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NCT Number: NCT06189209

Efficacy and Safety of Tenalisib in Patients With Metastatic Triple Negative Breast Cancer (TNBC)

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

HCG City Cancer Center, Vijayawada, Andhra Pradesh, India

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients who have histologically confirmed TNBC.
  • Patients who have received at least 1 but not more than 3 prior chemotherapy regimens in a metastatic setting.
  • Patients with at least one measurable lesion, per RECIST version 1.1 at baseline . Bone-only disease is not permitted.
  • ECOG performance status 0 to 2.
  • Adequate bone marrow, liver, and renal function

Exclusion criteria

  • Cancer therapy/ any cancer investigational drug within 3 weeks (21 days) or 5 half-lives (whichever is shorter).
  • Patient who has not recovered from acute toxicities of previous therapy except treatment-related alopecia.
  • Prior exposure to PI3K inhibitors (e.g., alpelisib, buparlisib) for breast cancer.
  • Major surgery within 4 weeks of starting study treatment.
  • Patient with symptomatic uncontrolled brain metastasis.
  • Ongoing immunosuppressive therapy including systemic corticosteroids.
  • History of severe cutaneous reactions.
  • Concurrent disease or condition that would interfere with study participation
  • Pregnancy or lactation.
  • Any severe and/or uncontrolled medical conditions or other conditions that could affect patient participation

Treatment and study plan

Tenalisib

Drug

Tenalisib will be administered 800mg/ 400mg BID, orally

Other names: RP6530

Primary outcomes

  1. Clinical Benefit Rate (CBR)

    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.

  2. Duration of Clinical Benefit (DoCB)

    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.

  3. Overall Response Rate (ORR)

    Time frame: 1 year

    Overall Response is defined as sum of CR and PR.

  4. Progression Free Survival (PFS)

    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.

Secondary outcomes

  1. Number of Participants With Treatment-emergent Adverse Events as Assessed by CTCAE v5.0

    Time frame: 1 year

    Number of adverse events reported by the patients

  2. Trough plasma concentrations of tenalisib/metabolite

    Time frame: 1 year

    plasma concentrations of drug

  3. Correlation of efficacy to baseline mutational status

    Time frame: 1 year

    Baseline mutational status and its correlation with efficacy

Study contacts

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

Prajak Barde, MD

CONTACT

[email protected]

+41325800175

Sponsors and collaborators

Lead sponsor

Rhizen Pharmaceuticals SA

Industry

Collaborators

  • Incozen Therapeutics Pvt Ltd

Registry information

Official study title

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)

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Jan 3, 2024
Registry last updated
Dec 2, 2025

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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