The approval makes Ogluo™ Europe’s first ready-to-use liquid glucagon for rescuing diabetic patients from severe hypoglycaemic events.
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The EMA's human medicines committee has released its results for the December meeting, suggesting which therapies should receive marketing authorisation.
Marketing authorisation in the EU for Baqsimi, the first non-injectable treatment for very low levels of blood sugar, has been recommended by an EMA committee.
Phase I trial results for ZP4207 support its further development as a rescue treatment for severe hypoglycaemia
Zealand has announced results from a clinical Phase I trial with a single-dose version of its novel, stable glucagon analogue, ZP4207.