Study of SRF617 With AB928 (Etrumadenant) and AB122 (Zimberelimab) in Patients With Metastatic Castration Resistant Prostate Cancer

Prostate Cancer Clinical Trial

Official title:

A Phase 2 Trial of SRF617 in Combination With AB928 (Etrumadenant) and AB122 (Zimberelimab) in Patients With Metastatic Castration-Resistant Prostate Cancer

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT05177770
• Other study ID #: SRF617-201
• Status: Terminated
• Phase: Phase 2
• Start date: January 17, 2022
• Est. completion date: April 5, 2023

Study information

• Verified date: May 2024
• Source: Coherus Biosciences, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This trial will look at the safety and preliminary efficacy of SRF617 in combination with etrumadenant and zimberelimab in patients with metastatic castration-resistant prostate cancer (mCRPC).

Description:

This is a phase 2, open-label, safety and preliminary efficacy trial in patients with mCRPC using the combination of SRF617, etrumadenant (AB928), and zimberelimab (AB122).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 16
• Est. completion date: April 5, 2023
• Est. primary completion date: April 5, 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• = 18 years of age.

• Metastatic CRPC with castrate levels of testosterone (= 50 ng/dL or = 1.7 nmol/L).

• Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.

• Progressed (by PSA or radiologic criteria) during or following treatment with a novel androgen receptor signaling inhibitor (ARSI, eg, abiraterone, enzalutamide, apalutamide, darolutamide), which may have been given for either hormone-sensitive prostate cancer or CRPC.

• Received 1 to 2 prior lines of taxane chemotherapy, unless the physician and patient believe the patient is medically ineligible or the patient refuses (ineligibility or refusal must be documented in the source documents).

• Progressed by PSA or radiologic criteria on or during last therapy for prostate cancer.

• Measurable or non-measurable disease as per radiographic evaluation. Lesions situated in a previously irradiated area are considered evaluable if progression has been demonstrated in such lesions since radiation.

• Note: If disease is considered non-measurable, a minimum PSA of 1 ng/dL is required with at least 1 confirmed rise at a minimum of a 1-week interval.

• Adequate hematologic function, defined as absolute neutrophil count = 1.5 × 109/L, hemoglobin = 9.0 g/dL, and platelet count = 100 × 109/L. Transfusions are permitted to meet hemoglobin and platelet criteria. However, the patient must have a stable hemoglobin level and platelet count for = 2 weeks prior to dosing without transfusion.

• Adequate renal function, defined as serum creatinine clearance = 30 mL/min per Cockcroft-Gault formula.

• Total bilirubin = 1.5 × upper limit of normal (ULN) (= 3 × ULN if elevated because of Gilbert's syndrome, and = 2 × ULN for patients with known liver metastases).

• Aspartate aminotransferase and alanine aminotransferase < 2.5 × ULN (< 5 × ULN if liver metastases present).

• Prothrombin time (PT) or international normalized ratio (INR) and activated partial thromboplastin time (aPTT) = 1.5 × ULN unless the patient is receiving anticoagulant therapy, in which case PT/INR or aPTT must be within therapeutic range of intended use of anticoagulants.

Exclusion Criteria:

• Currently participating in or has participated in a trial of an investigational device or has used an investigational device within 21 days before the first dose of study drug.

• Any component of small cell or neuroendocrine histology.

• Previously received an anti-CD39 antibody, anti-CD39 targeted therapy, or other agent targeting the adenosine pathway.

• Prior treatment with programmed death-ligand 1 (PD-L1)/programmed death receptor-1 (PD-1) inhibitors.

• Prior treatment with = 3 lines of taxane chemotherapy administered as a single agent or as part of a combination regimen.

• Symptomatic or untreated brain metastases (including leptomeningeal metastases). Patients previously treated for brain metastases must be at least 4 weeks from completion of radiation treatment with follow-up imaging showing no progression.

• Current pneumonitis with or without steroid requirement or history of pneumonitis requiring steroids.

• Another malignancy other than prostate within 2 years of trial entry, except for those with a low risk of spreading or negligible risk of death such as non-melanoma skin cancer or Ta superficial bladder cancer.

• Active autoimmune disease that has required systemic treatment in past 2 years (ie, with use of disease modifying agents, corticosteroids, or immunosuppressive drugs).

• Medical conditions requiring chronic steroid (ie, > 10 mg/day of prednisone or its equivalent).

• Note: Replacement therapy (eg, levothyroxine, insulin, or physiologic corticosteroid replacement therapy for thyroid, adrenal, or pituitary insufficiency) is allowed.

• Administration of a live attenuated vaccine within 6 weeks before the first dose of study drug.

• Exception: Health Authority approved COVID-19 vaccines are permitted.

• Any gastrointestinal condition that would preclude the use of oral medications (eg, difficulty swallowing, nausea, vomiting, or malabsorption).

