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NASDAQ, CRSP: Crispr Therapeutics Ag

23 Sep 26 07:05
LAST:

59.17

CHANGE:
 0.14		OPEN:
59.08		HIGH:
59.17		ASK:
20.25		VOLUME:
875
CHG(%):
0.24		PREV:
59.03		LOW:
58.80		BID:
17.88		 

CHART

RECENT END OF DAY PRICES

DateOpenHighLowCloseVolume
23 Sep 2659.0859.1758.8059.17875
22 Sep 2658.7360.7257.6459.032.08M
21 Sep 2657.9859.2456.8758.331.81M
18 Sep 2658.0059.3455.6356.563.38M
17 Sep 2653.9059.2153.1257.333.0M
16 Sep 2652.1653.6751.8352.212.67M
15 Sep 2652.5752.8551.4951.831.25M
14 Sep 2651.3353.8051.3352.961.53M
11 Sep 2652.3553.2151.6251.72856.7K
10 Sep 2652.5052.6351.7252.261.26M

PROFILE

Name:Crispr Therapeutics Ag
About:CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious human diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. The company's CRISPR/Cas9 is a revolutionary technology for gene editing which is the process of precisely altering specific sequences of genomic DNA. It has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, CAR T cell therapies, in vivo, and type 1 diabetes, as well as develops investigational CAR T programs, including an autologous, gene-edited CAR T program targeting glypican-3 (GPC3) for the potential treatment of solid tumors. The company's lead product candidate is CASGEVY, an ex vivo CRISPR/Cas9 gene-edited cell therapy for treating patients suffering from transfusion-dependent beta-thalassemia, severe sickle cell disease (SCD), and hemoglobinopathies in which a patient's hematopoietic stem and progenitor cells are edited to produce high levels of fetal hemoglobin in red blood cells. It also develops CAR T cell therapies, including CTX112 targeting cluster of differentiation 19 (CD19) and CTX131 targeting CD70 for oncology and autoimmune indications; CTX310 and CTX320, in vivo gene editing to address the cardiovascular disease by disrupting the validated targets angiopoietin-like protein 3 and lipoprotein; and CTX211, an allogeneic, gene-edited, hypoimmune stem cell-derived product candidate for the treatment of T1D. It has strategic partnerships with Vertex Pharmaceuticals Incorporated, Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland.
Sector:Healthcare
Industry:Biotechnology
Address:Baarerstrasse 14, Zug, Switzerland, 6300
Website:https://www.crisprtx.com
CUSIP:H17182108
CIK:0001674416
ISIN:CH0334081137
FIGI:BBG00DBBGRX1
LEI:506700O6IRRIQLT3W370

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FUNDAMENTALS

Trailing P/E:-14.28 
Forward P/E:-16.01 
PEG Ratio:-0.23 
Price to Sales:152.95 
Price to Book:3.29 
Profit Margin:-2.15 
Operating Margin:-149.18 
Return on Assets:-0.13 
Return on Equity:-0.25 
EPS Ratio:-6.17 
Revenue:38.05M 
Shares:98.48M 
Market Cap:5.827B 

TECHNICAL INDICATORS

MA5:58.081.9%
MA10:55.147.3%
MA20:55.955.8%
MA50:53.4710.7%
MA100:53.3610.9%
MA200:53.3710.9%
STO9:82.78 
STO14:82.78 
RSI14:56.84
MTM14:2.68
ROC14:0.05 
ATR:2.46 
Week High:60.722.6%
Week Low:51.8314.2%
Month High:61.554.0%
Month Low:51.3310.9%
Year High:78.4832.6%
Year Low:44.1234.1%
Volatility:48.50 

RECENT SPLITS

Date Ratio
19 Jul 2016333333-100000