CovidResearchTrials by Shray Alag


CovidResearchTrials Covid 19 Research using Clinical Trials (Home Page)


Selitrectinib (BAY2731954)Wiki

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


Correlated Drug Terms (1)


Name (Synonyms) Correlation
drug1978 Questionnaire Wiki 0.21

Correlated MeSH Terms (3)


Name (Synonyms) Correlation
D007239 Infection NIH 0.06
D045169 Severe Acute Respiratory Syndrome NIH 0.05
D018352 Coronavirus Infections NIH 0.04

Correlated HPO Terms (0)


Name (Synonyms) Correlation

There is one clinical trial.

Clinical Trials


1 An Open-label, Non-randomized, Phase I Study to Evaluate the Pharmacokinetics of Selitrectinib (BAY 2731954) and Food Effects in Healthy Adult Male Participants

The researchers in this study want to gather information in healthy adult male participants about how the human body absorbs, distributes and excretes the drug selitrectinib including the effect of the interaction of food with the study drug on the human body. Selitrectinib is a new drug under development for the treatment of patients with solid tumor caused by a genetic abnormality known as an NTRK gene fusion which cannot be cured by currently available treatment options or has spread to other parts of the body. The drug blocks the action of the NTRK gene fusion and prevents the activation of certain proteins (TRK fusion proteins), which can cause cancer cells to multiply and form a tumor. Researchers also want to find out if the participants have any medical problems during this study. Participants in this study will receive the study drug twice with at least 6 days in between. The study drug will be taken orally as a liquid before or after meal. Observation will last for up to 8 weeks, and blood samples will be taken from the participants to measure the blood levels of the study drug.

NCT04275960 Solid Tumors Harboring NTRK Fusion Drug: Selitrectinib (BAY2731954)

Primary Outcomes

Measure: Maximum concentration of selitrectinib in plasma in fasted state (Cmax_fasted)

Time: Up to 3 days

Measure: Area under the concentration-time curve of selitrectinib in plasma from time 0 to 24 hours in fasted state (AUC(0-24)_fasted)

Time: Up to 1 day

Measure: Area under the concentration-time curve of selitrectinib in plasma from time 0 to infinity in fasted state (AUC_fasted)

Time: Up to 3 days

Measure: Maximum concentration of selitrectinib in plasma in fed state (Cmax_fed)

Time: Up to 3 days

Measure: Area under the concentration-time curve of selitrectinib in plasma from time 0 to 24 hours in fed state (AUC(0-24)_fed)

Time: Up to 1 days

Measure: Area under the concentration-time curve of selitrectinib in plasma from time 0 to infinity in fed state (AUC_fed)

Time: Up to 3 days

Secondary Outcomes

Measure: Number of participants with treatment-emergent adverse events (TEAEs)

Time: Up to 23 weeks


No related HPO nodes (Using clinical trials)