InterMune Reports Phase 3 ASCEND Trial Results of Pirfenidone in Idiopathic Pulmonary Fibrosis (IPF)

 InterMune Reports Phase 3 ASCEND Trial Results of Pirfenidone in Idiopathic
                           Pulmonary Fibrosis (IPF)

- Study Meets Primary and Both Key Secondary Endpoints -

- Company to Conduct Conference Call and Webcast Today at 8:00 a.m. EST -

PR Newswire

BRISBANE, Calif., Feb. 25, 2014

BRISBANE, Calif., Feb. 25, 2014 /PRNewswire/ --InterMune, Inc. (NASDAQ: ITMN)
today announced that top-line data from ASCEND, a Phase 3 trial evaluating
pirfenidone in patients with idiopathic pulmonary fibrosis (IPF), demonstrated
that pirfenidone significantly reduced IPF disease progression as measured by
change in percent predicted forced vital capacity (FVC) from Baseline to Week
52 (rank ANCOVA p<0.000001). Additionally, significant treatment effects were
demonstrated on both of the key secondary endpoints of six-minute walk test
distance (6MWD) change (p=0.0360) and progression-free survival (PFS)
(p=0.0001).

(Logo: http://photos.prnewswire.com/prnh/20120827/SF62570LOGO)

"We are pleased to report these top-line ASCEND Phase 3 results," said Dan
Welch, Chairman, Chief Executive Officer and President of InterMune. "Based
on the strength of the ASCEND results, InterMune is preparing a resubmission
of our New Drug Application for pirfenidone to the U.S. Food and Drug
Administration (FDA), which we expect to submit by early third quarter of this
year. We would like to thank our collaborators, patients and their families
for their participation in ASCEND and their contributions to IPF research."

Primary Endpoint

The magnitude of the treatment effect of pirfenidone was measured by comparing
the proportion of patients in the pirfenidone and placebo groups experiencing
either a clinically meaningful change in FVC, or death. A 10% decline in FVC
in an individual IPF patient is considered clinically meaningful and strongly
predicts mortality. At Week 52, 16.5% of patients in the pirfenidone group
experienced an FVC decline of 10% or more or death, compared with 31.8% in the
placebo group, representing a 47.9% reduction in the proportion of patients
who experienced a meaningful change in FVC or death. Additionally, at Week 52
the data demonstrated that 22.7% of patients in the pirfenidone group
experienced no decline in FVC, compared with 9.7% in the placebo group,
representing a 132.5% increase in the proportion of patients whose FVC did not
decrease between Baseline and Week 52.

Dr. Talmadge King, Chair, Department of Medicine, University of California San
Francisco and Co-chair of the ASCEND protocol steering committee, said, "IPF
is an unpredictable, debilitating and ultimately fatal disease, and safe and
effective treatments are desperately needed to alter the course of this
challenging and complex condition. The ASCEND data demonstrated that
pirfenidone significantly reduced decline in lung function and significantly
increased the proportion of patients who had no decline, which is an important
advance in the field. The results for 6MWT distance, PFS and mortality
provide important supportive evidence of pirfenidone's efficacy."

Key Secondary Endpoints

The ASCEND protocol pre-specified 6MWD and PFS as the two key secondary
endpoints. Change from Baseline to Week 52 in 6MWD is a measure of exercise
tolerance. A 50-meter decrement in walk distance is considered an independent
predictor of mortality in an individual patient with IPF. In ASCEND,
pirfenidone reduced by 27.5% the proportion of patients who experienced a
decline in 6MWD of 50 meters or greater (p=0.0360).

PFS is a measure of time before death or a disease-progression event. A PFS
event was defined in the protocol as any of the following: death, percent
predicted FVC decrement of 10% or greater or 6MWD decrement of 50 meters or
greater. In ASCEND, pirfenidone reduced the risk of death or disease
progression by 43% compared to placebo (Hazard Ratio [HR]=0.57; 95% confidence
interval, 0.43-0.77; p=0.0001).

