Opening the door for the development of new treatment of the lethal disease sepsis, scientists have identified a gene that triggers the inflammatory condition.
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Opening the door for the development of new treatment of the lethal disease sepsis, scientists have identified a gene that triggers the inflammatory condition.
Prime Minister Narendra Modi on Sunday highlighted the need for organ donation in the country and encouraged people for it.
The number of opiate receptors in the brain, critical in the modulation of pain behaviour, increase to combat severe pain in arthritis sufferers, according to a study.
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Young adults with genetically-increased Alzheimer's risk have altered activation patterns in a brain region that is crucial for spatial navigation, a study has found.
Danish researchers have discovered a previously unknown function in histones -- responsible for packaging the DNA into structural units -- that will help improve understanding of how cells protect and repair DNA damage.
One stop diagnostics and patient management system "Healthcube Pro" capable of executing 32 tests at the same time was the showstopper at the fourth edition of Indian Pharma Expo 2015 which opened on Saturday.
The Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of Novartis' Cosentyx (secukinumab) in Europe to treat ankylosing spondylitis (AS) and psoriatic arthritis (PsA) patients. Cosentyx is the first of a new class of medicines called interleukin-17A (IL-17A) inhibitors to be recommended for AS and PsA - conditions that affect around five million people in Europe.
U.S. Food and Drug Administration approved Yondelis (trabectedin), a chemotherapy, for the treatment of specific soft tissue sarcomas (STS) – liposarcoma and leiomyosarcoma – that cannot be removed by surgery (unresectable) or is advanced (metastatic). This treatment is approved for patients who previously received chemotherapy that contained anthracycline.
Ambry Genetics (Ambry), a leader in clinical genetic diagnostics and genetics software solutions, announced that it is launching a new suite of seven genetic testing panels for epilepsy.
Tests can be ordered from November 6 with the first samples expected to be tested on November 9.
In consultation with the U.S. Food and Drug Administration (FDA), the U.S. Product Inserts (USPI) for VIEKIRA PAK® (ombitasvir, paritaprevir, and ritonavir tablets; dasabuvir tablets) and TECHNIVIE™ (ombitasvir, paritaprevir, and ritonavir tablets) have been updated from 'not recommended in Child Pugh B patients' to a contraindication in patients with Child-Pugh B cirrhosis. The updated USPI for VIEKIRA PAK also includes a recommendation for physicians to assess evidence of hepatic decompensation prior to treatment and during treatment in cirrhotic patients.