Form 6-K
FORM 6-K
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
Report of Foreign Private Issuer
Pursuant to Rule 13a-16 or 15d-16
of the Securities Exchange Act of 1934
Month of September 2011
Commission File Number 1-15182
DR. REDDYS LABORATORIES LIMITED
(Name of Registrant)
8-2-337, Road No. 3, Banjara Hills
Hyderabad, Andhra Pradesh 500 034, India
+91-40-4900-2900
(Address of Principal Executive Offices)
Indicate by check mark whether registrant files or will file annual reports under cover of Form
20-F or Form 40-F.
Form 20-F þ Form 40-F o
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by
Regulation S-T Rule 101(b)(1): o
Note: Regulation S-T Rule 101(b)(1) only permits the submission in paper of a Form 6-K if submitted
solely to provide an attached annual report to security holders.
Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by
Regulation S-T Rule 101(b)(7): o
Note: Regulation S-T Rule 101(b)(7) only permits the submission in paper of a Form 6-K if submitted
to furnish a report or other document that the registrant foreign private issuer must furnish and
make public under the laws of the jurisdiction in which the registrant is incorporated, domiciled
or legally organized (the registrants home country), or under the rules of the home country
exchange on which the registrants securities are traded, as long as the report or other document
is not a press release, is not required to be and has not been distributed to the registrants
security holders, and, if discussing a material event, has already been the subject of a Form 6-K
submission or other Commission filing on EDGAR.
Indicate by check mark whether by furnishing the information contained in this Form, the registrant
is also thereby furnishing the information to the Commission pursuant to Rule 12g3-2(b) under the
Securities Exchange Act of 1934.
Yes
o No
þ
If Yes is marked, indicate below the file number assigned to registrant in connection with Rule
12g3-2(b):
Not applicable.
Table of Contents
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Press Release, Dr. Reddys announces start of Phase II study with the CETP inhibitor, DRL-17822 in
dyslipidemia patients, September 2, 2011. |
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Press Release, Dr. Reddys announces the Launch of Rivastigmine Tartrate Capsules, September 22, 2011. |
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Press Release, Dr. Reddys and JB Chemicals & Pharmaceuticals (JBCPL) terminate Rx business deal in
Russia and other CIS, September 26, 2011. |
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Press Release
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Dr. Reddys Laboratories Ltd. |
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8-2-337, Road No. 3 |
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Banjara Hills, Hyderabad 500 034 |
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Andhra Pradesh, India |
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Tel: 91-40-4900-2900 |
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Fax: 91-40-4900-2999 |
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www.drreddys.com |
Dr. Reddys announces start of Phase II study with the CETP inhibitor, DRL-17822 in dyslipidemia
patients
Hyderabad, India, September 02, 2011:
Dr Reddys Laboratories (NYSE: RDY) announced the initiation of dosing with DRL-17822 in patients
with diagnosis of type II dyslipidaemia. DRL-17822, is a selective, orally bioavailable inhibitor
of cholesteryl ester transfer protein (CETP), for the treatment and/or prevention of dyslipidaemia,
atherosclerosis and associated cardiovascular disease.
The current study is being conducted under a CTA in a number of countries in Europe. The objective
of the study is to evaluate the efficacy and safety of DRL-17822 in patients with Type-II
dyslipidemia. This is a randomized, double blind, placebo controlled, parallel group study in 160
subjects. The primary outcome measure is to assess the elevation in HDL cholesterol and reduction
in LDL cholesterol from baseline to end of treatment compared to placebo. Three doses (50, 150 &
300 mg) of DRL-17822 given once daily for 4 weeks will be evaluated during this study.
Three human Phase I studies with DRL-17822 had already been conducted in Europe, where DRL-17822
was shown to be safe and well tolerated. In these studies, the proof of mechanism had been
demonstrated by dose-dependent inhibition of plasma CETP activity as well as by significant
increase in HDL cholesterol & decrease in LDL cholesterol levels.
