Tech Millionaire: "Here's Where I'd Put $10,000 After the Selloff"

A little-known breakthrough is already showing up in Amazon's 1,285 warehouses... could soon be in every middle-class household in America... and might create more millionaires in the coming years than any other investment.

CRISPR Therapeutics AG
NASDAQ:CRSP
$35.97
Open 36.52 Prev Close 36.14
High 37.34 Low 35.54
Volume 1,012,462 Volume (Avg) 2,283
52 Week High 67.88 52 Week Low 30.04
Market Cap 3.1B PE Ratio

General

NameCRISPR Therapeutics AG
TickerCRSP
ExchangeNASDAQ
SectorHealthcare
IndustryBiotechnology
CurrencyUSD
CountryUSA
Fiscal Year EndDecember
Full Time Employees393

About CRISPR Therapeutics AG

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.

Highlights

Analyst Target78.20
Market Cap3,106,500,000
PEG Ratio-0.21
EBITDA-447,307,008

Valuation

Forward PE23.36
Price/Sales (Trailing 12 Mt.)87.07
Price/Book (Most Recent Quarter)1.68

Technicals

Beta1.80
52 Week High67.88
52 Week Low30.04
50 Day Average-6.99%
200 Day Average-19.47%

Earnings

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