Efficacy and Safety of Tenalisib (RP6530), in Patients With Locally Advanced or Metastatic Breast Cancer

NCT ID: NCT05021900

Last Updated: 2024-08-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-10-13
• Study Completion Date: 2023-03-31

Brief Summary

Phase II, randomized, open-label study, designed to evaluate the preliminary efficacy and safety of tenalisib at two dose levels in 40 patients with locally advanced or metastatic breast cancer.

Detailed Description

The study will have two groups, Group 1 with a treatment option of 800mg RP6530 BID and Group 2 with a treatment option of 1200mg RP6530 BID, where the subjects will be randomly assigned to each group in 1:1 and continued on each group of treatment till disease progressed.

Conditions

Locally Advanced Breast Cancer; Metastatic Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Tenalisib 800 mg BID

Single agent at a dose of 800 mg BID

Group Type: EXPERIMENTAL

Tenalisib 800mg

Intervention Type: DRUG

Tenalisib will be administered 800mg BID, orally

Tenalisib 1200 mg BID

Single agent at a dose of 1200 mg BID

Group Type: EXPERIMENTAL

Tenalisib 1200mg

Intervention Type: DRUG

Tenalisib will be administered 1200mg BID, orally

Interventions

Tenalisib 800mg

Tenalisib will be administered 800mg BID, orally

Intervention Type: DRUG

Tenalisib 1200mg

Tenalisib will be administered 1200mg BID, orally

Intervention Type: DRUG

Other Intervention Names

RP6530; RP6530

Eligibility Criteria

Inclusion Criteria

1. Patients must be ≥18 years of age, at the time of signing informed consent.

2. Female patients who have histologically and/or cytologically confirmed locally advanced or metastatic breast cancer that has progressed following at least one line of therapy.

3. Patients with at least one measurable lesion per RECIST version 1.1 at baseline that can be accurately assessed by CT scan or MRI and is suitable for repeated assessment at follow up-visits.

4. ECOG performance status 0 to 2.

5. Life expectancy of at least 3 months.

6. Adequate bone marrow, liver, and renal functions

7. Female patients of childbearing potential should be willing to use a medically acceptable method of contraception

Exclusion Criteria

1. Patients with HER-2 positive breast cancer.

2. Patients receiving anticancer therapy within 4 weeks or 5 half-lives of the drug prior to C1D1, whichever is shorter.

3. Patient who has not recovered from acute toxicities (defined as NCI-CTCAE grade > 1) of previous therapy except treatment-related alopecia.

4. Patients who have had disease progression within 8 weeks of platinum chemotherapy.

5. Prior exposure to investigational or marketed PI3K inhibitors given for the treatment of breast cancer.

6. Major surgery within 4 weeks of starting study treatment OR any patient who has not recovered from the effects of major surgery.

7. Patient with symptomatic uncontrolled brain metastasis.

8. HIV-positive patients who are on antiretroviral therapy OR active hepatitis C OR active hepatitis B virus infections.

9. Ongoing immunosuppressive therapy including systemic corticosteroids except as allowed per concomitant medication.

10. Known history of severe liver injury as judged by the investigator.

11. History of severe cutaneous reactions in the past.

12. Active gastrointestinal tract disease with malabsorption syndrome or uncontrolled inflammatory gastrointestinal disease such as Crohn's disease or ulcerative colitis.

13. Pregnancy or lactation.

14. Patient with other active malignancies at the time of screening.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Rhizen Pharmaceuticals SA

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

High Technology Hospital Medcenter

Batumi, , Georgia

LLC Caucasus Medical Center

Tbilisi, , Georgia

Simon Khechinashvili University Hospital

Tbilisi, , Georgia

Countries

Georgia

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Statistical Analysis Plan

View Document

Other Identifiers

RP6530-2101

Identifier Type: -

Identifier Source: org_study_id