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French drug company Sanofi SA (SAN.FR) Monday said results from the pivotal Phase III Velour study evaluating Zaltrap showed improvement in overall survival rate to colorectal cancer.
MAIN FACTS:
- Sanofi said the Journal of Clinical Oncology published the results of the study evaluating Zaltrap effects.
- In the Velour trial evaluating metastatic colorectal cancer patients previously treated with an oxaliplatin-containing regimen, Zaltrap in combination with the Folfiri chemotherapy regimen (5-fluorouracil, leucovorin, irinotecan) showed a statistically significant improvement in overall survival, progression-free survival, and the overall tumor response rate versus placebo plus Folfiri.
- The Velour data supported the regulatory approval of Zaltrap by the U.S. Food and Drug Administration (FDA) on August 3, 2012 after a Priority Review.
- Zaltrap is under review at the European Medicines Agency and other regulatory agencies worldwide, Sanofi says.
-Write to Inti Landauro at inti.landauro@dowjones.com
Subscribe to WSJ: online.wsj.com?mod=djnwires
(END) Dow Jones Newswires
October 08, 2012 01:43 ET (05:43 GMT)
© 2012 Dow Jones & Company, Inc.

AAND SANOFI ADR
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WEST CHESTER, Pa., Oct. 05, 2012 -- (BUSINESS WIRE) -- A new approach to musculoskeletal care appears to be on the horizon with the recent formation of a company aiming to regenerate human bone and other skeletal tissue. The company, called SkelRegen, LLC (short for Skeletal Regeneration), has already identified several compounds that it believes could transform musculoskeletal care.

SkelRegen results from a collaboration between Scott D. Boden, MD, Chief Medical Officer at the Emory University Orthopaedic & Spine Hospital and Professor of Orthopaedics, Emory University School of Medicine and Stephen R. LaNeve, former President of a multi-billion dollar Spinal & Biologics division of a leading global medical device company.

A major challenge in orthopaedic surgery, trauma, and plastic surgery is dealing with damaged skeletal tissues (bone, cartilage, ligament, tendon). Current options are limited to biologically inactive space fillers or expensive recombinant proteins, peptides, and antibodies. The best possible solution to this challenge would be a less expensive small molecule capable of regenerating skeletal tissues using the body’s own mechanisms; and by using compounds with known acceptable safety and toxicity profiles, the company expects to greatly reduce the time and expense needed for commercialization.

SkelRegen is the first company to focus on newly identified small molecules that target different aspects of the skeletal tissue formation pathway. Several of its discoveries have been shown to be successful in blocking specific intracellular/extracellular inhibitors of BMPs, the key regulators of bone and soft tissue growth. Blocking the inhibitors of BMPs dramatically enhances the body’s own stem cells and growth factors that lead to regeneration of bone and soft tissue. Other discoveries also include molecules that can activate the BMP pathway directly.

Boden, SkelRegen’s Co-Founder and Chief Medical, Science & Technology Officer, says, “We discovered several small molecules that simply help the body’s own regeneration machinery do its job. We are basically building bone from scratch now, with the expectation of building cartilage and other soft tissue in the near future. This technology has broad application throughout the field of orthopaedics and holds promise for transforming musculoskeletal care.” Dr. Boden oversaw the research team led by Emory Orthopaedics researcher Sreedhara Sangadala, PhD, that discovered the molecules.

The company anticipates addressing the unique clinical and economic needs of several major market segments, including Spine, Trauma, Scaffold & Bone Void Filler, Soft Tissue Repair, and Osteoporosis.

LaNeve, SkelRegen’s Co-Founder and CEO, adds, “These compounds are inexpensive to manufacture and many have already been cleared by the FDA for other uses, which means they have acceptable safety and toxicity profiles. It’s very attractive from a development perspective.”

SkelRegen is the only company to have identified such compounds with all of these key attributes.

