Vidutolimod (CMP-001) in Combination With Nivolumab for the Treatment of Metastatic Castration Resistant Prostate Cancer

NCT05445609 | Suspended Phase 2 DMC FDA Drug

• 3 other identifiers: STUDY00004226NCI-2022-05290WINSHIP5576-22
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

This phase II trial tests whether vidutolimod with nivolumab works to destroy tumor cells in patients with castration resistant prostate cancer that has spread to other places in the body (metastatic). Nivolumab is an antibody working by attaching to and blocking a molecule called PD 1. PD 1 is a protein that is present on different types of cells in the immune system and controls parts of the immune system by shutting it down. Antibodies (proteins in the immune system which act to stop infection harming the body) that block PD 1 can potentially prevent PD 1 from shutting down the immune system, thus allowing immune cells to recognize and destroy cancer cells. Vidutolimod (CMP-001) is a Toll-like receptor 9 (TLR9) agonist, with the ability to generate tumor-targeted T cells capable of killing a tumor both locally and systemically in combination with checkpoint inhibitors (nivolumab, in this case), thus potentially improving outcomes for people whose tumors are progressing. Giving nivolumab and vidutolimod may kill more cancer cells in patients with metastatic prostate cancer.

Conditions

Metastatic Prostate Adenocarcinoma; Stage IV Prostate Cancer AJCC v8

Outcome Measures

Primary Outcomes (1)

• Safety of Treatment

  Will be summarized descriptively using frequencies and percentages of all captured toxicities by severity and relevance.

  Up to 24 months

Secondary Outcomes (5)

• Serum prostate-specific antigen (PSA) response

  Up to 24 weeks from treatment initiation

• Radiographic progression free survival (rPFS)

  At 1 year

• Overall survival (OS)

  At 1 year

• Objective response rate (ORR)

  Up to 24 months

• ORR

  Up to 24 months

Study Arms (1)

Treatment ((vidutolimod, nivolumab)

EXPERIMENTAL

Patients receive vidutolimod SC on days 1 and 7 of cycle 1, IT on day 14 of cycle 1 and days 1 and 14 of cycle 2, and then SC on day 1 of subsequent cycles. Patients also receive nivolumab IV over 30 minutes on days 1 and 14 of cycle 2 and on day 1 of subsequent cycles. Cycles of nivolumab repeat every 4 weeks for up to 24 months in the absence of disease progression or unacceptable toxicity. Cycles of vidutolimod repeat every 4 weeks for up to 6 months in the absence of disease progression or unacceptable toxicity.

Drug: VLP-encapsulated TLR9 Agonist CMP-001,; Biological: Nivolumab

Interventions

VLP-encapsulated TLR9 Agonist CMP-001, DRUG

Given SC or IT

Also known as: ARB-1598, CMP-001, CYT 003, CYT-003

Treatment ((vidutolimod, nivolumab)

Nivolumab BIOLOGICAL

Given IV

Also known as: 946414-94-4, BMS-936558, CMAB819, MDX-1106, NIVO, Nivolumab Biosimilar CMAB819, ONO-4538, Opdivo

Treatment ((vidutolimod, nivolumab)