Related Conditions & MeSH terms

• Metastatic Castration-resistant Prostate Cancer
• Prostate Cancer
• Prostatic Neoplasms

Intervention

Drug:
• SRF617
SRF617 is a fully human antibody designed to inhibit the enzymatic activity of CD39.
• etrumadenant
Etrumadenant is an A2aR and A2bR antagonist.
• zimberelimab
Zimberelimab is a fully human anti-PD-1 monoclonal antibody.

Locations

Country	Name	City	State
Canada	Université de Montreal - Centre de Recherche du Centre Hospitalier de L'Université de Montreal (CRCHUM)	Montréal	Quebec
Canada	BC Cancer - The Vancouver Centre	Vancouver	British Columbia
United States	University of Michigan Health System	Ann Arbor	Michigan
United States	UT Southwestern	Dallas	Texas
United States	Comprehensive Cancer Centers of Nevada	Las Vegas	Nevada
United States	University of Miami - Sylvester Comprehensive Cancer Center	Miami	Florida
United States	START South Texas Accelerated Research Therapeutics, LLC	San Antonio	Texas
United States	Fred Hutchinson Cancer Research Center	Seattle	Washington
United States	START Mountain Region, Utah Cancer Specialists	West Valley City	Utah

Sponsors (3)

Lead Sponsor	Collaborator
Coherus Biosciences, Inc.	Arcus Biosciences, Inc., Surface Oncology

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants With Response	Response was defined as Prostate-Specific Antigen (PSA) decline of = 50% (PSA50) and/or radiographic objective response of Complete Response (CR) or Partial Response (PR) per Prostate Cancer Working Group 3 (PCWG3) Criteria. The number of participants with response shows participants with any one or combination of these response types.; CR: Disappearance of all extranodal target lesions. All pathological lymph nodes must have decreased to < 10 millimeters (mm) in short axis; PR: At least a 30% decrease in the sum of diameters of target lesions, taking as reference the Baseline sum of diameters	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Primary	Number of Participants With Adverse Events (AEs)	An AE was defined as any untoward medical occurrence in a participant who received study drug without regard to possibility of causal relationship. Serious Adverse Events (SAEs) were defined as death, a life-threatening AE, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant disability or incapacity, a congenital anomaly or birth defect, or an important medical event that jeopardized participant and required medical intervention to prevent 1 of the outcomes listed in this definition. A summary of other non-serious AEs and all serious AEs, regardless of causality is located in Reported AE section.	From date of first dose until 90 days after the last dose of treatment (maximum treatment exposure: 168 days)
Secondary	Number of Participants With Response Per PCWG3 Criteria	The number of participants achieving CR or PR by PCWG3 criteria is reported: CR: Disappearance of all extranodal target lesions. All pathological lymph nodes must have decreased to < 10 millimeters (mm) in short axis; PR: At least a 30% decrease in the sum of diameters of target lesions, taking as reference the Baseline sum of diameters; Progressive Disease (PD): At least a 20% increase in the sum of diameters of target lesions from the smallest value on trial (including Baseline, if that is the smallest). The sum of diameters must also demonstrate an absolute increase of at least 5 mm. Or, the appearance of one or more lesions; Stable Disease (SD): Neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Duration of Response (DOR)	DOR was defined as the time from first documented response (PSA50 and/or CR/PR) to documented disease progression as determined by applicable disease criteria, or documented death due to any cause, whichever occured first.	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Disease Control Rate (DCR)	DCR was defined as the percentage of participants with CR, PR, or SD lasting a minimum of 12 weeks by PCWG3 or PSA50 criteria.	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Number of Participants With PSA50 Response	PSA50 response is defined as a confirmed PSA decrease from Baseline of 50% or more based on 2 consecutive assessments measured 3 to 4 weeks apart.	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Number of Participants With PSA Decline of = 30% (PSA30) Response	PSA30 response is defined as a confirmed PSA decrease from Baseline of 30% or more based on 2 consecutive assessments measured 3 to 4 weeks apart.	From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Time to PSA Progression		From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Radiographic Progression Free Survival (PFS)		From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Landmark PFS Rate	Landmark PFS was defined as the percentage of participants who have not developed PFS events of death or documented disease progression as determined by applicable disease criteria.	Months 6 and 12
Secondary	Maximum Observed Serum Concentration of SRF617 (Cmax)		From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Minimum Observed Serum Concentration of SRF617 Prior to Administration of Subsequent Dose (Cmin)		From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Number of Participants With Antidrug Antibodies (ADAs)		From the date of first dose administration to the end of treatment (maximum exposure: 168 days)
Secondary	Number of Participants With Symptomatic Skeletal Events (SSEs)	Number of participants with SSEs per PCWG3 criteria, defined as symptomatic fracture, radiation or surgery to bone, or spinal cord compression, is reported.	From date of first dose until 90 days after the last dose of treatment (maximum treatment exposure: 168 days)