A detailed history of Lindbrook Capital, LLC transactions in Crispr Therapeutics Ag stock. As of the latest transaction made, Lindbrook Capital, LLC holds 50 shares of CRSP stock, worth $2,394. This represents 0.0% of its overall portfolio holdings.

Number of Shares
50
Previous 32 56.25%
Holding current value
$2,394
Previous $1,000 100.0%
% of portfolio
0.0%
Previous 0.0%

Shares

16 transactions
Quarter Operation Price Per share shares change shares Held SEC Form
Q3 2024

Nov 01, 2024

BUY
$44.62 - $62.75 $803 - $1,129
18 Added 56.25%
50 $2,000
Q4 2023

Jan 31, 2024

BUY
$38.62 - $72.18 $1,042 - $1,948
27 Added 540.0%
32 $2,000
Q3 2023

Oct 25, 2023

SELL
$45.39 - $59.0 $408 - $531
-9 Reduced 64.29%
5 $0
Q2 2023

Jul 28, 2023

SELL
$43.47 - $67.77 $999 - $1,558
-23 Reduced 62.16%
14 $0
Q1 2023

Apr 26, 2023

BUY
$41.0 - $56.12 $164 - $224
4 Added 12.12%
37 $1,000
Q4 2022

Jan 24, 2023

BUY
$39.19 - $65.67 $627 - $1,050
16 Added 94.12%
33 $0
Q3 2022

Nov 10, 2022

SELL
$61.1 - $83.78 $1,222 - $1,675
-20 Reduced 54.05%
17 $1,000
Q2 2022

Aug 01, 2022

SELL
$43.23 - $73.83 $778 - $1,328
-18 Reduced 32.73%
37 $2,000
Q1 2022

Apr 21, 2022

BUY
$53.19 - $79.24 $1,861 - $2,773
35 Added 175.0%
55 $3,000
Q4 2021

Jan 18, 2022

BUY
$70.09 - $111.29 $1,401 - $2,225
20 New
20 $2,000
Q2 2021

Jul 27, 2021

SELL
$100.84 - $161.89 $2,924 - $4,694
-29 Closed
0 $0
Q1 2021

Apr 28, 2021

SELL
$110.72 - $210.04 $2,325 - $4,410
-21 Reduced 42.0%
29 $4,000
Q4 2020

Jan 27, 2021

BUY
$79.67 - $173.23 $3,186 - $6,929
40 Added 400.0%
50 $8,000
Q3 2020

Nov 03, 2020

BUY
$78.5 - $100.64 $785 - $1,006
10 New
10 $1,000
Q4 2019

Jan 27, 2020

SELL
$36.68 - $73.13 $2,017 - $4,022
-55 Closed
0 $0
Q4 2018

Feb 07, 2019

BUY
$22.73 - $42.34 $1,250 - $2,328
55 New
55 $1,000

Others Institutions Holding CRSP

About CRISPR Therapeutics AG


  • Ticker CRSP
  • Exchange NASDAQ
  • Sector Healthcare
  • Industry Biotechnology
  • Shares Outstandng 78,009,296
  • Market Cap $3.74B
  • Description
  • CRISPR Therapeutics AG, a gene editing company, focuses on developing gene-based medicines for serious diseases using its proprietary 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....
More about CRSP
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