Recruiting
Phase 2

DOC1021 vs. SOC

Sponsor:

Diakonos Oncology Corporation

Code:

NCT06805305

Conditions

Glioblastoma (GBM)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

DOC1021

Tumor resection

Temodar (Temozolomide)

SOC cranial radiation

Study Details

Brief summary:

The goal of this clinical trial is to learn if DOC1021 + pIFN alongside standard of care (SOC) will improve survival in adult patients newly diagnosed with glioblastoma (IDH-wt). It will also evaluate the safety of DOC1021 + pIFN. Researchers will compare DOC1021 dendritic cell immunotherapy regimen added to SOC compared to SOC treatment alone.

Participants in the DOC1021 + pIFN + SOC arm will:

  • Take filgrastim subcutaneously x 5 doses and subsequently undergo a leukapheresis collection
  • Undergo ultrasound guided perinodal DOC1021 injections every 2 weeks for a total of 3 doses
  • Receive subcutaneous pIFN injections weekly for a total of 6 doses in parallel with the DOC1021 injections

Both arms of the trial will:

\- Visit the clinic regularly to assess quality of life, symptoms, medication use, imaging, bloodwork, and to receive SOC treatment with surgery, temozolomide chemotherapy and radiation

Conditions

Glioblastoma (GBM)

Study ID

NCT06805305

Start date

Mar 17, 2025

Status verified date

Jun, 2026

Completion date

Mar, 2032

Anticipated

Primary completion date

Mar, 2030

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Provision of signed and dated informed consent form
2. Stated willingness to comply with all study procedures and availability for the duration of the study
3. Age 18 years or older
4. Presumed diagnosis of glioblastoma IDH-wt (as per the 2021 WHO Classification of CNS Tumors) deemed to be potentially resectable and deemed to be a good candidate for post-operative standard of care temozolomide and radiation therapy.

1. Surgical objective is for gross total resection (GTR)/near-total resection (NTR) de-fined as ≥ 95% of contrast enhancing (CE) tumor removed plus ≤ 1 cm3 residual CE tumor. Patients with subtotal resection will still be eligible if at least 70% of the CE tumor is resected.
2. Eligibility will be confirmed after surgery when diagnosis of glioblastoma IDH-wt confirmed prior to randomization. Randomization can occur with only IDH1 immunohistochemistry and when additional molecular testing is available, if glioblastoma IDH-wt is not confirmed, the participant will be deemed a screen failure and replaced.
3. Patients with prior biopsy or subtotal resection are eligible if no other anti-cancer treatment received for glioblastoma and additional resection indicated.
5. Ability to receive filgrastim (e.g., Neupogen), leukapheresis and 3 bi-weekly injections of DOC1021 near deep cervical lymph nodes + weekly pIFN x 6 weeks.
6. Females of reproductive potential must have a negative serum pregnancy test and agree to use effective contraception (as determined appropriate for the patient by the investigator) during study treatment.
7. Adequate kidney, liver, bone marrow function, and immune function, as follows:

1. Hemoglobin ≥ 8.0 gm/dL
2. Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3
3. Platelet count ≥ 75,000/mm3
4. Calculated creatinine clearance (CrCl) > 30 mL/min using Cockcroft and Gault for-mula:

i. For males = (140 - age\[years\]) x (body weight \[kg\]) / (72 x serum creatinine \[mg/dL\]) ii. For females = 0.85 x value from male formula e. Total bilirubin ≤ 1.5 times upper limit of normal (ULN) except in patients with Gilbert's disease for which total bilirubin must be ≤ 2 times ULN f. Aspartate transaminase AST (SGOT) and alanine aminotransferase ALT (SGPT) ≤ 3 times the ULN
8. Karnofsky Performance Score ≥ 70

Exclusion Criteria:

1. Infratentorial, recurrent, leptomeningeal or extracranial disease.
2. Patients who are pregnant or breastfeeding.
3. Known active HIV or hepatitis infection. Patients with HIV that is well-controlled and have undetectable viral titers remain eligible. Patients with history of HCV adequately treated such that RNA viral load is negative also remain eligible.
4. Any severe or uncontrolled medical condition or other condition that could affect participation in this study as determined by the investigator, including but not limited to: uncontrolled or severe cardiac disease, systemic autoimmune disorders requiring immunosuppression in the past 2 years\*, autoimmune hyper/hypothyroidism, untreated viral hepatitis, autoimmune hepatitis. \*autoimmune disorders include but are not limited to rheumatoid arthritis, psoriasis and inflammatory bowel disease and immunosuppressive medications include DMARDs like methotrexate, TNF inhibitors, IL-6 receptor blockers, CD80/86 inhibitors, anti-CD20 and JAK inhibitors
5. Treatment with another investigational drug or other experimental intervention within the last 30 days.