Additional Secondary Endpoints

Three additional secondary endpoints were pre-specified in the ASCEND
protocol: all-cause mortality, treatment-emergent IPF-related mortality and
change from Baseline to Week 52 in dyspnea (shortness of breath). The two
mortality analyses were pre-specified for both the ASCEND study and the pooled
population of the ASCEND study and the previous Phase 3 CAPACITY studies
through 52 weeks. Due to the relatively low overall mortality rate in patient
populations in the time frames studied in a single IPF study such as ASCEND,
pooled analyses of ASCEND and CAPACITY data provide more statistical power and
a more precise estimate of the treatment effect of pirfenidone on mortality.

In the pre-specified mortality analysis of the ASCEND study alone, there were
fewer events of all-cause mortality (HR=0.55, log rank p=0.1045) and of
treatment-emergent IPF-related mortality (HR=0.44, log rank p=0.2258) in the
pirfenidone group compared to the placebo group. ASCEND was not powered to
show a difference on these endpoints. The relationship of death to IPF was
determined in ASCEND by a blinded adjudication committee.

The pre-specified analyses of the pooled population (N=1,247) across ASCEND
and the two Phase 3 CAPACITY studies (taking CAPACITY mortality data through
Week 52) showed that the risk of all-cause mortality was reduced by 48% in the
pirfenidone group compared to the placebo group (HR=0.52, log rank p=0.0107).
Additionally, in the pooled population the risk of treatment-emergent
IPF-related death in the pirfenidone group compared to placebo was reduced by
68% (HR=0.32, log rank p=0.0061).

The secondary endpoint of dyspnea, measured by the UCSD SOBQ questionnaire,
was not achieved (p=0.1577).

Safety and Tolerability

In ASCEND, pirfenidone showed a favorable safety profile and was generally
well tolerated.

A total of 93.5% and 94.6% of patients completed the study, died or had a lung
transplant by study day 365 in the pirfenidone and placebo groups,
respectively. The percentage of patients discontinuing treatment due to an
adverse event was 14.4% in the pirfenidone group and 10.8% in the placebo
group. Serious adverse events (SAEs) were reported in 19.8% of patients in
the pirfenidone group and 24.9% in the placebo group. Hospitalizations due to
respiratory, thoracic and mediastinal SAEs were reported in 3.6% of patients
in the pirfenidone group and 11.2% in the placebo group.

The most common AEs with higher incidence in the pirfenidone group were
primarily gastrointestinal (e.g., nausea and dyspepsia) and skin-related
(e.g., rash). The GI and rash AEs were generally mild to moderate in
severity, manageable, reversible and only infrequently led to treatment
discontinuations.

Elevations of aminotransferase levels at least 3 times the upper limit of
normal occurred in 2.9% of pirfenidone patients (including one case associated
with a bilirubin increase) vs. 0.7% of placebo patients. In general, these
elevations occurred early, were manageable and reversible, and were similar to
those observed in previous pirfenidone studies.

The safety and tolerability profile of pirfenidone was generally consistent
with observations from the previous Phase 3 CAPACITY studies, open-label
extension studies and post-marketing experience.

"These results from the ASCEND trial provide compelling evidence of a
clinically meaningful treatment effect of pirfenidone with generally favorable
safety and tolerability findings, which is very encouraging for patients
suffering from this fatal and relentless disease," said Paul W. Noble, Chair,
Department of Medicine, Cedars-Sinai Medical Center, Los Angeles, Calif. and
Co-chair of the ASCEND protocol steering committee. "Importantly, the overall
safety observations from ASCEND complement and corroborate the robust safety
database that already exists from the InterMune-sponsored clinical studies of
pirfenidone and extensive post-marketing experience outside the United
States."

InterMune intends to present additional data from the ASCEND study at the 2014
American Thoracic Society International Conference in May.

About ASCEND

ASCEND (Assessment of Pirfenidone to Confirm Efficacy and Safety in IPF) is a
multinational, randomized, double-blind, placebo-controlled Phase 3 trial
designed to evaluate the safety and efficacy of pirfenidone in patients with
IPF. Patients (N=555) were randomly assigned 1:1 to receive oral pirfenidone
(2403 mg/day) or placebo and were enrolled at 127 centers in the United
States, Australia, Brazil, Croatia, Israel, Mexico, New Zealand, Peru and
Singapore.

