Tibotec Data Presented at ICAAC and HIV9 Follow key Regulatory Approvals for Anti-HIV Compounds

Glasgow, Scotland, November 12 (ots/PRNewswire) -

- Not Intended for Journalists in the UK or Ireland

- New Findings From ARTEMIS and TITAN Studies Demonstrate Growth
of the Tibotec Virology Franchise

New data on PREZISTA(R) (darunavir), a protease inhibitor from
Tibotec, will be presented at the Ninth International Congress on
Drug Therapy in HIV Infection (HIV9) in Glasgow, U.K., from 09-13
November 2008. The company also presented new data on PREZISTA(R) at
the 48th Interscience Conference on Antimicrobial Agents and
Chemotherapy (ICAAC) in Washington, D.C., from 25-28 October 2008.
These presentations follow key regulatory approvals and decisions for
PREZISTA(R) and INTELENCE(TM) (etravirine), a next-generation
non-nucleoside reverse transcriptase inhibitor (NNRTI). The company
continues to research various compounds in hepatitis C, tuberculosis
and HIV.

"The Tibotec data being presented at HIV9 culminate an exciting
three months for the company and for the entire HIV community," said
Roger Pomerantz, President, Tibotec Research & Development. "The data
we've amassed and the regulatory milestones we've achieved this year
are signs of our dedication to finding innovative ways to meet the
needs of people with HIV."

Recent Regulatory Milestones for Tibotec in HIV

- 28 August 2008 - The European Commission approved etravirine, in
combination with a boosted protease inhibitor and other antiretroviral
medicinal products, for the treatment of human immunodeficiency virus
type 1 (HIV-1) infection in antiretroviral treatment-experienced adult
patients.
- 21 October 2008 - The U.S. FDA granted traditional approval to
darunavir, coadministered with low dose ritonavir, for twice-daily use in
treatment-experienced adult patients, as well as an expanded indication
for once-daily dosing as part of HIV combination therapy in treatment-
naïve adults (those who have never taken HIV medication before).
- 23 October 2008 - Darunavir received a positive opinion from the
European Medicines Agency's (EMEA) Committee for Medicinal Products for
Human Use (CHMP) to extend the drug's indication to treat human
immunodeficiency virus (HIV-1) infection to include treatment-experienced
adult patients. Darunavir, coadministered with low dose ritonavir, is
currently indicated for the treatment of HIV-1 in combination with other
antiretroviral medicines in highly pre-treated adult patients who failed
more than one regimen containing a protease inhibitor.

Tibotec Data at ICAAC and HIV9 Data from multiple studies
examining the use of darunavir in patients with varying levels of
treatment experience were presented at ICAAC and will be presented at
HIV9. Highlights include:

- A new analysis of ARTEMIS (AntiRetroviral Therapy with TMC114 ExaMined
In Naive Subjects), a randomised, controlled, open-label Phase III trial
that compares the 96-week efficacy and safety of darunavir/ritonavir
with lopinavir/ritonavir in treatment-naive adults. ARTEMIS is the first
study to examine darunavir/ritonavir in a once-daily dose in treatment-
naive patients with HIV. These data were presented at ICAAC on 26
October.
- A new analysis of TITAN (TMC114/r In Treatment-experienced pAtients
Naive to lopinavir), a randomised, controlled, open-label Phase III
study that compares the 96-week efficacy and safety of
darunavir/ritonavir with lopinavir/ritonavir in treatment-experienced,
lopinavir-naive patients. These data will be presented at HIV9 on 13
November.

The ARTEMIS and TITAN studies are ongoing. Darunavir and
etravirine were developed by Tibotec Pharmaceuticals, Cork, Ireland.
Tibotec, a division of Janssen-Cilag, is responsible for marketing
the brand in Europe.

Please see full Prescribing Information for more details.

About Tibotec Pharmaceuticals

Tibotec Pharmaceuticals, based in Cork, Ireland, is a
pharmaceutical research and development company, with offices in
Yardley, PA and main research and development operations/labs in
Belgium. Tibotec is dedicated to the discovery and development of
innovative HIV/AIDS drugs and anti-infectives for diseases of high
unmet medical need.

About Tibotec

Tibotec, a division of Janssen-Cilag, will bring innovative
products for HIV/AIDS to patients in Europe, the Middle East and
Africa This new division was created within the Janssen-Cilag
companies in October 2005 to focus on patients' and healthcare
providers' specific needs in this disease domain. The company will
also commercialise medicine to combat other viral diseases in the
future.

Janssen-Cilag

Janssen-Cilag is a leader in traditional and biological medicines
for disorders such as gastroenterology, women's health, mental health
and neurology as well as for pain, oncology, haematology and
nephrology.

(This press release contains "forward-looking statements" as
defined in the Private Securities Litigation Reform Act of 1995.
These statements are based on current expectations of future events.
If underlying assumptions prove inaccurate or unknown risks or
uncertainties materialize, actual results could vary materially from
the Company's expectations and projections. Risks and uncertainties
include general industry conditions and competition; economic
conditions, such as interest rate and currency exchange rate
fluctuations; technological advances and patents attained by
competitors; challenges inherent in new product development,
including obtaining regulatory approvals; domestic and foreign health
care reforms and governmental laws and regulations; and trends toward
health care cost containment. A further list and description of these
risks, uncertainties and other factors can be found in Exhibit 99 of
Johnson & Johnson's Annual Report on Form 10-K for the fiscal year
ended December 30, 2007. Copies of this Form 10-K, as well as
subsequent filings, are available online at http://www.sec.gov,
http://www.jnj.com or on request from Johnson & Johnson. The Company
does not undertake to update any forward-looking statements as a
result of new information or future events or developments.)

Contact: Hans Vanavermaete
Mobile: +32(0)478-447-278
Office: +32(0)15-461-017

ots Originaltext: Tibotec Pharmaceuticals
Im Internet recherchierbar: http://www.presseportal.de

Contact:
Contact: Hans Vanavermaete, Mobile: +32(0)478-447-278, Office:
+32(0)15-461-017