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A novel human disease model of alopecia areata to evaluate benefit of the DHODH inhibitor farudodstat (San Diego Convention Center (Upper Level, Sails Pavilion, Poster Center 1)) - Feb 20, 2024 - Abstract #AAD2024AAD_2409; In addition, farudodstat did not induce catagen, nor did it cause cytotoxicity, affect keratinocyte proliferation, or IP marker expression in healthy HFs. These preliminary data demonstrate anti-CD3/CD28 treatment induced features of AA in an ex vivo disease model and provide promising evidence for the therapeutic potential of farudodstat in patients suffering from AA.
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Phase classification, Trial completion date, Trial primary completion date: FAST-AA: Investigate the Efficacy and Safety of Farudodstat Compared With Its Placebo in Adult Alopecia Areata Participants (clinicaltrials.gov) - Dec 18, 2023 P2, N=60, Recruiting, These preliminary data demonstrate anti-CD3/CD28 treatment induced features of AA in an ex vivo disease model and provide promising evidence for the therapeutic potential of farudodstat in patients suffering from AA. Phase classification: P2a --> P2 | Trial completion date: Apr 2024 --> Oct 2024 | Trial primary completion date: Feb 2024 --> Sep 2024
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Journal: Discovery of potent human dihydroorotate dehydrogenase inhibitors based on a benzophenone scaffold. (Pubmed Central) - Nov 2, 2022 Furthermore, 7d exhibited favorable safety profiles in mice and displayed effective antitumor activities with tumor growth inhibition (TGI) rates of 58.3% and 42.1% at an oral dosage of 30 mg/kg in Raji and HCT116 cells xenograft models, respectively. Taken together, these findings provide a promising hDHODH inhibitor 7d with potential activities against some tumors.
- |||||||||| farudodstat (ASLAN003) / Almirall, ASLAN Pharma, ONC201 / Chimerix
Preclinical, Journal: IMP075 targeting ClpP for colon cancer therapy in vivo and in vitro. (Pubmed Central) - Oct 12, 2022 ONC201 is a well-known caseinolytic protease (ClpP)activator with established benefits against multiple tumors, including colorectal cancer (CRC)...Our findings substantiate that IMP075 exerts excellent antitumor effects against CRC by activating ClpP-mediated impairment of mitochondrial function. Due to its superior properties, IMP075 appears to be have huge prospects for application.
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Trial completion, Enrollment change: A Dose Optimisation Study of ASLAN003 in Acute Myeloid Leukemia (clinicaltrials.gov) - Jul 2, 2021 P2a, N=24, Completed, Combining Molnupiravir with DHODH inhibitors may thus improve available therapy options for COVID-19. Recruiting --> Completed | N=56 --> 24
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Enrollment change, Trial completion date, Trial primary completion date: A Dose Optimisation Study of ASLAN003 in Acute Myeloid Leukemia (clinicaltrials.gov) - Jan 11, 2019 P2a, N=56, Recruiting, ASLAN003 is currently being evaluated in phase 2a clinical trial in acute myeloid leukemia patients. N=38 --> 56 | Trial completion date: Dec 2019 --> Aug 2020 | Trial primary completion date: Jun 2019 --> Apr 2020
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Enrollment change: A Dose Optimisation Study of ASLAN003 in Acute Myeloid Leukemia (clinicaltrials.gov) - May 31, 2018 P2a, N=38, Recruiting, N=38 --> 56 | Trial completion date: Dec 2019 --> Aug 2020 | Trial primary completion date: Jun 2019 --> Apr 2020 N=18 --> 38
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