Janssen Collaborates With ViiV Healthcare to Develop Two-Drug Single Tablet Regimen for the Maintenance Treatment of People Living With HIV

Cork, Ireland (ots/PRNewswire) -

Janssen R&D Ireland Ltd announced today that they have entered
into a collaboration with ViiV Healthcare to develop and
commercialize a new single tablet regimen containing Janssen's
Non-Nucleoside Reverse Transcriptase Inhibitor rilpivirine (marketed
as EDURANT(R)) and ViiV's Integrase Inhibitor dolutegravir(marketed
as TIVICAY(R)) as the sole active ingredients for the maintenance
treatment of people living with Human Immunodeficiency Virus (HIV).
The companies will further investigate development of this drug
combination for pediatric use.

If successfully developed and approved by regulatory authorities,
this treatment could offer people living with HIV who are
virologically suppressed an option to switch from a standard
three-drug therapy to a two-drug, Nucleoside Reverse Transcriptase
Inhibitor (NRTI)-sparing antiviral regimen.

"HIV remains a significant medical challenge, and our goal is to
find new treatment regimens for patients," says Paul Stoffels, Chief
Scientific Officer, Johnson & Johnson and Worldwide Chairman,
Janssen. "We are pleased to collaborate with ViiV Healthcare in
pursuing this shift in the HIV treatment paradigm and reaffirm our
commitment to collaborate and develop new HIV treatments and
fixed-dose regimens."

Formulation and clinical development for the single tablet regimen
will begin in the coming months.

Since the beginning of the HIV epidemic, almost 75 million people
have been infected with the HIV virus.[1] It is estimated that 35
million people are currently living with HIV globally, with 2.5
million people becoming newly infected each year.[1],[2],[3]

Standard HIV-drug therapy contains three active components: a
backbone of two NRTIs, plus either a Non-Nucleoside Reverse
Transcriptase Inhibitor (NNRTI), Protease Inhibitor (PI) or Integrase
Inhibitor (INI).

About EDURANT(R)

EDURANT(R) (rilpivirine) is a prescription HIV medicine that is
used with other antiretroviral medicines to treat Human
Immunodeficiency Virus-1 (HIV-1)in adults:

- Who have never taken HIV medicines before, and
- Who have an amount of HIV in their blood (called "viral load") that is no more
than 100,000 copies/mL. Your healthcare professional will measure your viral load
- EDURANT(R) should be taken in combination with other HIV medicines. Your
healthcare professional will work with you to find the right combination of HIV
medicines
- It is important that you remain under the care of your healthcare professional
during treatment with EDURANT(R)
- EDURANT(R) is not recommended for patients less than 18 years of age

EDURANT(R) does not cure HIV infection or AIDS. You should remain
on your HIV medications without stopping to ensure that you control
your HIV infection and decrease the risk of HIV-related illnesses.
Ask your healthcare professional about how to prevent passing HIV to
other people.

Please read Important Safety Information below, and talk to your
healthcare professional to learn if EDURANT(R) is right for you.

Important Safety Information

Can EDURANT(R) be taken with other medicines?

EDURANT(R) may affect the way other medicines work and other
medicines may affect how EDURANT(R) works and may cause serious side
effects. If you take certain medicines with EDURANT(R), the amount of
EDURANT(R) in your body may be too low and it may not work to help
control your HIV infection, and the HIV virus in your body may become
resistant to EDURANT(R) or other HIV medicines that are like it. To
help get the right amount of medicine in your body, you should always
take EDURANT(R) with a meal. A protein drink alone does not replace a
meal.

