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Compare ARMOUR Residential REIT, Inc. (ARR) vs Crispr Therapeutics AG (CRSP) Price & Performance

ARMOUR Residential REIT, Inc.Trade
Crispr Therapeutics AGTrade

Price performance (Past 24H)

Key statistics

ARMOUR Residential REIT, Inc. vs Crispr Therapeutics AG — how do they compare? ARMOUR Residential REIT, Inc. trades at $16.7 (market cap $2.05B), while Crispr Therapeutics AG trades at $53.88 (market cap $5.17B). The key difference: Crispr Therapeutics AG is far larger — about 2.5× ARMOUR Residential REIT, Inc.'s market cap, and ARMOUR Residential REIT, Inc. pays a 17.41% dividend while Crispr Therapeutics AG pays none. Which is the better fit depends on your goals.

ARRCRSP
Market Cap
$2.05B$5.17B
Sector
FinancialsHealth
52-Week High
$19.12$76.78
52-Week Low
$14.05$44.34
Dividend Yield
17.41%
Enterprise Value
$3.59B

Returns comparison

Trailing returns across standard periods

About ARMOUR Residential REIT, Inc.

ARMOUR Residential REIT Inc is a real estate investment trust that invests in residential mortgage-backed securities or RMBS. These are issued or guaranteed by U.S.-government-sponsored enterprises, such as Fannie Mae, Freddie Mac, or Ginnie Mae. The company's investment portfolio is composed of mortgage-backed securities, adjustable-rate mortgage securities, and multifamily mortgage-backed securities. In terms of total fair value, most Armour's investments are long-term, fixed-rate agency RMBS. Multifamily RMBS also represents a substantial amount. Fannie Mae guarantees most of the company's holdings. Armour derives substantially all its revenue as interest income from its investments.

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About Crispr Therapeutics AG

CRISPR Therapeutics is a gene editing company focused on the development of CRISPR/Cas9-based therapeutics. CRISPR/Cas9 stands for Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9), which is a revolutionary technology for precisely altering specific sequences of genomic DNA. The company is focused on using this technology to treat genetically defined diseases. CRISPR's most advanced pipeline candidate, CTX001, is in collaboration with Vertex Pharmaceuticals and targets sickle cell disease and transfusion-dependent beta-thalassemia, which have high unmet medical needs. The company is progressing additional gene editing programs for immuno-oncology, as well as a stem cell-derived therapy for the treatment of Type 1 diabetes.

Read more on CRSP