32 Participants NeededMy employer runs this trial

Sapanisertib + Serabelisib for Breast Cancer

Recruiting at 6 trial locations
MM
Overseen ByMedical Monitor
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests two drugs, sapanisertib and serabelisib, to determine their effectiveness with fulvestrant in treating advanced breast cancer that is hormone receptor-positive (HR+) and human epidermal growth factor receptor 2-negative (HER2-). The goal is to assess the safety and efficacy of these drugs for individuals whose cancer has spread or recurred after treatment. It targets those diagnosed with HR+/HER2- breast cancer that cannot be treated with surgery or radiation and have undergone at least one other therapy. As a Phase 1, Phase 2 trial, the research focuses on understanding the treatment's effects and measuring its efficacy in an initial, smaller group, offering participants a chance to contribute to early-stage cancer treatment advancements.

Do I have to stop taking my current medications for the trial?

The trial requires that you stop taking strong CYP3A4 inhibitors, strong CYP1A2 inhibitors or inducers, or clinically significant CYP3A4 inducers at least 7 days before starting the study. If you are on these medications, you will need to stop them before participating.

Is there any evidence suggesting that this trial's treatments are likely to be safe?

Earlier research tested the combination of sapanisertib and serabelisib with another drug, paclitaxel. These studies showed that the combination was safe and generally well-tolerated by patients. Participants did not report major safety issues, indicating that most people could handle the treatment. Overall, the combination demonstrated promising results in terms of safety and effectiveness. This suggests that sapanisertib and serabelisib are safe options for those considering joining the trial.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about the combination of Sapanisertib and Serabelisib for breast cancer because it targets cancer cells in a unique way. Unlike traditional treatments like hormone therapies or chemotherapy, this combo specifically inhibits mTOR and PI3K pathways, which are key players in cancer cell growth and survival. This targeted approach could minimize damage to healthy cells, potentially leading to fewer side effects. Additionally, the combination is taken orally, offering a convenient alternative to some intravenous treatments. By combining these drugs with fulvestrant, which is a standard hormonal therapy, researchers hope to enhance treatment effectiveness against resistant types of breast cancer.

What evidence suggests that this trial's treatments could be effective for breast cancer?

Research has shown that combining the drugs sapanisertib and serabelisib may help treat certain cancers. These drugs target key pathways in cancer cells, potentially stopping their growth. In this trial, participants will receive sapanisertib and serabelisib, along with fulvestrant, in varying dosages across two cohorts. Early results indicated that 73% of patients experienced some benefit, with their cancer not growing for about 11 months on average. Although more research is needed, these findings offer hope that these drugs could also be effective for advanced breast cancer.13678

Are You a Good Fit for This Trial?

This trial is for adults with HR+/HER2- advanced or metastatic breast cancer that can't be cured by surgery or radiation. Participants must have had at least one prior treatment, be in good physical condition, and not be pregnant or breastfeeding.

Inclusion Criteria

My breast cancer is HR positive and HER2 negative.
My cancer is advanced or has come back and cannot be cured with surgery or radiation.
I am fully active or have only minor limitations in daily activities.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive sapanisertib and serabelisib (PIKTOR) with fulvestrant and/or other anticancer therapies

6 months
Regular visits for dose escalation and monitoring

Follow-up

Participants are monitored for safety and effectiveness after treatment

6 months
Periodic visits for safety and efficacy assessments

Long-term follow-up

Participants are monitored for progression-free survival and overall survival

Up to 5 years

What Are the Treatments Tested in This Trial?

Interventions

  • Sapanisertib
  • Serabelisib

Trial Overview

The study tests different combinations of sapanisertib and serabelisib (PIKTOR) with fulvestrant and possibly other cancer drugs to find safe doses and see how well they work against this type of breast cancer.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Group I: Cohort A2 - Sapanisertib and serabelisib (PIKTOR) with fulvestrantExperimental Treatment3 Interventions
Group II: Cohort A1 - Sapanisertib and serabelisib (PIKTOR) with fulvestrantExperimental Treatment3 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Faeth Therapeutics

Lead Sponsor

Trials
4
Recruited
170+

Citations

Sapanisertib and Serabelisib (PIKTOR) in Various ...

The study is a Phase 1b/2, multi-center, open-label, dose escalation trial evaluating the safety and preliminary efficacy of sapanisertib and serabelisib ( ...

2.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/35843739/

Phase I dose escalation study of dual PI3K/mTOR ...

The combination of sapanisertib, serabelisib, and paclitaxel was safe and generally well tolerated. Preliminary efficacy was remarkable in an area of unmet ...

Sapanisertib and serabelisib (PIKTOR) with paclitaxel and ...

This study evaluates whether PIKTOR with paclitaxel improves efficacy outcomes in participants with advanced/recurrent endometrial cancer.

Serabelisib, sapanisertib (PIKTOR) and paclitaxel

The Phase 1 study combined the targeted PI3K-alpha and mTOR inhibitors serabelisib and sapanisertib (PIKTOR) with paclitaxel showing reasonable safety and ...

Sapanisertib and Serabelisib (PIKTOR) in Various ...

The study is a Phase 1b/2, multi-center, open-label, dose escalation trial evaluating the safety and preliminary efficacy of sapanisertib ...

Final results of phase 1 evaluation of the safety and clinical ...

Conclusions: Overall, the combination of sapanisertib, serabelisib, and paclitaxel was safe and efficacious throughout the first 4 cohorts.

Patient Reported Outcomes and Final Results of Phase 1 ...

Conclusions: Overall, the combination of sapanisertib, serabelisib, and paclitaxel was safe and well-tolerated throughout the first four cohorts. Preliminary ...

Results of a phase Ib trial evaluating the safety and clinical ...

The combination proved to be well tolerated in the doses and schedules used in cohorts 1-4 and exhibited very promising clinical activity in heavily pretreated ...