CRISPR Therapeutics AG

CH

CRSP

Health Care

55.66 ₽

Current price

Buy
55.66 ₽

Target price 00%

Ranks rating

76

  • Position in sub-industry

    225 / 1361

  • Position in country

    202 / 449

  • Return on Assets, %

    -7

    -40.3

  • Net income margin, %

    44.4

    -180

  • EBITDA margin, %

    37

    -168.2

  • Debt to Equity, %

    0

    3.2

  • Intangible assets and goodwill, %

    0

    0.2

  • Revenue CAGR 3Y, %

    702.2

    12.5

  • Total Equity change 1Y, %

    0.3

    -9

  • Revenue Y, % chg

    30885.4

    0

  • P/BV

    2.5

    1.8

  • P/S

    13.8

    10.3

  • EV/S

    9.3

    7.5

  • EV/EBITDA

    -16.2

    -1.6

  • Average Analyst recommendation

    Hold

    Hold

  • Average upside forecasts, %

    36.8

    131.1

  • Expected dividend per share

    0

    0

Get an analytical review of this company

Competitors

Ranks

  • MoonLake Immunotherapeutics

    00%

  • Vertex Pharmaceuticals Inc

    00%

  • CSL Ltd

    00%

  • Regeneron Pharmaceuticals Inc

    00%

  • Gilead Sciences Inc

    00%

  • CRISPR Therapeutics AG

    00%

  • Seagen Inc

    00%

  • Amgen Inc

    00%

  • Moderna Inc

    00%

  • AbbVie Inc

    00%

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Company information

  • Country

    Switzerland

  • Sector

    Health Care

  • Industry group

    Pharmaceuticals, Biotechnology & Life Sciences

  • Industry

    Biotechnology

  • Sub-sector

    Health Care

  • Capitalization (millions of $)

    5149.8

  • Ticker

    CRSP.O

  • ISIN

    CH0334081137

  • IPO date

    2016-10-19

  • Availability on Russian exchanges

    Yes

  • Reporting for

    2024-02-21

  • Date fact. publication of reports

    2023-12-31

Company Description

CRISPR Therapeutics AG is a Switzerland-based gene-editing company. It focuses on the development of transformative gene-based medicines for serious diseases. The Company develops its products using Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/Cas9 gene-editing platform, which allows for precise directed changes to genomic deoxyribonucleic acid (DNA). The Company has a portfolio of therapeutic programs in a range of disease areas, including hemoglobinopathies, oncology, regenerative medicine and rare diseases. Its lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta thalassemia or severe sickle cell disease in which a patient’s hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. The Company has business operations in London and the United Kingdom, as well as research and development operations in the United States.