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  • Roche and Ignyta, Inc have entered into a definitive merger agreement for Roche to fully acquire Ignyta at a price of US$ 27.00 per share in an all-cash transaction. This corresponds to a total transaction value of US$ 1.7 billion on a fully diluted basis. This price represents a premium of 74% to Ignyta’s closing price on 21 December 2017 and a premium of 71% and 89% to Ignyta’s 30-day and 90-day volume weighted average share price on 21 December 2017, respectively. The merger agreement has been unanimously approved by the boards of Ignyta and Roche.

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  • Allergan plc a leading global pharmaceutical company, announced that the United States Court of Appeals for the Federal Circuit affirmed the United States District Court for the Eastern District of Texas' earlier decision that that each of three Allergan patents (U.S. Patent Nos. 7,030,149, 7,320,976 and 8,748,425) that are listed in the Orange Book for COMBIGAN® is valid. The Federal Circuit also affirmed the district court's finding that Sandoz' proposed generic version of COMBIGAN® does not infringe the '149 and '976 patents, and reversed the district court's decision that Sandoz' proposed generic product infringes the '425 patent.

  • AMAG Pharmaceuticals, Inc announced the issuance of U.S. Patent Number 9,844,558 entitled “Methods of Reducing Risk of Preterm Birth.” This newly issued patent is directed to subcutaneous administration and dosing of Makena® (hydroxyprogesterone caproate injection) and is expected to expire on May 2, 2036. Makena is a treatment to reduce the risk of preterm birth in women who are pregnant with one baby and who spontaneously delivered one preterm baby in the past.

  • Suven Life Sciences Ltd (Suven) granted of one product patent from Canada (2932428) and one product patent from India (289123) corresponding to the New Chemical Entities (NCEs) for the treatment of disorders associated with Neurodegenerative diseases and these Patents are valid through 2034 and 2028 respectively.

  • Lincoln Pharmaceuticals Ltd. has been awarded a Patent for “An Arteether Injection For Treatment of Malaria”, Patent No.258915 by Government of India for Antimalarial Drug. In the present time, this formulation, “Arteether !njection”are available in market in 3ml and 2ml ampoules form. At the time of injecting “Arteether Injection” to the patient by doctors , it is very painful for a long time. Patient will have to take this injection at least for a period of three days to control the malaria.

  • F. Hoffmann-La Roche Ltd. obtained approval from the European Commission, for Alecensa® as monotherapy indicated for “the first-line treatment of adult patients with anaplastic lymphoma kinase (ALK)-positive advanced non-small cell lung cancer (NSCLC)”. In addition, the EU marketing authorisation for Alecensa has been switched from conditional approval (given in February 2017) to a full approval for the treatment of people with ALK-positive, metastatic NSCLC who have progressed on or are intolerant to crizotinib (second-line).

  • The Indian Pharmaceutical Association (IPA) Anantapuramu Local Branch, Head Quarters at Raghavendra Institute of Pharmaceutical Education and Research (RIPER), Anantapuramu celebrated the National Pharmacy Week (NPW) 2017, in association with University College of Pharmaceutical Sciences - Sri Krishnadevaraya University and Oil Technological and Pharmaceutical Research Institute - [OTPRI], Anantapuramu, Andhra Pradesh.

  • The US subsidiary of Dr. Reddy’s Laboratories Ltd. announced that it has reached a settlement with the US Government, in a case that is more than six years old, involving packaging for five blister-packed prescription products. In a joint filing by the parties, Dr. Reddy’s and the US Department of Justice agreed to the settlement of the action without any adjudication of any issue of fact or law.

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