COMMITMENT TO A CURE
Investor Presentation
January 2021
cellectis.com
FORWARD-LOOKING STATEMENTS
This presentation contains "forward-looking" statements that are based on our management's current expectations and assumptions and on information currently available to management.
Forward-looking statements involve known and unknown risks, uncertainties and other factors that may cause our actual results, performance or achievements to be materially different from those expressed or implied by the forward-looking statements.
Factors that may cause actual results to differ from those in any forward-looking statement, include the duration and severity of the COVID-19 pandemic and responsive measures; inconclusive clinical trial results or clinical trials failing to achieve one or more endpoints; early data not being repeated in ongoing or future clinical trials; failures to secure required regulatory approvals; disruptions from failures by third-parties on whom we rely in connection with our clinical trials; delays or negative determinations by regulatory authorities; changes or increases in oversight and regulation; increased competition;
manufacturing delays problems; inability to achieve enrollment disagreements with our collaboration partners of collaboration partners to pursue product legal challenges or intellectual property disputes; disruptions to access to raw materials or starting material.
Further information on risks and factors that may affect company business and financial performance, is included in our annual report on form 20-F and the financial report (including the management report) for the year ended December 31, 2019 and subsequent filings Cellectis makes with the Securities and Exchange Commission from time to time.
Except as required by law, we assume no obligation to update these forward-looking statements publicly, or to update the reasons actual results could differ materially from those anticipated in the forward-looking statements, even if new information becomes available in the future.
Cellectis proprietary information. Not to be copied, distributed or used without Cellectis' prior written consent.
P2
WRITING THE HISTORY OF ALLOGENEIC CAR T-CELLS
21 years | 9 years | 7 clinical trials |
of expertise in | of experience in allogeneic | ongoing as of 2020; |
gene editing | CAR-T manufacturing | 3 Cellectis-sponsored |
4 partnered |
INVENTORS / PIONEERS OF GENE EDITING & ALLOGENEIC CAR T-CELLS
In 2012 . .
Mission to develop allogeneic CAR T-cells begins
In 2015 . .
First-in-man compassionate use of an allogeneic CAR-T product candidate occurs
P3
ADVANTAGES OF ALLOGENEIC VS. AUTOLOGOUS CAR-T
Autologous process: | Manufacturing variability + several weeks before treatment is available | |||
1. | 2. | 3. | 4. |
CANCER TREATMENT | CANCER | MANUFACTURING OF A | INDIVIDUAL CAR-T |
DECISION | PATIENT APHERESIS | SINGLE PATIENT | THERAPY |
PRODUCT |
Allogeneic process:
Consistent manufacturing + quality | Immediate treatment | |||
HEALTHY DONOR | SCALABLE | MASS PRODUCED | 1. | 2. |
APHERESIS | MANUFACTURING | ALLOGENEIC CAR-T | CANCER TREATMENT | OFF-THE-SHELF |
OF 100+ DOSES/BATCH | THERAPIES | DECISION | CAR-T THERAPY |
- TIME SAVED
- COST EFFECTIVE
- MARKET ACCESS
P4
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Cellectis SA published this content on 08 January 2021 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 08 January 2021 21:15:04 UTC