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Home » Newsletters » BioWorld

BioWorld

July 23, 2024

View Archived Issues
Coin stacks layered with charts

Seed and series As down but not out: Brenig, Third Arc at bat

After reaching a height in 2021, seed and series A rounds have fallen in recent years, and 2024 is no exception, although amounts raised are tracking slightly ahead of last year. On July 23, the numbers were given a boost when two new companies – namely Dover, Del.-based Brenig Therapeutics Inc. and Boston-based Third Arc Bio Inc. – raised $65 million and $165 million, respectively, in series A financings. A third new company, Abiologics Inc., also received $50 million in initial funding. Read More
Avak Kahvejian, CEO, Abiologics

Supranatural: Synteins being the platform, Abiologics nets $50M

With $50 million in hand from Flagship Pioneering, Abiologics Inc. is pairing generative artificial intelligence with high-throughput chemical protein synthesis to attack oncology and immunology indications with Synteins, synthetic proteins that represent a new class of programmable medicines. Avak Kahvejian, co-founder and CEO of Abiologics and general partner at Flagship, told BioWorld that Abiologics stands “at the precipice of a completely new modality.” Read More
Tape measure wrapped around scale

Gan & Lee’s long-acting GLP-1 shows weight loss in phase IIb

Gan & Lee Pharmaceuticals’ long-acting GLP-1 receptor agonist (GLP-1 RA), GZR-18, achieved as much as 17.29% weight loss in a phase IIb trial in obese and overweight Chinese patients. Developed independently by Shanghai-based Gan & Lee, GZR-18 is a once-weekly or potentially biweekly GLP-1 RA being developed to treat adults with type 2 diabetes and for weight management for obese or overweight patients. Read More
Infant receiving vaccine

Merck’s RSV antibody for infants hits late-stage study endpoints

Many respiratory syncytial virus (RSV) disease vaccines are for older adults but Merck & Co. Inc.’s monoclonal antibody, MK-1654 (clesrovimab), which just produced positive top-line phase IIb/III data, aims at a far smaller and younger market. Data for protecting healthy preterm and full-term infants from RSV disease show the double-blind, randomized, placebo-controlled clinical trial hit all its primary efficacy and safety endpoints, including the incidence of RSV-associated medically attended lower respiratory infection for 150 days compared to placebo. Read More
Prescription drug bottle, pills shaped in $ sign

House Oversight hearing cuts through PBM blame game with warning

Noting that the median list price of new drugs that entered the U.S. market last year hit $300,000, senior officials of the three biggest pharmacy benefit managers (PBMs) in the country once again denied responsibility for those prices as they testified before the House Oversight Committee July 23 in the third hearing the committee has held on PBM practices. Read More
FDA website and logo

FDA approves second Soliris biosimilar

Samsung Bioepis Co. Ltd., of Incheon, South Korea, gained U.S. FDA approval of Epysqli (eculizumab-aagh) as the second biosimilar product to Alexion Pharmaceuticals Inc.’s Soliris (eculizumab) to treat two rare diseases. The regulatory clearance July 22 grants use of Epysqli to treat paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome – two rare hematologic- and kidney-related disorders known to affect about 50,000 and 5,000 patients in the U.S., respectively. Read More

HHS posts negative opinion on Bluebird’s fertility support program

The U.S. Department of Health and Human Services’ Office of the Inspector General disclosed an advisory opinion finding Bluebird Bio Inc.’s fertility support program for a gene therapy treatment could run afoul of federal anti-kickback statutes. That follows a similar opinion against Vertex Pharmaceuticals Inc., and its fertility program associated with gene-editing therapy Casgevy (exagamglogene autotemcel). Vertex subsequently filed a lawsuit. Read More

BioWorld Insider Podcast – The cost of delays in development and sales: It’s probably not what you think

Two costs of developing drug candidates have been upended by new research from the Tufts University School of Medicine’s Center for the Study of Drug Development. New data have produced some very different numbers than you might expect in the cost of a single day of a clinical trial and of missing a day to generate prescription drugs sales. The center’s director, Ken Getz, spoke to the BioWorld Insider podcast about updating the outdated numbers and what it means for companies and investors. Read More

‘We're always on the lookout for what's next’

From no hope to viable treatments, BioWorld  is there to cover the breakthroughs in medicine. Listen to Randy Osborne explain why the BioWorld  team is ‘always on the lookout for what's next.’ Read More

Appointments and advancements for July 23, 2024

New hires and promotions in the biopharma industry, including: Bridgebio, Metrion, Moderna, Ovid, Pharmaessentia, Precision Neuroscience, Scilex, Vedanta. Read More

Financings for July 23, 2024

Biopharmas raising money in public or private financings, including: Hepion, Pharma Two B, Rani. Read More

In the clinic for July 23, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Cannamore, Destiny. Read More

Other news to note for July 23, 2024

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Addex, Apollo, Evotec, J&J, MEI, Mymd, Synaptixbio, TME, Valneva. Read More

Regulatory actions for July 23, 2024

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Certa, Immutep, J&J, Samsung Bioepis. Read More

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