“We are very pleased to be able to commercialize this new technology,” says Todd Sherer, Executive Director of Emory's Office of Technology Transfer. “I look forward to the results of this partnership and its potential to improve the lives of patients with musculoskeletal disease and injury.”
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Study Findings of Desirudin for DVT Prophylaxis Published in Clinical and Applied Thrombosis and Hemostasis

PARSIPPANY, N.J., Oct. 09, 2012 -- (BUSINESS WIRE) -- DESIR-ABLE, a multicenter, open-label, single-arm study of desirudin (Revasc®, Iprivask®) demonstrated the clinical utility and safety profile of desirudin for prevention of dangerous blood clots in a broad population of surgical and medically ill patients.

Results of the study, entitled Multi-Center Trial of Desirudin for the Prophylaxis of Thrombosis: an Alternative to Heparin-Based Anticoagulation (DESIR-ABLE), were published in Clinical and Applied Thrombosis and Hemostasis.

“This study adds to our overall body of knowledge of desirudin, which has been shown to be safe and effective in preventing blood clots after total hip replacement surgery,” commented Jerrold Levy, MD, Professor and Deputy Chair for Research at Emory University and Chair of the DESIR-ABLE Steering Committee. “The safety profile of desirudin appears to be acceptable in many patients requiring deep vein thrombosis (DVT) prophylaxis who may not be good candidates for heparin-based anticoagulation due to low platelet counts, renal impairment or other high risk features.”

“As we have seen time and time again, despite the many treatment options to prevent blood clots in hospitalized patients, large groups of patients remain underserved,” said Dawn Bell, PharmD, Senior Vice President and General Manager of Canyon Pharmaceuticals, desirudin’s manufacturer. “The DESIR-ABLE study provides important information about the safety of desirudin in a population of patients at high risk for complications from standard drugs used for DVT prophylaxis.” Canyon provided support for the study.

Desirudin is approved in the US and Europe for the prevention of blood clots in patients undergoing hip or knee replacement surgery. It is sold under the trade name Iprivask® in the US and Revasc® in Europe. Desirudin was the first direct thrombin inhibitor (DTI) approved for DVT prophylaxis in Europe, where it has been available for over 10 years.

Study Design

This was a multi-center, single-arm, open-label study of desirudin 15 mg BID in hospitalized patients requiring anticoagulation to prevent blood clots, such as a deep vein thrombosis, or DVT. The primary endpoint was major bleeding.

Results

516 patients were enrolled at 19 centers and required anticoagulation after non-cardiac major surgery (331, 64%), cardiac surgery (45, 9%) or due to medical illness (139, 27%). The study population included many patients at high risk for bleeding or blood clots including patients with low platelet counts, morbid obesity and moderate to severe renal impairment. No patients in the study experienced a major bleed.

About Canyon

Canyon PharmaceuticalsTM is a privately held specialty biopharma company focused on delivering innovative therapeutic solutions that target important cellular pathways in thrombosis, tumor growth, and metastasis. Canyon holds exclusive world-wide rights to desirudin, a subcutaneous (SC) recombinant DTI, and to pegmusirudin, a pegylated recombinant DTI with a longer duration of action than desirudin.
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Thrombotic events associated with c1 esterase inhibitor products in patients with hereditary angioedema: investigation from the United States food and drug administration adverse event reporting system database.
Gandhi PK, Gentry WM, Bottorff MB.
Source

Department of Pharmacy Practice, School of Pharmacy, South College, Knoxville, Tennessee.
Abstract
STUDY OBJECTIVE:

To investigate reports of thrombotic events associated with the use of C1 esterase inhibitor products in patients with hereditary angioedema in the United States.
DESIGN:

Retrospective data mining analysis.
SOURCE:

The United States Food and Drug Administration (FDA) adverse event reporting system (AERS) database.
MEASUREMENTS AND MAIN RESULTS:

