ONC201 and Atezolizumab in Obesity-Driven Endometrial Cancer

Sponsor

UNC Lineberger Comprehensive Cancer Center (Other)

Overall Status

Not yet recruiting

CT.gov ID

NCT05542407

Collaborator

Genentech, Inc. (Industry), Oncoceutics, Inc. (Industry)

Enrollment

Arms

Anticipated Duration (Months)

Study Details

Study Description

Brief Summary

Endometrial cancer (EC) is the fourth most common cancer in United States women, and alarmingly, the frequency and mortality from EC continues to rise, in part due to the obesity epidemic. Obese women with EC have a 6.3-fold increased risk of death from this disease, as compared to their non-obese counterparts. Patients with advanced/recurrent EC are unlikely to be cured by surgery, conventional chemotherapy (paclitaxel + carboplatin is the standard first-line treatment), radiation, or a combination of these. Thus, new treatments for EC are desperately needed as well as a better understanding of the impact of obesity on EC biology and treatment.

The purpose of this study is to test the safety of a combination of treatments, atezolizumab and ONC201, given based on body weight, to treat endometrial cancer. Using the combination of atezolizumab and ONC201, has not been approved by the Food and Drug Administration (FDA) for the treatment of endometrial cancer. This clinical trial will examine the treatment of atezolizumab + ONC201 in obese and non-obese subjects with metastatic/recurrent EC.

Condition or Disease	Intervention/Treatment	Phase
Endometrial Cancer Metastasis	Drug: Atezolizumab Drug: ONC201	Phase 1

Study Design

Study Type:

Interventional

Anticipated Enrollment :

58 participants

Allocation:

Non-Randomized

Intervention Model:

Parallel Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

Phase 1 Clinical Trial of ONC201 and Atezolizumab in Obesity-Driven Endometrial Cancer

Anticipated Study Start Date :

Oct 15, 2022

Anticipated Primary Completion Date :

Jan 15, 2025

Anticipated Study Completion Date :

Jan 15, 2025

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Obese Subjects with BMI > 30 kg/m2	Drug: Atezolizumab 10 mg/kg- 20 mg/kg Atezolizumab will be administered by intravenous, on day 1 of each 21-day cycle. Drug: ONC201 375 mg once weekly - 625 mg ONC201 will be administered orally, once or twice weekly.
Experimental: Non-Obese Subjects with BMI ≤ 29.9 kg/m2	Drug: Atezolizumab 10 mg/kg- 20 mg/kg Atezolizumab will be administered by intravenous, on day 1 of each 21-day cycle. Drug: ONC201 375 mg once weekly - 625 mg ONC201 will be administered orally, once or twice weekly.

Arm

Intervention/Treatment

Experimental: Obese

Subjects with BMI > 30 kg/m2

Drug: Atezolizumab

10 mg/kg- 20 mg/kg Atezolizumab will be administered by intravenous, on day 1 of each 21-day cycle.

Drug: ONC201

375 mg once weekly - 625 mg ONC201 will be administered orally, once or twice weekly.

Experimental: Non-Obese

Subjects with BMI ≤ 29.9 kg/m2

Drug: Atezolizumab

10 mg/kg- 20 mg/kg Atezolizumab will be administered by intravenous, on day 1 of each 21-day cycle.

Drug: ONC201

375 mg once weekly - 625 mg ONC201 will be administered orally, once or twice weekly.

Outcome Measures

Primary Outcome Measures

Recommended phase 2 dose (RP2D) [Up to 3 weeks]
The RP2D will be determined based on the incidence of dose-limiting toxicities (DLT)s. A DLT is defined as all grade 3 or above toxicities that are related to study treatment and occur within the first cycle of therapy. Adverse events are assessed using NCI Common Terminology Criteria for Adverse Events (CTCAE). A grading (severity) scale is provided for each AE term. Grade 1 Mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not indicated. Grade 2 Moderate; minimal, local, or noninvasive intervention indicated; limiting age-appropriate Instrumental Activities of Daily Living (ADL). Grade 3 Severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limiting self-care ADL. Grade 4 Life-threatening consequences; urgent intervention indicated. Grade 5 Death related to AE.

Secondary Outcome Measures

Overall Response Rate (ORR) [Up to 2 years]
ORR is defined as the proportion of subjects achieving response complete response (CR) or partial response(PR) assessed by RECIST v1.1. Complete Response (CR): Disappearance of all target lesions; Partial Response (PR): >=30% decrease in the sum of the longest diameter of target lesions.
Progression Free Survival (PFS) [Up to 2 years]
PFS is defined as time from first day of treatment until disease progression as defined by RECIST v1.1 or death from any cause.
Overall Survival (OS) [Up to 2 years]
OS is defined as the time of the start of study treatment to death from any cause.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

Female

Accepts Healthy Volunteers:

In order to participate in this study a subject must meet all of the eligibility criteria outlined below.

Inclusion Criteria

Ability to understand and willingness to sign a written informed consent obtained to participate in the study and HIPAA authorization for release of personal health information.
Age ≥ 18 years at the time of consent.
ECOG Performance Status of 0, 1, or 2
Histologically confirmed metastatic or recurrent EC (endometrioid, serous, clear cell, adeno-squamous and mixed histologies).
Subjects must have measurable disease, defined as at least one lesion that can be accurately measured in at least one dimension in accordance with RECIST criteria
Must have radiographic disease progression after at least 1 line of systemic cytotoxic therapy for metastatic disease or with progression within 12 months of completing adjuvant chemotherapy.
Life expectancy of at least 3 months.
Demonstrate adequate organ function as defined in the table below; all screening labs to be obtained within 72 hours prior to initiating study treatment.

Exclusion Criteria

Prior treatment with ONC201.
Prior treatment with CD137 agonists or immune checkpoint blockade therapies, including antiCTLA-4, and anti PD-L1 therapeutic antibodies
Treatment with another investigational agent or participation in another clinical trial within the last 28 days prior to initiating protocol therapy.
Subjects who have had chemotherapy or radiotherapy within 4 weeks prior to study treatment or those who have not recovered from adverse events due to agents administered more than 4 weeks prior to initiating protocol therapy.
Treatment with therapeutic oral or IV antibiotics within 2 weeks prior to initiation of protocol therapy Subjects receiving prophylactic antibiotics (e.g., to prevent a urinary tract infection or chronic obstructive pulmonary disease exacerbation) are eligible for the study.
Treatment with systemic immunostimulatory agents (including, but not limited to, interferon and interleukin 2 [IL-2]) within 4 weeks or 5 half-lives of the drug (whichever is longer) prior to initiation of protocol therapy.
Treatment with systemic immunosuppressive medication (including, but not limited to, corticosteroids, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti TNF-agents) within 2 weeks prior to initiation