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Biomarker, Enrollment change, Trial completion date, Trial withdrawal, Trial primary completion date: A Biomarker Evaluation Trial of UAB30 in Renal Transplant Recipients at High Risk for Non-melanoma Skin Cancer (clinicaltrials.gov) - Dec 27, 2023 P1/2, N=0, Withdrawn, Our data also show the critical role of miRs responsive to UAB30 treatment in cancer chemoprevention. N=84 --> 0 | Trial completion date: Aug 2025 --> Aug 2023 | Recruiting --> Withdrawn | Trial primary completion date: Aug 2024 --> Aug 2023
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Biomarker, Trial completion date, Trial primary completion date, IO biomarker: A Biomarker Evaluation Trial of UAB30 in Renal Transplant Recipients at High Risk for Non-melanoma Skin Cancer (clinicaltrials.gov) - Aug 30, 2023 P1/2, N=84, Recruiting, Conclusions The RXR agonists have an immunostimulatory role with plasmid cancer vaccines, but further modification of the immune environment may be needed for prevention vaccines. Trial completion date: Aug 2024 --> Aug 2025 | Trial primary completion date: Aug 2023 --> Aug 2024
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Epigenetic mechanism underlying pathogenesis of skin photo-damage and actinic keratoses (Section 36; Poster Board #5) - Mar 14, 2023 - Abstract #AACR2023AACR_3322; 9cUAB30 treatment attenuates growth of human SCC xenograft tumors in highly immune-suppressed mice, a response which was significantly more profound when the drug was administered with a survivin inhibitor, LQZ-7I. These translational studies demonstrate that UVB-induced cutaneous BRD4 drives AK pathogenesis and their progression to invasive SCCs.
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PIM Kinase Inhibition Results in Neuroblastoma Differentiation (H0100: Section on Surgery) - Nov 10, 2022 - Abstract #AAPNCE2022AAP_NCE_1748; These findings are potentially mediated through increased HOXC9. These data support the need for further studies of the role of PIM kinase inhibition as a therapeutic strategy to improve RA-induced differentiation, potentially mitigating disease relapse in high risk neuroblastoma.
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Biomarker, Trial completion date, Trial primary completion date, IO biomarker: A Biomarker Evaluation Trial of UAB30 in Renal Transplant Recipients at High Risk for Non-melanoma Skin Cancer (clinicaltrials.gov) - Aug 31, 2022 P1/2, N=84, Recruiting, These data support the need for further studies of the role of PIM kinase inhibition as a therapeutic strategy to improve RA-induced differentiation, potentially mitigating disease relapse in high risk neuroblastoma. Trial completion date: Aug 2022 --> Aug 2024 | Trial primary completion date: Aug 2022 --> Aug 2023
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Clinical, Journal: Methods to Assess Activity and Potency of Rexinoids Using Rapid Luciferase-Based Assays: A Case Study with NEt-TMN. (Pubmed Central) - Mar 31, 2020 These methods have general applicability beyond this NEt-TMN case study, and can be employed to characterize and biologically evaluate other putative RXR agonists (rexinoids), and benchmarked against perhaps the most common rexinoid known as bexarotene (Bex), a drug awarded FDA approval for the treatment of cutaneous T-cell lymphoma in 1999 but that is also prescribed for non-small cell lung cancer and continues to be explored in multiple human cancer types...Notable examples of potent rexinoids in addition to Bex and NEt-TMN include CD3254, LGD100268, and 9-cis-UAB30...In addition, a second, more sensitive assay is also detailed that utilizes activation of RXR-RXR homodimers in the context of a mammalian two-hybrid (M2H) luciferase assay. Methods for applying the M2H assay at different rexinoid concentrations are further described for the determination of EC values for rexinoids from dose-response curves.
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Clinical, Journal: Methods to Generate an Array of Novel Rexinoids by SAR on a Potent Retinoid X Receptor Agonist: A Case Study with NEt-TMN. (Pubmed Central) - Mar 31, 2020 These methods have been extensively applied beyond the present case study to generate several analogs of other potent RXR agonists (rexinoids), particularly the RXR agonist known as bexarotene (Bex), a Food and Drug Administration (FDA) approved drug for cutaneous T-cell lymphoma that is also often prescribed, off-label, for breast, lung, and other human cancers...Some of the more prominent examples include LGD100268, CD3254, and 9-cis-UAB30, to name only a few...For the synthesis of the modified base-structure analogs, often identical synthetic strategies used to access the base-structure are applied; however, reasonable alternative synthetic routes may need to be explored if the modified analog intermediates encounter bottlenecks where yields are negligible for a given step in the base-structure route. In fact, this particular problem was encountered and successfully resolved in our case study for generating an array of NEt-TMN analogs.
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Preclinical, Journal: A novel retinoid X receptor agonist, UAB30, inhibits rhabdomyosarcoma cells in vitro. (Pubmed Central) - Jun 7, 2019 Both CD133-enriched and CD133-depleted medulloblastoma cell populations demonstrated sensitivity to UAB30, indicating its potential as a therapeutic option for group 3 medulloblastoma. The results of these studies suggest a potential therapeutic role for the low-toxicity synthetic retinoid X receptor selective agonist, UAB30, in RMS treatment.
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Enrollment closed, Trial initiation date: Retinoid 9cUAB30 in Preventing Cancer in Healthy Volunteers (clinicaltrials.gov) - Aug 16, 2016 P1, N=40, Active, not recruiting, Active, not recruiting --> Completed Initiation date: Sep 2015 --> Aug 2013 | Recruiting --> Active, not recruiting
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Enrollment open, Trial initiation date, Trial primary completion date: Retinoid 9cUAB30 in Preventing Cancer in Healthy Volunteers (clinicaltrials.gov) - Oct 22, 2015 P1, N=40, Recruiting, Initiation date: Sep 2015 --> Aug 2013 | Recruiting --> Active, not recruiting Terminated --> Recruiting | Initiation date: Aug 2013 --> Sep 2015 | Trial primary completion date: Sep 2014 --> Nov 2016
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Phase classification: Study of 9cUAB30 in Healthy Participants (clinicaltrials.gov) - Jun 18, 2015 P1, N=15, Completed, Terminated --> Recruiting | Initiation date: Aug 2013 --> Sep 2015 | Trial primary completion date: Sep 2014 --> Nov 2016 Phase classification: P=N/A --> P1
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