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Home » Newsletters » BioWorld

BioWorld

May 26, 2017

View Archived Issues

In the clinic

Trovagene Inc., of San Diego, reported summary data from a phase I study conducted by Nerviano Medical Sciences Inc., of Nerviano, Italy, with PCM-075, a polo-like kinase inhibitor, with thrombocytopenia and neutropenia identified as the primary dose-limiting toxicities, which the company described as consistent with the expected mechanism of action and results from preclinical studies. Read More

Other news to note

Pharmamar SA, of Madrid, Spain, said it inked a licensing deal with Eczacıbaşı Group, of Istanbul, to commercialize marine-derived cancer drug Aplidin (plitidepsin) in Turkey. Read More

Financings

Antibe Therapeutics Inc., of Toronto, filed for a best efforts offering intended to raise between $3 million and $5 million. The proposed offering will consist of yet-to-be-priced units of the company comprising one common share and one-half of one common share purchase warrant. Read More

Holiday Notice

BioWorld's offices will be closed Monday, May 29, in observance of the Memorial Day holiday in the U.S. Read More

Gottlieb vows action on drug cost issue in budget hearing

The latest FDA commissioner may be in an uncomfortable place where the Trump administration's budget proposal is concerned, but Scott Gottlieb told a congressional committee that the agency will undertake several actions to bolster competition in the drug marketplace, including the publication of a list of off-patent drugs that are not represented by a generic. Read More

Regulatory reforms in China rapidly closing the gap on global norms

SHANGHAI – The hot topic at the 9th DIA China annual meeting was China's proposed entry into the ICH, a global body that facilitates the harmonizing of drug regulations across countries. Read More

Harpoon lands $45M in series B funding for trispecific protein drugs

DUBLIN – Harpoon Therapeutics Inc. has landed a $45 million series B round to enable it to further develop its distinctive approach to the discovery of post-antibody scaffolds with multiple specificities. Read More

ODAC says yes to Hospira biosimilar, urges vigilance

With an FDA advisory committee voting 14-1 Thursday to recommend licensure of Hospira Inc.'s epoetin biosimilar, the U.S. is one step closer to catching up with other markets that are nearly a decade ahead on the biosimilar path. Read More

Appointments and advancements

Chromocell Corp., of North Brunswick, N.J., appointed Heikki Mansikka vice president, clinical development. Read More

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