Cardiovascular disease is a leading cause of death among men and women worldwide. Among
cardiovascular disorders, coronary heart disease (CHD), caused by atherosclerosis is the most
common cause of morbidity and mortality. Stabilization and/or regression of atherosclerotic plaques
may have a major impact on reducing the risk of acute coronary events. Low-density lipoprotein
cholesterol lowering agents, primarily the statins, are the current mainstay in the pharmacological
management of dyslipidaemia. However, significant residual cardiovascular risk remains despite use
of statins.
Epidemiological and observational studies demonstrate that reduced high density lipoprotein
cholesterol levels are a strong, independent predictor of CHD, suggesting that raising HDL
cholesterol levels might afford clinical benefit in the reduction of cardiovascular risk. One
approach to raise HDL level has been inhibition of CETP activity. Currently it is believed that,
raising HDL cholesterol and lowering LDL cholesterol through CETP inhibition would lead to a
significant benefit in terms of CHD risk reduction.
Dr. K. Anji Reddy, Founder Chairman, Dr. Reddys Laboratories added, We are committed to
delivering products of differentiated value in this area of high global clinical unmet need. We
are excited to continue to advance our CETP program and look forward to the data from our Phase II
study. This class of therapy could transform the treatment of CHD and DRL 17822 is in a position to
be one of the front-running products in the class.
Disclaimer
This press release includes forward-looking statements, as defined in the U.S. Private Securities
Litigation Reform Act of 1995. We have based these forward-looking statements on our current
expectations and projections about future events. Such statements involve known and unknown risks,
uncertainties and other factors that may cause actual results to differ materially. Such factors
include, but are not limited to, changes in local and global economic conditions, our ability to
successfully implement our strategy, the market acceptance of and demand for our products, our
growth and expansion, technological change and our exposure to market risks. By their nature, these
expectations and projections are only estimates and could be materially different from actual
results in the future.
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About Dr. Reddys
Dr. Reddys Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed
to providing affordable and innovative medicines for healthier lives. Through its three businesses
Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products Dr.
Reddys offers a portfolio of products and services including APIs, custom pharmaceutical services,
generics, biosimilars, differentiated formulations and NCEs. Therapeutic focus is on
gastro-intestinal, cardiovascular, diabetology, oncology, pain management, anti-infective and
pediatrics. Major markets include India, USA, Russia and CIS, Germany, UK, Venezuela, S. Africa,
Romania, and New Zealand. For more information, log on to: www.drreddys.com
For more information please contact:
Investors and Financial Analysts:
Kedar Upadhye at kedaru@drreddys.com / +91-40-66834297
Raghavender R at raghavenderr@drreddys.com / +91-40-49002135
Milan Kalawadia (North America) at mkalawadia@drreddys.com / +1-908-203-4931
Media:
Rajan S at rajans@drreddys.com / +91-40-49002445
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Press Release
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Dr. Reddys Laboratories Ltd. |
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8-2-337, Road No. 3 |
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Banjara Hills, Hyderabad 500 034 |
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Andhra Pradesh, India |
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Tel: 91-40-4900-2900 |
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Fax: 91-40-4900-2999 |
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www.drreddys.com |
Dr. Reddys announces the Launch of Rivastigmine Tartrate Capsules
Hyderabad, India, September 22, 2011
Dr. Reddys Laboratories (NYSE: RDY) announced today that it has launched Rivastigmine Tartrate
Capsules (1.5 mg, 3 mg, 4.5 mg and 6 mg), a bioequivalent generic version of EXELON®*
Capsules in the US market on September 15, 2011 following the approval by the United States Food &
Drug Administration (USFDA) of Dr. Reddys ANDA for Rivastigmine tartrate capsules.
The EXELON®* brand and generic Rivastigmine tartrate had U.S. sales of approximately
$92.6 million for the most recent twelve months ending June 2011 according to IMS Health.
Dr. Reddys Rivastigmine tartrate capsules 1.5 mg, 3 mg, 4.5 mg and 6 mg strengths are available in
60 count bottles.
