Tenalisib
DrugTenalisib will be administered 800mg/ 400mg BID, orally
Other names: RP6530
NCT Number: NCT06189209
This is a Phase II, open-label, single-arm, study, designed to evaluate the efficacy and safety of tenalisib in patients with metastatic TNBC, who have received at least one but not more than 3 prior therapies in a metastatic setting.
Interested in participating?
Request Info18 year and older
Female
Interventional
Phase 2
HCG City Cancer Center, Vijayawada, Andhra Pradesh, India
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tenalisib will be administered 800mg/ 400mg BID, orally
Other names: RP6530
Time frame: 1 year
It is defined as the percentage of patients achieving complete response (CR), partial response (PR), or stable disease (SD) for 16 weeks or longer.
Time frame: 1 year
It is defined as the time from the first dose to disease progression or death on study from any cause, whichever occurs first in patients who achieve CR, PR or SD for 16 weeks or longer.
Time frame: 1 year
Overall Response is defined as sum of CR and PR.
Time frame: 1 year
It is defined as the time from the first dose to disease progression or death on study from any cause, whichever occurs first.
Time frame: 1 year
Number of adverse events reported by the patients
Time frame: 1 year
plasma concentrations of drug
Time frame: 1 year
Baseline mutational status and its correlation with efficacy
Contact information is provided by the study sponsor or research team.
Rhizen Pharmaceuticals SA
Industry
A Phase II, Multi-center, Single-arm, Open-label Study to Assess the Efficacy and Safety of Tenalisib, a PI3K δ/γ, and SIK3 Inhibitor, in Patients With Metastatic Triple Negative Breast Cancer (TNBC)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07652242
Breast Diseases, Breast Neoplasms
Grand Rapids, Michigan, United States
View Trial DetailsNCT07630961
Breast Diseases, Breast Neoplasms
Chuo Ku, Tokyo, Japan
View Trial DetailsNCT06606730
Breast Cancers, Breast Diseases
Brussels, Belgium
View Trial DetailsNCT07705334
Adenoma, Advanced or Metastatic Solid Tumors
Denver, Colorado, United States
View Trial Details