Gross Profit, Operating Income, and Net Income as a percentage of Revenue

Operating Margin

Profit Margin

Margins

An operating expense is an expense a business incurs through its normal business operations. Often abbreviated as OPEX.

Collaboration expense, net

Operating Expenses

Year over year growth in Revenue and Operating Expenses.

Revenue Y/Y

OpEx Y/Y

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Shares outstanding refer to a company's stock currently held by all its shareholders, including share blocks held by institutional investors and restricted shares owned by the company's officers and insiders.

Outstanding Shares

Market Cap

Also known as Price/Sales Ratio. Calculated using Average market cap for the quarter / Annualized quarterly revenue.

Revenue Multiple

CRISPR Therapeutics

CRISPR Therapeutics AG is a gene editing company, which engages in the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. Its CRISPR/Cas9 platform is a gene editing technology that allows for precise, directed changes to genomic DNA. The firm offers a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company was founded by Rodger Novak, Emmanuelle Charpentier, Shaun Patrick Foy, Matthew Porteus, Daniel Anderson, Chad Cowan and Craig Mellow on October 31, 2013 and is headquartered in Zug, Switzerland.

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CRISPR Therapeutics AG is a gene editing company, which engages in the development of transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 platform. Its CRISPR/Cas9 platform is a gene editing technology that allows for precise, directed changes to genomic DNA. The firm offers a portfolio of therapeutic programs across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company was founded by Rodger Novak, Emmanuelle Charpentier, Shaun Patrick Foy, Matthew Porteus, Daniel Anderson, Chad Cowan, and Craig Mellow on October 31, 2013 and is headquartered in Zug, Switzerland.

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Block

CRISPR Therapeutics is blazing new trails in the promising area of gene editing. Block's two central ecosystems and several other ventures promise a bright future.

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CRISPR Therapeutics and Vertex Pharmaceuticals just launched a gene therapy. For now, it's a pricey medicine, and there aren't many eligible patients.

CRISPR Therapeutics Just Made History. So Why Did Its Stock Fall?

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AbbVie's rally has already begun and could continue into the new year. CRISPR Therapeutics received a holiday gift recently with U.S. approval of its first product.

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The main reason to consider buying CRISPR Therapeutics has little to do with its newly approved gene-editing therapy. Instead, the biotech's promising pipeline is the key factor that should be attractive.

Here's the 1 Key Reason You Might Want to Buy CRISPR Therapeutics Stock on the Dip

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The pharma stock leaders can at times seem overly risk averse with their approach to developing new medicines and cures. With the difficulty of clinical trials and the uncertainty of Federal Drug Administration (FDA) approval, many pharma companies prefer to play it safe rather than bet big.

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CRISPR Therapeutics won regulatory approval of its first product, Casgevy, for blood disorders. This is also the world's first approval of a treatment based on CRISPR gene editing.

After This Landmark Win, Is CRISPR Therapeutics a Buy?

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Amgen's pioneering efforts in antibody drug development turned out to be a game changer for early shareholders. CRISPR Therapeutics could follow a similar path, following its historic approval for Casgevy this month.

1 Biotech Stock That Could Be the Next Amgen

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Gene editing stocks have received a lot of attention throughout 2023. The intense focus on gene editing therapies and CRISPR technology is likely only to increase moving forward: The U.S. Food and Drug Administration (FDA) just approved the world's first medicine employing CRISPR technology.

3 Gene-Editing Stocks With the Potential to Mint Millionaires

Vertex Pharmaceuticals

Biotech stocks could be at a major turning point after FDA approval of the first gene editing drug using Crispr technology. But gene editing therapies aren't without risk, and questions remain about the safety and cost effectiveness of these experimental treatments.

Here's What The FDA Approval Of Gene Editing For Sickle Cell Means For CRSP Stock And The Future Of Medicine

Crispr Therapeutics AG ( NASDAQ:CRSP) stock is down 7.2% to trade at $59.89 at last check, despite its gene therapy treatment for sickle cell disease in partnership with Vertex (VRTX) last week receiving approval from the U.S. Food and Drug Administration (FDA).

Crispr Therapeutics Stock Sinks Despite FDA Approval

bluebird bio

The FDA approves two one-time gene therapies for treating sickle cell disease. One of them utilizes the Nobel prize-winning CRISPR/Cas9 gene-editing technology.

