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NCT Number: NCT05753657

A Pilot Study of Monitoring Insulin Levels and Treating Hyperinsulinemia and Hyperglycemia With Pioglitazone in Patients Treated With Alpelisib for Metastatic Breast Cancer.

The goal of this study is to test whether monitoring insulin levels and using pioglitazone to treat hyperglycemia and hyperinsulinemia in patients treated with Alpelisib for metastatic breast cancer is feasible and safe, and to assess the rates of glycemic control, dose reductions and treatment discontinuation and the progression free survival of patients treated with this regimen.

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Key information

Age range

18 year–85 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

Primary location

Rambam Health Care Campus

Haifa, 3109601, Israel

Location status: Recruiting

Location contact

Ayalet Shai, MD

CONTACT

[email protected]

About this study

  • To assess the feasibility and safety of monitoring insulin levels alongside glucose levels and of directing antidiabetic treatment according to insulin and fasting glucose levels in patients treated with Alpelisib for metastatic breast cancer.
  • To assess the feasibility and safety of treatment with pioglitazone in these patients.
  • To assess the rate of severe (grade 3-4) hyperglycemia in patients treated according to this protocol.
  • To assess the rates of dose reductions and treatment discontinuation due to hyperglycemia in patients treated according to this protocol.
  • To assess the median progression free survival of patients treated according to this protocol

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with ER positive HER2 negative metastatic breast cancer, harboring an activating PIK3CA mutation, scheduled to start treatment with Alpelisib and fulvestrant.
  • Ages 18 - 85
  • ECOG performance status 0, 1 or 2
  • Ability to understand and willingness to sign a written informed consent.

Exclusion criteria

  • Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of Alpelisib
  • Uncontrolled diabetes mellitus, defined as HbA1c above 8%
  • Diabetes mellitus controlled by insulin
  • Uncontrolled intercurrent illness including, but not limited to: active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • Pregnancy
  • Known allergy to pioglitazone

Treatment and study plan

pioglitazone

Drug

hyperinsulinemia and hyperglycemia

Primary outcomes

  1. Rate of severe (grade 3 and 4) hyperglycemia in patients enrolled in the study and in patients treated per protocol

    Time frame: through study completion, an average of 1 year

  2. Rate of all grade hyperglycemia in patients enrolled in the study and in patients treated per protocol

    Time frame: through study completion, an average of 1 year

  3. Progression free survival in patients enrolled in the study and in patients treated per protocol

    Time frame: through study completion, an average of 1 year

Study contacts

Contact information is provided by the study sponsor or research team.

Ayelet Shai, MD

CONTACT

[email protected]

+972-4-777-6700

Sponsors and collaborators

Lead sponsor

Rambam Health Care Campus

Other

Registry information

Important dates

Study start
2022
Primary completion
2026
Study completion
2027
First posted
Mar 3, 2023
Registry last updated
Mar 3, 2023

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.

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