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male \>= 18 years of age
• Histologically confirmed adenocarcinoma of the prostate with metastatic disease
• Subjects who are refractory to a novel antiandrogen therapy (abiraterone, darolutamide, enzalutamide and/or apalutamide) and have failed at least 1 taxane based chemotherapy regimen (or who are deemed medically unsuitable to be treated with a taxane regimen or have actively refused treatment with a taxane regimen)
• Prior orchiectomy or serum testosterone levels \< 50 ng/dL determined within 4 weeks prior to start of study drug
• Having measurable disease per RECIST 1.1 (at least one additional lesion \>= 0.5 cm amenable to repeated IT injection per investigator)
• Eastern Cooperative Oncology Group performance status of 0 or 1
• Neutrophil count \>= 1,000/mm\^3 (within 4 weeks prior to the first dose of CMP-001)
• Platelet count \>= 100,000/mm\^3 (within 4 weeks prior to the first dose of CMP-001)
• Hemoglobin concentration \>= 9 g/dL (within 4 weeks prior to the first dose of CMP-001)
• Total bilirubin =\< 1.5 times the upper limit of normal (ULN) with the following exception: subjects with Gilbert Disease serum bilirubin \>= 3 times ULN (within 4 weeks prior to the first dose of CMP-001)
• Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 times the ULN or =\< 5 times the ULN for patients with active liver metastases (within 4 weeks prior to the first dose of CMP-001)
• Serum creatinine =\< 1.5 times the ULN or calculated creatinine clearance \>= 40 mL/min (\>= 0.67 mL/sec) using the Cockcroft-Gault equation (within 4 weeks prior to the first dose of CMP-001)
• Subjects should have an international normalized ratio (INR) or a partial thromboplastin time (PTT) =\< 1.5 x ULN unless the subject is receiving anticoagulant therapy (within 4 weeks prior to the first dose of CMP-001). Subjects on anticoagulant therapy should have a prothrombin time (PT) or PTT within therapeutic range of intended use and no history of severe hemorrhage. Patients who require therapeutic anticoagulation and cannot discontinue anticoagulation safely during the day prior, day of, and day after injection are excluded. Patients requiring anticoagulation with warfarin are excluded unless they can be transitioned to an alternative anticoagulant (e.g., low molecular weight heparin or direct oral anticoagulants) prior to enrollment. Antiplatelet agents (e.g., aspirin, clopidogrel, etc.) are not considered anticoagulants for the purposes of this study (i.e., they are allowed)
• Willingness to provide pre- and post-treatment fresh tumor biopsies, if safe and medically feasible
• Male subjects must be surgically sterile or must agree to use adequate method of contraception from the time of consent until at least 120 days after the last dose of CMP-001

You may not qualify if:

• Pathological finding consistent with pure small cell, neuroendocrine carcinoma of prostate or any other histology different from adenocarcinoma
• Requires systemic pharmacologic doses of corticosteroids \> 10 mg/day prednisone within 7 days prior to the first dose of CMP-001 on C1D1
• Subjects who are currently receiving steroids at a prednisone-equivalent dose of =\< 10 mg/day do not need to discontinue steroids prior to enrollment
• Replacement doses, topical, ophthalmologic and inhalational steroids are permitted
• History of immune-related adverse event (AE) that required permanent discontinuation of anti-PD1/PDL1 antibody
• History of (non-infectious) pneumonitis that required steroids or current pneumonitis
• Patients with active autoimmune disease
• Known history of immunodeficiency
• Known additional malignancy that is progressing or requires active treatment within the past 3 years. Exceptions include basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy, ductal carcinoma in situ, non-invasive bladder cancer and thyroid cancer (except anaplastic)
• Untreated, symptomatic, or growing central nervous system (CNS) metastases
• Patients with treated and stable (defined as non-progression on a restaging contrast enhanced magnetic resonance imaging (MRI) or computed tomography (CT) at least 30 days after CNS directed therapy) CNS disease are eligible to enroll
• Patients with treated and stable CNS disease enrolled on study must be willing to undergo restaging contrast-enhanced CT or MRI every 12 weeks
• Prior allogenic tissue/solid organ transplant
• Known infection with human immunodeficiency virus, hepatitis B virus or hepatitis C virus; testing is not required unless suspected
• Received a live virus vaccination within 30 days prior to the first dose of CMP-001 on D1. Seasonal flu vaccines that do not contain live virus or COVID vaccines that administered more than 1 week prior to first dose of CMP-001 on D1 the are permitted

Sponsors & Collaborators

• Emory University: lead
• National Cancer Institute (NCI): collaborator
• Prostate Cancer Foundation: collaborator

Study Sites (1)

Emory University Hospital/Winship Cancer Institute

Atlanta, Georgia, 30322, United States

Location

MeSH Terms

Conditions

Prostatic Neoplasms

Interventions

CYT003-QbG10; Nivolumab

Condition Hierarchy (Ancestors)

Genital Neoplasms, Male; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Genital Diseases, Male; Genital Diseases; Urogenital Diseases; Prostatic Diseases; Male Urogenital Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins

Study Officials

• Mehmet A Bilen, M.D.

  Emory University Hospital/Winship Cancer Institute

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Principal Investigator

Study Record Dates

• First Submitted: June 28, 2022
• First Posted: July 6, 2022
• Study Start: June 7, 2023
• Primary Completion (Estimated): June 23, 2027
• Study Completion (Estimated): June 23, 2028
• Last Updated: September 19, 2025

Record last verified: 2025-09

Locations

US (1)