BLUE, CRSP & VRTX Down Despite FDA Nod to SCD Therapies

On Friday, the FDA approved CRISPR's Casgevy gene-editing treatment for sickle cell anemia. Analysts are mixed in their opinions on how big a deal this is for CRISPR.

Why CRISPR Stock Keeps Falling

CRISPR (CRSP) and Vertex announce the FDA approval of the first-ever CRISPR-based gene-editing therapy, Casgevy, for the treatment of sickle cell disease.

CRISPR (CRSP), Vertex Fall Despite FDA Nod to SCD Drug Casgevy

After reaching an important support level, CRISPR Therapeutics AG (CRSP) could be a good stock pick from a technical perspective. CRSP recently experienced a "golden cross" event, which saw its 50-day simple moving average breaking out above its 200-day simple moving average.

After Golden Cross, CRISPR Therapeutics AG (CRSP)'s Technical Outlook is Bright

CRISPR Therapeutics ( CRSP ) just made history on Friday with the first FDA-approved gene-editing medicine based on the Nobel Prize-winning discovery that targets disease with the billion-year old defense mechanism bacteria use to battle viruses. CRISPR -- which stands for clustered regularly interspaced short palindromic repeats -- was discovered and described as a potential gene modifying treatment in a paper published in 2012 by biochemist Jennifer Doudna and microbiologist Emmanuelle Charpentier.

Bull of the Day: CRISPR Therapeutics (CRSP)

CRISPR Therapeutics received marketing approval from the U.S. Food and Drug Administration for its first drug, called Casgevy, on Dec. 8. Shares of CRISPR Therapeutics fell sharply in response to what seemed like great news.

Is CRISPR Therapeutics a Good Stock to Buy Following Approval of Its First Drug?

The FDA approved the first gene therapies for sickle cell anemia. The two approved treatments, Casgevy and Lyfgenia, will cost $2.2 million and $3.1 million.

The FDA just approved the first gene editing therapy for sickle cell anemia, but it'll cost $2.2 million per person

The FDA has granted approval to a CRISPR-based gene editing therapy for the first time in history, validating the approach. The therapy, called Casgevy, is approved to treat Sickle Cell Disease after showing positive results in clinical trials, functionally curing patients. Despite the approval, the stock prices of CRISPR Therapeutics AG and Vertex Pharmaceuticals Incorporated did not surge today, possibly due to concerns about market potential and competition from another approved therapy.

Vertex And CRISPR Therapeutics: Historic Exa-cel Approval, Why Market Is Nonplussed

Vertex Pharmaceuticals (VRTX) and CRISPR Therapeutics (CRSP) announced Friday that the Food and Drug Administration (FDA) gave them approval for use of the first-ever gene-editing therapy using CRISPR technology in the U.S.

Vertex, CRISPR Therapeutics Get FDA Approval for First CRISPR Gene-Editing Therapy in US

Vertex Pharmaceuticals and its partner CRISPR Therapeutics said on Friday their sickle cell disease gene therapy Casgevy would be available at a list price of $2.2 million in the United States.

Vertex/CRISPR price sickle cell disease gene therapy at $2.2 mln

BOSTON & ZUG, Switzerland--(BUSINESS WIRE)--Vertex Pharmaceuticals Incorporated (Nasdaq: VRTX) and CRISPR Therapeutics (Nasdaq: CRSP) announced today that the U.S. Food and Drug Administration (FDA) has approved CASGEVY™ (exagamglogene autotemcel [exa-cel]), a CRISPR/Cas9 genome-edited cell therapy, for the treatment of sickle cell disease (SCD) in patients 12 years and older with recurrent vaso-occlusive crises (VOCs). This approval means that for the first time, approximately 16,000 patients.

Vertex and CRISPR Therapeutics Announce US FDA Approval of CASGEVY™ (exagamglogene autotemcel) for the Treatment of Sickle Cell Disease

Crispr Therapeutics AG CRSP, -5.37% and Vertex Pharmaceuticals Inc. VRTX, -1.25% on Friday got U.S. regulatory approval for a treatment for sickle-cell disease based on the transformative gene-editing technology Crispr.

News for CRISPR Therapeutics Stock (CRSP)