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Agios provides update on Phase 2 trial of tebapivat in sickle cell disease
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Agios announces that the FDA has accepted its sNDA for mitapivat in sickle cell disease with a Priority Review
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Agios showcases RISE UP Phase 3 results at EHA 2026 Plenary Session reinforcing strong anti-hemolytic profile of mitapivat in sickle cell disease
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Agios announces the submission of its sNDA to the FDA for the U.S. accelerated approval of mitapivat in sickle cell disease
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Agios announces new data on mitapivat will be featured in oral and poster presentations at EHA 2026 in Stockholm, Sweden, June 11-14, 2026
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Agios announces first quarter 2026 financial results and provides business update.
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Exicure enters co-development agreement with Adbiotech to advance Burixafor (GPC-100) combination therapies across multiple indications.
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Etavopivat showed a 27% reduction in vaso-occlusive crisis events and ~4-month delay to first vaso-occlusive crisis event on top of standard of care1Haemoglobin response was superior with...
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Agios announces it will pursue U.S. accelerated approval for mitapivat in sickle cell disease
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Agios (Nasdaq: AGIO) announces financial results and updates for the fourth quarter and year ended December 31, 2025.