IBRX-042 In Subjects With HPV-Associated Tumors

Trial Title: IBRX-042 In Subjects With HPV-Associated Tumors

NCT ID: NCT05976828

Condition: HPV-Related Carcinoma

Conditions: Official terms:
Vaccines

Study type: Interventional

Study phase: Phase 1

Overall status: Recruiting

Study design:

Allocation: Non-Randomized

Intervention model: Sequential Assignment

Intervention model description: Determination of the MTD of IBRX-042 vaccine will utilize 3 + 3 dose escalation design. Subjects will be sequentially enrolled to 1 of 3 dosing cohorts (up to 3-6 subjects per arm). - Dose cohort 1: 1e11 virus particles (VP)/dose - Dose cohort 2: 5e11 VP/dose - If needed, dose cohort -1 (de-escalation): 5e10 VP/dose

Primary purpose: Treatment

Masking: None (Open Label)

Intervention:

Intervention type: Drug
Intervention name: IBRX-042
Description: - Dose cohort 1: 1e11 virus particles (VP)/dose - Dose cohort 2: 5e11 VP/dose - If needed, dose cohort -1 (de-escalation): 5e10 VP/dose
Arm group label: De-escalation Dose Level
Arm group label: First Dose Level
Arm group label: Second Dose Level

Other name: IBRX-042 (hAd5-HPV E6.ETSD-IRES-E7.ETSD Vaccine)

Summary: The goal of this clinical trial is to determine the maximum tolerated dose and to find out the side effects of a drug called IBRX-042 at different dose levels in patients with recurrent or progressive Human Papillomavirus (HPV) associated tumors. The main questions it aims to answer are: - What is the maximum tolerated dose of IBRX-042? - How well does the study drug treat cancer? - What effects the study drug may have on the human body and cancer? Participants will receive IBRX-042 at one of three dose levels every 3 weeks for a total of 3 injections. Participants will undergo tests, exams, and procedures that are part of standard of care and for study purposes. IBRX-042 will be administered by injection every 3 weeks for a total of 3 injections.

Detailed description: Up to 60 subjects may be screened for up to 18 subjects to receive at least 1 dose of study drug. Subjects will be administered IBRX-042 by injection once every 3 weeks for a total of 3 injections. Subjects will receive study treatments until they report progressive disease (PD), unacceptable toxicity, withdraw consent, or if the Investigator feels it is no longer in their best interest to continue treatment. Subjects who progress, discontinue treatment, or complete the study will attend an end-of-treatment (EOT) visit 30 days after the last study assessment. Additionally, subjects will attend a follow-up visit 6 months following administration of the last dose of IBRX-042. After the subject completes or withdraws from the study, the study team will contact subjects approximately every 3 months for a minimum of 1 year post administration of the first dose of study drug and then yearly until death to collect follow-up information, including survival status, collection of adverse events, and any current cancer treatment regimen. A clinic visit will be scheduled for 6 months after the last injection administered for collection of whole blood for exploratory immune and molecular profiling.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. 18-75 years of age. 2. Able to understand and provide a signed informed consent that fulfills the relevant Institutional Review Board (IRB) or Independent Ethics Committee (IEC) guidelines. 3. Histologically confirmed HPV-associated cancer documented as HPV- or p16-positive carcinoma (measurable or nonmeasurable disease). 4. Subjects must have received at least one standard of care therapy per National Comprehensive Cancer Network (NCCN) guidelines for their HPV-associated cancer > 28 days prior to enrollment. 5. Availability of a representative formalin fixed, paraffin embedded tumor specimen or fresh frozen tissue specimen that enables the definitive diagnosis of an HPV- or p16- positive carcinoma, accompanied by an associated pathology report. Specimens can be collected by surgical resection, biopsy of the primary tumor or biopsy or resection of a metastatic lesion. 6. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 7. Resolution of all toxic side effects of prior therapy for their HPV-associated cancer to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 5 grade ≤ 1. 8. Ability to attend required study visits and return for adequate follow-up, as required by this protocol. 9. Agreement to practice effective contraception for female subjects of child-bearing potential and nonsterile males. Female subjects of child-bearing potential must agree to use effective contraception for up to 30 days after last dose of study drug. Nonsterile male subjects must agree to use a condom while on study and for up to 30 days after the last dose of study drug. Effective contraception includes surgical sterilization (eg, vasectomy, tubal ligation), two forms of barrier methods (eg, condom, diaphragm) used with spermicide, and intrauterine devices (IUDs). 10. Adequate organ function, evidenced by the following laboratory results: 1. Absolute neutrophil count (ANC): 1.5 x 109/L 2. Absolute lymphocyte count (ALC) > institutional lower limit of normal 3. Hemoglobin ≥ 10.0 g/dL. 4. Platelet count: 100 × 109/L 5. Total bilirubin ≤ 1.5 × upper limit of normal (ULN; unless the subject has documented Gilbert's syndrome). 6. Aspartate aminotransferase [serum glutamic-oxaloacetic transaminase] (AST [SGOT]) or alanine aminotransferase [serum glutamic-pyruvic transaminase] (ALT [SGPT]) ≤ 3.0 × ULN. For patients with significant hepatic involvement by tumor, ALT ≤ 5 × ULN is acceptable. 7. Albumin < 3.0 g/dL. Note: Each study site should use its institutional ULN to determine eligibility Exclusion Criteria: 11. History of autoimmune disease as determined by the Investigator (eg, lupus erythematosus, rheumatoid arthritis, Addison's disease, or autoimmune disease associated with lymphoma). 12. Serious uncontrolled concomitant disease that would contraindicate the use of the investigational drugs used in this study or that would put the subject at high risk for treatment-related complications. 13. Serious pulmonary disease. 14. Platelet count < 100,000 cells/mm3. 15. Active hepatitis. 16. Positive results of screening test for human immunodeficiency virus (HIV), hepatitis B virus, and/or hepatitis C virus. 17. Current chronic daily treatment (continuous for > 3 months) with systemic corticosteroids (dose equivalent to or greater than 10 mg/day methylprednisolone), excluding inhaled steroids. Short-term steroid use to prevent IV contrast allergic reaction or anaphylaxis in subjects who have known contrast allergies is allowed. 18. Known hypersensitivity to any component of the study medication(s). 19. Subjects taking any medication(s) (herbal or prescribed) known to have an adverse drug reaction with any of the study medications. 20. Participation in an investigational drug study or receiving any investigational treatment within 28 days prior to study treatment. Approved drugs for the prevention and treatment of COVID-19 are permitted. 21. Concurrent participation in any interventional clinical trial. 22. Assessed by the Investigator to be unable or unwilling to comply with the requirements of the protocol. 23. Pregnant and nursing women.

Gender: All

Minimum age: 18 Years

Maximum age: 75 Years

Healthy volunteers: No

Locations:

Facility:
Name: Chan Soon-Shiong Institute for Medicine (CSSIFM)

Address:
City: El Segundo
Zip: 90245
Country: United States

Status: Recruiting

Contact:
Last name: Mini Gill

Phone: 213-266-5639
Email: Jaya.Gill@cssifm.org

Contact backup:
Last name: Jacqui Parnin

Phone: 213-266-5604
Email: Jacqueline.Parnin@cssifm.org

Investigator:
Last name: Chaitali Nangia
Email: Principal Investigator

Start date: June 14, 2024

Completion date: August 14, 2033

Lead sponsor:
Agency: ImmunityBio, Inc.
Agency class: Industry

Source: ImmunityBio, Inc.

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05976828