Case reports of C1 esterase inhibitor products, thrombotic events, and C1 esterase inhibitor product-associated thrombotic events (i.e., combination cases) were extracted from the AERS database, using the time frames of each respective product's FDA approval date through the second quarter of 2011. Bayesian statistical methodology within the neural network architecture was implemented to identify potential signals of a drug-associated adverse event. A potential signal is generated when the lower limit of the 95% 2-sided confidence interval of the information component, denoted by IC(025) , is greater than zero. This suggests that the particular drug-associated adverse event was reported to the database more often than statistically expected from reports available in the database. Ten combination cases of thrombotic events associated with the use of one C1 esterase inhibitor product (Cinryze) were identified in patients with hereditary angioedema. A potential signal demonstrated by an IC(025) value greater than zero (IC(025) = 2.91) was generated for these combination cases.
CONCLUSION:

The extracted cases from the AERS indicate continuing reports of thrombotic events associated with the use of one C1 esterase inhibitor product among patients with hereditary angioedema. The AERS is incapable of establishing a causal link and detecting the true frequency of an adverse event associated with a drug; however, potential signals of C1 esterase inhibitor product-associated thrombotic events among patients with hereditary angioedema were identified in the extracted combination cases.

© 2012 Pharmacotherapy Publications, Inc.

:-)
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bovenstaand bericht is oud nieuws, kan het niet meer weghalen, excuus hiervoor...
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Gastrointestinal Drugs Advisory Committee Meeting Scheduled for October 16, 2012

BEDMINSTER, N.J., Oct. 12, 2012 -- (BUSINESS WIRE) -- NPS Pharmaceuticals, Inc. (NASDAQ: NPSP), a biopharmaceutical company developing innovative therapeutics for rare gastrointestinal and endocrine disorders, announced today that the U.S. Food and Drug Administration (FDA) has posted briefing materials for the October 16, 2012 Gastrointestinal Drugs Advisory Committee meeting to review Gattex® (teduglutide). Gattex is a novel, recombinant analog of human glucagon-like peptide 2 (a protein involved in the rehabilitation of the intestinal lining) being developed for the treatment of adults with short bowel syndrome.

The Advisory Committee meeting is scheduled for 8:00 a.m. ET on Tuesday, October 16, 2012. The briefing materials can be found on the FDA website at www.fda.gov/AdvisoryCommittees/Commit... The Prescription Drug User Fee Act (PDUFA) date for completion of the review of the company’s New Drug Application (NDA) for Gattex is December 30, 2012.

The Gastrointestinal Drugs Advisory Committee reviews and evaluates available data concerning the safety and effectiveness of marketed and investigational human drug products for use in the treatment of gastrointestinal diseases and makes appropriate recommendations to the FDA.

About Short Bowel Syndrome

Short bowel syndrome (SBS) is a highly disabling condition that can impair a patient's quality of life and lead to serious life-threatening complications. SBS typically arises after extensive resection of the bowel due to Crohn's disease, ischemia or other conditions. SBS patients often suffer from malnutrition, severe diarrhea, dehydration, fatigue, osteopenia, and weight loss due to the reduced intestinal capacity to absorb nutrients, water, and electrolytes. The usual treatment for SBS is nutritional support, including parenteral nutrition (PN) and/or intravenous (IV) fluids to supplement and stabilize nutritional needs.

Although PN can provide nutritional support for SBS patients, it does not improve the body's own ability to absorb nutrients. PN is associated with serious complications, such as infections, blood clots or liver damage, and the risks increase the longer patients are on PN. Patients on PN often experience poor quality of life with difficulty sleeping, and frequent urination, and patients receiving chronic PN often experience a loss of independence.

About Gattex ® (teduglutide)

Gattex (teduglutide) is a novel, recombinant analog of human glucagon-like peptide 2, a protein involved in the rehabilitation of the intestinal lining. It has been developed to reduce dependence on parenteral nutrition (PN) in adult patients with short bowel syndrome (SBS). Significant reductions in mean PN/IV infusion volume from baseline to end of treatment were seen in the Phase 3 studies of teduglutide. In addition, some patients were able to be weaned off PN during these trials. The most common treatment-emergent adverse events with Gattex in the placebo-controlled studies that occurred at a higher frequency with Gattex were abdominal pain, upper respiratory tract infections, nausea, injection site reactions, abdominal distension, headaches, and gastrointestinal stoma complications.

