Month: September 2016
GW Pharmaceuticals, a UK based company, believes in growing its own cannabis plants, search for its ingredients and then come up with medicines that help the company in taking one more step towards approval of Epidiolex, as seen in the announcement of positive phase 3 trial results earlier this week.
The drug is for the treatment of epilepsy including Dravet syndrome and lennox-Gastaut syndrome. Pateints who were on 20mg dosage of Epidiolex had 42% reduction in monthly seizures compared to 17% of control patients. The company is expecting to submit a new drug application with US FDA in the first half of 2017. On Monday, a sudden rise of more than 16% in the stocks of the company was noted.
The drug so far has got Orphan Drug Designation from FDA for the treatment of Dravet syndrome and lennox-Gastaut syndrome and Fast track designation for Dravet syndrome. The company has, thus, set a new standard in the market by announcing promising results of Epidiolex.
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Bayer AG and Evotec AG enter a multi-target research partnership agreement
Bayer and Evotec have agreed to develop novel treatments for chronic kidney disease in diabetic patients. According to the agreement, Bayer will have all the rights to select clinical candidates and Evotec’s Cure Nephron target pipeline. It will pay approximately $15.64m to Evotec during the contract period.
Plasticell and CellSpring AG have entered into an agreement
Plasticell and CellSpring have entered an agreement which aims to examine and validate the capability of osteogenic cell therapy and 3D cell cultures in drug screening. According to this agreement, the companies will be responsible for developing 3D tissue models that accurately respond to the drug treatment. These 3D models are used in pharmaceutical industry in all stages of drug discovery, to evaluate the efficacy of lead compounds.
Allergan Acquires Akarna Therapeutics
Allergan plans to develop novel treatments for non-alcoholic steatohepatitis (NASH) and other liver diseases through the acquisition of Akarna Therapeutics. The acquisition has been completed for a purchase consideration of $50m. Allergan will gain all rights to AKN-083 and a portfolio of additional development stage FXR compounds. Akarna Therapeutics will receive additional clinical, regulatory, developmental and commercialisation milestones of its drug candidate.
Cambrex Acquires Pharmacore
Cambrex Corporation, a manufacturer of small molecule innovator and generic active pharmaceutical ingredients (APIs), has acquired PharmaCore, which specializes in developing, manufacturing and scaling up small molecule APIs for clinical phase projects, for approximately $25 million. The company is licensed with the US Drug Enforcement Administration (DEA) to manufacture Schedule II to Schedule V controlled substances.
Merck is a leading science and technology company, and has many projects that are involved in research to find treatments for diseases that are hard to treat. Keeping in view with this agenda, Merck has announced that the new research that has been conducted from their marketed and pipeline compounds will be presented at this year’s European Society for Medical Oncology annual meeting in Denmark. The presentations are to be focussed on hard-to-treat cancers, and will include results for Erbitux® (cetuximab) in metastatic colorectal cancer (mCRC) and squamous cell carcinoma of the head and neck (SCCHN); preliminary study results in bladder cancer and renal cell carcinoma (RCC) for avelumab, which is being developed in collaboration with Pfizer; and updates on the Phase II program for tepotinib* in non-small cell lung cancer (NSCLC).
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US FDA grants approval for Novartis’ Ilaris to treat Periodic Fever Syndromes
Novartis received approval to market its Periodic Fever Syndrome drug Ilaris (cancakinumab). The drug targets the syndrome, and will be used to treat a group of diseases that cause serious recurrent fever and pathogenic inflammation through non-infectious activation of the immune system. Ilaris inhibits Interleukin-1 (IL-1) beta, and is already approved in the US to treat Cryopyrin-Associated Periodic Syndromes (CAPS) and Systemic Juvenile Idiopathic Arthritis (SJIA).
Sanaria receives FDA fast-track designation for malaria vaccine
PfSPZ, the malaria vaccine of Sanaria, has received fast-track designation from the US Food and Drug Administration (FDA).PfSPZ is currently in clinical trials that are intended to finalise an immunisation regimen to be taken forward into pivotal Phase III clinical trials. If successful, the clinical trials provide the necessary data for licensing the vaccine, according to the company.
Sanofi and Regeneron’s next wannabe blockbuster tagged ‘priority’ by Regulators
FDA has accepted the application for atopic dermatitis candidate dupilumab, from Sanofi and Regeneron, and have given it a priority review tag that should hasten its trip to approval. Dupilumab has already shown it can beat out those topical steroids, too. In June, its makers rolled out Phase III data showing that a dupilumab/corticosteroid combo topped steroids alone. analysts see dupilumab generating more than $2.5 billion a year–with some predicting up to $4 billion or $5 billion.
Allele receives NIH grant to develop new antibody therapy for Alzheimer’s disease
Allele Biotechnology and Pharmaceuticals (Allele) has secured a grant from the US National Institutes of Health’s (NIH) National Institute on Aging to develop a new antibody therapy for Alzheimer’s disease. Allele will develop a panel of antibodies that identify this protein, one of which would be used as a therapeutic drug candidate. The antibodies will feature a distinct shape and size, allowing them to pass the blood-brain barrier to reach the critical areas of the brain. Allele researchers also aim to modify and engineer each antibody to enhance its therapeutic potential.
