CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


RifampinWiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (5)


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

Correlated MeSH Terms (10)


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

Correlated HPO Terms (6)


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

Clinical Trials


1 Antibiotic Treatment Trial Directed Against Chlamydia Pneumonia in Multiple Sclerosis

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.

NCT00043264 Multiple Sclerosis Drug: Rifampin Drug: Azithromycin
MeSH:Pneumonia Multiple Sclerosis Sclerosis
HPO:Pneumonia


2 A Phase 1 Open-Label, Fixed-Sequence Drug-Drug Interaction Study to Evaluate the Effects of Steady-state Itraconazole and Rifampin on the Single-dose Pharmacokinetics of Lazertinib Tablets in Healthy Adult Participants

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.

NCT04410094 Healthy Drug: Lazertinib Drug: Itraconazole Drug: Rifampin

Primary Outcomes

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 dose

Description: 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 dose

Description: 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 dose

Description: 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 dose

Description: %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 dose

Secondary Outcomes

Description: 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)


Related HPO nodes (Using clinical trials)