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BioWorld - Wednesday, March 25, 2026
Home » Newsletters » BioWorld

BioWorld

Feb. 18, 2015

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VBL shares tumble on phase II misses of VB-201 in psoriasis, ulcerative colitis

VBL Therapeutics shares (NASDAQ:VBLT) plummeted 65.5 percent Tuesday to $4.87, more than a dollar under the company's recent initial public offering (IPO) price, as investors digested news that VB-201, an experimental autoimmune therapy that had appeared to help patients with psoriasis in an earlier midstage study, failed to significantly benefit both psoriasis and ulcerative colitis sufferers in separate phase II trials. Read More

Not-blue Laguna: $30M series B funds phase III in a-fib with vanoxerine

Formerly known as Chanrx Corp., Laguna Pharmaceuticals Inc. raised $30 million in series B money for phase III work in atrial fibrillation (AF) and atrial flutter with vanoxerine, moving operations from Cleveland to San Diego while bringing aboard as CEO well-known biotech player Bob Baltera. Read More

Don't stop Ebola drug R&D efforts despite slowing infection rate, biodefense chief urges

SAN JOSE, Calif. – The push to develop vaccines and antivirals against Ebola must go on, even though the falling infection rate may reduce the chances of getting definitive phase III efficacy data during the current outbreak. Read More

Alzheimer's research moving toward early diagnoses, biomarkers

SAN JOSE, Calif. – The industry's expensive attempts to develop treatments for Alzheimer's disease have been confounded by the difficulties of diagnosis, and multiple drugs targeting amyloid plaques, administered once overt symptoms are well established, have failed in development. Read More

Clinical data reporting requirements next on path to transparency

SAN JOSE, Calif. – As momentum increases behind the movement for greater transparency of clinical trials data, attention is turning to ensuring that when information is made available it is accessible and consistent, and that confidentiality is respected when patient-level data are disclosed. Read More

China's 3SBio expands footprint, prepares for IPO on HK exchange

HONG KONG – In the wake of a pair of deals in just two months that would expand its European footprint, Chinese biopharmaceutical company 3SBio Inc. is getting ready for an initial public offering (IPO) in Hong Kong. Read More

Potent breast cancer candidate targets stem, bulk tumor cells

HONG KONG – A highly potent small-molecule inhibitor designed by Korean scientists has been shown both in vivo and in vitro to be a promising candidate treatment for breast cancer that preferentially targets both breast cancer stem cells (BCSCs) and bulk tumor cells, thereby potentially reducing the chances of relapse. Read More

Bills to improve drug regulatory, development scene make their debut

With 2015 shaping up as the year to reform the drug development and approval process, a raft of related legislation is floating through Congress. Read More

Financings

Ultragenyx Pharmaceutical Inc., of Novato, Calif., said underwriters of the previously disclosed offering of 3 million shares of common stock have exercised in full their option to purchase an additional 450,000 shares from the company at the public offering price of $54 each, before underwriting discounts. Read More

Stock movers

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In the clinic

Cynata Therapeutics Ltd., of Melbourne, Australia, said earlier it has engaged an undisclosed contract research organization to begin clinical trial planning and logistics development for a phase I study of its mesenchymal stem cell product. Read More

Other news to note

Hyperion Therapeutics Inc., of Brisbane, Calif., said it amicably resolved its disputes, and entered a completion of phase III trial, option and mutual release agreement with Clal Biotechnology Industries Ltd. (CBI), of Ramat Gan, Israel, and Yeda Research and Development Co. Ltd. regarding Diapep277, a product candidate developed by Andromeda Biotech Ltd., a company which Hyperion acquired from CBI in June 2014. Read More

Pharma: Other news to note

Eisai Inc., of Woodcliff Lake, N.J., said the FDA approved the company's receptor tyrosine kinase inhibitor Lenvima (lenvatinib) for the treatment of locally recurrent or metastatic, progressive, radioactive iodine-refractory differentiated thyroid cancer. Read More

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