An Open-label, Multi-center, Phase I/II Study of ERW316 as a Single Agent or in Combination With Endocrine Therapy in Patients With HR+/HER2- Breast Cancer and Other Advanced Solid Tumors
Trial Snapshot
- Phase
- Phase 1
- Status
- Withdrawn
- Sponsor
- Novartis Pharmaceuticals
- Enrollment
- 217
- Primary Endpoint
- Phase I: Incidence and severity of dose-limiting toxicities (DLTs)
Study Overview
Brief Summary
Phase I: Characterize safety and tolerability of ERW316 as a single agent and in combination with fulvestrant or letrozole. Identify dose range for optimization/recommended dose for further clinical evaluation.
Phase II: Further characterize the safety and tolerability of ERW316 in combination with fulvestrant in patients with hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) advanced breast cancer.
Detailed Description
This is a first-in-human, open-label, Phase I/II, multi-center study consisting of an ERW316 single agent arm in patients with advanced HR+/HER2- breast cancer, other advanced solid tumors harboring CCNE1 amplification, and metastatic castration-resistant prostate cancer, and a combination treatment arm of ERW316 with fulvestrant or letrozole in patients with advanced HR+/HER2- breast cancer. Single agent escalation may be followed by an expansion part stratified by disease indication. The escalation of the fulvestrant combination arm may continue into a randomized, open-label, Phase II with optional dose optimization in advanced HR+/HER2- breast cancer patients.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Sequential
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Age ≥ 18 years old
- •Eastern Cooperative Oncology Group (ECOG) performance status of ≤
- •Patients with one of the following histologically or cytologically confirmed advanced cancers:
- •Phase I (patients with one of the following cancers, for whom no standard therapy is available or appropriate in the judgment of the investigator):
- •HR+/HER2- advanced breast cancer (aBC) with disease progression on or following at least one line of hormone-based therapy in combination with a CDK4/6i and at least one additional line of systemic therapy for metastatic disease.
- •Locally advanced or metastatic cancer with CCNE1- amplification. For dose expansion only: no more than 5 prior lines of therapy (ovarian cancer) or 3 prior lines of therapy (gastric or esophageal adenocarcinoma).
- •Metastatic castration-resistant prostate adenocarcinoma (mCRPC), with no documented neuroendocrine component, castrate level of testosterone, disease progression on or after at least one line of androgen receptor pathway inhibitor therapy (ARPI) and at least one line of taxane-based chemotherapy, and no more than 3 total prior lines of systemic therapy for metastatic disease.
- •HR+/HER2- aBC with disease progression on or after an endocrine therapy in combination with a CDK4/6 inhibitor for advanced disease, with no more than 2 total lines of endocrine therapy and no prior cytotoxic chemotherapy or antibody-drug conjugate therapy for advanced disease.
- •Phase I and Phase II:
- •- Measurable disease as determined by RECIST v1.1, with the following exceptions: aBC only: If no measurable disease is present, then at least one predominantly lytic bone lesion must be present that can be accurately assessed at baseline and is suitable for repeated assessment.
- •mCRPC only: If no measurable disease is present per PCWG3 modified RECIST, then at least one metastatic lesion must be present on bone scan imaging
Exclusion Criteria
- •Patients with inadequate bone marrow and/or organ function
- •Presence of symptomatic central nervous system (CNS) metastases or CNS metastases that require local therapy or increasing doses of corticosteroids within 2 weeks prior to study entry.
- •Patients with symptomatic visceral disease, including visceral crisis.
- •For patients with breast cancer only: Patient is concurrently using hormone replacement therapy.
- •Women of childbearing potential (WOCBP) who are unwilling to use highly effective contraception methods
- •Pregnant or nursing women
- •Other protocol-defined inclusion/exclusion criteria may apply.
Arms & Interventions
Phase II, RD-2 (optional dose optimization): ERW316 in combination with Fulvestrant (Arm E)
ERW316 in combination with fulvestrant.
Intervention: ERW316 (Drug)
Phase II, RD-2 (optional dose optimization): ERW316 in combination with Fulvestrant (Arm E)
ERW316 in combination with fulvestrant.
Intervention: Fulvestrant (Drug)
Phase II, recommended dose (RD)-1: ERW316 in combination with Fulvestrant (Arm D)
ERW316 in combination with fulvestrant.
Intervention: ERW316 (Drug)
Phase I: ERW316 in combination with letrozole (Arm C)
ERW316 in combination with letrozole.
Intervention: Letrozole (Drug)
Phase I: ERW316 single agent (Arm A)
ERW316
Intervention: ERW316 (Drug)
Phase I: ERW316 in combination with Fulvestrant (Arm B)
ERW316 in combination with fulvestrant.
Intervention: ERW316 (Drug)
Phase I: ERW316 in combination with Fulvestrant (Arm B)
ERW316 in combination with fulvestrant.
Intervention: Fulvestrant (Drug)
Phase I: ERW316 in combination with letrozole (Arm C)
ERW316 in combination with letrozole.
Intervention: ERW316 (Drug)
Phase II, recommended dose (RD)-1: ERW316 in combination with Fulvestrant (Arm D)
ERW316 in combination with fulvestrant.
Intervention: Fulvestrant (Drug)
Outcomes
Primary Outcomes
Phase I: Incidence and severity of dose-limiting toxicities (DLTs)
Time Frame: 28 days
Number of participants with DLTs. A DLT is defined as an adverse event or abnormal laboratory value of Common Terminology Criteria for Adverse Events (CTCAE) grade ≥ 3, unless clearly and inconvertibly assessed as due to disease progression, inter-current illness/injury, concomitant medications, or extraneous causes, that occurs within the first 28 days of treatment in the Phase I part. Other clinically significant toxicities may be considered to be DLTs, even if not CTCAE grade 3 or higher.
Phase I and Phase II: Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Time Frame: Up to approximately 2 years
Number of participants with AEs and SAEs, including changes in laboratory values, vital signs and echocardiograms (ECGs) qualifying and reported as AEs.
Phase I and Phase II: Frequency of dose interruptions, reductions and discontinuations
Time Frame: Up to approximately 2 years
Number of participants with dose adjustments (interruptions, reductions, or permanent discontinuation) as a measure of tolerability.
Phase I and Phase II: Dose intensity
Time Frame: Up to approximately 2 years
Dose intensity defined as the ratio of actual cumulative dose received and actual duration of exposure.
Secondary Outcomes
- Phase I and Phase II: Best Overall Response (BOR)(Up to approximately 2 years)
- Phase I and Phase II: Overall Response Rate (ORR)(Up to approximately 2 years)
- Phase I and Phase II: Disease Control Rate (DCR)(Up to approximately 2 years)
- Phase I and Phase II: Clinical Benefit Rate (CBR)(Up to approximately 2 years)
- Phase I and Phase II: Progression Free Survival (PFS)(Up to approximately 2 years)
- Phase II: Duration of Response (DOR)(Up to approximately 2 years)
- Phase I and Phase II: Area under the plasma concentration-time curve (AUC) of ERW316(From pre-dose up to 24 hours after dosing on Cycle 1 Day 1 and Day 22. 1 cycle = 28 days)
- Phase I and Phase II: Maximum plasma concentration (Cmax) of ERW316(From pre-dose up to 24 hours after dosing on Cycle 1 Day 1 and Day 22. 1 cycle = 28 days)
- Phase I and Phase II: Time to reach maximum plasma concentration (Tmax) of ERW316(From pre-dose up to 24 hours after dosing on Cycle 1 Day 1 and Day 22. 1 cycle = 28 days)