Advanced CCNE1-amplified Solid Tumors, Advanced HR+/HER2- Breast Cancer, Metastatic Castration-resistant Prostate Cancer (mCRPC)
Conditions
Keywords
ERW316, fulvestrant, letrozole, hormone receptor positive, HER-2 negative, Breast cancer, CCNE1 amplification, Prostate cancer
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.
Interventions
DRUGERW316
Oral administration
DRUGFulvestrant
Intramuscular injection. Approved medication.
DRUGLetrozole
Oral administration. Approved medication.
Sponsors
Novartis Pharmaceuticals
Study design
Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Age ≥ 18 years old * Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1. * 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. Phase II: • 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/
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Phase I: Incidence and severity of dose-limiting toxicities (DLTs) | 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) | 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 | 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 | Up to approximately 2 years | Dose intensity defined as the ratio of actual cumulative dose received and actual duration of exposure. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Phase I and Phase II: Best Overall Response (BOR) | Up to approximately 2 years | BOR per RECIST v1.1 is defined as the best overall confirmed response recorded from the start of the treatment until progressive disease (PD), death, start of new therapy, withdrawal of consent or end of study, whatever comes first. Efficacy will be based on the investigator assessment per Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1), or Prostate Cancer Working Group 3 (PCWG3) criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| Phase I and Phase II: Overall Response Rate (ORR) | Up to approximately 2 years | ORR per RECIST v1.1 is defined as the proportion of patients with a BOR of Complete response (CR) or Partial response (PR). Efficacy will be based on the investigator assessment per RECIST v1.1, or PCWG3 criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| Phase I and Phase II: Disease Control Rate (DCR) | Up to approximately 2 years | DCR per RECIST v1.1 is defined as the proportion of patients with a BOR of CR, PR, or Stable disease (SD). Efficacy will be based on the investigator assessment per RECIST v1.1, or PCWG3 criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| Phase I and Phase II: Clinical Benefit Rate (CBR) | Up to approximately 2 years | CBR per RECIST v1.1 is defined as the proportion of patients with a BOR of CR, PR, or an overall lesion response of SD or Non-CR/Non-PD which lasts for at least 24 weeks. Efficacy will be based on the investigator assessment per RECIST v1.1, or PCWG3 criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| Phase I and Phase II: Progression Free Survival (PFS) | Up to approximately 2 years | PFS per RECIST 1.1 is defined as the time from the date of start of study treatment (Phase I) or the date of randomization (Phase II) to the date of the first documented progression or death due to any cause. Efficacy will be based on the investigator assessment per RECIST v1.1, or PCWG3 criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| Phase II: Duration of Response (DOR) | Up to approximately 2 years | DOR per RECIST v1.1 is the time between the first documented response (CR or PR) and the date of progression by local review as applicable or death due to any cause. Efficacy will be based on the investigator assessment per RECIST v1.1, or PCWG3 criteria including PCWG3-modified RECIST v1.1 (only for patients with prostate cancer). |
| 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 | Pharmacokinetic (PK) parameters based on plasma concentrations of ERW316. |
| 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 | PK parameters based on plasma concentrations of ERW316. |
| 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 | PK parameters based on plasma concentrations of ERW316. |
Outcome results
None listed