Onconova Therapeutics Inc (ONTX)

2.02
0.01 0.50
NASDAQ : Health Care
Prev Close 2.01
Open 2.04
Day Low/High 1.98 / 2.06
52 Wk Low/High 3.30 / 40.00
Volume 29.25K
Avg Volume 191.40K
Exchange NASDAQ
Shares Outstanding 9.49M
Market Cap 19.35M
EPS -4.40
P/E Ratio N/A
Div & Yield N.A. (N.A)

Latest News

Onconova Therapeutics, Inc. To Provide Corporate Update And First Quarter 2017 Financial Results

Onconova Therapeutics, Inc. To Provide Corporate Update And First Quarter 2017 Financial Results

Company to Hold Conference Call and Webcast at 9:00 a.m. Eastern Time on Monday, May 15, 2017

Onconova Therapeutics Announces Pricing Of Public Offering Of Common Stock

Onconova Therapeutics Announces Pricing Of Public Offering Of Common Stock

Gross Proceeds to Support Phase 3 Trials of Rigosertib for Patients with Myelodysplastic Syndromes

Onconova Therapeutics Announces Proposed Public Offering Of Common Stock

Onconova Therapeutics Announces Proposed Public Offering Of Common Stock

Gross Proceeds to Support Phase 3 Trials of Rigosertib for Patients with Myelodysplastic Syndromes

Onconova Therapeutics, Inc. To Provide Corporate Update And Full Year 2016 Financial Results

Onconova Therapeutics, Inc. To Provide Corporate Update And Full Year 2016 Financial Results

Company to Hold Conference Call and Webcast at 9:00 a.m. Eastern Time on Monday, March 27, 2017

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Onconova And Cellworks Announce Presentation Of Rigosertib Predictive Signature For Clinical Response In Myelodysplastic Syndromes (MDS) At 2016 ASH Annual Meeting

Onconova And Cellworks Announce Presentation Of Rigosertib Predictive Signature For Clinical Response In Myelodysplastic Syndromes (MDS) At 2016 ASH Annual Meeting

Computational Subgroup Analysis of Phase 3 ONTIME Trial Provides Insights into Clinical Response to Rigosertib in Higher-risk MDS

Onconova Announces Successful End-of-Phase 2 Meeting With FDA For Oral Rigosertib And Azacitidine Combination

Onconova Announces Successful End-of-Phase 2 Meeting With FDA For Oral Rigosertib And Azacitidine Combination

Pivotal Randomized Trial in 1st-line MDS Patients will Assess Overall Response Rate as Approval Endpoint

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