Clinical Trials Directory

Trials / Completed

CompletedNCT05904730

Phase I Clinical Trials Investigating the Potential Efficacy of Axitinib in Patients With a BRCA 1/2 Mutations

Phase I Clinical Trials Investigating the Potential Efficacy of Axitinib in Patients With a BRCA 1/2 Mutations Independent of HER2 Expression With Progression After Previous Treatment

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Lynkcell Europe · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This Clinical Trial is investigating the potential efficacy of axitinib after genetic testing in BRCA 1/2 Mutation patients, regardless of HER2 expression, who have progressed after at least one line of standard treatment or for whom there is no consensus treatment approach. The use of Axitinib may help physicians plan for more effective patient care in combination with existing treatment protocols.

Detailed description

This Clinical Trial is investigating the potential efficacy of axitinib after genetic testing in BRCA 1/2 Mutation patients, regardless of HER2 expression, who have progressed after at least one line of standard treatment or for whom there is no consensus treatment approach. The use of Axitinib may help physicians plan for more effective patient care in combination with existing treatment protocols. The addition of Axitinib to existing treatment protocols and to fractionated irradiation without functional normalization of the tumor vasculature can significantly improve response to therapy, contributing to the breakdown of the metabolic symbiosis of adaptive drug resistance.

Conditions

Interventions

TypeNameDescription
DRUGAxitinibThe starting dose of axitinib is 5 mg twice daily by mouth with meals. (reception is desirable at the same time every day)

Timeline

Start date
2023-07-11
Primary completion
2024-11-09
Completion
2024-12-26
First posted
2023-06-15
Last updated
2024-12-30

Locations

2 sites across 1 country: Ukraine

Source: ClinicalTrials.gov record NCT05904730. Inclusion in this directory is not an endorsement.