Name (Synonyms) | Correlation | |
---|---|---|
drug1326 | Lazertinib Wiki | 0.71 |
drug1269 | Itraconazole Wiki | 0.50 |
drug332 | Best Practice Wiki | 0.41 |
drug2527 | Tocilizumab Wiki | 0.13 |
drug262 | Azithromycin Wiki | 0.12 |
Name (Synonyms) | Correlation | |
---|---|---|
D003324 | Coronary Artery Disease NIH | 0.35 |
D007676 | Kidney Failure, Chronic NIH | 0.29 |
D012598 | Scoliosi NIH | 0.25 |
D029424 | Pulmonary Disease, Chronic Obstructive NIH | 0.25 |
D009103 | Multiple Sclerosis NIH | 0.24 |
D008173 | Lung Diseases, Obstructive NIH | 0.24 |
D020521 | Stroke NIH | 0.22 |
D009369 | Neoplasms, NIH | 0.16 |
D011014 | Pneumonia NIH | 0.04 |
D007239 | Infection NIH | 0.04 |
Name (Synonyms) | Correlation | |
---|---|---|
HP:0001677 | Coronary artery atherosclerosis HPO | 0.35 |
HP:0006510 | Chronic pulmonary obstruction HPO | 0.25 |
HP:0006536 | Pulmonary obstruction HPO | 0.24 |
HP:0001297 | Stroke HPO | 0.22 |
HP:0002664 | Neoplasm HPO | 0.16 |
HP:0002090 | Pneumonia HPO | 0.04 |
There are 2 clinical trials
Multiple sclerosis (MS) is an inflammatory, demyelinating disease which affects the central nervous system (CNS). The etiology of MS is unknown, although the immune system appears to play a role. Many different infectious agents have been proposed as potential causes for MS, including Epstein-Barr virus, human herpesvirus 6, and coronaviruses. Recently Dr. Sriram at Vanderbilt University has found evidence for active Chlamydia pneumonia infection in the CNS of MS patients. These findings have been replicated in part by other laboratories. The purpose of the current study is to test whether antibiotic treatment aimed at eradicating Chlamydia infection will reduce the disease activity in MS. The primary outcome measure will be reduction in new enhancing MS lesions on brain MRI. Forty patients will be entered into the trial. To be eligible, patients must have evidence of chlamydia infection in their spinal fluid and enhancing lesions on their pre-randomization MRI scans. Patients who meet these criteria will be randomized to either placebo or antibiotic therapy, and followed for 6 months on treatment.
The purpose of this study is to evaluate the effects of multiple doses of strong cytochrome P450 (CYP) 3A4 inhibitor itraconazole and strong CYP3A4 inducer rifampin on the single dose pharmacokinetics (PK) of lazertinib in healthy adult participants.
Description: Cmax is defined as maximum plasma concentration.
Measure: Cohort 1 and 2: Maximum Plasma Concentration (Cmax) of Lazertinib Time: Predose up to 120 hours post doseDescription: AUC (0-120h) is defined as area under the plasma concentration-time curve from time 0 to 120 hours postdose.
Measure: Cohort 1 and 2: Area Under the Plasma Concentration-time Curve from Time 0 to 120 Hours (AUC [0-120h]) of Lazertinib Time: Predose up to 120 hours post doseDescription: AUC (0-last) is defined as area under the plasma concentration-time curve from time 0 to time of last quantifiable timepoint.
Measure: Cohort 1 and 2: Area Under the Plasma Concentration-time Curve from Time Zero to Time of Last Quantifiable Timepoint (AUC [0-last]) of Lazertinib Time: Predose up to 120 hours post doseDescription: AUC (0-inf) is defined as area under the plasma concentration-time curve from time 0 to infinity, calculated as the sum of AUC(0-last)+C(last)/ lambda(z), where C(last) is the last observed measurable (non-below limit of quantification) concentration.
Measure: Cohort 1 and 2: Area Under the Plasma Concentration-time Curve from Time Zero to Infinity (AUC [0-inf]) of Lazertinib Time: Predose up to 120 hours post doseDescription: %AUC (0-inf),ex is defined as percentage of area under the plasma concentration from time zero to infinite time obtained by extrapolation, calculated as (AUC [0-infinity] minus AUC [0-last]/AUC [0-infinity])*100.
Measure: Cohort 1 and 2: Percentage of Area Under the Plasma Concentration from time Zero to Infinite time obtained by Extrapolation (%AUC [0-inf],ex) of Lazertinib Time: Predose up to 120 hours post doseDescription: An AE is any untoward medical occurrence in a clinical study participant administered a investigational or non investigational medicinal product. An AE does not necessarily have a causal relationship with the treatment.
Measure: Cohort 1 and Cohort 2: Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability Time: Up to 65 days (Cohort 1) and up to 70 days (Cohort 2)