Do not take EDURANT(R) if:

Your HIV infection has been previously treated with HIV medicines

You are taking any of the following medicines:

- Anti-seizure medicines: carbamazepine (Carbatrol(R), Equetro(R),
Tegretol(R), Tegretol-XR(R), Teril(R), Epitol(R)), oxcarbazepine (Trileptal(R)),
phenobarbital (Luminal(R)), phenytoin (Dilantin(R), Dilantin-125(R), Phenytek(R))
- Anti-tuberculosis (anti-TB) medicines: rifampin (Rifater(R), Rifamate(R),
Rimactane(R), Rifadin(R)), rifapentine (Priftin(R))
- Proton pump inhibitor (PPI) medicine for certain stomach or intestinal
problems: esomeprazole (Nexium(R), Vimovo(R)), lansoprazole (Prevacid(R)), omeprazole
(Prilosec(R), Zegerid(R)), pantoprazole sodium (Protonix(R)), rabeprazole (Aciphex(R))
- More than 1 dose of the steroid medicine dexamethasone or dexamethasone sodium
phosphate
- St. John's wort (Hypericum perforatum)

Especially tell your doctor if you take:

- Rifabutin (Mycobutin(R), a medicine to treat some bacterial infections).
Talk to your doctor or pharmacist about the right amount of EDURANT(R) you should take
if you also take rifabutin.
- Medicines used to treat HIV
- An antacid medicine that contains aluminum, magnesium hydroxide, or calcium
carbonate. Take antacids at least 2 hours before or at least 4 hours after you take
EDURANT(R)
- Medicines to block acid in your stomach, including cimetidine (Tagamet(R)),
famotidine (Pepcid(R)), nizatidine (Axid(R)), or ranitidine hydrochloride (Zantac(R)).
Take these medicines at least 12 hours before or at least 4 hours after you take
EDURANT(R)
- Any of these medicines (if taken by mouth or injection): clarithromycin
(Biaxin(R)), erythromycin (E-Mycin(R), Eryc(R), Ery-Tab(R), PCE(R), Pediazole(R),
Ilosone(R)), fluconazole (Diflucan(R)), itraconazole (Sporanox(R)), ketoconazole
(Nizoral(R)), methadone (Dolophine(R)), posaconazole (Noxafil(R)), telithromycin
(Ketek(R)),voriconazole (Vfend(R))

This is not a complete list of medicines. Before starting
EDURANT(R), be sure to tell your healthcare professional about all
the medicines you are taking or plan to take, including prescription
and nonprescription medicines, vitamins, and herbal supplements.

Before taking EDURANT(R), also tell your healthcare professional
if you have had or currently have liver problems (including hepatitis
B or C), have ever had a mental health problem, are pregnant or
planning to become pregnant, or breastfeeding. It is not known if
EDURANT(R) will harm your unborn baby.

You and your healthcare professional will need to decide if taking
EDURANT(R)is right for you.

- Do not breastfeed if you are taking EDURANT(R). You should not breastfeed
if you have HIV because of the chance of passing HIV to your baby

What are the possible side effects of EDURANT(R)?

EDURANT(R) can cause serious side effects including:

- Depression or mood changes. Tell your doctor right away if you have any of
the following symptoms: feeling sad or hopeless, feeling anxious or restless, have
thoughts of hurting yourself (suicide), or have tried to hurt yourself
- Liver problems. People with a history of hepatitis B or C virus infection or
who have certain liver function test changes may have an increased risk of developing
new or worsening liver problems during treatment. Liver problems were also reported
during treatment in some people without a history of liver disease. Your healthcare
professional may need to do tests to check liver function before and during treatment
- Changes in body shape or body fat have been seen in some patients taking HIV
medicines. The exact cause and long-term health effects of these conditions are not
known
- Changes in your immune system (immune reconstitution syndrome).

Your immune system may get stronger and begin to fight infections.
Tell your healthcare professional right away if you start having any
new symptoms of infection.

Other common side effects of EDURANT(R) include depression,
headache, trouble sleeping (insomnia), and rash.

This is not a complete list of all side effects. If you experience
these or other symptoms, contact your healthcare professional right
away. Do not stop taking EDURANT(R) or any other medications without
first talking to your healthcare professional.

You are encouraged to report negative side effects of prescription
drugs to the FDA. Visit http://www.fda.gov/medwatch, or call
1-800-FDA-1088.

Please see full Product Information for more details:

http://www.edurant.com/sites/default/files/EDURANT-PI.pdf

About EDURANT(R) (rilpivirine)

Rilpivirine was developed by Janssen R&D Ireland Ltd, one of the
Janssen Pharmaceutical Companies.

