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IRLAB is Granted an End-of-Phase 2 Meeting with the FDA for the Phase III-Ready Mesdopetam Program

GOTHENBURG, SWEDEN / ACCESSWIRE / January 3, 2024 / IRLAB Therapeutics (STO:IRLAB-A) (FRA:6IRA) Gothenburg, Sweden, January 3, 2024 - IRLAB Therapeutics AB (Nasdaq Stockholm: IRLAB A), a company discovering and developing novel treatments for Parkinson's . ....

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A year of hits and misses for the Indian pharma sector

Even as pharma exports grew in terms of volumes and value, the cloud of inadequate hygiene and safety in some pharma companies continued to hang over the industry, forcing the government to put in place more stringent inspections and processes. ....

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Zealand Pharma submits New Drug Application to the US FDA for glepaglutide in short bowel syndrome

Press release – No. 18 / 2023 Zealand Pharma submits New Drug Application to the US FDA for glepaglutide in short bowel syndrome Copenhagen, Denmark, December 22, 2023 – Zealand Pharma A/S (Nasdaq: ZEAL) (“Zealand”) (CVR-no. 20045078), a biotechnology company focused on the discovery and development of innovative peptide-based medicines, today announced the submission of a New Drug Application (NDA) to the US Food and Drug Administration (FDA) for glepaglutide, a long-acting GLP-2 analog, for th ....

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Aurobindo subsidiary in Tirupati classified as VAI by US FDA

Aurobindo Pharma shares hit their record high of Rs 1,081.95 a piece around 1 pm today, December 20. ....

Andhra Pradesh , Naidupeta Mandal , Aurobindo Pharma , Drug Administration , Aurobindo Pharma Ltd , Menakuru Village , Tirupati District , Voluntary Action Indicated , Cash Market , S Fda ,

Lupin secures US FDA approval for generic allopurinol tablets

The newly approved product will be manufactured at Lupin s facility in Pithampur, India ....

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