ViiV Healthcare has initiated a rolling submission of a new drug application (NDA) to the US Food and Drug Administration (FDA) for long-acting cabotegravir to prevent human immunodeficiency
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Specialty life sciences company Revive Therapeutics has signed a research agreement with University of California, San Francisco (UCSF) to study Bucillamine as a potential treatment for severe Covid-19.
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The US Food and Drug Administration (FDA) has expanded the emergency use authorisation (EUA) for Pfizer and BioNTechs Covid-19 vaccine to include adolescents aged 12 to 15 years.
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Under the terms of the deal, CDR will pay 10.23 in cash per share in UDG. Headquartered in Dublin, UDG Healthcare provide healthcare advisory, communications, commercial, clinical and
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Biopharmaceutical company CANbridge Pharmaceuticals has signed a licensing agreement with Mirum Pharmaceuticals for the development and commercialisation of maralixibat in Greater China. Maralixibat is a minimally absorbed, orally
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The Russian Direct Investment Fund (RDIF) has announced that a single dose Covid-19 vaccine called Sputnik Light, obtained authorisation for use in the country. With recombinant human adenovirus
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The companies will leverage MiNA Therapeutics small activating RNA (saRNA) technology platform to develop the drug candidates. Using its saRNA platform, MiNA Therapeutics will research up to five
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Indias Defence Research and Development Organisation (DRDO) lab Institute of Nuclear Medicine and Allied Sciences (INMAS) developed the drug in alliance with Dr Reddys Laboratories (DRL). The drug
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Besides acquiring the exclusive rights to commercialise PRG1801 inIndia, Dr. Reddys will be responsible for future development including clinical trials, inthe country. Pregene will be the sole supplier
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World Health Organization (WHO) has granted emergency use listing (EUL) for Modernas Covid-19 vaccine to prevent the infection in people aged 18 years and above. The Covid-19 Vaccine
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