Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: 2025 Eurostat Trade Data and Economic Impact
Recruiting Phase 1

Phase 1 Study of Intratumoral Administration of VAX014 With Expansion in Combination With a Checkpoint Inhibitor in Subjects With Advanced Solid Tumors

NCT05901285 · tracked via the Priya Life Science USA tracker
Sponsor
Vaxiion Therapeutics
Phase
Phase 1
Started
2023-11-02
Last updated
2026-08-24

Condition(s) studied

Advanced Solid TumorAdvanced Solid Tumors Appropriate for Treatment With Either Nivolumab or Pembrolizumab

Investigational drug(s) / intervention(s)

VAX014Nivolumab or pembrolizumab

VAX014: Intratumorally administered oncolytic agent comprised of recombinant bacterial minicells. VAX014 is not infectious and is not capable of replication

Nivolumab or pembrolizumab: VAX014 will be given in combination with Investigator's choice of nivolumab or pembrolizumab.

Study summary

The purpose of this research study is to evaluate the safety, tolerability and activity of VAX014 for intratumoral injections (VAX014) as a single agent as well as in combination with Investigator's choice of nivolumab or pembrolizumab in patients with advanced solid tumors. VAX014 is a targeted oncolytic agent designed to kill tumor cells following intratumoral injection into advanced solid tumors.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Age 18+ 2. Informed consent 3. Histological or cytopathological confirmed diagnosis of a locally advanced or metastatic solid tumor 4. Progression following at least one prior standard treatment or intolerant of standard treatments. 5. \[Dose Escalation\] Availability of archival or fresh tumor tissue 6. \[Expansion\] Willing to undergo biopsy of the tumor to be injected prior to the initial VAX014 injection (may provide archival tissue instead if approved by Medical Monitor) 7. No available SOC therapy that would confer clinical benefit 8. \[Dose escalation\] At least one cutaneous, subcutaneous, or nodal injectable tumor (between 1 and 10 cm in largest diameter) that can be injected by direct palpation or with the assistance of ultrasound without the need for interventional radiology 9. \[Expansion\] At least one injectable tumor (\>=0.5cm in largest diameter) that can be injected either with or without the need for interventional radiology 10. \[Expansion\] Appropriate for treatment with either nivolumab or pembrolizumab 11. \[Expansion\] Progression following at least one prior regimen containing PD-1 directed immune checkpoint blockade 12. Measurable disease by RECIST v1.1 13. ECOG Performance Status of 0, 1, or 2 14. Resolution of any toxicity associated with prior therapy to ≤ Grade 1 (Residual toxicity of Grade 2 may be allowed following discussion with Medical Monitor) 15. Adequate hematologic function defined as: 1. Absolute neutrophil count \>=1,500/uL 2. Platelet count \>=100,000/uL 3. \[Expansion\] Hemoglobin \>=9 gm/dL 16. Adequate hepatic function defined as: 1. Total bilirubin ≤ 1.5 x ULN 2. Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 x ULN 17. Adequate coagulation defined as: 1. International normalized ratio (INR) ≤ 1.5 x ULN or prothrombin time (PT) ≤ 1.5 x ULN 2. Partial thromboplastin time (PTT) or activated PTT (aPTT) ≤ 1.5 x ULN 18. Serum creatinine ≤ 1.5 x ULN or estimated GFR ≥ 60 mL/min/1.73 m2 (per MDRD GFR formula) 19. Women of childbearing potential must have a negative serum pregnancy test 20. All subjects of childbearing potential must be willing to consent to using effective contraception (as determined by the Investigator) while on treatment and for 3 months after their participation in the study ends Exclusion Criteria: 1. Injectable tumor not sufficiently distanced from critical structures (e.g., major airway, neurovascular structure) where post injection swelling may place the subject at unacceptable risk 2. ≤ 21 days or ≤ five half-lives (whichever is shorter) between any prior anticancer therapy (e.g., chemotherapy, immunotherapy, intralesional therapy, irradiation) and the first injection of VAX014 3. Known CNS metastases or leptomeningeal carcinomatosis, unless adequately treated and clinically stable off steroids for ≥ 14 days from the first injection of VAX014 4. Severe infection requiring systemic antibiotic therapy or hospitalization for treatment of injection 5. Need for systemic immunosuppressive therapy (≤10 mg of prednisone equivalent, or one time pulse steroids excepted) 6. Active autoimmune disease requiring systemic immunosuppressive therapy 7. Active lung disease or pneumonitis 8. History of Grade 4 toxicity in response to prior PD-1 blockade 9. Any other malignancy likely to require treatment in the next 2 years (exceptions include cancer such as basal or squamous cell skin cancers, noninvasive cancer of the cervix, and local prostate cancer) 10. Known active infection with tuberculosis or HIV 11. Active Hepatitis B or C 12. \[Females\] pregnant or breastfeeding 13. Clinically significant cardiovascular abnormalities including: 1. ≤ 12 months from prior MI 2. Unstable angina pectoris 3. ≤ 6 months from NYHA classification \>=3 CHF 14. Electrocardiogram (ECG) with QTcF \> 450 msec (males) and QTcF \> 470 msec (females) based on an average of triplicate ECGs (triplicate ECGs performed only if initial QTcF exceeds male/female limits) 15. Medical or psychological condition that places the subject at undue risk with study participation

Primary outcome measure(s)

  • Maximum tolerated dose (MTD) of VAX014 — up to 21 days
    The MTD will be defined as the dose level at which at most one of six patients experiences a dose limiting toxicity (DLT) after 21 days of treatment have occurred, with the next higher dose having at least 2/3 or 2/6 patients experiencing a DLT
  • Incidence of Treatment-Emergency Adverse Events (Safety and Tolerability) — Through study completion, an average of 20 weeks
    Toxicities will be assessed in each subject by tracking the occurrence of graded Adverse Events (AEs). AEs will be graded according to the National Cancer Institute Common Terminology for Adverse Events (NCI CTCAE) v5.0
  • Recommended Phase 2 Dose (RP2D) for single agent intratumoral VAX014 — up to 5 weeks
    The RP2D will be determined following the determination of the MTD and with agreement by the Safety Review Committee
  • Acceptable dose of VAX014 in combination with PD-1 Inhibitor — 3 months
    Determine the acceptable dose of VAX014 when used in combination with Investigator's choice of nivolumab or pembrolizumab
  • Evaluation of efficacy of VAX014 in combination with either nivolumab or pembrolizumab — 18 months
    Evaluate efficacy including overall response rate (ORR), response of injected tumor(s) of VAX014 in combination with Investigator's choice of nivolumab or pembrolizumab

Trial sites (8)

FacilityCityRegionStatus
University of Arizona Cancer Center Tucson Arizona Recruiting
Melanoma & Skin Cancer Institute Denver Colorado Recruiting
Sarah Cannon Research Institute at HealthONE Denver Colorado Recruiting
George Washington University Washington D.C. District of Columbia Recruiting
Dana Farber Cancer Institute Boston Massachusetts Recruiting
Dartmouth Cancer Center Lebanon New Hampshire Recruiting
Atlantic Health System Morristown New Jersey Recruiting
Cleveland Clinic Cleveland Ohio Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05901285 on ClinicalTrials.gov ↗ ← All trials in the USA