Gattex has received orphan drug designation for the treatment of SBS from the European Medicines Agency (EMA) and the FDA.

In 2007, NPS granted Nycomed, a Takeda company, the rights to develop and commercialize teduglutide outside the United States, Canada, Mexico and Israel. NPS retains all rights to teduglutide in North America. A positive opinion was issued on June 21, 2012 by the Committee for Medicinal Products for Human Use, followed by the European Commission granting European market authorization on August 30, 2012 for the medicinal product teduglutide (trade name in Europe: Revestive®) as a once-daily treatment for adult patients with short bowel syndrome.

About NPS Pharmaceuticals

NPS Pharmaceuticals is a biopharmaceutical company focused on bringing orphan products to patients with rare disorders and few, if any, therapeutic options. NPS is advancing two late-stage registration programs. A New Drug Application is undergoing FDA review for Gattex® (teduglutide) as a treatment for adults with short bowel syndrome (SBS) and a Phase 3 registration study has been completed for Natpara® (recombinant human parathyroid hormone (rhPTH [1-84]) in adult hypoparathyroidism. NPS' earlier stage pipeline includes two calcilytic compounds, NPSP790 and NPSP795, with potential application in rare disorders involving increased calcium receptor activity, such as autosomal dominant hypocalcemia with hypercalciuria (ADHH). NPS complements its proprietary programs with a royalty-based portfolio of products and product candidates that includes agreements with Amgen, GlaxoSmithKline, Janssen Pharmaceuticals, Kyowa Hakko Kirin, and Nycomed, a Takeda company.
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hm...
A new 3rd generation recombinant factor VIII (rFVIII), GreenGene F (WHO INN: beroctocog alfa), which is a highly homogenous B-domain deleted FVIII protein comprising of two peptides as heavy chain (A1 and A2 domain) and light chain (A3, C1, and C2 domain) at 80 and 90 kDa, was developed from its predecessor product GreenGene (2nd generation product previously approved by Korea FDA after clinical studies in South Korea) by process improvements of i) addition of Solvent/Detergent treatment for virus inactivation, ii) nanofiltration (20 nm pore size) for viral removal and iii) alterations to an albumin-free formulation to minimize the risk of viral contamination. An assessment of comparability between the two products was made to see if process improvements for safer product manufacturing affected the rFVIII structural and functional characteristics. Physicochemical and physiological characteristics were observed, in vivo efficacy following a single intravenous administration to FVIII knock-out mice and toxicity by various GLP in vivo tests were evaluated. All results showed equivalence, proving that no changes in protein characteristics of rFVIII occurred from process changes in formulation, viral inactivation, and viral removal which minimize the risk of pathogen transmission to enhance safety.
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Host cell lines used for recombinant protein expression differ in their ability to perform post-translational modifications (PTMs). The currently available recombinant human FVIII (rhFVIII) products are produced in mammalian, non-human cell lines. For rhFVIII, glycosylation and sulfation are vital for functionality and von Willebrand factor (VWF)-binding affinity. Here we present the characterisation of the PTMs of a novel, human cell line-derived recombinant human FVIII (human-cl rhFVIII). rhFVIII expression in a human cell line avoids expression of undesirable mammalian glycoforms like Gala1-3Galß1-GlcNAc-R (a-Gal) and N-glycolylneuraminic acid (Neu5Gc), which constitute epitopes antigenic to humans. We describe sulfation analysis, glycan profiling and characterisation using liquid chromatography-mass spectrometry and high performance anion exchange chromatography with pulsed amperometric detection. Human-cl rhFVIII is confirmed to be sulfated and glycosylated comparable to human plasma-derived FVIII. Most importantly, human-cl rhFVIII is devoid of the antigenic Neu5Gc or a-Gal epitopes observed in Chinese Hamster Ovary- and Baby Hamster Kidney-derived rFVIII products. Both the avoidance of non-human glycan structures and the achievement of complete sulfation are proposed to lower the intrinsic immunogenicity of human-cl rhFVIII compared with current rFVIII products.
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'The Medical and Scientific Advisory Council of the National Hemophilia Foundation encourages the use of recombinant clotting factor products because they are safer'

www.hemophilia.org/NHFWeb/MainPgs/Mai...
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Novo Nordisk files for regulatory approval of turoctocog alfa for haemophilia A in the US and EU
Source Press Release
Company Novo Nordisk
Tags Europe, USA, Filing & Registration, Protein Therapeutic, Blood
Date October 16, 2012

