Monday, April 17, 2017

OncoMed (OMED)'s lung cancer drug fails mid-stage study

  • To also discontinue enrollment in colorectal cancer drug trial
  • CEO says to review portfolio immediately


A week earlier:

One month later:

April 17 (Reuters) - OncoMed Pharmaceuticals Inc's shares were jolted for a second time in a week after the company said on Monday its experimental lung cancer drug failed a mid-stage study.
The company's stock was down 22 percent in early trading. Including those losses, OncoMed's market valuation has halved since the company said last week it would discontinue a trial testing another cancer drug.
"Based on the events of today and last week, we will be undertaking a comprehensive portfolio prioritization review immediately," said Chief Executive Paul Hastings.
The company said on Monday the mid-stage trial was testing a combination of its drug, tarextumab, and chemotherapy, compared with chemotherapy and a placebo.
The main goal for Tarextumab, which the company is developing in partnership with GlaxoSmithKline Plc, was to slow the progression of the disease.
The company said the tarextumab study also failed the secondary goal of overall survival benefit.
OncoMed's management will need to focus on rebuilding the research and development pipeline in a capital-efficient manner, Leerink Partners analyst Michael Schmidt wrote in a research note.
OncoMed also said on Monday it would also discontinue enrollment in an early-stage trial testing its drug, brontictuzumab, in combination with chemotherapy in patients with colorectal cancer due to toxicity issues.
The company said last week it would discontinue a trial testing demcizumab as an initial treatment for advanced pancreatic cancer.
Dealing another blow last week, Germany's Bayer AG said it would not exercise an option to license two of OncoMed's other experimental therapies, vantictumab and ipafricept, for "strategic reasons."
OncoMed had cash and short-term investments totaling about $156.9 million as of the first quarter of 2017.
Lung cancer (both small cell and non-small cell) is the second most common cancer in men and women and is by far the leading cause of cancer death, according to the American Cancer Society. 

OncoMed Pharmaceuticals, Inc. discovers and develops cancer stem cell (CSC) and immuno-oncology therapeutics. The company's product candidates and preclinical programs include demcizumab (anti-DLL4, OMP-21M18), a humanized monoclonal antibody, in Phase II trial for pancreatic cancer, a randomized Phase II trial in non-small cell lung cancer, and a Phase Ib trial for solid tumor; tarextumab (anti-Notch2/3, OMP-59R5) that targets the Notch2 and Notch3 receptors, which is in Phase II clinical trial for small cell lung cancer; vantictumab (anti-Fzd, OMP-18R5) in two Phase Ib clinical trials for breast and pancreatic cancer; ipafricept (Fzd8-Fc, OMP-54F28), a fusion protein based on Frizzled8 receptor, which is in two Phase Ib clinical trials for ovarian and pancreatic cancer; and navicixizumab (anti-DLL4/VEGF Bispecific, OMP-305B83), a monoclonal antibody that targets DLL4 and vascular endothelial growth factor, which is in Phase Ia single-agent clinical trial for solid tumors, and two Phase Ib clinical trial for ovarian and metastatic colorectal cancer. It is also developing anti-RSPO3 (OMP-131R10), a monoclonal antibody, in Phase Ia/b clinical trial for solid tumor and metastatic colorectal cancer; brontictuzumab (anti-Notch1, OMP-52M51) targeting the Notch1 receptor, in Phase Ib clinical trial for colorectal cancer; anti-tigit (OMP-313M32), a T-cell immunoglobulin and ITIM domain protein, in Phase I clinical trial for tumor; and GITRL-Fc trimer (OMP-336B11), a preclinical product candidate targeting glucocorticoid-induced tumor necrosis factor receptor and its ligand. The company has strategic alliances with GlaxoSmithKline LLC to develop and commercialize antibody therapeutics targeting the Notch signaling pathway; Bayer Pharma AG for biologic and small molecule therapeutics targeting the Wnt signaling pathway; and Celgene Corporation for anti-CSC product candidates. The company was founded in 2004 and is headquartered in Redwood City, California.

Key stats and ratios

Q1 (Mar '17)2016
Net profit margin-363.88%-409.90%
Operating margin-366.30%-411.03%
EBITD margin--404.02%
Return on average assets-50.04%-47.58%
Return on average equity--
Employees122

Address

800 Chesapeake Dr
REDWOOD CITY, CA 94063-4748
United States 

No comments:

Post a Comment