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Business
11 Startups Selected for National Life Sciences Accelerator Program
Of the 11 companies participating in the spring cohorts of the Drive program run by MassBio and SCbio, eight have locations in Massachusetts. One cohort focuses on biotech and the other on biomarkers and diagnostics.
April 1, 2026
·
2 min read
·
Angela Gabriel
Press Releases
Resverlogix Corp. Provides Bi-Weekly MCTO Status Update
April 1, 2026
·
4 min read
Press Releases
Dr. Christina Rahm Named One of MSN’s “Top 10 Trailblazing Women in 2026"
April 1, 2026
·
2 min read
Press Releases
Cardiol Therapeutics Announces Year-End 2025 Update on Operations
April 1, 2026
·
14 min read
Press Releases
Envoy Medical Announces First Patients Successfully Reaching 12-Month Endpoint in Pivotal Clinical Trial for Fully Implanted Cochlear Implant
Company Remains on Schedule for PMA Submission to FDA
April 1, 2026
·
8 min read
Press Releases
Scryb Reports 2026 AGM Results and Welcomes Veteran Capital Markets and Finance Directors
April 1, 2026
·
4 min read
Press Releases
Advanced Therapy Medicinal Products CDMO Market Size to Hit USD 53.11 Billion by 2035
April 1, 2026
·
1 min read
Podcast
Biopharma M&A Heats Up, Rare Diseases Win Three Approvals, Wave Crashes
Biogen, Eli Lilly, Merck and Novartis spent more than $20 billion to absorb biotechs with promising or approved drugs; the rare disease space notched approvals for therapies from Denali Therapeutics, Rocket Pharmaceuticals and Biogen; and Wave’s stock lost half its value after its RNA-based obesity candidate failed to impress investors.
April 1, 2026
·
1 min read
·
Heather McKenzie
Funding
Ambrosia Eyes Next-Generation Small Molecule GLP-1s With $100M Series B
While peptides are currently the dominant approach to GLP-1 agonism, Ambrosia Biosciences is pursuing a small-molecule approach.
April 1, 2026
·
2 min read
·
Tristan Manalac
Regulatory
FDA Ties Amgen’s Rare Inflammatory Disease Drug to Eight Deaths, Dozens of Liver Injuries
The FDA in January asked Amgen to pull Tavneos from the market, citing liver toxicity issues that affected the drug’s overall risk-benefit profile. The pharma refused.
April 1, 2026
·
2 min read
·
Tristan Manalac
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