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News Breaks
March 6, 2014
07:20 EDTKPTIKaryopharm price target raised to $50 from $25 at JMP Securities
JMP Securities raised its price target on Karyopharm after it provided an outline of planned pivotal trials in AML, DLBCL, and Richterís syndrome, and formally stated that it is broadening its Phase II development plans in various solid tumor malignancies. The firm sees unmet need in these indications and its confidence in the company's chances of success has increased. It increased its estimate of peak U.S. sales for selinexor to $3.6B from $1.8B and reiterates an Outperform rating.
News For KPTI From The Last 14 Days
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December 15, 2014
10:18 EDTKPTIKaryopharm management to meet with JMP Securities
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December 12, 2014
08:16 EDTKPTIKaryopharm sell-off overdone, says JMP Securities
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December 11, 2014
16:30 EDTKPTIOn The Fly: Closing Wrap
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08:10 EDTKPTIKaryopharm initiates third registration-directed clinical trial of Selinexor
Karyopharm Therapeutics announced the initiation of the SADAL study, or Selinexor and Dexamethasone in Aggressive Lymphoma, a registration-directed, Phase 2b study of Selinexor, or KPT-330, in patients with relapsed/refractory diffuse large B-cell lymphoma, or DLBCL. This randomized, multi-center study of Selinexor, one of the company's novel, oral Selective Inhibitor of Nuclear Export/SINE compounds, is being evaluated as a single agent in combination with dexamethasone for supportive care and is expected to enroll approximately 200 patients in approximately 90 sites worldwide. Karyopharm has received Orphan Drug Designation from the FDA and European Medicines Agency, or EMA, for Selinexor for the treatment of patients with DLBCL. This open-label Phase 2b study will evaluate the safety and efficacy of high dose versus mid dose Selinexor in combination with low dose dexamethasone for supportive care, each given orally to approximately 200 patients with relapsed/refractory DLBCL. Overall response rate, or ORR, is the primary endpoint. The study is expected to take approximately two years to complete and is intended to support accelerated regulatory approval. This study was designed in consultation with the FDA and on the basis of data from Karyopharm's ongoing Phase 1 study of Selinexor in patients with advanced hematologic malignancies.
December 9, 2014
10:19 EDTKPTIHigh option volume stocks
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10:08 EDTKPTIHigh option volume stocks
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December 8, 2014
13:03 EDTKPTIKaryopharm reports positive combination data for Selinexor
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December 7, 2014
14:48 EDTKPTIKaryopharm to hold an investor dinner and a clinical data presentation
Investor Dinner and a clinical data presentation being held in conjunction with the American Society of Hematology's 56th Annual Meeting in San Francisco on December 8 at 10:15 pm.

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