Novo Nordisk today announced the submission of the regulatory application for turoctocog alfa (NN7008) to the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA). Turoctocog alfa is a third-generation recombinant coagulation factor VIII intended for prevention and treatment of bleeding in people with haemophilia A.

"We are very excited about having reached this goal. Turoctocog alfa represents a new treatment alternative for people with haemophilia A and is one of the first important outcomes of the haemophilia research strategy we embarked upon in 2006," says Mads Krogsgaard Thomsen, executive vice president and chief science officer of Novo Nordisk.

Turoctocog alfa demonstrates Novo Nordisk’s commitment to the wider haemophilia community as the new alternative in factor VIII treatment. Based on the most advanced protein and purification technology, the product has been designed to expand reliability, safety and portability for people with haemophilia A.

The decision to apply for marketing authorisation for turoctocog alfa is based upon the results of the clinical trials guardian™1 and guardian™3, which were completed in 2011. More than 200 people with haemophilia A around the world were enrolled, making guardian™ the largest clinical pre-registration trial programme conducted in haemophilia A.

The phase 3 trials included previously treated adults and children with severe haemophilia A and demonstrated efficacy in preventing and treating bleeds with no development of inhibitors.

the coming months, applications for regulatory approval in other countries will be submitted.

Novo Nordisk today announced the submission of the regulatory application for turoctocog alfa (NN7008) to the European Medicines Agency (EMA) and the US Food and Drug Administration (FDA). Turoctocog alfa is a third-generation recombinant coagulation factor VIII intended for prevention and treatment of bleeding in people with haemophilia A.

"We are very excited about having reached this goal. Turoctocog alfa represents a new treatment alternative for people with haemophilia A and is one of the first important outcomes of the haemophilia research strategy we embarked upon in 2006," says Mads Krogsgaard Thomsen, executive vice president and chief science officer of Novo Nordisk.

Turoctocog alfa demonstrates Novo Nordisk’s commitment to the wider haemophilia community as the new alternative in factor VIII treatment. Based on the most advanced protein and purification technology, the product has been designed to expand reliability, safety and portability for people with haemophilia A.

The decision to apply for marketing authorisation for turoctocog alfa is based upon the results of the clinical trials guardian™1 and guardian™3, which were completed in 2011. More than 200 people with haemophilia A around the world were enrolled, making guardian™ the largest clinical pre-registration trial programme conducted in haemophilia A.

The phase 3 trials included previously treated adults and children with severe haemophilia A and demonstrated efficacy in preventing and treating bleeds with no development of inhibitors.

In the coming months, applications for regulatory approval in other countries will be submitted.

About haemophilia A

Haemophilia is a chronic, inherited bleeding disorder that affects males. People with haemophilia A are either missing or have a malfunctioning factor VIII protein, which is essential for proper blood clotting. People with haemophilia A have a tendency to bleed longer than most, or to bleed internally, because they are missing this clotting factor. To manage the disease and stop bleeding, people with haemophilia A must replace the missing factor VIII protein, which is accomplished by intravenous infusion of the clotting factor.

Globally, it is estimated that 500,000 people have haemophilia A. The disease is severely under-diagnosed in developing countries.

About turoctocog alfa

Turoctocog alfa (NN7008) is a third-generation recombinant coagulation factor VIII in development for the prevention and treatment of people with haemophilia A, and could provide a reliable and portable treatment option. The product is manufactured using the latest recombinant technology.