More than 95 percent of eligible patients (those patients who remained on
blinded pirfenidone or placebo therapy) who completed the ASCEND study decided
to enter the open-label RECAP extension study. RECAP is a study in which all
patients receive pirfenidone. RECAP also includes patients rolled over from
the company's prior CAPACITY studies which completed in late 2008 and enrolled
779 patients in two Phase 3 studies. RECAP provides valuable long-term safety
data that further expands the already large safety database for pirfenidone in
patients with IPF.

About CAPACITY

Pirfenidone has been studied in multiple Phase 3 clinical trials in patients
with IPF, including the two Phase 3 CAPACITY trials sponsored by InterMune.

The CAPACITY program consisted of two concurrent 72-week trials which enrolled
a total of 779 patients. Both trials were multinational, randomized,
double-blind, and placebo-controlled. The studies were designed to evaluate
the safety and efficacy of pirfenidone in IPF patients with mild to moderate
impairment in lung function. The primary endpoint in both studies was the
change from Baseline to Week 72 in percent predicted FVC. This endpoint was
met with statistical significance in CAPACITY 2 (p=0.001). The secondary
endpoints of PFS and categorical change in FVC also achieved statistical
significance (p<0.05). Although the primary endpoint was not met in CAPACITY
1 (p=0.501), supportive evidence of a pirfenidone treatment effect was
observed on a number of measures, including percent predicted FVC at weeks 24,
36 and 48, and on 6MWD.

Pirfenidone demonstrated a favorable safety profile and was generally well
tolerated in both CAPACITY studies. The most frequent side effects reported
were photosensitivity rash, gastrointestinal symptoms such as nausea and
dyspepsia, and dizziness.

About Esbriet® (pirfenidone)

Pirfenidone is an orally active, anti-fibrotic agent that inhibits the
synthesis of TGF-beta, a chemical mediator that controls many cell functions
including proliferation and differentiation, and plays a key role in
fibrosis. Pirfenidone also inhibits the synthesis of TNF-alpha, a cytokine
that is known to have an active role in inflammation.

On February 28, 2011, the European Commission (EC) granted marketing
authorization for Esbriet® (pirfenidone) for the treatment of adults with mild
to moderate IPF. The approval authorized marketing of Esbriet in all 28 EU
member states. Esbriet has since been approved for marketing in Norway and
Iceland. In 2011, InterMune launched commercial sales of pirfenidone in
Germany under the trade name Esbriet, and Esbriet is now also commercially
available in various European countries, including key markets such as France,
Italy and the UK.

On October 1, 2012, Health Canada approved Esbriet for the treatment of mild
to moderate IPF in adult patients. Health Canada designated Esbriet for
Priority Review and completed the accelerated review according to target
guidelines of 180 days. InterMune launched Esbriet in Canada in January 2013.

Pirfenidone has been marketed as Pirespa® since 2008 in Japan and since 2012
in South Korea by Shionogi & Co. Ltd. Under different trade names,
pirfenidone is also approved for the treatment of IPF in China, India,
Argentina and Mexico.

Pirfenidone is not approved for sale in the United States.

About IPF

Idiopathic pulmonary fibrosis (IPF) is an irreversible and ultimately fatal
disease characterized by progressive loss of lung function due to fibrosis
(scarring) in the lungs, which hinders the ability of lungs to absorb oxygen.
IPF inevitably causes shortness of breath, and a deterioration in lung
function and exercise tolerance. IPF patients follow different and
unpredictable clinical courses and it is not possible to predict if a patient
will progress slowly or rapidly, or when the rate of decline may change.
Periods of transient clinical stability in IPF, when they occur, inevitably
give way to continued disease progression. The median survival time from
diagnosis is two to five years, with a five-year survival rate of
approximately 20-40 percent, which makes IPF more rapidly lethal than many
malignancies, including breast, ovarian and colorectal cancers. IPF typically
occurs in patients over the age of 45, and tends to affect slightly more men
than women.

