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Wave Life Sciences offers support for monthly dosing of its AATD RNA therapy Read in browser
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top stories
1. Q&A: Novo Nordisk research chief discusses streamlined R&D, asset integration and role of AI
2. Wave aims for monthly dosing with RNA editing treatment for AATD
3.
news briefing
Full-Life Technologies raises $150M; Quince's reboot with pulmonary drug
4. Relay's PI3Kα inhibitor clears efficacy bar in Phase 2 vascular anomalies study
5. BioMarin's rare disease therapy shows no clinical benefit in Phase 3 test
6. FDA's unreleased Covid vaccine deaths report is published by lawmaker
7. Nourish raises $100M for virtual nutrition care
more stories
 
Karen Weintraub
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Last year, Novo Nordisk rejigged its R&D activities with the aim of becoming faster and more agile. Elizabeth Cairns talks with the company's head of global research Jacob Sten Petersen about AI, RNAi and integrating bought-in assets.

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Karen Weintraub
Deputy Editor, Endpoints News
Jacob Sten Petersen, Novo Nordisk head of global research
1
by Elizabeth Cairns

Just as Maziar Mike Doust­dar took the helm at No­vo Nordisk in the sum­mer of 2025, the com­pa­ny said it would re­or­ga­nizeits R&D ac­tiv­i­ties...

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Paul Bolno, Wave Life Sciences CEO
2
by Lei Lei Wu

Wave Life Sci­ences re­port­edan up­dat­ed cut of da­ta from its ear­ly-stage study of an RNA edit­ing treat­ment for al­pha-1 an­tit­rypsin de­fi­cien­cy, sug­gest­ing it can...

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News Briefing: Quick hits from the biopharma web
3
by ENDPOINTS

Plus, news about Ac­cro Bio­science, Hansa Bio­phar­ma, Shang­hai Best-Link Bio­science and UCB.

Full-Life Tech­nolo­gies gets $150M: The ra­dio­ther­a­py com­pa­ny has raised$110 mil­lion in a...

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LGBTQ+ LEADERSHIP IN 2026
LGBTQ+ diversity drives innovation in biopharma — but transgender and non-binary professionals face rising challenges. Endpoints is going live with our fourth annual special report celebrating the honorees giving voice and visibility while forging ahead across life sciences. Join us.
4
by Ayisha Sharma

Re­lay Ther­a­peu­tics’ first da­ta read­out for zove­g­al­is­ib in a rare ge­net­ic dis­ease beat Wall Street ex­pec­ta­tions, ex­pand­ing the PI3Kα in­hibitor’s R&D prospects be­yond breast can­cer...

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5
by Reynald Castaneda

Bio­Marin’s en­zyme re­place­ment ther­a­py for a rare ge­net­ic dis­or­der called ENPP1 de­fi­cien­cy de­liv­ered mixed re­sults in a late-stage study.

Pa­tients with the con­di­tion don't pro­duce...

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