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Dillingh M, et al. Front. Immunol. 2016;7(508):1-9. * Data on file. 25 - No serious adverse events or adverse events that led to discontinuation of study medication - All adverse events were mild in severity and did not interfere with everyday activities - A trend of a decrease in absolute neutrophil count was observed; no correlation with clinical sequelae o This effect is consistent with the pharmacodynamic profile of certain anti-TNF therapies1 Copyright 2020 Aclaris Therapeutics, Inc.
Wang C, et al. J Exp Med. 2018;215(5):1315-1325. 2. Strasser S, et al. Integrative Biology. 2019;11(7):301-314. 0.8 1 1.2 1.4 1.6 1.8 2 2.2 2.4 2.6 2.8 0 5 10 15 20 Paw Volume - ml Study Day Vehicle CDD450 - 10 MPK CDD450 - 5 MPK CDD110 - 1.5 MPK Oral dosing initiated vehicle ATI-450 IL1 (bone marrow fluid) CDD-450 - + - + 0 10 20 30 40 50 60 70 ( p g ) ( n g / m l ) 0 0.5 1.0 1.5 2.0 2.5 3.0 Normal NOMID CDD-450 - + - + Normal NOMID IL6 (serum) ( p g ) 0 10 20 30 40 50 60 70 CDD-450 - + - + Normal NOMID IL18 (bone marrow fluid) ATI-450 ATI-450 ATI-450 ATI-450 PLACEBO 17 Copyright 2020 Aclaris Therapeutics, Inc.
J Exp Med. 2018;215(5):1315-1325. Inflammatory Bowel Disease Adoptive transfer mouse model of colitis - Endoscopy scores show disease control - Decreased inflammatory infiltrate - Protected structural integrity of mucosa Strasser S, et al. Integrative Biology. 2019;11(7):301-314. Cryopyrin-Associated Periodic Syndromes (CAPS) Murine NOMID (severe form of CAPS) transgenic model Human CAPS PBMC* IL1 modulation Wang C, et al.
Wang C, et al. J Exp Med. 2018;215(5):1315-1325. * Data on file. ** Optimized p38 peptide substrate ATI-450 is highly selective for the p38 /MK2 complex vs. other p38 substrates1 Assay Fold Selective p38 /MK2 1 p38 /ATF2 700 p38 /PRAK 750 ATI-450 binds to the p38 /MK2 complex with higher affinity than either p38 or MK2 alone* 0 20 40 60 80 100 120 1 3 5 7 9 11 13 15 1719 21 23 25 27 29 31 33 35 37 39 41 43 45 47 49 51 53 55 57 59 61 63 65 67 69 71 73 75 77 79 81 83 85 87 89 91 93 95 97 99 101 p38 p38 103 105 107 109 111 113 115 117 119 121 123 125 127 131 129 133 135 137 139 141 143 145 147 151 149 153 155 157 159 161 163 165 167 171 169 173 175 177 179 181 183185189 191 193 14 Copyright 2020 Aclaris Therapeutics, Inc.
Director of Chemistry at Mnemosyne, Luc, Cadent. -Inventor of 6 clinical candidates and author of 40 peer reviewed publications and patents David R Anderson, PhD Sr. Director, Discovery, Early Development -Former Exec. Director, Pfizer. Site Head for Medicinal & Structural Chemistry. ->100 patents. -Co-inventor of multiple drug candidates Gary DeCrescenzo SVP, Pharm R&D Experienced R&D Leadership Team Proven Track Record in Immunology and Inflammation 5 * All trademarks are the property of their respective owners.
Data on file. 2. Oprea TI, et al. Unexplored opportunities in the druggable human genome. Nature Rev Drug Discov. Poster Jan. 2017. 3. Manning G, et al. Science. 2002;298(5600):1912-1934. 4. Oprea TI, et al. Nat Rev Drug Discov. 2018;17(5):317-332. ** All trademarks are the property of their respective owners. 4 3 Copyright 2020 Aclaris Therapeutics, Inc.
This data involves a number of assumptions and limitations, and you are cautioned not to give undue weight to such estimates. In addition, projections, assumptions and estimates of our future performance and the future performance of the markets in which we operate are necessarily subject to a high degree of uncertainty and risk. Cautionary Note Regarding Forward-Looking Statements 2 Copyright 2020 Aclaris Therapeutics, Inc.
Securities and Exchange Commission from time to time. These documents are available under the SEC filings" section of the Investors page of Aclaris' website at http://www.aclaristx.com. Any forward-looking statements speak only as of the date of this presentation and are based on information available to Aclaris as of the date of this presentation, and Aclaris assumes no obligation to, and does not intend to, update any forward-looking statements, whether as a result of new information, future events or otherwise This presentation also contains estimates and other statistical data made by independent parties and by us relating to market size and other data about our industry.
These statements involve risks and uncertainties that could cause actual results to differ materially from those reflected in such statements. Risks and uncertainties that may cause actual results to differ materially include uncertainties inherent in the conduct of clinical trials, Aclaris' reliance on third parties over which it may not always have full control, the uncertainty regarding the COVID-19 pandemic including its impact on the timing of Aclaris' regulatory and research and development activities, and other risks and uncertainties that are described in the Risk Factors section of Aclaris' Annual Report on Form 10-K for the year ended December 31, 2019, Aclaris' Quarterly Report on Form 10-Q for the quarter ended June 30, 2020 and other filings Aclaris makes with the U.S.
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