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Argo Biopharma's siRNA Therapy BW-20805 Gets FDA Fast Track for HAE
Argo Biopharma has received FDA Fast Track designation for BW-20805, with an ongoing global phase-II study in adult HAE patients and primary completion expected in the second half of 2026.
Dr Dongxu Shu | 17/03/2026 | By News Bureau
Argo Biopharma to Present Phase II Interim Data on BW-20805 for HAE at AAAAI 2026
Argo Biopharma’s investigational siRNA therapy BW-20805 showed sustained reduction in hereditary angioedema attack rates and plasma prekallikrein levels, with favorable safety, in Phase II interim data selected for AAAAI 2026.
Dr Dongxu Shu | 27/02/2026 | By News Bureau | 152
Argo Biopharma and Novartis Partner on Novel Cardiovascular Therapies
Argo to receive $160 million upfront as Novartis licenses pipeline assets, explores ANGPTL3 in dyslipidemia, and secures options for future siRNA candidates.
Dr Dongxu Shu | 05/09/2025 | By Dineshwori | 310
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