter T[max ]which will address the need for a faster tadalafil product.

Development and Commercialization Agreement with Par Pharmaceutical, Inc.

In December 2011 we announced the execution of a co-development and
commercialization agreement with Par Pharmaceutical, Inc. ("Par") for a new
product utilizing one of our proprietary oral drug delivery platform
technologies. This program continues to make progress. For commercial reasons,
and in order to protect both Par's and IntelGenx' competitive advantage, the
agreement stipulates that all information pertaining to the product, together
with financial terms of the agreement, are to remain confidential.

Antihypertensive VersaTab™ product

We recently completed a pilot bioequivalence study for our antihypertensive
project, INT0001, a generic equivalent to a major cardiovascular product,
using our proprietary VersaTab™ delivery technology. We continue to make
progress with the project and, together with our strategic partner, Dava
Pharmaceuticals Inc., are working diligently towards the filing of an ANDA
with the FDA.

Financial Results:

The cash balance of $2.1 million as at December 31, 2012 compares with cash of
$3.5 million at December 31, 2011. Net funds used in operations totaled $1.6
million in 2012, compared with net funds used of $2.3 million in 2011, and
funds used in investing activities totaled $0.3 million and $0.2 million in
2012 and 2011 respectively. Funds generated from financing activities were
$0.4 million in 2012 compared with $4.8 million in 2011, including $3.2
million from private placements completed in June 2011.

Accounts receivable of $1.3 million as at December 31, 2012 (December 31, 2011
- $0.3 million) includes an amount of $1.0 million related to the launch of
Forfivo XL™ that was invoiced to Edgemont Pharmaceuticals in the fourth
quarter of 2012. Payment against the invoice was received in February 2013.

Revenue improved from $0.4 million in fiscal 2011 to $1.2 million in 2012,
primarily due to the milestone payment of $1.0 million invoiced to Edgemont
Pharmaceuticals for the launch of Forfivo XL™ in the fourth quarter of 2012.

Total expenses increased from $2.9 million in fiscal 2011 to $3.5 million in
2012. The increase is primarily attributable to additional R&D expenditure of
$0.3 million related to costs associated with the technical transfer of
activities in preparation of the manufacture of Forfivo XL™ and a Product Fee
for Forfivo XL™ payable to the FDA.

The net loss decreased from $2.5 million in fiscal 2011 to a loss of $2.3
million in 2012, and the loss per share decreased from $0.05 per share in 2011
to $0.04 per share in 2012.

About IntelGenx:

IntelGenx is a drug delivery company focused on the development of oral
controlled-release products as well as novel rapidly disintegrating delivery
systems. IntelGenx uses its unique multiple layer delivery system to provide
zero-order release of active drugs in the gastrointestinal tract. IntelGenx
has also developed novel delivery technologies for the rapid delivery of
pharmaceutically active substances in the oral cavity based on its experience
with rapidly disintegrating films. IntelGenx' development pipeline includes
products for the treatment of severe depression, hypertension, erectile
dysfunction, benign prostatic hyperplasia, migraine, insomnia, idiopathic
pulmonary fibrosis, allergies and pain management. More information is
available about the company at

Forward Looking Statements:

This document may contain forward-looking information about IntelGenx'
operating results and business prospects that involve substantial risks and
uncertainties. Statements that are not purely historical are forward-looking
statements within the meaning of Section 21E of the Securities Exchange Act of
1934, as amended, and Section 27A of the Securities Act of 1933, as amended.
These statements include, but are not limited to, statements about IntelGenx'
plans, objectives, expectations, strategies, intentions or other
characterizations of future events or circumstances and are generally
identified by the words "may," "expects," "anticipates," "intends," "plans,"
"believes," "seeks," "estimates," "could," "would," and similar expressions.
All forward looking statements are expressly qualified in their entirety by
this cautionary statement. Because these forward-looking statements are
subject to a number of risks and uncertainties, IntelGenx' actual results
could differ materially from those expressed or implied by these forward
looking statements. Factors that could cause or contribute to such differences
include, but are not limited to, those discussed under the heading "Risk
Factors" in IntelGenx' annual report on Form 10-K for the fiscal year ended
December 31, 2011, filed with the United States Securities and Exchange
Commission and available at, and also filed with Canadian
securities regulatory authorities and IntelGenx assumes no
obligation to update any such forward-looking statements.

Each of the TSX Venture Exchange and OTCQX has neither approved nor
disapproved the contents of this press release.

CONTACT: Dr. Horst G. Zerbe,
         President and CEO
         IntelGenx Technologies Corp.
         T: +1 514-331-7440 (ext. 201)
         F: +1 514-331-0436
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