Publications by authors named "Janice Jia Ni Goh"

Background: Phase 2a trials in tuberculosis typically use early bactericidal activity (EBA), the decline in sputum CFU over 14 days, as the primary end-point for testing the efficacy of drugs as monotherapy. However, the cost of phase 2a trials can range from USD 7 million to USD 19.6 million on average, while >30% of drugs fail to progress to phase 3.

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Background: Phase 2a trials in tuberculosis typically use early bactericidal activity (EBA), the decline in sputum colony forming units (CFU) over 14 days, as the primary outcome for testing the efficacy of drugs as monotherapy. However, the cost of phase 2a trials can range from 7 to 19.6 million dollars on average, while more than 30% of drugs fail to progress to phase 3.

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Cytochrome P450 1A1 (CYP1A1) metabolizes estrogens, melatonin, and other key endogenous signaling molecules critical for embryonic/fetal development. The enzyme has increasing expression during pregnancy, and its inhibition or knockout increases embryonic/fetal lethality and/or developmental problems. Here, we present a virtual screening model for CYP1A1 inhibitors based on the orthosteric and predicted allosteric sites of the enzyme.

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The objectives of this study are to compare steady-state trough (Cmin,ss) and peak (Cmax,ss) concentrations of rivaroxaban between Asians and Caucasians and to evaluate the relationship between rivaroxaban concentrations and prothrombin time/international normalized ratio (PT/INR). Recruited patients were advised on the time to take rivaroxaban. Cmin,ss and PT/INR were taken when patients arrived.

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Article Synopsis
  • - Rivaroxaban is a medication used to prevent strokes in patients with nonvalvular atrial fibrillation, and its clearance mainly involves enzymes CYP3A4, CYP2J2, and P-glycoprotein (P-gp).
  • - Antiarrhythmic drugs like amiodarone and dronedarone, while managing atrial fibrillation, can inhibit these enzymes, potentially increasing rivaroxaban levels in the body by reducing its clearance.
  • - In vitro studies showed that dronedarone and its metabolite affected rivaroxaban metabolism more significantly than amiodarone, predicting an increase in rivaroxaban exposure by 37% and 31%, with additional
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