Novo Nordisk in haemophilia

Turoctocog alfa is one of several compounds from Novo Nordisk that are in development for various bleeding disorders. Its regulatory submission is an important accomplishment in our effort to increase the range of therapeutic options available to the bleeding disorder community. For full overview of molecules under development, please visit novonordisk.com/science/pipeline/rd_p...
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Roche's KW3 omzet stijgt op verkoop kankermedicijn, zwakkere frank


ZURICH (Dow Jones)--Roche Holding AG (ROG.VX) heeft ondanks een aanhoudende prijsdruk in het door bezuinigingen geteisterde Europa in het derde kwartaal een omzetstijging van 15% geboekt. De omzetstijging werd gegenereerd dankzij een stabiele verkoop van zijn kankerbestrijdingsmedicijn in de Verenigde Staten en in opkomende markten, en een constante uitoefening van zijn klinische laboratoriumpraktijken.

Het Zwitserse farmaceutische concern meldt dat de omzet in de drie maanden die eindigden in september toenam naar 11,27 miljard Zwitserse frank van CHF9,82 miljard in diezelfde periode een jaar geleden, waarmee de verwachting van CHF11,05 miljard overtroffen werd.

"Met de sterke groei in het derde kwartaal blijven we goed op koers om onze doelstellingen over het gehele jaar te bereiken," stelt bestuursvoorzitter Severin Schwan.

Roche is in tegenstelling tot andere farmaceuten weinig blootgesteld aan patenten die in de nabije toekomst verlopen. Het verlopen van patenten kan de omzet aanzienlijk aantasten, aangezien goedkopere kopieen van het geneesmiddel op de markt gebracht zullen worden.

Daarnaast werkt het concern aan nieuwe geneesmiddelen die de huidige goed verkochte producten tegen die tijd kunnen vervangen.

De omzet uit medicijnen steeg in de recente verslagperiode met 16% naar CHF8,79 miljard, aangedreven door kankerbestrijdende medicijnen, evenals de depreciatie van de Zwitserse frank ten opzichte van de dollar en de Japanse yen.

Roche gaf het startsein aan het cijferseizoen binnen de farmaceutische branche, maar verschafte geen details over de winst, die slechts eenmaal in de zes maanden wordt vrijgegeven.

Het aandeel Roche sloot maandag op CHF183,90.


- Door Marta Falconi. Vertaald door Ellen Proper; Dow Jones Newswires; +31 20 571 52 00; ellen.proper@dowjones.com


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Johnson & Johnson verhoogt winstprognose
Gepubliceerd op 16 okt 2012 om 14:07 | Views: 387

Johnson & Johnson 19:28
USD 69,50 +0,90 (+1,31%)

NEW BRUNSWICK (AFN) - Het Amerikaanse farmacieconcern Johnson & Johnson heeft zijn winstverwachting voor het lopende boekjaar verhoogd. Dat maakte het bedrijf dinsdag bekend bij de presentatie van de resultaten over het derde kwartaal.

Johnson & Johnson gaat nu voor heel 2012 uit van een winst per aandeel tussen de 5,05 en 5,10 dollar. In een eerdere prognose was dat 5 tot 5,07 dollar per aandeel.

De omzet nam in het derde kwartaal toe met 6,5 procent op jaarbasis tot 17,1 miljard dollar (13,1 miljard euro). De nettowinst daarentegen daalde met 7,3 procent tot 3 miljard dollar. Per aandeel komt dat neer op 1,05 dollar.
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Crucell levert Italië griepmedicijn niet
Gepubliceerd op 17 okt 2012 om 20:51 | Views: 1

LEIDEN (AFN) - Vaccinmaker Crucell, een in Nederland gevestigd onderdeel van het Amerikaanse Johnson & Johnson, heeft de levering van een griepmedicijn aan Italië opgeschort. Dat werd woensdag bekendgemaakt door de Italiaanse gezondheidsautoriteiten.

Volgens het Italiaanse ministerie van Volksgezondheid stopte Crucell de geplande levering van 2,36 miljoen doses griepvaccin, nadat bij kwaliteitscontroles onregelmatigheden aan het licht waren gekomen. Bij Crucell was woensdagavond niemand bereikbaar voor commentaar.

