Grifols completes phase 3 SPARTA study
The study evaluated emphysema due to alpha-1 antitrypsin deficiency and is the largest randomized, double-blind, placebo-controlled augmentation therapy study in this population.
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Global healthcare company providing plasma-derived medicines, diagnostics, and transfusion solutions
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In short: Grifols posted solid first-half results and refinanced debt, while facing a Canadian plasma safety crisis.
The study evaluated emphysema due to alpha-1 antitrypsin deficiency and is the largest randomized, double-blind, placebo-controlled augmentation therapy study in this population.
Joanna Susan Le Couilliard replaces Iñigo Sánchez-Asiaín Mardones as independent director and Audit Committee Chair
Revenue grew from immunoglobulins, debt refinanced, organizational transformation advanced.
Adjusted EBITDA reached €854 million with margin improvement, and free cash flow pre-M&A turned positive to €91 million.
The European Medicines Agency (EMA) has opened an investigation into the safety of normal human immunoglobulins after detecting an increase in the...
The judge states that the temporary halt of the information exchange phase to prepare for the trial causes no harm...
Grifols faces a new health alert in the United States that could slow sales of its plasma-derived medicines in its main market of...
The bassist's defense, which has just been reinforced with a new law firm, warns that the court lacks jurisdiction because Daniel Yu is...
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