Cervical cancer is the second most common cause of death in women globally. Increased awareness and early diagnosis has reduced the death toll over the years; but still there is considerable risk that exists. According to the estimated of American Cancer Society, approximately 12,990 new cases of invasive cervical cancer will be diagnosed and about 4,120 women might die from cervical cancer in United States in 2016. There are many risk factors associated with the cause of cervical cancer and the most common is the persistent HPV (Human papillomavirus) infection which accounts 90% of the total cases.
Research showed that psychosocial stress is one of the crucial contributors of the prolonged infection of HPV. Women who smoke, take drugs etc. are more prone to HPV infection which further increases the chances of developing cervical cancer. Women suffering from Systemic Lupus Erythematosus (SLE) and Inflammation Bowel Syndrome (IBD) like Crohn’s disease should take extra care as they can be more likely to develop cervical cancer. Age is also an important factor. Trends indicate that occurrence of cervical cancer rises between late teens and mid 30s. Women with lowered immunity are at high risk of developing this cancer. Other factors such as multiple pregnancies, oral contraceptives, more than one sex partners etc. are more likely to contribute to the occurrence of cervical cancer.
Since cervical cancer has a large scope for treatment if detected in early stages, researchers are focusing on developing better ways of detecting precancer and cervical cancer. Prevention has always been better than cure, and in case of cancer early diagnosis increases the survival rate. Regular screening (Pap test and HPV Test) and vaccination is suggested for prevention. Cervical Cancer treatment is based on use of surgery, Chemotherapy, Radiation therapy and targeted therapy.
Several chemotherapeutics such as Cisplatin (Platinol; Bristol-Myers Squibb Company), Carboplatin (Paraplatin; Bristol-Myers Squibb Company), Paclitaxel (Taxol; Bristol-Myers Squibb), Topotecan (Hycamtin; GlaxoSmithKline), Gemcitabine (Gemzar; Eli Lilly and Company), Bevacizumab (Avastin; Genentech) are available for the treatment of advanced stages of cervical cancer. Researchers and pharmaceutical companies are focusing on targeted therapies, drugs for treating early detection, palliative care and use of biomarkers for accurate detection of cervical cancer.
DelveInsight Business Research, LLP
The Food and Drug Administration approved the recent controversial drug to treat Duchenne muscular Dystrophy, which is a rare disease that confines boys to wheelchairs and condemns them to an early death. The decision was made after months of debate between the Agency and Sarepta Therapeutics, regarding the evidence needed to demonstrate that its medication, called eteplirsen, had a meaningful impact on patients. Sarepta said the drug would be priced at about $300,000 a year in the US. As a condition of the approval, Sarepta will have to conduct a two-year, randomized controlled trial to verify the clinical benefit of the drug. The purpose is to determine whether the drug actually improves motor functions. If the trial fails, the FDA could move to withdraw approval.
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Collaboration between Sygnis AG and ECACC for licensing and distribution of Caco-2 cell line
Sygnis AG enters into a collaboration agreement with ECACC to significantly expand Sygnis’ Caco-2 business. Under the collaboration, ECACC will organize that companies obtain the license for the use of the Caco-2 cell line from Sygnis in the US and afterwards will provide the Caco-2 materials directly.
Partnership between BioNTech and Genentech to develop individualized mRNA cancer therapies
BioNTech has agreed to collaborate with Roche’s Genentech to develop and commercialize mRNA based, individualized cancer vaccines. The agreement will see the companies jointly develop individually tailored mRNA cancer vaccines applicable against a wide range of cancers, in a bid to potentially provide a new treatment paradigm for cancer patients.
Partnership between Zydus Cadila and Takeda to develop vaccine for Chikungunya virus
Zydus Cadila and Takeda Pharmaceutical have agreed to partner to develop a vaccine for an emerging infectious disease known as Chikungunya. The agreement will see both parties collaborating from an early stage development of the vaccine up to its final commercialization.
Global Agreement between Regeneron Pharmaceuticals, Inc. and Teva Pharmaceutical to develop Regeneron’s Fasinumab
Regeneron and Teva entered a global agreement for the development and commercialization of the former’s NGF antibody, fasinumab. According to the developmental deal, Regeneron will receive payment of $250 million along with development and regulatory milestone payments, plus additional payments based on net sales. Regeneron will be responsible for the global development and commercialization of fasinumab in the U.S., and Teva will be responsible for the candidate’s development and commercialization outside the U.S.
Big Pharma companies including Cipla & Wockhardt in global alliance to fight drug resistance
13 global pharmaceutical companies have joined hands in laying out a roadmap to combat antimicrobial resistance (AMR) by 2020. The roadmap by these 13 drug firms follows the Industry Declaration signed in January 2016 at the World Economic Forum by more than 100 companies and trade associations, the companies said in a joint statement. The other companies in the alliance include global majors such as Johnson & Johnson, Novartis, Pfizer, Sanofi and AstraZeneca.