The registered formulation of rilpivirine is a 25 mg film-coated
tablet taken orally once daily. Marketed as EDURANT(R), rilpivirine
is indicated, in combination with other ARVs, for the treatment of
HIV-1 in ARV treatment-naive adult patients. In most countries,
including US and EU, this indication is further restricted to
patients with a viral load < 100,000 copies/ mL.

Rilpivirine is available in the United States (US) and the
European Union as part of a once daily fixed dose antiretroviral
combination with Gilead Sciences Inc's tenofovir and emtricitabine.
This combination, known as COMPLERA(R) (US) or EVIPLERA(R), was
granted marketing authorisation from the Food and Drug Administration
in August 2011, with Gilead Sciences Inc being the marketing
authorisation holder in the US, and from the European Commission in
November 2011, with Gilead Sciences International Ltd. being the
marketing authorisation holder in Europe, Middle East and Africa.

About TIVICAY(R) (dolutegravir)

TIVICAY(R) (dolutegravir) is an integrase inhibitor indicated for
use in combination with other antiretroviral agents for the treatment
of HIV-1 in adults and children aged 12 years and older weighing at
least 40 kg. Integrase inhibitors block HIV replication by preventing
the viral DNA from integrating into the genetic material of human
immune cells (T-cells). This step is essential in the HIV replication
cycle and is also responsible for establishing chronic infection. It
is available as a small, yellow, 50 mg tablet. Importantly, it can be
taken with or without food and at any time of the day.

About Janssen

At Janssen, we are dedicated to addressing and solving some of the
most important unmet medical needs of our time in infectious diseases
and vaccines, oncology, immunology, neuroscience, and cardiovascular
and metabolic diseases. Driven by our commitment to patients, we
develop innovative products, services and healthcare solutions to
help people throughout the world.

(This press release contains "forward-looking statements" as
defined in the Private Securities Litigation Reform Act of 1995. The
reader is cautioned not to rely on these forward-looking statements.
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 expectations and projections of Janssen R&D Ireland Ltd, any of
the Janssen Pharmaceutical Companies and/or Johnson & Johnson.

Risks and uncertainties include, but are not limited to: economic
factors, such as interest rate and currency exchange rate
fluctuations; competition, including technological advances, new
products and patents attained by competitors; challenges inherent in
new product development, including obtaining regulatory approvals;
challenges to patents; changes in behavior and spending patterns or
financial distress of purchasers of health care products and
services; changes to governmental laws and regulations and domestic
and foreign health care reforms; general industry conditions
including trends toward health care cost containment; and increased
scrutiny of the health care industry by government agencies.

A further list and description of these risks, uncertainties and
other factors can be found in Johnson & Johnson's Annual Report on
Form 10-K for the fiscal year ended December 29, 2013, including in
Exhibit 99 thereto, and our subsequent filings with the Securities
and Exchange Commission. Copies of these filings are available online
at http://www.sec.gov, http://www.jnj.com or on request from Johnson
& Johnson. None of the Janssen Pharmaceutical Companies nor Johnson &
Johnson undertakes to update any forward-looking statements as a
result of new information or future events or developments.)

1. World Health Organization. Global summary of the AIDS epidemic.
Available at: http://www.who.int/gho/hiv/en/
[http://www.who.int/gho/hiv/en ]. Last accessed June 2014.

2. Hui Dy. Effects of HIV protease inhibitor therapy on lipid
metabolism. Prog Lipid Res 2003;
http://www.ncbi.nlm.nih.gov/pubmed/12547652 42(2):81-92.

3. World Health Organization. Global summary of the AIDS epidemic.
Available at: http://www.who.int/hiv/data/2012_epi_core_en.png. Last
accessed June 2014.

MEDIA CONTACT:
Ronan Collins
+47-488-42500
rcollin5@its.jnj.com

INVESTOR RELATIONS:
Stan Panasewicz
+1-732-524-2524

Louise Mehrotra
+1-732-524-6491

ots Originaltext: Janssen R&D Ireland Ltd
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