Trump Signs Law to Launch Dollar 2.0

Trump just signed law S.1582, unleashing the biggest money shift in 100+ years. For the first time since 1913, private firms - not the Fed - can mint a "Dollar 2.0." Treasury says it could drain $6.6T from banks and pay 10X current savings rates. Early investors in minting firms could see 40X returns by 2032.

CRSP
CRISPR Therapeutics AG
NASDAQ
50.23
Open 48.48 Prev Close 49.29
High 51.45 Low 48.02
Volume 2,753,748 Volume (Avg) 2,448
52 Week High 78.48 52 Week Low 30.04
Market Cap 4.8B PE Ratio

Shares Stats

Shares Outstanding93,870,000
Shares Float91,320,000
Shares Short21,030,000
Insider Holdings161%
Institution Holdings77.95%

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.

General

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

Highlights

Analyst Target78.00
Market Cap4,786,900,000
PEG Ratio-0.21
EBITDA-459,481,984

Financials

Curr Year EPS Estimate-6.23
Next Quarter EPS Estimate-1.18
Profit Margin-1273.70%
Operating Margin-1,247.21
Return on Assets-0.13
Return on Equity-0.25
Revenue38.3M
Earnings Per Share-5.54
Revenue Per Share0.44
Gross Profit-430,665,984
Quarterly Revenue Growth0.48

Valuation

Forward PE23.36
Price/Sales (Trailing 12 Mt.)122.53
Price/Book (Most Recent Quarter)2.52

Earnings

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