Disclaimer
This press release includes forward-looking statements, as defined in the U.S. Private Securities
Litigation Reform Act of 1995. We have based these forward-looking statements on our current
expectations and projections about future events. Such statements involve known and unknown risks,
uncertainties and other factors that may cause actual results to differ materially. Such factors
include, but are not limited to, changes in local and global economic conditions, our ability to
successfully implement our strategy, the market acceptance of and demand for our products, our
growth and expansion, technological change and our exposure to market risks. By their nature, these
expectations and projections are only estimates and could be materially different from actual
results in the future.
About Dr. Reddys
Established in 1984, Dr. Reddys Laboratories (NYSE: RDY) is an emerging global pharmaceutical
company. We fulfill our purpose of providing affordable and innovative medicines through three core
businesses: Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary
Products. Our products are marketed globally, with a focus on India, US, UK, Germany and Russia.
www.drreddys.com
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EXELON is a registered trademark of Novartis Pharmaceuticals Corporation |
IMS National Sales Perspectives: Retail and Non-Retail MAT JUNE 2011
For more information please contact:
Investors and Financial Analysts:
Kedar Upadhye at kedaru@drreddys.com / +91-40-66834297
Raghavender R at raghavenderr@drreddys.com / +91-40-49002135
Milan Kalawadia (North America) at mkalawadia@drreddys.com / +1-908-203-4931
Media:
Rajan S at rajans@drreddys.com / +91-40-49002445
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Press Release
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Dr. Reddys Laboratories Ltd. |
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8-2-337, Road No. 3 |
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Banjara Hills, Hyderabad 500 034 |
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Andhra Pradesh, India |
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Tel: 91-40-4900-2900 |
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Fax: 91-40-4900-2999 |
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www.drreddys.com |
Dr. Reddys and JB Chemicals & Pharmaceuticals (JBCPL) terminate Rx business deal in Russia and
other CIS
September 26, 2011, Hyderabad, India
Dr. Reddys Laboratories (NYSE: RDY) announced today that the proposed business deal to acquire the
pharmaceutical prescription portfolio of JB Chemicals & Pharmaceuticals in Russia and other CIS
countries has been mutually terminated in the overall business interest of both parties. Dr.
Reddys and JBCPL had entered into an agreement on July 22, 2011.
Russia is one of Dr. Reddys focus markets where we continue to improve our market ranks and we are
committed to expanding our presence in the region.
Disclaimer
This press release includes forward-looking statements, as defined in the U.S. Private Securities
Litigation Reform Act of 1995. We have based these forward-looking statements on our current
expectations and projections about future events. Such statements involve known and unknown risks,
uncertainties and other factors that may cause actual results to differ materially. Such factors
include, but are not limited to, changes in local and global economic conditions, our ability to
successfully implement our strategy, the market acceptance of and demand for our products, our
growth and expansion, technological change and our exposure to market risks. By their nature, these
expectations and projections are only estimates and could be materially different from actual
results in the future.
About Dr. Reddys
Dr. Reddys Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed
to providing affordable and innovative medicines for healthier lives. Through its three businesses
- Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products Dr.
Reddys offers a portfolio of products and services including APIs, custom pharmaceutical services,
generics, biosimilars, differentiated formulations and NCEs. Therapeutic focus is on
gastro-intestinal, cardiovascular, diabetology, oncology, pain management, anti-infective and
pediatrics. Major markets include India, USA, Russia and CIS, Germany, UK, Venezuela, S. Africa,
Romania, and New Zealand. For more information, log on to: www.drreddys.com
For more information please contact:
Investors and Financial Analysts:
Kedar Upadhye at kedaru@drreddys.com / +91-40-66834297
Raghavender R at raghavenderr@drreddys.com / +91-40-49002135
Milan Kalawadia (North America) at mkalawadia@drreddys.com / +1-908-203-4931
Media:
Rajan S at rajans@drreddys.com / +91-40-49002445
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Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused
this report to be signed on its behalf by the undersigned, thereunto duly authorized.
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DR. REDDYS LABORATORIES LIMITED
(Registrant)
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By: |
/s/ Sandeep Poddar
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Date: September 30, 2011 |
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Name: |
Sandeep Poddar |
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Title: |
Company Secretary |
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