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BioWorld - Thursday, December 11, 2025
Home » Newsletters » BioWorld

BioWorld

Jan. 20, 2017

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In the clinic

Catabasis Pharmaceuticals Inc., of Cambridge, Mass., said phase I data published in The Journal of Clinical Pharmacology showed that edasalonexent (CAT-1004), an oral inhibitor of NF-kB, was safe, well-tolerated and inhibited activated NF-kB in adult subjects with Duchenne muscular dystrophy (DMD). Read More

Other news to note

Ethypharm SA, of Saint-Cloud, France, signed a definitive agreement to acquire Martindale Pharma, of Wooburn Green, U.K., which specializes in the fields of opioid addiction, emergency care and sterile injectables. Read More

Financings

Zynerba Pharmaceuticals Inc., of Devon, Pa., said it priced a public offering of 2.8 million shares of common stock at $18 per share for gross proceeds of $50.4 million. Read More

Regulatory front

The NIH has finalized the Common Rule for human subject protections in federally funded research, stripping away a provision in the draft rewrite of the common rule that would have required researchers to obtain consent to use non-identified tissue specimens. Read More

One-third of foreign drug plants never inspected by the FDA

The FDA still has a ways to go to ensure the safety and quality of the U.S. drug supply chain, as it has yet to inspect nearly 1,000 foreign plants that manufacture drug substances for the market. Read More

Octimet closes $12M series A round for oral Met inhibitor

DUBLIN – Octimet Oncology NV, a spinout from the Janssen Pharmaceutica NV arm of Johnson & Johnson, raised €11.3 million (US$12 million) in a series A round for clinical development of a drug that hits c-Met (cellular mesenchymal-epithelial transition factor), a receptor tyrosine kinase that is one of the most beguiling targets in cancer. Read More

In some tumors, heterogeneity only in passenger mutations

Tumor heterogeneity, the diverging evolution of both different subparts of primary tumors and of metastases compared to the primary tumor, is often named among the challenges for targeted treatment. Read More

PASIng lane? Dermira wins again with Cimzia phase III; high dose conquers Enbrel

Dermira Inc.’s third positive phase III trial with Cimzia (certolizumab pegol) in moderate to severe psoriasis turned up “market-leading type” results at the 400-mg dose, the firm’s chief development officer, Luis Peña, told BioWorld Today, and enables a regulatory filing in Europe. Read More

Cytori taps Azaya for potential revenue, nanotech platform

The acquisition of two partner-ready nanoparticle cancer candidates developed by Azaya Therapeutics Inc. and an associated nanotech platform could yield potential near-term revenue for Cytori Therapeutics Inc. as well as further-afield promise in the use of Azaya’s nanoparticle liposomal technology for the delivery of targeted regenerative therapies to sites of acute or chronic injury, the company said. Read More

Appointments and advancements

The Female Health Co., of Chicago, an affiliate Veru Healthcare, of Miami, named Brian J. Groch chief commercial officer. Read More

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