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Abbott Laboratories to acquire Russian firm Petrovax Farm?
Article | 15 October 2012 Print This ShareThis
Although the US health care major has declined to comment on Russian media reports, Abbott Laboratories (NYSE: ABT) is expanding in Russia, through the filing of an application to the Russian Federal Antimonopoly Service (FAS) for the acquisition of Petrovax Farm, a well-known pharmaceutical producer, according to sources in the FAS.

Abbott reportedly plans to acquire 100% of Petrovax. The value of the deal is not disclosed but, according to some Russian analysts, it could be in the range of $250-$300 million. The annual turnover of the Russian company is currently estimated at $100 million.

Enjoying this article? Have the leading Biopharma news & analysis delivered daily on email by signing up for our FREE email newsletter here.

Existing links between Abbott and Petrovax

Through its acquisition of Belgian drugmaker Solvay, Abbott already has an established position in the lucrative Russian influenza vaccine market with Petrovax Pharm, which was seen as a major attraction for Abbott’s vaccine business which it failed to divest (The Pharma Letter September 6, 2010). Petrovax also has an agreement with Pfizer to manufacture the US drugs behemoth’s innovative pneumococcal vaccine in the Moscow region.

This deal is expected to be among the three largest transactions in the Russian pharmaceutical market following the planned acquisition of 100% of Natur Produkt International, by Canada’s Valeant Pharmaceuticals International for $180 million (which, however is currently at risk of failure; TPL October 2) and the acquisition of local producer Masterlek by Pharmstandard, one of Russia’s largest drugmakers for $146 million in 2009.

Russian analysts believe that the acquisition of Petrovax Farm will provide an opportunity for Abbott to start an active expansion in the Russian market, including through the participation in the State Reimbursement Program.

In addition, this will also allow Abbott to localize its production in the Russian market and to get preferences from the local government. So far, according to DSM, a Russian consulting agency in the field of pharmaceuticals, total sales of Abbott in Russia do not exceed $430 million, which is significantly lower, compared to major competitors.
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Door Ben Zwirs
Van DOW JONES NIEUWSDIENST
AMSTERDAM (Dow Jones)--De Indiase farmaceut Dr. Reddy's wil Octoplus nv (OCTO.AE) overnemen voor EUR0,52 per aandeel, waarmee het biotechconcern uit Leiden wordt gewaardeerd op EUR27,4 miljoen, maken de bedrijven maandag bekend.
De Raad van Bestuur en Raad van Commisarissen van Octoplus steunen het bod van Dr. Reddy's unaniem. Aandeelhouders van het bedrijf, waaronder A. Van Herk en Omni Investments, die in totaal iets meer dan 50% van het bedrijf bezitten, hebben reeds toegezegd hun stukken aan te bieden.
Het bod van EUR0,52 per aandeel biedt een premie van 30% op de slotkoers van afgelopen vrijdag en vertegenwoordigt de waarde van Octoplus na de recente 'waarde-erosie' van zijn medicijn Locteron, licht het concern toe.
"De laatste paar maanden hebben we een aantal alternatieve strategieen voor ons bedrijf bestudeerd", licht Octoplus toe. "We zijn tot de conclusie gekomen dat het voorgenomen bod van Dr. Reddy's de belangen van onze stakeholders, waaronder werknemers en aandelehouders, het best dient."
Door Ben Zwirs; Dow Jones Nieuwsdienst; +31-20-5715200; ben.zwirs@dowjones.com
(END) Dow Jones Newswires
October 22, 2012 02:16 ET (06:16 GMT)
© 2012 Dow Jones & Company, Inc.

AAND OCTOPLUS @ EUR 0.12
NL0000345718

dit scenario zal er ook komen voor pharming ,denk ik.
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ma 22 okt 2012, 07:32 Bijna 14 miljoen extra aandelen Pharming LEIDEN (AFN) - Het aantal uitstaande aandelen Pharming is met bijna 14 miljoen toegenomen tot ruim 980,8 miljoen stuks als gevolg van de uitoefening van warrants. Dat maakte het biotechbedrijf maandag bekend.

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