-- Genentech will discuss results with the U.S. Food and Drug Administration (FDA) as part of atezolizumab’s Breakthrough Therapy Designation in lung cancer -- Genentech, a member of the...
-- Regulatory applications for venetoclax are planned for submission to the U.S. Food and Drug Administration (FDA) and European Medicines Agency (EMA) by the end of 2015...
-- Results showed that high levels of PD-L1 expression were associated with greater responses to atezolizumab -- -- Genentech will discuss results with the U.S. Food and Drug...
Studies showed superiority on primary and major secondary endpoints in people with relapsing forms of multiple sclerosis Genentech will submit data to the U.S. Food and Drug...
Systemic sclerosis affects approximately 75,000 to 100,000 people in the U.S. and has highest mortality rate of any autoimmune rheumatic disease1,2 There is no FDA-approved therapy...
-- New data from Phase II NeoSphere study provide additional evidence on the role of Perjeta in the neoadjuvant (pre-surgery) treatment of HER2-positive early breast cancer -- Genentech...
-- GADOLIN is the second positive Phase III study in the Gazyva clinical development program -- -- Genentech and Roche will submit data from the GADOLIN study to regulatory authorities...
-- Alectinib showed response rates of up to 69 percent in the central nervous system (CNS) in people with advanced ALK-positive non-small cell lung cancer -- -- Genentech plans to...
Period | Change | Change % | Open | High | Low | Avg. Daily Vol | VWAP | |
---|---|---|---|---|---|---|---|---|
1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
4 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
12 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
26 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
52 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
156 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |
260 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | CS |