Search Results for: Clinical Roundup
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As Markets Fancy Biotech, PTC Therapeutics Joins IPO Queue
On Friday, the Vetex's shares (NASDAQ:VRTX) gained $1.60, closing at $79.49.By Marie Powers | BioWorld Today | Monday, May 20, 2013 -
Isis Peers Beyond Kynamro, Seeks $171M for Pipeline
clinical development plan and financial terms relating to ISIS-TTRRx to reflect an accelerated development plan for that antisense drug...Isis has 28 candidates in preclinical and clinical development across a wide variety of indications, with nine scheduled to report data in the next 12 monthsBy Marie Powers | BioWorld Today | Friday, May 10, 2013 -
ActoGeniX Series B to Move IBD Program to IND Stage
AG014 comprises oral delivery of an anti-TNF antibody with proven clinical efficacy in IBD, resulting in local efficacy and an improved safety profile over systemic drugs...Shares of Northwest (NASDAQ:NWBO) fell 13 cents to close Thursday at $3.77.By Marie Powers | BioWorld Today | Friday, April 19, 2013 -
Revance Adds $33M for BoNTA Alternative to Botox
The latest round is expected to support ongoing clinical development of lead candidate, LiRIS (lidocaine releasing intravesical system), in development for patients with interstitial cystitis.By Marie Powers | BioWorld Today | Wednesday, April 3, 2013 -
Following Ravicti Win in UCD, Hyperion Seeks $59.7M for HE
at the same unit price.By Marie Powers | BioWorld Today | Monday, March 11, 2013 -
Immunomedics Seeks $14M as Bridge to Milestones
UCB also picked up clinical development and commercialization costs. (See BioWorld Today, May 11, 2006.) In 2009, the companies reported results from a Phase IIb dosing study of the drug showing a 24.9 percent treatment advantage over placebo in systemic lupus erythematosus (SLE) patients...Closing of the private placement is subject to customary conditions, including acceptance by the TSX Venture Exchange.By Marie Powers | BioWorld Today | Monday, February 25, 2013 -
Jounce Gets $47M Series A, Seeks to Jolt Cancer Therapy
The transaction is expected to close on Feb. 19.By Marie Powers | BioWorld Today | Thursday, February 14, 2013 -
Celldex Seeks $90M, End Zone for Rindopepimut
The company will receive proceeds of $8 million, which it expects to use to fund clinical trials and for working capital and general corporate purposes.By Marie Powers | BioWorld Today | Thursday, February 7, 2013 -
Aileron $12M Raise to Propel Stapled Peptide into Clinic
Together, the three collaborated in the seminal discovery of the first biologically active stapled peptide and translation into a potential clinical application...Proceeds from any offering are expected to support general corporate purposes, including to R&D costs, payment obligations and capital expenditures.By Marie Powers | BioWorld Today | Tuesday, January 15, 2013 -
HC Royalty Inks Hefty Deals to Propel Nuron and Raptor
As a small biotech with one foot in infectious disease and the other in neurology while having one hand in commercial products and the other in clinical development, "we have a unique strategy, and so far it's working well," Musunuri said...Proceeds will be used for general corporate purposes, including the company's ongoing trials of NX-1207, in late-stage development for benign prostatic hyperplasia and in Phase II testing in prostate cancer.By Marie Powers | BioWorld Today | Friday, December 21, 2012 -
To 'Infinity' and Beyond: $150M to Propel PI3K Inhibitor IPI-145
The company plans to use the proceeds to fund research and development, clinical trials and for other corporate purposes.By Marie Powers | BioWorld Today | Friday, December 14, 2012 -
Zafgen $21M Raise to Move Beloranib Beyond Phase IIa
The Series D enables Zafgen to move clinical and regulatory activities forward without the distraction of additional fundraising, Hurwitz added...Proceeds will support a Phase III trial of Multikine (leukocyte interleukin, injection).By Marie Powers | BioWorld Today | Wednesday, December 5, 2012 -
MEI Pharma to Advance HDAC Inhibitor with $27.5M Raise
The company laid groundwork for clinical trials in advance of the financing and plans to begin a "very substantial" randomized Phase II study in the U.S...The company also received $25.0 million from the sale of common stock in a private placement to strategic partner AstraZeneca plc, of London, that closed concurrently with the IPO, and $5.0 million from the sale of a convertible note to research collaborator Biogen Idec Inc., of Weston, Mass., which was converted into shares of common stock atBy Marie Powers | BioWorld Today | Tuesday, November 6, 2012 -
Supremes to Hear Arguments on 'Fraud-on-the-Market' Claims
The study, by scientists at the National Cancer Institute, and colleagues, appeared in Cancer Research.By Marie Powers | BioWorld Today | Monday, November 5, 2012 -
Hydrocodone Combo Products Come Under FDA Microscope
Thus, Calderon said she "would recommend requiring clinical studies to fully evaluate the abuse potential" of products submitted for review that exceed that levelBy Marie Powers | BioWorld Today | Monday, October 29, 2012 -
Antibody Firm KaloBios Enters IPO Queue, Aims to Raise $60M
KaloBios has three mAbs at the clinical development stage...Shares of Cell Therapeutics (NASDAQ:CTIC) dropped 51 cents, or 25 percent, to close Friday at $1.53.By Marie Powers | BioWorld Today | Monday, October 8, 2012 -
PCAST to FDA: Double New Drug Output in 10 Years
Clinical trials now represent an aggregate expense of approximately $31.3 billion, or nearly 40 percent of the R&D budget of major drug developers – much of that due to systemic inefficiency, according to the report...362, has been introduced in the Senate.By Marie Powers | BioWorld Today | Thursday, September 27, 2012 -
Relypsa Loads $80M Series C to Fund Patiromer Phase III
is acting as sole book-running manager.By Marie Powers | BioWorld Today | Thursday, August 16, 2012 -
MAP Seeks $52M, Prepares to Resubmit Levadex NDA
The FDA did not cite clinical safety or efficacy issues and did not request additional pre-approval studies, but the agency did raise questions relating to chemistry, manufacturing and controls, as well as issues related to a facility inspection at a third-party manufacturer. (See BioWorld Today, March 28, 2012.) The company completed an end-of-review meeting with the FDA in June to seek clarity from the agency in developing its response...LLC acted as joint book-running managers, with NeedhamBy Marie Powers | BioWorld Today | Thursday, August 2, 2012 -
Synageva Rides Stock Crest, Seeks $100M Public Offering
The company plans to use the proceeds to complete clinical development of lead candidate dalbavancin, currently in a second pivotal Phase III trial in skin infections, and to fund commercialization activities in the U.S...LLC and CRT Capital Group LLC served as initial purchasers in the private placement. (See BioWorld Today, March 1, 2012.)By Marie Powers | BioWorld Today | Wednesday, July 11, 2012
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