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

BioWorld

Dec. 13, 2017

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In the clinic

Proteostasis Therapeutics Inc., of Cambridge, Mass., disclosed positive study results across all three of the company's cystic fibrosis (CF) pipeline programs. Those include a study in CF subjects for PTI-428, a cystic fibrosis transmembrane conductance regulator (CFTR) amplifier; interim data for a study in CF subjects for PTI-801, a new generation CFTR corrector; and studies in healthy volunteers for PTI-808, a CFTR potentiator, and the combination of PTI-428, PTI-801 and PTI-808. Read More

News from ASH

Actinium Pharmaceuticals Inc., of New York, reported results from a study of 865 samples from U.S. patients with multiple myeloma (MM), which showed that 25 percent had CD33 expression. Read More

Other news to note

Cyclenium Pharma Inc., of Montreal, said it signed a drug discovery agreement with Ono Pharmaceutical Co. Ltd., of Osaka, Japan. Read More

Financings

Soleno Therapeutics Inc., of Redwood City, Calif., said it entered a definitive agreement with certain institutional and accredited investors to raise aggregate gross proceeds of about $15 million through the private placement of its equity securities. Read More

Sanofi's Dengvaxia faces legal threat, investigations after Philippines suspension

HONG KONG – Controversy has continued to mount in the Philippines around Sanofi Pasteur Ltd.'s dengue vaccine, Dengvaxia, which is now facing questions about its effectiveness and the manner and speed with which the government adopted it in its national vaccination program. Read More

Psioxus enters clinic with tumor-targeting gene therapy, earns milestone from BMS

LONDON – Psioxus Therapeutics Ltd. has received approval for a phase I trial of NG-348, the first of its gene therapy for tumor products, triggering a $15 million milestone from partner Bristol-Myers Squibb Co. (BMS). Read More

As U.S. pays global tab on drug innovation, golden age could be wearing thin

Are drug prices turning what's being called the golden age of science into the gilded age in the U.S.? That's the question Sen. Tim Kaine (D-Va.) posed Tuesday as the Senate Health, Education, Labor and Pensions (HELP) Committee held its third hearing on high drug prices. Read More

Dezima team regroups in startup Northsea to advance NASH candidate

LONDON – Newco Northsea Therapeutics BV has sailed onto the scene with a portfolio of structurally engineered fatty acids and a €25 million (US$29.4 million) series A funding round to take the lead product, icosabutate (PRC-4016), through phase IIb in the treatment of nonalcoholic steatohepatitis (NASH). Read More

Clementia starts first global phase III trial in ultra-rare bone disorder

Just four months out from its $128.2 million August IPO, Montreal-based Clementia Pharmaceuticals Inc. is moving palovarotene, its lead candidate, into a registrational phase III trial testing its ability to treat fibrodysplasia ossificans progressiva (FOP), an ultra-rare bone disorder. Read More

Bioverativ compass points True North with BIVV-009 pivotal effort in CAgD

ATLANTA – Bioverativ Inc. wasted little time moving the monoclonal antibody (MAb) BIVV-009 into phase III development after picking up the complement C1s subcomponent inhibitor, previously known as TNT-009, in its potential $825 million acquisition of True North Therapeutics Inc. (See BioWorld Today, May 24, 2017.) Read More

Lagoon boon swoon: Data from Murano helps Abbvie, waters in CLL still churning

ATLANTA – Abbvie Inc.'s vice president of oncology, Gary Gordon, told BioWorld that his firm aims to "restate the standard of care" in chronic lymphocytic leukemia (CLL), and the firm moved another step closer with full results from the phase III Murano trial, detailed in a late-breaking session at the American Society of Hematology meeting. Read More

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