Crispr Therapeutics AG
A biotech company that turns the CRISPR gene-editing discovery into medicines for serious inherited diseases. Its first approved therapy, Casgevy, treats sickle cell disease and beta-thalassemia by editing a patient's own blood stem cells. Co-founded in 2013 by Emmanuelle Charpentier — one of the scientists who shared the Nobel Prize for discovering CRISPR — along with Rodger Novak and Shaun Foy, the company takes its name directly from the gene-editing system it commercializes.
| Holder | Schedule | % of class | Shares | Filed |
|---|---|---|---|---|
| ORBIS INVESTMENT MANAGEMENT LTD | 13G/APassive | 5.6% | 5.43M | Aug 14, 2026 |
| Allan Gray Australia Pty Ltd | 13G/APassive | 0% | 15.8K | Aug 14, 2026 |
| BlackRock, Inc. | 13G/APassive | 8.3% | 7.99M | Jul 27, 2026 |
| Capital World Investors | 13GPassive | 5.1% | 4.93M | May 14, 2026 |
| ARK Investment Management LLC | 13G/APassive | 11.79% | 11.31M | Apr 30, 2026 |
| Catherine D. Wood | 13G/APassive | 11.79% | 11.31M | Apr 30, 2026 |
| Capital International Investors | 13G/APassive | 1.2% | 1.19M | Feb 5, 2026 |