As on 28-Nov-2023 16:05 EST
$71.61
$71.17
$71.74
$69.44
1,852,962
$37.55 - 76.19
YTD
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1 Month
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3 Months
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1 Year
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3 Years
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5 Years
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10 Years
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Crispr Therapeutics AG (CRSP)
| 73.83 | 82.40 | 39.92 | 28.50 | -16.54 | 14.24 | -- |
S&P BSE Sensex*
| 10.91 | 5.65 | 4.09 | 6.94 | 15.19 | 13.27 | 12.49 |
S&P Small-Cap 600#
| -5.82 | -5.34 | -13.90 | -6.30 | 5.30 | 2.98 | 5.53 |
2022
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2021
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2020
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2019
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2018
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2017
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Crispr Therapeutics AG (CRSP)
| -46.36 | -50.51 | 151.39 | 113.18 | 21.55 | 15.89 |
S&P Small-Cap 600
| -17.42 | 25.27 | 9.57 | 20.86 | -9.70 | 11.73 |
S&P BSE Sensex
| 4.44 | 21.99 | 15.75 | 14.38 | 5.87 | 27.91 |
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The total asset value of Crispr Therapeutics AG (CRSP) stood at $ 2,330 Mln as on 30-Jun-23
The share price of Crispr Therapeutics AG (CRSP) is $70.66 (NASDAQ) as of 28-Nov-2023 16:05 EST. Crispr Therapeutics AG (CRSP) has given a return of -16.54% in the last 3 years.
Crispr Therapeutics AG (CRSP) has a market capitalisation of $ 3,920 Mln as on 11-Aug-2023. As per Value Research classification, it is a Small Cap company.
The P/B ratio of Crispr Therapeutics AG (CRSP) is 2.01 times as on 11-Aug-2023, a -0.21% premium to its peers’ median range of 2.54 times.
Since, TTM earnings of Crispr Therapeutics AG (CRSP) is negative, P/E ratio is not available.
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CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. Its CRISPR/Cas9 is a gene editing technology that allows for precise directed changes to genomic DNA. The company has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company's 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. It also develops CTX110, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting cluster of differentiation 19; CTX120, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting B-cell maturation antigen for the treatment of relapsed or refractory multiple myeloma; and CTX130, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting Cluster of Differentiation 70 to treat various solid tumors and hematologic malignancies. In addition, the company develops VCTX210, a gene-edited immune-evasive stem cell-derived product candidate for the treatment of treatment of type 1 diabetes; and VCTX211, an investigational, allogeneic, gene-edited, stem cell-derived product candidate for the treatment of T1D. It has strategic partnerships with Bayer Healthcare LLC, Vertex Pharmaceuticals Incorporated, ViaCyte, Inc., Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland.
The CEO & director of Dr. Samarth Kulkarni Ph.D.. is Crispr Therapeutics AG (CRSP), and CFO & Sr. VP is Mr. Brendan Smith M.B.A..
The promoters of Crispr Therapeutics AG (CRSP) have pledged 0% of the total equity as on Jun-23.
Some of the close peers are:
Company | Market Cap($ Mln) |
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313
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299
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226
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100
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Crispr Therapeutics AG (CRSP) | Ratios |
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Return on equity(%)
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-22.53
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Return on capital employed(%)
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--
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Debt-to-equity ratio
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0
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Dividend yield(%)
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0
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No, TTM profit after tax of Crispr Therapeutics AG (CRSP) was $-338 Mln.
CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious diseases using its Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) platform. Its CRISPR/Cas9... is a gene editing technology that allows for precise directed changes to genomic DNA. The company has a portfolio of therapeutic programs across a range of disease areas, including hemoglobinopathies, oncology, regenerative medicine, and rare diseases. The company's 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. It also develops CTX110, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting cluster of differentiation 19; CTX120, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting B-cell maturation antigen for the treatment of relapsed or refractory multiple myeloma; and CTX130, a donor-derived gene-edited allogeneic CAR-T investigational therapy targeting Cluster of Differentiation 70 to treat various solid tumors and hematologic malignancies. In addition, the company develops VCTX210, a gene-edited immune-evasive stem cell-derived product candidate for the treatment of treatment of type 1 diabetes; and VCTX211, an investigational, allogeneic, gene-edited, stem cell-derived product candidate for the treatment of T1D. It has strategic partnerships with Bayer Healthcare LLC, Vertex Pharmaceuticals Incorporated, ViaCyte, Inc., Nkarta, Inc., and Capsida Biotherapeutics. CRISPR Therapeutics AG was incorporated in 2013 and is headquartered in Zug, Switzerland. Read more
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