Study Design

Enrollment

180 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: DOC1021 + pIFN + SOC

DOC1021 administered by injection near deep-cervical lymph nodes + pIFN adjuvant with standard of care treatment

active comparator: SOC

Standard of Care treatment alone

Interventions

DOC1021

Double-loaded dendritic cell vaccine, loaded with tumor lysate and mRNA using proprietary method

Tumor resection

SOC brain tumor resection

Temodar (Temozolomide)

SOC concomitant temozolomide during radiation and adjuvant temozolomide after radiation

SOC cranial radiation

60Gy radiation over 6 weeks in 2Gy fractions

Primary outcome measure

  • Overall survival (time in months from randomization until death for each participant) [ Time Frame: 5 years ]

Central Contacts and Locations

Locations

City of Hope

Recruiting

Duarte, California, United States, 91010

Contacts

Principal Investigator:

Jana Portnow, MD

HOAG

Recruiting

Newport Beach, California, United States, 92663

Contacts

Principal Investigator:

Simon Khagi, MD

UCSF

Recruiting

San Francisco, California, United States, 94143

Contacts

Principal Investigator:

Thomas Nelson, MD

Baptist MD Anderson Cancer Center

Recruiting

Jacksonville, Florida, United States, 32207

Contacts

Principal Investigator:

Robert Cavaliere, MD

Dana-Farber Cancer Institute

Recruiting

Boston, Massachusetts, United States, 02115

Contacts

Cooper University Health Care

Recruiting

Camden, New Jersey, United States, 08103

Contacts

Principal Investigator:

Alan Turtz, MD

Rutgers Cancer Institute

Recruiting

New Brunswick, New Jersey, United States, 08901

Contacts

Principal Investigator:

Morana Vojnic, MD

Atlantic Health

Recruiting

Summit, New Jersey, United States, 07901

Contacts

Principal Investigator:

Robert Aiken, MD

Lenox Hill Hospital

Recruiting

New York, New York, United States, 10075

Contacts

UNC Lineberger Comprehensive Cancer Center

Recruiting

Chapel Hill, North Carolina, United States, 27599

Contacts

Principal Investigator:

Dominique Higgins, MD

Wake Forest University Health Sciences

Recruiting

Winston-Salem, North Carolina, United States, 27157

Contacts

Principal Investigator:

Roy E Strowd III, MD

The Ohio State University Comprehensive Cancer Center

Recruiting

Columbus, Ohio, United States, 43210

Contacts

Clinical Research Coordinator

800-293-5066jamesline@osumc.edu

Principal Investigator:

J. Bradley Elder, MD

UPMC Presbyterian Hospital

Recruiting

Pittsburgh, Pennsylvania, United States, 15213

Contacts

Principal Investigator:

Costas Hadjipanayis, MS, MD, PhD

Vanderbilt-Ingram Cancer Center

Recruiting

Nashville, Tennessee, United States, 37203

Contacts

VICC CTIP (Clinical Trials Info Program)

800-811-8480cip@vumc.org

Principal Investigator:

Ryan Merrell, MD

UTHealth Houston

Recruiting

Houston, Texas, United States, 77030

Contacts

Principal Investigator:

Nitin Tandon, MD

Baylor College of Medicine

Recruiting

Houston, Texas, United States, 77057

Contacts

Principal Investigator:

Jacob Mandel, MD

The University of Texas Health Science Center at San Antonio

Recruiting

San Antonio, Texas, United States, 78229

Contacts

Principal Investigator:

Andrew Brenner, MD, PhD

More Information

Sponsor

Diakonos Oncology Corporation

Last update posted

Jul 1, 2026

Last verified

Jun, 2026

Keywords

  • Dendritic Cell Vaccine
  • Immunotherapy
  • Tumor vaccine

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Diakonos Oncology Corporation on 2026-07-01.