Breast Cancer Clinical Trial

Study of TTI-101 in Combination for Participants With Metastatic Hormone Receptor-Positive and Human Epithelial Receptor 2 (HER2)-Negative Breast Cancer

Summary

The primary objectives of the Phase 1b part of this study are to evaluate the safety and tolerability of TTI-101 when added to palbociclib and aromatase inhibitor (AI) administered orally to participants with estrogen receptor-positive (ER+) human epithelial receptor 2-negative (HER2-) palbociclib-resistant breast cancer, and to determine the recommended Phase 2 dose (RP2D) for TTI-101 when added to palbociclib and AI.

The primary objective of the Phase 2 part of this study is to evaluate tumor response by Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 criteria in participants who receive TTI-101 added to palbociclib and AI.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Participants must meet all the following criteria to be eligible:

Age ≥18 years at the time of informed consent.
Metastatic or locally advanced breast cancer not amenable to curative treatment by surgery or radiotherapy.

Currently receiving palbociclib and AI therapy in the metastatic setting with evidence of progressive disease. In addition:

Must have remained on palbociclib and AI therapy for ≥6 months for advanced breast cancer or metastatic disease prior to evidence of progression that in the opinion of the treating physician warrants continued therapy with palbociclib and AI.
Must be continuing on palbociclib at a dose of 125, 100, or 75 mg administered orally for 21 days every 28-day cycle.
All men and premenopausal women must be on medical gonadal suppression therapy with a gonadotropin analog (e.g, goserelin or leuprolide) and have estrogen levels in the postmenopausal range by institutional criteria at baseline.
Has an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Has documented confirmation of histological or cytological hormone receptor-positive (estrogen receptor-positive [ER+], human epithelial receptor 2-negative [HER2-]) breast cancer per local laboratory testing.
Only 1 prior line of systemic treatment (palbociclib and AI) in the locally advanced or metastatic setting is allowed; the participant must have shown evidence of progressive disease on palbociclib and AI in the locally advanced or metastatic setting prior to enrollment.
Willing to provide a representative fresh tumor tissue specimen prior to enrollment. The fresh tumor specimen must be obtained after evidence of progression on first-line palbociclib and AI.
The presence of measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 is required. Lesions in a previously irradiated area that have not progressed are not considered measurable.

Exclusion Criteria:

Participants meeting any of the following exclusion criteria will not be eligible:

Has received more than 1 line of prior systemic therapy for locally advanced/metastatic breast cancer.
Had prior exposure to any signal transducer and activator of transcription 3 (STAT3) inhibitor.
Had radiotherapy within 3 weeks prior to Cycle 1 Day 1 (cycle is 28 days). Participants must have recovered from radiotherapy toxicities prior to starting study treatment and recovered to Grade 1 or better from related side effects of such therapy (with the exception of alopecia).
Has human epithelial receptor 2 (HER2) overexpression by local laboratory testing (immunohistochemical [IHC] 3+ or in situ hybridization positive).
Has known loss of retinoblastoma tumor suppressor gene (Rb) or estrogen receptor 1 (ESR1) activating mutation (testing not mandatory).
Has had disease progression on more than one cyclin-dependent kinase (CDK)4/6 inhibitor or has progressed more than once on the same CDK4/6 inhibitor.
Concurrently using other anticancer therapy. Participants should continue palbociclib and AI therapy.

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

53

Study ID:

NCT05384119

Recruitment Status:

Recruiting

Sponsor:

Tvardi Therapeutics, Incorporated

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There are 3 Locations for this study

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Washington University School of Medicine Siteman Cancer Center
Saint Louis Missouri, 63110, United States
Gabrail Cancer Center Research
Canton Ohio, 44718, United States
University of Texas MD Anderson Cancer Center
Houston Texas, 77030, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 1

Estimated Enrollment:

53

Study ID:

NCT05384119

Recruitment Status:

Recruiting

Sponsor:


Tvardi Therapeutics, Incorporated

How clear is this clinincal trial information?

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