About InterMune

InterMune is a biotechnology company focused on the research, development and
commercialization of innovative therapies in pulmonology and orphan fibrotic
diseases. In pulmonology, the company is focused on therapies for the
treatment of idiopathic pulmonary fibrosis (IPF), a progressive, irreversible,
unpredictable and ultimately fatal lung disease. Pirfenidone, the only
medicine approved for IPF anywhere in the world, is approved for marketing by
InterMune in the EU and Canada under the trade name Esbriet®. Pirfenidone is
not approved for sale in the United States but has completed three Phase 3
clinical trials to support regulatory registration in the United States.
InterMune's research programs are focused on the discovery of targeted,
small-molecule therapeutics and biomarkers to treat and monitor serious
pulmonary and fibrotic diseases. For additional information about InterMune
and its R&D pipeline, please visit www.intermune.com.

Conference Call and Webcast Details

InterMune will host a live webcast of a conference call today at 8:00 a.m. EST
to discuss the top-line ASCEND Phase 3 results. Interested investors and
others may participate in the conference call by dialing 800-738-1032 (U.S.)
or +1-212-231-2905 (international), conference ID# 21709573. A replay of the
webcast and teleconference will be available approximately three hours after
the call.

To access the webcast, please log on to the company's website at
www.intermune.comat least 15 minutes prior to the start of the call to ensure
adequate time for any software downloads that may be required.

A telephonic replay will be available for 10 business days following the call
and can be accessed by dialing 800-633-8284 (U.S.) or +1 402-977-9140
(international), and entering conference ID# 21709573.

Forward-Looking Statements

This news release contains forward-looking statements within the meaning of
section 21E of the Securities Exchange Act of 1934, as amended, that reflect
InterMune's judgment and involve risks and uncertainties as of the date of
this release, including without limitation InterMune's expectations regarding
the timing for resubmission of its new drug application with the FDA for
pirfenidone; the potential to make pirfenidone available as a medicine to IPF
patients in the United States and InterMune's intention to present additional
data on the ASCEND trial at the American Thoracic Society meeting in May
2014. All forward-looking statements and other information included in this
press release are based on information available to InterMune as of the date
hereof, and InterMune assumes no obligation to update any such forward-looking
statements or information. InterMune's actual results could differ materially
from those described in InterMune's forward-looking statements.

Other factors that could cause or contribute to such differences include, but
are not limited to, those discussed in detail under the heading "Risk Factors"
in InterMune's most recent annual report on Form 10-K filed with the
Securities and Exchange Commission (SEC) on February 21, 2014 (the "Form
10-K") and other periodic reports filed with the SEC, including but not
limited to the following: (i) the risks related to the uncertain, lengthy and
expensive clinical development process for the company's product candidates,
including having no unexpected safety, toxicology, clinical or other issues
and having no unexpected clinical trial results such as unexpected new
clinical data and unexpected additional analysis of existing clinical data;
(ii) risks related to the regulatory process for the company's product
candidates, including the possibility that the results of the new 52-week
Phase 3 clinical trial (ASCEND) having an FVC endpoint may not be satisfactory
to the FDA for InterMune to receive regulatory approval for pirfenidone in the
United States; (iii) risks related to unexpected regulatory actions or delays,
in particular in connection with our planned resubmission of a Class 2 NDA
with the FDA seeking approval of pirfenidone or other government regulation
generally; (iv) risks related to our ability to successfully launch and
commercialize pirfenidone in the United States, if approved by the FDA and (v)
InterMune's ability to obtain or maintain patent or other proprietary
intellectual property protections. The risks and other factors discussed
above should be considered only in connection with the fully discussed risks
and other factors discussed in detail in the Form 10-K and InterMune's other
periodic reports filed with the SEC, all of which are available via
InterMune's web site at www.intermune.com.

SOURCE InterMune, Inc.

Website: http://www.intermune.com
Contact: Investors: Jim Goff, InterMune, Inc., 415-466-2228,
jgoff@intermune.com, orMedia: Geoff Curtis, Edelman, 312-550-8138,
geoff.curtis@edelman.com
 
Press spacebar to pause and continue. Press esc to stop.