AMXI-5001 / AtlasMedx 
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  • ||||||||||  AMXI-5001 / AtlasMedx
    Journal, Combination therapy:  Novel dual action PARP and microtubule polymerization inhibitor AMXI-5001 powerfully inhibits growth of esophageal carcinoma both alone and in combination with radiotherapy. (Pubmed Central) -  Feb 7, 2024   
    We found that AMXI-5001 was the most potent growth inhibitor of 8 out of 9 different esophageal carcinoma cell lines compared to other clinically available PARP inhibitors, Olaparib, Niraparib, Rucaparib, and Talazoparib...To further assess AMXI-5001's potential as a therapeutic for esophageal carcinoma we evaluated the effect of AMXI-5001 in combination with standard chemotherapy agents, Cisplatin and 5 Fluorouracil...Compared to vehicle control, and those treated with either AMXI-5001 alone or radiation alone, mice treated with both AMXI-5001 and radiation had significant tumor response. In conclusion, AMXI-5001 is an orally bioavailable dual-action PARP and microtubule polymerization inhibitor that holds promise in the treatment of esophageal carcinoma.
  • ||||||||||  AMXI-5001 / AtlasMedx
    Enrollment change, Trial completion date, Trial primary completion date, Metastases:  ATLAS-101: A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies (clinicaltrials.gov) -  Jul 21, 2023   
    P1/2,  N=122, Recruiting, 
    In conclusion, AMXI-5001 is an orally bioavailable dual-action PARP and microtubule polymerization inhibitor that holds promise in the treatment of esophageal carcinoma. N=80 --> 122 | Trial completion date: Jan 2023 --> Jan 2025 | Trial primary completion date: Jan 2023 --> Jan 2025
  • ||||||||||  AMXI-5001 / AtlasMedx
    Journal, BRCA Biomarker, PARP Biomarker:  AMXI-5001, a novel dual parp1/2 and microtubule polymerization inhibitor for the treatment of human cancers. (Pubmed Central) -  Sep 10, 2020   
    AMXI-5001 resulted in superior anti-tumor effects compared to either single agent (PARP or microtubule) inhibitor or combination with both agents. AMXI-5001 will enter clinical trial testing soon and represents a promising, novel first in class dual PARP1/2 and microtubule polymerization inhibitor that delivers continuous and synchronous one-two punch cancer therapy with one molecule.